Submission of the manuscript is online via e-mail
ecgarticle@gmail.com or
cholerez@mail.ru

Tel: +7 903 250 5288

Editorial Correspondence e-mail
gastrossr@gmail.com


Publishing, Subscriptions, Sales and Advertising, Correspondence e-mail
journal@cniig.ru

Tel: +7 917 561 9505

SCImago Journal & Country Rank

№ 05 (153) 2018

  • Уважаемые коллеги !
    В номер, посвященном заболеваниям кишечника, мы постарались осветить максимальное количество проблем, с которыми может встретиться как врач-гастроэнтеролог, так и врач любой специальности.
    Открывает номер статья с результатами большого 5 центрового наблюдательного российского исследования по оценке эффективности лактитола.
    Продолжает номер оригинальная работа О. В. Крапивной и С. А. Алексеенко (Дальневосточный государственный медицинский университет) » Минздрава России, оценивающая эффективность комбинированной терапии при различных вариантах СРК в сочетании с синдромом избыточного бактериального роста.
    Тему влияния избыточного бактериального роста и бактериальной эндотоксинемии на течение неалкогольной жировой болезни печени продолжают в следующей статье М. Д. Ардатская, Г. В. Гарушьян, Р. П. Мойсак (Москва).
    Профессор И. Л. Халиф и соавторы (Государственный научный центр колопроктологии им. А. Н. Рыжих) установили, что наиболее информативным УЗ-параметром для оценки активности воспаления у пациентов с язвенным колитом (ЯК) является площадь под кривой (AUC). Для данного параметра получена положительная корреляция с эндоскопической активностью ЯК.
    Очень актуальной, на наш взгляд, является работы Л. В. Поддубной, Т. В. Зыряновой, Т. И. Петренко, В. Г. Кононенко, Т. А. Колпаковой и Е. М. Жуковой (Новосибирск), которые сравнили частоту и структуру поражения туберкулезом органов брюшной полости у больных туберкулезом органов дыхания в период неблагополучной эпидемической ситуации (2006–2008 гг.) и в период снижения общей заболеваемости туберкулезом (2015–2017 гг.). Установлен факт, что несмотря на улучшение эпидемической ситуации, обусловленной снижением общей заболеваемости, доля больных туберкулезом легких с абдоминальным туберкулезом, лечившихся в туберкулезном стационаре, увеличилась почти в 2 раза (3,5±0,6% и 1,95±0,3%).
    Поддубная О. А., Привалова Н. И. (г. Томск) разработали высокоэффективный комплекс реабилитационных мероприятий у лиц молодого возраста с синдромом раздраженного кишечника с использованием СМТ-терапии и КВЧ-терапии, которые назначались с учетом типа функциональных нарушений, способствует значительному улучшению клинико-лабораторных показателей в виде купирования жалоб и симптомов, на фоне повышения адаптационного потенциала и нормализации показателей психовегетативного статуса.
    Группа ученых из Научного центра проблем здоровья семьи и репродукции человека (Иркутск), проанализировав структуру кишечных дисбиозов у взрослого населения с учетом гендерных различий, пришли к выводу, что у более 90% взрослого населения наблюдались дисбиотические изменения различной степени тяжести.
    Лычкова А. Э., Ручкина И. Н., Полева Н. И., Пузиков А. М. (Московский клинический научно-практический центр им. А. И. Логинова) выявили особенности моторной функции толстой и тонкой кишки при синдроме раздраженного кишечника с запором и у больных с долихосигмой.
    А. П. Годовалов, А. А. Антонян, Е. А. Горбунова (Пермский государственный медицинский университет им. акад. Е. А. Вагнера) рассматривают кишечную микрофлору как основную детерминанту здоровья и болезней людей. Проведенное ими исследование показало, что обнаружение в толстокишечном биотопе S. aureus и/или C. albicans может существенно менять состав микробиоты, что, возможно, отражается на функциональной активности слизистой оболочки толстого кишечника и в целом всего организма человека.
    Родионов Г. Г., Шантырь И. И., Колобова Е. А., Светкина Е. В. (Санкт-Петербург) свою работу также посвятили изучению микробиоты и выявили, что у лиц пожилого возраста по сравнению с молодыми общее количество микробных маркеров снижено на 40%; а доля условно-патогенной флоры существенно увеличена (у пожилых лиц 48%, а у молодых только 34%);
    Коллектив авторов из Красноярска (ФГБНУ «Федеральный исследовательский центр «Красноярский научный центр СО РАН» НИИ Медицинских проблем Севера) изучали спонтанную и индуцированную хемилюминесцентную активность нейтрофильных гранулоцитов у больных раком прямой кишки, функциональная активация которой коррелировала со стадией рака.
    В. Сагынбаева и соавт. рассмотрела иерсиниоз как причину развития внекишечных воспалительных заболеваний кишечника и как признак реактивации оппортунистических инфекций на фоне биологической терапии.
    Сотрудники кафедры поликлинической терапии МГМСУ им. А. И. Евдокимова предложили свои варианты рациональной фармакотерапии, основанные на результатах многолетнего наблюдения за больными дивертикулярной болезнью толстой кишки и оценке эффективности различных групп препаратов в зависимости от возраста больных, длительности анамнеза заболевания и наличия сопутствующих заболеваний.
    В разделе «Хирургическая гастроэнтерология» эндоскописты Ярославской областной онкологической больницы предложили пути решения проблемы неадекватной подготовки к колоноскопии. В лекции К. А. Шемеровского представлена новая хронобиологическая стратегия лечения больных с запорами. Выделено четыре основных аспекта этой стратегии: физиологический, патологический, общебиологический и терапевтический.
    В обзоре И. Д. Лоранской и соавторов рассмотрены современные представления о состоянии микробиома у здоровых людей и его изменение при воспалительных заболеваниях кишечника.
    Группа ученых под руководством член-корр. РАН, профессора Ю. А. Шелыгина приводит обзор публикаций об использовании метода планиметрической импедансометрии в исследовании аноректальной функции. Впервые в России появилась возможность использовать данный метод у колопроктологических пациентов в ФГБУ «ГНЦК им. А. Н. Рыжих Минздрава России».
    Скворцов В. В., Тумаренко А. В., Павлов В. К. из Волгограда еще раз подняли вопрос диагностики и лечения болезни Уиппла. М. Л. Чуркова, С. В. Костюкевич (Санкт-Петербург) посвятили свой обзор анализу структурных изменений эпителия слизистой оболочки различных отделов толстой кишки человека в условиях нормы и при функциональных и воспалительных заболеваниях кишечника. Анализ структурных изменений выявил основные характеристики дистрофических и регенераторных процессов, развивающихся в эпителии. Изменения захватывают многие структуры (микроворсинки, клеточные контакты, органеллы, ядро), образующих его клеток и являются неспецифическими. Они различаются степенью выраженности, что зависит от тяжести заболевания и индивидуальных особенностей организма.
    Осадчук А. М., Давыдкин И. Л., Гриценко Т.А, Лебедева Е. А., Петрушин А.Е (Самара) еще раз подняли вопрос об изменении микробиоты ЖКТ, которая ассоциирована с различными заболеваниями внутренних органов, и о перспективах коррекции нарушенного микробного баланса.
    Частные вопросы патогенеза воспалительных заболеваний кишечника затронули Першко А. М., Гриневич В. Б., Соловьев И. А., Шотик А. В., Курило Д. П. (Военно-Медицинская Академия им. С. М. Кирова, Санкт-Петербург). Рассмотрены принципиальные закономерности изменений генома, иммунной системы, роль и участие кишечной микрофлоры в патогенезе этих заболеваний.
    В рубрике История медицины наши постоянные авторы из Крымского федерального университета имени В. И. Вернадского С. А.Кутя и соавт. рассказали о биографии Н. Тульпа и его вклад медицину, в частности в описании илеоцекального клапана.
    Завершает номер статья М. А. Бутова о выдающемся А. М. Ногаллере.

    Желаем вам приятного, а главное, полезного прочтения, дорогие коллеги!
    Ответственный за выпуск редактор,

      профессор кафедры гастроэнтерологии
    ФГБУ ДПО «Центральная государственная медицинская академия» УПД Президента РФ

    доктор медицинских наук, профессор 
      Мария Дмитриевна Ардатская
       
    1. FGBOU VPO MGMSU named after A. I. Evdokimov of the Ministry of Health of Russia (Moscow, Russia)
    2. FGBOU VPO DVGMU of the Ministry of Health of Russia (Khavarovsk, Russia)
    3. FGBOU VPO “Omsk State Medical University Ministry of Health of Russia” (Omsk, Russia)
    4. Pirogov Russian National Research Medical University (RNRMU) (Moscow, Russia)
    5. The Loginov Moscow Clinical Scientific Center (Moscow, Russia)
    6. Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences, “Scientific research institute of medical problems of the North” (FRC KSC SB RAS, SRI MPN) (Krasnoyarsk, Russia)
    7. FGBOU VO Voronezh State Medical University named after N. N. Burdenko (Voronezh, Russia)
    8. Kazan State Medical University (Kazan, Russia)
    9. Kazan (Volga region) Federal University (Kazan, Russia)
    10. FGBOU VO IvGMA of the Ministry of Health of Russia (Ivanovo, Russia)
    11. FGBOU VO “North-Western State Medical University n. a. I. I. Mechnikov” of the Ministry of Health of Russia (St. Petersburg, Russia)
    12. GAUZ “Municipal Polyclinic № 6” (Ulan-Ude, Russia)
    13. FGBOU VPO “Altai State Medical University” of the Ministry of Health of Russia (Barnaul, Russia)
    14. GBU RS(Ya) “Yakutsk municipal hospital” (Yakutsk, Russia)
    15. FGBOU VO “Ulyanovsk State University” (Ulyanovsk, Russia)
    16. FGBOU VO “PIMU” of the Ministry of Health of Russia (Nizhny Novgorod, Russia)
    17. Far Eastern State Medical University of the Ministry of Health of Russia (Khabarovsk, Russia)
    18. Peoples’ Freindship University of Russia (PFU) (Moscow, Russia)
    19. FGBOU VO “Bashkir State Medical University” of the Ministry of Health of Russia (Ufa, Russia)
    20. Federal Research Center “Institute of Cytology and Genetics” of the Siberian Branch of the Russian Academy of Sciences (FRC ICG SB RAS) (Novosibirsk, Russia)
    21. “Scientific research institute of Internal and Preventive Medicine” (SRI TPM) (Novosibirsk, Russia)
    22. FGBOU VO “Smolensk State Medical University” of the Ministry of Health of Russia (Smolensk, Russia)
    23. Office No. 10 PKU “Main Bureau of medical-social examination of the Belgorod region” The Ministry of labour and social protection of the Russian Federation (Belgorod, Russia)
    24. Federal State Autonomous Educational Institution of Higher Education “Belgorod National Research University” (Belgorod, Russia)
    25. FGBOU VO Siberian State Medical University (Tomsk, Russia)
    26. FGAOU VO Federal State Autonomous Educational Institution of Higher Education I. M. Sechenov First Moscow State Medical University of the Ministry of Health of Russian Federation (Moscow, Russia)
    27. FGBOU VO RostGMU of the Ministry of Health of Russia (Rostov on Don, Russia)
    28. FGBOU VO RyazGMU (Ryazan, Russia)
    29. FGBOU VO ChGMA of the Ministry of Health of Russia (Chita, Russia)
    30. FGBOU VO Saratov State Medical University named after V. I. Razumovsky (Saratov, Russia)
    31. GBUZ NO “The City Clinical Hospital No. 13” (Nizhny Novgorod, Russia)
    32. FGBOU VO “Irkutsk State Medical University” of the Ministry of Health of Russia (Irkutsk, Russia)
    33. KGBUZ DPO “Institute of advanced training of health professionals” MZKH (Khabarovsk, Russia)
    34. GBUZ BUT they NOCB N. A. Semashko (Nizhny Novgorod, Russia)
    35. Kuban State Medical University, Ministry of Health of the Russian Federation
    36. FGBOU VO “Tver State Medical University” MH of Russia (Tver, Russia)
    37. FGBOU VO PSMU of the Ministry of Health of Russia (Vladivostok, Russia)
    38. Medical Center “MEDGARD”, the branch in Tolyatti (Tolyatty, Russia)
    39. Multidisciplinary medicine center Bank of Russia (Moscow, Russia)
    40. FGBOU VO Orenburg State Medical University of the Ministry of Health of Russia (Orenburg, Russia)
    41. FGBOU VO Kemerovo State Medical University of the Ministry of Health of Russia (Kemerovo, Russia)
    42. FGBOU VO NGMU of the Ministry of Health of Russia (Novosibirsk, Russia)
    43. FGBOU VO Krasnoyarsk State Medical University named after prof. Voyno-Yasenetsky Ministry of Health of Russia (Krasnoyarsk, Russia)
    44. IGMAPO- branch of the FGBOU DPO RMANPO of the Ministry of Health of Russia (Irkutsk, Russia)
    45. PIUV — branch of FGBOU DPO RMANPO Ministry of health of the Russian Federation (Penza, Russia)
    46. LTD “Zdorovje” (V. Novgorod, Russia)
    47. Non-state health care institution “Separate Clinical Hospital at Barnaul Station” of the Open Joint-Stock Company Russian Railways (Barnaul, Russia)
    48. FGBOU VO “StGMU of the Ministry of Health of Russia” (Stavropol, Russia)
    49. KSMA — Branch Campus of the FSBEI of FPE “Russian Medical Academy of Continuing Professional Education” of the Ministry of Healthcare of the Russian Federation (Kazan, Russia)
    50. FGBOU VO South-Ural State Medical University (Chelyabinsk, Russia)
    51. FGBOU VO KGMU of the Ministry of Health of Russia (Kursk, Russia)
    52. FGBOU VO Volgograd State Medical University (Volgograd, Russia)
    53. Orel State University named after I. S. Turgenev (Orel, Russia)
    54. FGBOU VO Federal State Budgetary Educational Institution of Higher Education “Kabardino-Balkarian State University named after H. M. Berbekov” (NalchiK, Russia)
    55. GUZ Regional clinical hospital of the Ministry of Health of Russia (Chita, Russia)
    56. LLS “University Clinic” (Arkhangelsk, Russia)
    57. FGBOU VO “Astrakhan State Medical University of the Ministry of Health of Russia” (Astrakhan, Russia)
    58. GBUZ DKKB MZ KK, Krasnodar Regional Base Medical College of the Ministry of Health of Russia (Krasnodar, Russia)
    59. FGBOY VO Samara state medical university (SamGMU) of the Ministry of Health of Russia (Samara, Russia)
    60. FGBVOU VO “Military Medical Academy named after S. M. Kirov” of the Ministry of Defence of the Russian Federation (Moscow, Russia)
    61. National Medical Research Center for Preventive Medicine of the Ministry of Healthcare of the Russian Federation (Moscow, Russia)
    62. E. A. Wagner Perm State Medical University (Perm, Russia)
    63. FSBI “SCEEMP” of the Ministry of Health of the Russian Federation (Moscow, Russia)

    Keywords:Dyspepsia, risk of cancer, diagnosis, management, primary care

    Abstract:Aim: To develop evidence-based recommendations for primary care physicians and general practitioners (GP) on choosing the proper management tactics and making valuable & quick diagnostic decisions at outpatient phase for patients with symptoms of dyspepsia, and also reveal possible oncology on time. Summary of recommendations: Approximately 40% of the patients in Russia presenting to primary care with symptoms of dyspepsia. A doctor has to focus on the warning signs, which may require an urgent additional examination & the consultation with a surgeon/onco-surgeon or other specialists if required. With regard to a risk of cancer, a doctor should be more cautious in patients over 45 years of age. Early diagnosis of oncology depends mainly on cautiousness of GP, primary care physicians and their knowledge, future tactics with regard to the patients. From the mandatory diagnostic tests during the first visit, esophagogastroduodenoscopy and H. pylori diagnostics helps to exclude any organic esophagus and stomach pathology, possible oncology. While waiting for endoscopy results, a physician should use the preliminary diagnoses “Uninvestigated Dyspepsia” (ICD-10 К 31.9) (disease of stomach and duodenum, unspecified). After exclusion of all warning signs, therapy of dyspepsia should be in accordance to the order of the Ministry of Health No 248 which gives an option to use proton pump inhibitors (omeprazole or rabeprazole 20 mg daily) in combination with prokinetic (domperidone 30 mg daily). Fixed drug combination of omeprazole 20 mg and modified-release domperidone 30 mg/daily (Omez® DSR) is medically reasonable. Conclusion: The introduction of this recommendation into clinical practice will help clinicians to prevent diagnostic mistakes, unreasonable use of expensive diagnostic examinations and inappropriate treatment leads to improvement in the overall prognosis and quality of life for the patients.

      1. Hunt R., Quigley E., Abbas Z., Eliakim A., Emmanuel A., Goh K. L., et al. Coping with common gastrointestinal symptoms in the community: A global perspective on heartburn, constipation, bloating, and abdominal pain/discomfort May 2013. J Clin Gastroenterol 2014; 48(7):567-78
      2. Stanghellini V, Chan FK, Hasler WL, Malagelada JR, Suzuki H, Tack J, Talley NJ. Gastroduodenal Disorders. Gastroenterology. 2016 May;150(6):1380-92. doi: 10.1053/j.gastro.2016.02.011.
      3. Sugano K., Tack J., Kuipers E. J., et al. Kyoto global consensus report on Helicobacter pylori gastritis. Gut 2015; 64:1353-67.
      4. Ивашкин В.Т., Маев Ю. А. и соавт. Клинические рекомендации РГА по диагностике и лечению функциональной диспепсии. // РЖГГК. - 2017. - № 27(1).
      5. Ivashkin V. T., Mayev I. V., Kucheryavy Yu.A., Lapina T. L., et al. Management of abdominal pain: clinical guidelines of the Russian gastroenterological association. Ros zhurn gastroenterol gepatol koloproktol 2015; 25 (4): 71–80.
      6. Ivashkin V. T., Mayev I. V., Lapina T. L., Osipenko M. F., et al. Advisory board resolution on development of abdominal pain management algorithm. Ros zhurn gastroenterol gepatol koloproktol 2015; 25(3):104–6.
      7. Чиссов В.И., Старинский В. В., Мамонтов А.С, Данилова Т. В. Методические рекомендации для организаторов здравоохранения, врачей первичного звена, врачей-специалистов. Алгоритмы выявления онкологических заболеваний у населения Российской Федерации, 22.10.2009 (http://www.oncology.ru/service/organization/algorithms.pdf по состоянию на 03.08.2018).
      8. Mohammad Hasan Emami, Masoud Ataie-Khorasgani, and Nasim Jafari-Pozve Diagnostic value of alarm symptoms for upper GI malignancy in patients referred to GI clinic: A 7 years cross sectional study J Res Med Sci. 2017; 22: 76.
      9. Злокачественные новообразования в России в 2016 году (заболеваемость и смертность)/ Под ред. А. Д. Каприна, В. В. Старинского, Г. В. Петровой// М.: МНИОИ им. П. А. Герцена, филиал ФГБУ «НМИЦ радиологии» Минздрава России, – 2018. -илл. – 250 с.
      10. Thomson CS, Forman D. Cancer survival in England and the influence of early diagnosis: what can we learn from recent EUROCARE results? Br J Cancer. 2009;101(Suppl 2): S102–109.
      11. Paul M. Moayyedi, Brian E. Lacy, Christopher N. Andrews, Robert A. Enns, Colin W. Howden/ ACG and CAG Clinical Guideline: Management of Dyspepsia Am J Gastroenterol advance online publication, 20 June 2017; doi: 10.1038/ajg.2017.154.
      12. Приказ МЗ РФ № 248 «Об утверждении стандарта медицинской помощи больным хроническим гастритом, дуоденитом, диспепсией» (http://www.gastroscan.ru/literature/authors/2355, дата обращения 09.04.2018).
      13. John Robson, Luis Ayerbe, Rohini Mathur, Juliet Addo, and Andrew Wragg. Clinical value of chest pain presentation and prodromes on the assessment of cardiovascular disease: a cohort study Published online 2015 Apr BMJ Open. 2015; 5(4): e007251.
      14. The International statistical classification of diseases and related health problems. The 10th revision (ICD-10). Мoscow, 1995. Vol. 1 pp. 579–80.
      15. Ивашкин В.Т., Маев Ю. А. и соавт. Клинические рекомендации РГА по диагностике и лечению инфекции HР у взрослых. РЖГГК 2018; 28(1).
      16. Malfertheiner P, Megraud F, O’Morain C, et al. Management of Helicobacter pylori infection– the Maastricht V/Florence Consensus. Report. Gut 2017; 66(1): 6–30.
      17. Порядки и стандарты оказания медицинской помощи (http://www.gastroscan.ru/literature/108/, дата обращения 03.08.2018).
      18. Мараховский К.Ю., Василевская С. А., Карасева Г. А., Уласевич Д. Н., Мараховский Ю. Х. Гастроэзофагеальная рефлюксная болезнь: сопоставительная оценка эффективности и безопасности омепразола в комбинации с домперидоном в сравнении с омепразолом. Лечебное Дело, № 2 (42), 2015 г. / www.lech-delo.by
      19. Карева Е.Н., Сереброва С. Ю. Медикаментозное лечение нарушений моторики желудка – проблемы, пути решения, достижения. Экспериментальная и клиническая гастроэнтерология, № 7, 2017
     


    Full text is published :
    Lazebnik L.B., Alekseenko S.A., Lyalykova E.A., Samsonov A.A. et al. RECOMMENDATIONS ON MANAGEMENT OF PRIMARY CARE PATIENTS WITH SYMPTOMS OF DYSPEPSIA. Experimental and Clinical Gastroenterology Journal. 2018;153(05):04-18
    Read & Download full text

    1. Non-government healthcare institution “Khabarovsk-1 Road clinical hospital, Open Society “Russian Railways” (Khabarovsk, Russia)
    2. State educational government-financed institution of higher professional education “Far East state medical university”, Ministry of Healthcare of the Russian Federation (Khabarovsk, Russia)

    Keywords:irritable bowel syndrome with or without diarrhea, small intestinal bacterial overgrowth, mebeverin, rifaximin, probiotics

    Abstract:Aim. To assess the effect of therapy with mebeverine, rifaximin and probiotics on clinical symptoms, small intestinal bacterial overgrowth (SIBO) eradication, fecal calprotectin (FC) level and the quality of life in irritable bowel syndrome patients with (IBS-D) or without diarrhea (IBS without D). Material and methods. Patients with IBS-D (n=74) or IBS without D (n=127) were randomly divided into 2 subgroups homogeneous for sex, age, FC level and IBS severity. Patients of subgroup I received mebeverine 0,4 g/day for 1 month in combination with sequential therapy, including rifaximin 0,8 g/day 6 days followed by S. boulardii 0,5 g/day 10 days, and followed by probiotic “Bifiform” 2 capsules/day for 15 days. Patients of subgroup II received mebeverine 0,4 g/day for 3 months in combination with 3 courses of sequential therapy, without interruption, including rifaximin and probiotics in the same doses. IBS severity (IBS-SS), quality of life (SF-36), FC level and frequency SIBO eradication were estimated prior to onset of treatment and after its termination. Results. Differences between the 2 subgroups of IBS-D patients in clinical improvement and SIBO eradication after 1 or 3 months of therapy weren’t significant (р>0,05). Reduction of clinical symptoms and SIBO eradication were significantly more frequent in IBS patients without D after 3 months than 1 month (p<0.012). A significant decrease in the patient’s proportion with elevated FC levels occurred after 3 months (p <0.0001). Conclusions. The three-month therapy is significantly better than the monthly therapy in IBS patients without D in reducing the IBS severity, increasing the SIBO eradication frequency and the patient’s proportion with normal FC. Differences in clinical efficacy after 1 or 3 months of therapy in IBS-D patients with normal FC levels aren’t detected (p>0.05). Normalization of FC level in IBS-D patients with elevated FC levels (>100 μg/g) is significantly more likely to be detected after 3 months of therapy than in one (p <0.0001).

      1. Maev I. V., Cheremushkin S. V., Kucheryavyi Yu.A. et al. Pharmacotherapy for irritable bowel syndrome in the context of evidence-based medicine. Ter Arkh. – 2015. – Vol. 87, N2. – P. 4–10. (in Russian).
      2. Ivashkin V. T., Shelygin Yu.A., Baranskaya Ye.K. et al. Diagnosis and treatment of the irritable bowel syndrome: clinical guidelines of the Russian gastroenterological association and Russian association of coloproctology Rossiyskiy zhurnal gastroenterologii, gepatologii, koloproktologii. – 2017. – Vol. 27, N5. – P. 76–93. (in Russian).
      3. Lacy B. E., Mearin F., Chang L. et al. Bowel Disorders. Gastroenterology. – 2016. – Vol. 150, N6. – P. 1393–1407.
      4. Pimentel M., Lembo A., Chey W. D. et al. Rifaximin therapy for patients with irritable bowel syndrome without constipation. N Engl J Med. – 2011. – Vol. 364. – P. 22–32.
      5. Rosania R., Giorgio F., Principi M. et al. Effect of probiotic or prebiotic supplementation on antibiotic therapy in the small intestinal bacterial overgrowth: a comparative evaluation. Curr Clin Pharmacol. – 2013. – Vol. 8, N2. – Р. 169–172.
      6. Boltin D., Perets T. T., Shporn E. et al. Rifaximin for small intestinal bacterial overgrowth in patients without irritable bowel syndrome. Annals of Clinical Microbiology and Antimicrobials. – 2014. – Vol.13. – P. 49.
      7. Longstreth G. F., Thompson W. G., Chey W. D. et al. Functional bowel disorders. Gastroenterology. – 2006. – Vol. 130, N5. – Р. 1480–1491.
      8. Francis C. Y., Morris J., Whorwell P. J. The irritable bowel severity scoring system: a simple method of monitoring irritable bowel syndrome and its progress. Aliment Pharmacol Ther. – 1997. – Vol. 11, N2. – P. 395–402
      9. Ghoshal U. C., Shukla R., Ghoshal U. Small Intestinal Bacterial Overgrowth and Irritable Bowel Syndrome: A Bridge between Functional Organic Dichotomy. Gut Liver. – 2017. – Vol. 11, N2. – P. 196–208.
      10. Andreyev D. N., Zaborovsky A. V., Trukhmanov A. S. Evaluation of the functional gastrointestinal diseases concept from standpoints of Rome IV (2016) diagnostic criteria (review) Rossiyskiy zhurnal gastroenterologii, gepatologii, koloproktologii. – 2017. – Vol. 27, N1. – P. 4–11. (in Russian).
      11. Lee H. J., Choi J. K., Ryu H. S. et al. Therapeutic Modulation of Gut Microbiota in Functional Bowel Disorders. J Neurogastroenterol Motil. – 2017. – Vol. 23, N1. – P. 9–19.
      12. Lembo A., Pimentel M., Rao S. et al. Repeat Treatment With Rifaximin Is Safe and Effective in Patients With Diarrhea-Predominant Irritable Bowel Syndrome. Gastroenterology. – 2016. – Vol. 151, N6. – P. 1113–1121.
      13. Lee O. Y. Asian Motility Studies in Irritable Bowel Syndrome. J Neurogastroenterol Motil. – 2010. – Vol. 16, N2. – P. 120–130.
      14. Krapivnaya O. V. Clinical and prognostic significance of fecal calprotectin in patients with irritable bowel syndrome // Far East Medical Journal. – 2015. – № 4. – Р. 24–27. (in Russian).
      15. Xu D., Gao J., Gillilland M. et al. Rifaximin alters intestinal bacteria and prevents stress-induced gut inflammation and visceral hyperalgesia in rats. Gastroenterol. – 2014. – Vol. 146. – P. 484–496
      16. Collignon A., Sandré C., Barc M. C. Saccharomyces boulardii modulates dendritic cell properties and intestinal microbiota disruption after antibiotic treatment. Gastroenterol Clin Biol. – 2010. – Vol. 34, S. 1. – P. S71–78
      17. Madsen K. L. Enhancement of epithelial barrier function by probiotics. J Epithel Biol Pharmacol. – 2012. – Vol. 5. – P. 55–59.
     


    Full text is published :
    Krapivnaia O.V.Alexeenko S. A. EVALUATION OF THE EFFECTIVENESS OF COMBINATION THERAPY IN PATIENTS WITH DIFFERENT TYPES OF IRRITABLE BOWEL SYNDROME ASSOCIATED WITH SMALL INTESTINAL BACTERIAL OVERGROWTH.Experimental and Clinical Gastroenterology Journal. 2018;153(05):19-23
    Read & Download full text

    1. Central State Medical Academy of the Administrative Department of the President of Russia (Moscow, Russian Federation)

    Keywords:NAFLD, SIBO, intestinal microbiocenosis, endotoxemia, psyllium, rifaximin

    Abstract:Aim of investigation: to study the frequency of occurrence of small intestinal bacterial overgrowth (SIBO) and bacterial endotoxemia (BE) in patients with nonalcoholic fatty liver disease (NAFLD) of different stages. Material and methods: The survey included 100 patients (78 (78%) men, 28 (28%) women) with NAFLD of different stages (steatosis - 30 people, nonalcoholic steatohepatitis (NASH) of minimal activity - 30 people, NASH of moderate activity - 30 people, liver cirrhosis - 10 people) at the average age of 51,83±8,48 years old. SIBO was verified by hydrogen breath test with lactulose (LHBT). BE was diagnosed by method of activated particles with the use of test kits of “MAP-Endotox spp.”, Russia. According to the treatment type patients with NAFLD were divided in 3 groups. The first group of 36 people without SIBO (on the background of lifestyle modification) received a 6-month intake of psyllium. The second group of 35 people with SIBO in addition to lifestyle modification received a 7-day course of rifaximi(7 - days/800 mg/d) and psyllium during the period of observation (6 months). Comparison group to assess the prognosis of the disease consisted of 19 patients with NASH who refused therapy at different stages of the investigation. Results: SIBO was detected in 50% patients, including 38% people with recorded BE. In group of steatosis BE rate did not exceed normal values, in NASH groups it increased to 6.67% and 33.33%, respectively, in cirrhosis group - 70%. We analyzed the effectiveness of antibacterial (rifaximin) and prebiotic (psyllium) therapy in the course of 6 months. It is established that control LHBT and MAP-test after 6-months’ observation showed no SIBO and BE in all patients of two groups. The comparison group without therapy aimed at the normalization of intestinal microbiocenosis displayed negative dynamics in the course of the disease. According to the results of the control tests, the frequency of SIBO in this group increased by 20%. Conclusion: 1. Frequency of detection of intestinal microbiocenosis disorders, established by the results of LHBT and MAP-test, increases with the severity of pathological process that testifies the role of microbiota as one of the most important components in development and progression of NAFLD. 2. Combined course therapy of rifaximin and long-term intake of psyllium is effective for correction SIBO and BE as the control tests determine the normalization of their indicators.

      1. Ivashkin V.T., Drapkina O. M., Maev I. V. et al. Rasprostranennost’ nealkogol’noj zhirovoj bolezni pecheni u pacientov ambulatorno-poliklinicheskoj praktiki v Rossijskoj Federacii: rezul’taty issledovaniya DIREG 2 // RZhGGK. 2015; 25(6):31–41.
      2. Younossi Z.M., Blissett D., Blissett R., Henry L., Stepanova M., Younossi Y., Racila A., Hunt Sh., Beckerman R. The economic and clinical burden of nonalcoholic fatty liver disease in the United States and Europe // Hepatology. 2016 Nov;64(5):1577–1586.
      3. Byrne C.D., Targher G. et al. NAFLD: A multisystem disease // Journal of Hepatology. 2015;62(1):47–64.
      4. Loomba R., Sanyal A. J. et al. The global NAFLD epidemic // Nat Rev Gastroenterol Hepatol. 2013 Nov;10(11):686–90.
      5. Cua I.H., George J. Non-alcoholic fatty liver disease // Hosp. Med. 2005;66:106–111.
      6. Drapkina O.М., Smirin V. I., Ivashkin V. T. NAZhBP. Sovremennyj vzglyad na problemu // Lechashchij vrach. 2010;5(5):57–61.
      7. Drapkina О.М., Korneeva O. N. Kontinuum nealkogol’noj zhirovoj bolezni pecheni: ot steatoza pecheni do serdechno-sosudistogo riska // Racional’naya farmakoterapiya v kardiologii. 2016;12(4):424–429.
      8. Tilg H., Moschen A. R. et al. Evolution of inflammation in nonalcoholic fatty liver disease: The multiple parallel hits hypothesis // Hepatology. 2010;52(5)
      9. Zvyaginceva T.D., Chernobaj A. I., Gridneva S. V. Kishechnyj mikrobiom i nealkogol’naya zhirovaya bolezn’ pecheni: patogeneticheskiye svyazi i korrekciya probiotikami // Zdorov’ye Ukrainy. 2016;1(39). http://health-ua.com
      10. Kravchuk Y. A. Kliniko-morfologicheskiye osobennosti steatogepatita alkogol’noj i metabolicheskoj etiologii. Diss. …dokt. med. nauk. – S.-Pb. 2016; 286 s.
      11. Ardatskaya M. D., Bel’mer S. V., Dobrica V. P., Zaharenko S. M., Lazebnik L. B., Minushkin O. N., Oreshko L. S., Sitkin S. I., Tkachenko E. I., Suvorov A. N., Havkin A. I., Shenderov B. A. Disbioz (disbakterioz) kishechnika: sovremennoe sostoyanie problemy, kompleksnaya diagnostika i lechebnaya korrekciya // Eksperimental’naya i klinicheskaya gastrojenterologiya. 2015;117(5):13–50.
      12. Dzhulaj G. S., Shchelochenkov S. V. Mikrobiota zheludochno-kishechnogo trakta v razvitii nealkogol’noj zhirovoj bolezni pecheni // Tverskoj medicinskij zhurnal. 2015;5:41–52.
      13. Fedos’ina E.A., Zharkova M. S., Maevskaya M. V. Bakterial’naya kishechnaya mikroflora i zabolevaniya pecheni. // RZhGGK. 2009;19 (6):73–81.
      14. Kostyukevich O. I. Bylova N. A., Simbirceva A. S. Rol’ kishechnoj mikrobioty v razvitii zabolevanij pecheni i zhelchevyvodyashchih putej. // RMZh. 2016;11:713–20.
      15. Sajjad A., Mottershead M., Syn W. K. et al. Ciprofloxacin suppresses bacterial overgrowth, increases fasting insulin but does not correct low acylated ghrelin concentration in non-alcoholic steatohepatitis. // Aliment. Pharmacol. Ther. 2005; 22(4): 291–9.
      16. Zhdanov K. V., Gusev D. A., Zaharenko S. M., Kurtukov M. V., Sukachev V. S. Disbioz kishechnika pri cirroze pecheni // Eksperimental’naya i klinicheskaya gastrojenterologiya. 2011;6:38–44.
      17. Babasheva G. G. Klinicheskoe znachenie endotoksina i lipopolisaharid-svyazyvayushhego belka u bol’nyh nealkogol’noj zhirovoj bolezn’yu pecheni. – Diss. …kand.med.nauk. – Stavropol. 2015; 141 s.
      18. Kljaritskaya I. L., Semenihina E. V. Rol’ IL-8 i LBP v patogeneze sindroma izbytochnogo bakterial’nogo rosta u pacientov s nealkogol’nym steatogepatitom. // Krymskij terapevticheskij zhurnal. 2015;2: 54–60.
      19. Gäbele E., Dostert K., Hofmann C., Wiest R., Schölmerich J., Hellerbrand C., Obermeier F. DSS induced colitis increases portal LPS levels and enhances hepatic inflammation and fibrogenesis in experimental NASH // J Hepatol. 2011 Dec;55(6):1391–9.
      20. Harte A. L., da Silva N. F., Creely S. J., McGee K.C. et al. Elevated endotoxin levels in non-alcoholic fatty liver disease.// J Inflamm. 2010;30:7–15.
      21. Alisi A., Manco M., Devito R., Piemonte F., Nobili V. Endotoxin and plasminogen activator inhibitor-1 serum levels associated with nonalcoholic steatohepatitis in children // J Pediatr Gastroenterol Nutr. 2010; 50(6), 645–649.
      22. Thuy S., Ladurner R., Volynets V., Wagner S., Strahl S., Königsrainer A., Maier K.-P., Bischoff S. C., Bergheim I. Nonalcoholic fatty liver disease in humans is associated with increased plasma endotoxin and plasminogen activator inhibitor 1 concentrations and with fructose intake // J Nutr. 2008 Aug; 138(8):1452–5.
      23. Liu X., Lu L., Yao P., Ma Y., Wang F., Jin Q., Ye X., Li H., Hu F. B., Sun L., Lin X. Lipopolysaccharide binding protein, obesity status and incidence of metabolic syndrome: a prospective study among middle-aged and older Chinese // Diabetologia. 2014;57:1834–1841.
      24. Kucheryavyj Ju.A., Maevskaya E. A., Ahtaeva M. L., Krasnyakova E. A. Nealkogol’nyj steatogepatit i kishechnaya mikroflora: est’ li potencial prebioticheskih preparatov v lechenii? // Medicinskij sovet. Gastrojenterologiya. 2013;3:46–51.
      25. Loginov V. A. Sindrom izbytochnogo bakterial’nogo rosta u bol’nyh so snizhennoj kislotoproduciruyushchej funkciej zheludka (klinicheskoe znachenie, diagnostika i lechenie). – Diss. …kand.med.nauk. – 2015;126 s.
      26. Rusanova E.V., Niyazmatov A. G., Protas I. M. Rol’ jendotoksina v razvitii gnoyno-septicheskih zabolevanij i metody ego vyyavleniya v krovi // Al’manah klinicheskoj mediciny. 2013;2:70–73.
      27. Garbuzenko D. V., Mikurov A. A., Smirnov D. M. Bakterial’naya jendotoksinemiya i risk razvitiya krovotechenij iz varikozno-rasshirennyh ven pishhevoda u bol’nyh cirrozom pecheni // Klinicheskaya medicina. 2012;7:48–51.
      28. Klinicheskie rekomendacii po diagnostike i lecheniyu nealkogol’noj zhirovoj bolezni pecheni Rossijskogo obshchestva po izucheniyu pecheni i Rossijskoj gastroenterologicheskoj associacii / pod red. V. T. Ivashkina. – М. 2015; 38 s.
      29. EASL–EASD–EASO Clinical Practice Guidelines for the Management of Non-alcoholic Fatty Liver Disease // Journal of Hepatology. 2016;64(6):1388–1402.
      30. Ledochowski M., Ledochowski E., Eisenmann A. Hydrogen Breath tests. Innsbruck, 2008;59.
      31. Alisi A., Ceccarelli S., Panera N., et al. Causative role of gut microbiota in non-alcoholic fatty liver disease pathogenesis // Front Cell Infect. Microbiol. 2012;2:132.
     


    Full text is published :
    Ardatskaya M.D,Garushyan G.V, Moysak R.P.EFFECT OF SMALL INTESTINAL BACTERIAL OVERGROWTH AND BACTERIAL ENDOTOXEMIA ON THE COURSE OF NONALCOHOLIC FATTY LIVER DISEASE Experimental and Clinical Gastroenterology Journal. 2018;153(05):24-31
    Read & Download full text

    1. FSBI «A. N. Ryzhykh State scientific center of coloproctology» of Ministry of health of Russian Federation (Moscow, Russian Federation)

    Keywords:Ultrasonography examination, ulcerative colitis, contrast enhancement, therapy effectiveness

    Abstract:Aim of investigation: determination and selection of parameters of ultrasonography with contrast enhancement for evaluation of the effectiveness of the therapy in patients with ulcerative colitis (UC). Materials and methods: The study included 20 patients with active left-side UC or pancolitis. Before the treatment all patients underwent colonoscopy and ultrasonography in standard regimen and with contrast enhancement. All patients received systemic 5-aminosalicylic acid in granules at a dose of 4 g per day for 3 months. After treatment, patients were repeatedly underwent endoscopy and ultrasound. Based on the ultrasound obtained with a contrast enhancement curve, the contrast parameters were automatically calculated: the maximum intensity (Imax), the area under the contrast curve (AUC), rise time (RT), peak time (TTP) and mean transit time (mTT), time to half-wash (HTWo). Results: According to the results of the examination of patients before and after three months of treatment, it was established that the most informative US-parameter for assessing the activity of inflammation is the AUC. For this parameter, a positive correlation with the endoscopic activity of the UC was obtained. Conclusion: Ultrasonography with contrast enhancement may be a good alternative non-invasive method for assessing the efficacy of conservative therapy in patients with UC, but it is necessary to continue the study on a larger sample to identify the relationship between the other parameters and validate this technique.

      1. Shelygin Yu.A., Blagodarnyy L. A. Spravochnik po koloproktologii. [Reference book on coloproctology]. Moscow, Literra Publ., 2012. 460–522 p.
      2. Ivashkin VT, Shelygin Yu.A., Khalif IL et al. Clinical guide of russian association of gastroenterology and russian Association of coloproctology on diagnostics and treatment of Ulcerative colitis. Koloproktologia 2017;1(59): 6–30
      3. Schnitzler F., Fidder H., Ferrante M. et al. Mucosal healing predicts long-term outcome of maintenance therapy with infliximab in Crohn’s disease // Inflamm Bowel Dis. - 2009. - № 15. - Р.1295-1301
      4. Baert F., Moortgat L., Van Assche G. et al. Mucosal healing predicts sustained clinical remission in patients with early-stage Crohn’s disease // Gastroenterology. - 2010. - № 138. - Р.463-468
      5. Cellier C., Sahmoud T., Froguel E. et al. Correlations between clinical activity, endoscopic severity, and biological parameters in colonic or ileocolonic Crohn’s disease. A prospective multicentre study of 121 cases. The Groupe d’Etudes Therapeutiques des Affections Inflammatoires Digestives // Gut. - 1994. - № 35. - Р.231-235
      6. Panes J., Bouzas R., Chaparro M. et al. Systematic review: the use of ultrasonography, computed tomography and magnetic resonance imaging for the diagnosis, assessment of activity and abdominal complications of Crohn’s disease // Aliment Pharmacol Ther. - 2011. - № 34. - Р.125-145
      7. Horsthuis K., Bipat S., Bennink R. J., Stoker J. Inflammatory bowel disease diagnosed with US, MR, scintigraphy, and CT: meta-analysis of prospective studies // Radiology. - 2008. - № 247. - Р.64-79
      8. Quaia E., Migaleddu V., Baratella E. et al. The diagnostic value of small bowel wall vascularity after sulfur hexafluoride-filled microbubble injection in patients with Crohn’s disease. Correlation with the therapeutic effectiveness of specific anti-inflammatory treatment // Eur J Radiol. - 2009. - № 69. - Р.438-444
      9. Girlich C., Jung E. M., Iesalnieks I. et al. Quantitative assessment of bowel wall vascularisation in Crohn’s disease with contrast-enhanced ultrasound and perfusion analysis // Clin Hemorheol Microcirc. - 2009. - № 43. - Р.141-148
      10. Socaciu M., Badea R., Hagiu C. et al. Ultrasound Assessment Techniques and Quantification of Bowel Inflammation in Several Intestinal Diseases: Initial Experience // Automat Comput Appl Math. - 2009. - № 18. - Р.212-217.
      11. Badea R., Socaciu M., Ciobanu L. et al. Contrast-enhanced ultrasonography (CEUS) for the evaluation of the inflammation of the digestive tract wall // J Gastrointestin Liver Dis. - 2010. - № 19. - Р.439-444.
      12. Ripolles T., Rausell N., Paredes J. M. et al. Effectiveness of contrast-enhanced ultrasound for characterization of intestinal inflammation in Crohn’s disease: a comparison with surgical histopathology analysis // J Crohns Colitis. - 2013. - № 7. - Р.120-128.
      13. Wong D. D., Forbes G. M., Zelesco M. et al. Crohn’s disease activity: quantitative contrast-enhanced ultrasound assessment // Abdom Imaging. - 2012. - № 37. - Р.369-376.
      14. Malago R., D’Onofrio M., Mantovani W. et al. Contrast-enhanced ultrasonography (CEUS) vs. MRI of the small bowel in the evaluation of Crohn’s disease activity // Radiol Med. - 2012. - № 117. - Р.268-281.
      15. Goertz R. S., Heide R., Bernatik T. et al. Mesenteric transit time using contrast-enhanced ultrasound (CEUS) does not correlate with disease activity in Crohn’s disease // Ultraschall Med. - 2012. - № 33. - Р.164-169.
      16. Girlich C., Schacherer D., Jung E. M. et al. Comparison between a clinical activity index (Harvey-Bradshaw-Index), laboratory inflammation markers and quantitative assessment of bowel wall vascularization by contrast-enhanced ultrasound in Crohn’s disease // Eur J Radiol. - 2012. - № 81. - Р.1105-1109.
      17. Girlich C., Jung E. M., Huber E. et al. Comparison between preoperative quantitative assessment of bowel wall vascularization by contrastenhanced ultrasound and operative macroscopic findings and results of histopathological scoring in Crohn’s disease // Ultraschall Med. - 2011. - № 32. - Р.154-159.
      18. Ripolles T., Martinez M. J., Paredes J. M. et al. Crohn disease: correlation of findings at contrast-enhanced US with severity at endoscopy // Radiology 2009. - № 253. - Р.241-248.
      19. Migaleddu V., Scanu A. M., Quaia E. et al. Contrast-enhanced ultrasonographic evaluation of inflammatory activity in Crohn’s disease // Gastroenterology. - 2009. - № 137. - Р.43-52.
      20. Kumar P., Domjan J., Bhandari P. et al. Is there an association between intestinal perfusion and Crohn’s disease activity? A feasibility study using contrast-enhanced ultrasound // Br J Radiol. - 2009. - № 82. - Р.112-117.
      21. Serra C., Menozzi G., Labate A. M. et al. Ultrasound assessment of vascularization of the thickened terminal ileum wall in Crohn’s disease patients using a low-mechanical index real-time scanning technique with a second generation ultrasound contrast agent // Eur J Radiol. - 2007. - № 62. - Р.114-121.
      22. De Franco A., Di Veronica A., Armuzzi A. et al. Ileal Crohn disease: mural microvascularity quantified with contrast-enhanced US correlates with disease activity // Radiology. - 2012. - № 262. - Р.680-688.
      23. Girlich C., Schacherer D., Jung E. M. et al. Comparison between quantitative assessment of bowel wall vascularization by contrast-enhanced ultrasound and results of histopathological scoring in ulcerative colitis // Int J Colorectal Dis. - 2012. - № 27. - Р.193-198.
      24. Yamaguchi T., Yoshida S., Tanaka S. et al. Predicting the clinical response to cytapheresis in steroid-refractory or -dependent ulcerative colitis using contrast-enhanced ultrasonography // Scand J Gastroenterol. - 2009. - № 44. - Р.831-837.
     


    Full text is published :
    Khalif I.L., Shapina M.V.,Orlova L.P., Evgrafov P.G.ULCERATIVE COLITIS TREATMENT EFFICIENCY ASSESSED BY ULTRASONOGRAPHY WITH CONTRAST ENHANCEMENT. Experimental and Clinical Gastroenterology Journal. 2018;153(05):32-37
    Read & Download full text

    1. FSBEI Novosibirsk State Medical University of Ministry of Health of the Russian Federation (Novosibirsk, Russian Federation)
    2. FSBI Novosibirsk Tuberculosis Research Institute of Ministry of Health of the Russian Federation (Novosibirsk, Russian Federation)

    Keywords:abdominal tuberculosis, intestinal tuberculosis, mesenterial lymph node tuberculosis, disseminated pulmonary tuberculosis, HIV-infection, risk groups, diagnosis of abdominal tuberculosis

    Abstract:The goal of the study is determining of the prevalence and morbidity of tuberculosis (TB) lesions in organs of abdominal cavity in pulmonary TB patients during the period of unfavorable epidemic situation (2006-2008 years) and the period of reduction in TB incidence (2015-2017 years). Clinical records of patients with combined pulmonary and abdominal tuberculosis that underwent treatment in TB hospital during the periods of 2006-2008 and 2015-2017 years were analyzed. Despite a reduction in overall TB incidence from 2006-2008 to 2015-2017 years, the proportion of pulmonary TB patients with abdominal tuberculosis, treated in TB hospital, increased for this period almost twice (1,95±0,3% vs 3,5±0,6%). Abdominal tuberculosis is the result of generalization of TB. Abdominal TB was registered more often in 2015-2017 than in 2006-2008 (75,9±7,9% vs 20,5±6,1%, p=0,00001, Fischer exact test) and was less frequently associated with lung tissue destruction (27,4 and 81,8%, respectively, p=0,00001, Fischer exact test). Detection of Mycobacterium tuberculosis in feces increase significantly an efficiency of diagnosis of TB colitis (especially in patients without clinical intestinal symptoms).

      1. Global tuberculosis report 2017. – World Health Organization. [Электронный ресурс] URL: http://www.who.int/tb/publications/global_report/en/ (Дата обращения 28.03.2018).
      2. Rossiiskii statisticheskii iejegodnik, 2016. Federalnaiya slujba gosudarstvennoi statistiki. URL: http://www.gks.ru/wps/wcm/connect/rosstat_main/rosstat/ru/statistics/publications/catalog/doc_1135087342078
      3. Osnovnii pokasateli protivotuberkulosnoi deiatelnosti v Sibirskom I Dalnevostochnom federalnom okruge / Novosibirsk: IPC NGMU, 2017. – 92 s. URL: http://nsk-niit.ru/ru/nauchnaja-dejatelnost/publikacii-za-2010–2012-gg/metodicheskie-rekomendacii-i-posobija/
      4. Kulchavenia E. V., Jukova I. I. Vnelegochnii tuberkulos – voprosov bolshe, chem otvetov. Tuberkulos i bolesni legkih. 2017. N2. S.59–63.
      5. Sovetova N. A. Savin I. B., Malchenko O. V. i dr. Sovremennaia luchevaia diagnostika vnelegochnogo tuberkulosa. Problemi tuberkulosa i bolesnei legkih. 2006. N11. S. 6–9.
      6. Skopin M. S. Batirov F. A. Kornilova Z. H. Rasprostranennost tuberkulosa organov bruchnoi polosti i osobennosti ego viavlenia. Problemi tuberkulosa i bolesnei legkih. 2007. N1. S. 22–26.
      7. Panteleev A. M. Klinicheskoe predstavlenie o patogenese generalisacii tuberkulosa u bolnih HIV-infekciei. Tuberkulos i bolesni legkih. 2015. N2. S.26–30.
      8. Levashov Iu.N., Mushkin A. Iu., Grishko A. N. Vnelegochnii tuberkulos v Rossii: oficialnaia statistika i realnost. Problemi tuberkulosa i bolesnei legkih. 2006. N11. S. 3–6.
      9. Kiselevich O. K., Balashova N. A., Iusubova A. N., Shirshov I. V. Tuberkulos mnogestvennih lokalisacii u detei rannego vosrasta. Tuberkulos i bolesni legkih. 2015. N6. S.76.
      10. Guseinov A. G., Guseinov G. K. Atipichno tekuchii tuberkuliosnii mezadenit u pacienta s HIV-infekciei, narkomaniei i gepatitom C. Tuberkulos i bolesni legkih. 2015. N11. S.52–55.
      11. Holtobin D. P., Jukova I. I., Brijatiuk E. V. i soavt., Demograficheskie i klinicheskie osobennosti urogenitalnogo tuberkulosa na sovremennom etape. Sibirskii meicinskii vestnik. 2017. N1. S. 9–15.
      12. Barinov V. S., Prohorovich N. A. Differencialnaia diagnostika abdominalnogo tuberkulosa na osnove kliniko-laboratornih i laparoskopicheskih dannih: Posobie dlia ftisiatrov i hirurgov. – SPb., 1997. – S.4–6.
      13. Perelman M. I., Bogadelnikova I. V. Ftisiatria. Uchebnik. «GEOTAR-Media», 2010. – 266 s.
     


    Full text is published :
    Poddubnaya L.V.,Zyryanova T.V.,Petrenko T.I.,Kononenko V.G. et al. ABDOMINAL TUBERCULOSIS IN PULMONARY TUBERCULOSIS PATIENTS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):38-43
    Read & Download full text

    1. FSBI “SFSCC FMBA of Russia” (Novosibirsk, Russian Federation)
    2. SBEI HPE “Siberian State medical University of Minzdrav of Russia” (Novosibirsk, Russian Federation)

    Keywords:irritable bowel syndrome, psychovegetative status, drug-free rehabilitation, SMC-therapy, EHF-therapy

    Abstract:Complex of rehabilitation measures at persons of young age with clinical signs of irritable bowel syndrome using SMC-therapy and EHF-therapy, which was prescribed based on the type of functional disorders, contributes to a significant improvement of clinical and laboratory parameters in the form of relief of complaints and symptoms against the background of increasing adaptive capacity and normalization of psycho-autonomic status. The direct effectiveness of non-pharmacological rehabilitation amounted to 94.4% of constipation and 93.3% in diarrhea. The obtained results were associated with the peculiarities of rehabilitation facilities (χ2=to 34.94; p=0,004; r=0,45;), while the maximum contribution to the total statistics Pearson correlations were “significant improvements” and “improvements” with the rehabilitation complexes, including SMT-therapy and EHF-therapy (with diarrhea - χ2=3,59 and χ2=1,51; constipation - χ2=2,85 and χ2=1,37, respectively).

      1. Ivashkin V. T., Shelygin Y. A., Marshall, E. K., and others. Clinical guidelines of the Russian gastroenterological Association, Association of Coloproctology Russia on the diagnosis and treatment of patients with irritable bowel syndrome. Grew. Sib. of gastroenterology. hepatol. coloproctol. – 2014.-№ . 2. – P. 92–102.
      2. Samsonov A. A. Features of patients with irritable bowel syndrome, based on polyvalence of the disease background. Gastroenterology. – 2014.-№ 2. – P. 26–30
      3. Maev I. V., Cheremushkin S. V. irritable bowel Syndrome. Manual for doctors. – Moscow: “Forte-print”, 2012. – P. 6
      4. Loranskaya I. D., Kozlova Yu. A. The role of vegetative disorders in the pathogenesis of irritable bowel syndrome. Experimental and clinical gastroenterology. – 2014. – Issue 107, № 7. – P. 87–90.
      5. Stanislavchuk N. A. Kulchytska E. N. Features of the functional state of the autonomic nervous system in patients with irritable bowel syndrome. Pathogenesis. – 2013. – Vol. 11, № 3. – P. 74–77.
      6. Kozlov Yu. A. Irritable bowel Syndrome: clinical significance of autonomic status with refractory disease. The dissertation on competition of a scientific degree of candidate of medical Sciences. – Moscow, 2015. – 24p.
      7. Poluektova E. A., Kuchumova S. Yu., Shifrin O. S., Sheptulin A. A., Ivashkin V. T. Pathogenic role of intestinal microflora changes in patients with irritable bowel syndrome and the ways of its correction. Grew. Sib. of gastroenterology. Hepatol. coloproctol. – 2014. – № 3. – P. 89–96.
      8. Prikhodko E. M., Tsurtsumia D. B., Seliverstov P. V., Sitkin S. I., Radchenko V. G. The possibilities of modern therapy for patients with irritable bowel syndrome. Attending physician. – 2016. – № 8. – P. 76–80.
      9. Poluektova E. A., kuchumova S. Yu., Sheptulin A. A., Ivashkin V. T. Treatment of irritable bowel syndrome from the standpoint of modern ideas about the pathogenesis of the disease. Grew. Sib. of gastroenterology. Hepatol. coloproctol. – 2013. – № 1. – P. 57–64.
      10. Akhmedov V. A., Orlov I. N., Gaus, O. V. Modern methods of rehabilitation of patients with irritable bowel syndrome. Therapy. – 2017. – № 3. – P. 49–55.
      11. Danilov D. S., Morozova V. D., Korobkova I. G., Lukyanova T. V. Irritable bowel Syndrome in the practice of psychiatrist (the problem of nosological independence) and the possibility of its treatment with antidepressants (for example, the effectiveness of paroxetine). Neurology, neuropsychiatry, psychosomatics. – 2013. -№ 2. – P. 46–50.
      12. Lagunova N. In. Marchukova A. Yu., Lebedeva T. N. Application of frequency-resonance therapy in health-resort rehabilitation of children with irritable bowel syndrome. Bulletin of Belgorod state University. – 2017. – Volume 37, № 5 (254). – P. 52–58.
      13. Filimonov R. M., Faustova I. I., Filimonova T. R. Physical therapy in the irritable bowel syndrome. Issues of balneology, Physiotherapy and therapeutic physical training. – 2013.-№ 25. – P. 51–56.
      14. Filippova O. L., Statsenko E. V., Bikbova G. R., Labutina N. Sazonova E. I. Irritable bowel syndrome. The possibility of physical therapy. Sanatorium and resort organization: management, marketing, economics, finance. – 2015. – № 4. – P. 68–73.
      15. Abramovich S. G.(ed.), Kulikov A. G. Physiotherapy in Clinical gastroenterology. Part 1: practice benefit. Irkutsk: RIO GBOU DPO IGMAP, 2016. – 52 p.
      16. Kasinova A. C., Tekeeva F. I., Prosolenko B. A., Kazaryan T. S. Sanatorium-resort treatment of patients with irritable bowel syndrome. Spa medicine. – 2015. – № 2. – P. 104–107.
      17. Kazaryan T. S. Balneophysiotherapy of irritable bowel syndrome. Spa medicine. – 2016. -№ 1. – P. 63–67.
      18. Litvinova O. N. Physiotherapeutic methods used in the complex treatment of patients with chronic constipation in large intestine abnormalities. Physiotherapy, balneology and rehabilitation. – 2016. – Volume: 15, № 4. – P. 182–184.
      19. Efimenko N. I., Kazaryan T. S., Khapaeva F. M., Chalaya E. N. Dynamic electroneurostimulation in the complex sanatorium treatment of patients with irritable bowel syndrome with constipation. Physiotherapy, balneology and rehabilitation. – 2016. – Volume 15, № 2. – 86–91.
      20. Orda, T. A., P. V. Poruchikov, V. F. Horde Wave therapy. Occupational medicine. M.: Eksmo, 2008. – № 12. – P. 136,430.
      21. Poddubnaya O. A., Ugolnikov O. I., Levitskaya T. E. Chronophototherapy patients with dysfunctions of the gallbladder and dyscholia on the background of psycho-vegetative imbalance. Physiotherapy, balneology and re-habilitation. – 2014. – № 3. – P. 12–17.
      22. Rapoport S. I., Frolov V. A., Khetagurov L. G. Chronobiology and chronomedicine. Guide. M.: OOO “Medical in-formation Agency”, 2012. – P. 72.
      23. Garkavi L. H., Kvakina E. B., Kuzmenko T. S. Antistress reactions and activation therapy. M.,”IMEDIS”, 1998. – P. 28
      24. Wayne A. M., Solov’eva, A. D., Danilov A. B., Khaspekov N. B. Methods of study of vegetative nervous system. Vegetative disorders. – Moscow, 2003. – P. 752.
     


    Full text is published :
    Poddubnaya O.A.,Privalova N.I. THE EFFICIENCY OF THE COMPLEX NON-DRUG REHABILITATION OF YOUNG PATIENTS WITH IRRITABLE BOWEL SYNDROME. Experimental and Clinical Gastroenterology Journal. 2018;153(05):44-51
    Read & Download full text

    1. Scientific Сentre for Family Health and Human Reproduction Problems (Moscow, Russian Federation)

    Keywords:men, women, eubiosis, intestinal dysbiosis

    Abstract:Aims. Analyze the structure of intestinal dysbiosis in adults, taking into account gender differences. Materials and methods: in the period from 2013 to 2017 the coprological material from 572 patients aged from 22 to 74 years (134 men and 438 women) was studied. Results: Long-term studies have shown that more than 90% of the adult population observed dysbiotic changes of varying severity. The structure was dominated by mild and moderate disorders (I and II degree of dysbiosis). In women, on average, more often than in men, there were dysbiotic changes of I degree (in 67,1±2,2% and 58,2± 4,2%, respectively), the proportion of men with dysbiotic disorders of II and III severity was higher than in women. It was revealed that in men in 2017 there was a decrease in the frequency of registration of the II degree of dysbiosis to 10,5± 7,0%, but the number of severe dysbiotic disorders of the III degree increased (to 10,6±7,0%) (p<0,05). In 2015 and 2017 men’s and, in 2016, the women there was not a single case eubioz intestine. This circumstance can be connected both with decrease in a standard of living, and with the ecological pressure on an organism of negative factors of environment continuing in our territory.

      1. Global status report on non communicable diseases 2010; 1, Chronic disease – prevention and control. 2. Chronic disease – epidemiology 3. Chronic disease – mortality 4.Cost of illness. 5. Delivery of health care. World Health Organization. ISBN978 92 456422 6 (NLM classification: WT 500). Available at: http://www.who.int/nmh/publications/ncd_report2010/ru/
      2. Wang YR, Richter JE, Dempsey DT. Trends and Outcomes of Hospitalizations for Peptic Ulcer Disease in the United States, 1993 to 2006. Journal: Annals of Surgery Ann Surg. – 2010. – Т. 251, № 1. –С.51–58
      3. Lazebnik L. B., Masharova A. A., Bordin D. S., Vasil’ev Yu.V. et al. Rezul’taty mnogotsentrovogo issledovaniya «Epidemiologiya gastroezofageal’noy reflyuksnoy bolezni v Rossii» (MEGRE). Terapevticheskiy arkhiv. – 2011. – № 1. – S.45–50.
      4. Eganyan R. A., Kalinina A. M., Ipatov P. V., Drapkina O. M. Metodologicheskie aspekty i rezul’tativnost’ vyyavleniya zabolevaniy organov pishchevareniya pri dispanserizatsii vzroslogo naseleniya. Profilakticheskaya meditsina. – 2017. – № 1. – S.15–23
      5. Kostyukevich O. I. Vliyanie kishechnoy mikroflory na zdorov’e cheloveka. Ot patogeneza k sovremennym metodam korrektsii disbioza. RMZh. – 2011. – T. 19, № . 5. – S. 304–308
      6. Bellantani S., Saccoccio G., Masutti F., Croce LS. et al. Prevalence and risk factors for hepatic steatosis in northern Italy. Ann. Intern. Med. – 2000. –№ 132. – С. 112–117.
      7. Chikhacheva E. A., Seliverstov P. V., Teterina L. A., Dobritsa V. P. et al. Mikrobiotsenoz kishechnika pri khronicheskikh zabolevaniyakh pecheni: diagnostika i lechenie. Vrach. – 2011. – № . 7. – S. 18–21
      8. Bondarenko V. M., Matsulevich T. V. Disbakterioz kishechnika kak kliniko-laboratornyy sindrom: sovremennoe sostoyanie problemy. – M.: GEOTAR – Media, 2007. –S. 8–35.
      9. Sukhareva I. A. Sravnitel’naya kharakteristika zabolevaemosti, smertnosti i ozhidaemoy prodolzhitel’nosti zhizni muzhchin i zhenshchin v respublike Krym. Meditsinskiy al’manakh. – 2016. – № 1 (41). – S. 14–17
      10. Semutenko K. M., Cheshik I. A., Sharshakova T. M. Osnovnye faktory, opredelyayushchie sostoyanie zdorov’ya muzhchin. Voprosy organizatsii i informatizatsii zdravookhraneniya. – 2014. – № 2. – S.36–46.
      11. Ardatskaya M. V., Bel’mer S.V., Dobritsa V. P., Zakharenko S. M. et al. Disbioz (disbakterioz) kishechnika: sovremennoe sostoyanie problemy, kompleksnaya diagnostika i lechebnaya korrektsiya. Experimental’naya i klinicheskaya gastroenterologia – 2015. – № 5. – S. 13–50
      12. Ofitsial’nyy sayt Territorial’nogo organa Federal’noy sluzhby gosudarstvennoy statistiki po Irkutskoy oblasti. Available at: http://irkutskstat.gks.ru/
      13. Popkova S. M., Rakova E. B., Kichigina E. L., Nemchenko U. M. et al. Mikroekologicheskiy peyzazh u detey Irkutskoy oblasti na fone gigienicheskikh kharakteristik territorii. Izvestiya Irkutskogo gosudarstvennogo universiteta. Seriya: Biologiya. Ekologiya. – 2012. – № 5(4). – S.44–54.
      14. Krasnozhenov E. P., Akhremenko Ya. A. Kolonizatsionnaya rezistentnost’ organizma cheloveka v norme i pri patologii. Monografiya. – Kirov: MTsNIP, 2013. – S.115
      15. Savilov E. D., Il’ina S. V. Infektsionnaya patologiya v usloviyakh tekhnogennogo zagryazneniya okruzhayushchey sredy: klinikoepidemiologicheskie issledovaniya. – Novosibirsk: Nauka, 2010. – 248 s.
      16. Nemchenko U. M., Rakova E. B., Popkova S. M., Savel’kaeva M.V. et al. Struktura disbiozov kishechnika u detey doshkol’nogo vozrasta za mnogoletniy period nablyudeniy. Klinicheskaya laboratornaya diagnostika. – 2015. – T. 60, № 2. – S. 63–65
      17. Ivanova E.I., Rychkova L. V., Nemchenko U. M., Bukharova E. V., Savelkaeva M. V., Dzhioev Y. P. The structure of the intestinal microbiota of the intestine and the frequency of detection of pathogenicity genes (stx1, stx2, bfp) in Escherichia coli with normal enzymatic activity isolated from children during the first year of life. Molecular Genetics, Microbiology and Virology. – 2017. – Т. 32, № 1. – С. 42–48.
      18. Kozlova I. V., Pakhomova A. L. Sovremennyy patsient gastroenterologicheskogo profilya: shtrikhi k klinicheskomu portretu. Experimental’naya i klinicheskaya gastroenterologia. – 2015. –Vypusk 118. № 6. – S.4–10
     


    Full text is published :
    Nemchenko U. M., Ivanova E. I., Grigorova E.V, Voropaeva N. M. et al. CHANGES IN THE STRUCTURE OF THE DYSBIOSIS OF THE INTESTINE IN THE ADULT POPULATION FOR LONG-TERM OBSERVATION PERIOD. Experimental and Clinical Gastroenterology Journal. 2018;153(05):52-56
    Read & Download full text

    1. Moscow clinical scientific and practical center. A. I. Loginov (Moscow, Russian Federation)

    Keywords:constipation, dolichosigma, electromyography, motor bowel function

    Abstract:Irritable bowel syndrome (IBS) is a functional bowel disease in which recurrent abdominal pain is associated with defecation or a change in bowel function. Despite the numerous works devoted to the study of mechanisms of IBS development, intestinal motility in this disease has not been studied enough. The goal is to identify features of the motor function of the colon and small intestine in irritable bowel syndrome with constipation (IBS-C) and dolichosigma. Material and methods. The method of electromyography was used to study 84 patients with IBS-C in comparison with a group of 25 patients with dolichosigma and a group of 35 patients with functional constipation. The frequency of slow waves of the small and large intestine (patients with functional constipation) and left colon (patients with IBS-C and dolichosigma) was measured by the hardware-software complex “Conan-M”. Results and discussion. In electromyography patients with IBS-C showed a decrease in the frequency of slow waves to 5.4±0.2 V min (10%, p<0.05), the amplitude - to 0.09±0001 mV (46.6% p<0.05). The increase of spike activity was revealed: frequency 2.8±0.18 (40% p<0.05)., amplitude-0.13±0.02 mV (13.4% p<0.05). In patients with dolichosigma on electromyography revealed a decrease in the frequency of slow waves to 4.8±0.15 per minute (20%, p<0.05), the amplitude - to 0.07±0011 mV (53.3% p<0.05) with minimal spike activity. IBS-W is characterized by hypomotor dyskinesia of the left parts with pronounced spastic contractions of the smooth muscles of the circular layer of the intestine due to, perhaps, the activity of stimulating serotoninergic effects on the spastic activity of the circular muscle layer or inhibitory adrenergic neurons of the intermuscular (auerbachian) nerve plexus. When dolichosigma identified hypomotor dyskinesia of the left departments of the colon due to stretching of the mechanoreceptors in the afferent neurons of the intramural reflex arcs.

      1. Tokmulina G. M., et al. «Roman criteria for the IV syndrome of irritable bowel: the evolution of views on pathogenesis, diagnosis and treatment.» Lech the doctor «2017; 3: 61–67.
      2. Gershon M.D, Tack J. The serotonin signaling system: from basic understanding to drug development for functional GI disorders. Gastroenterology 2007; 132:397-414.
      3. Hoffman J.M, Tyler K, MacEachern SJ, et al. Activation of colonic mucosal 5-HT(4) receptors accelerates propulsive motility and inhibits visceral hypersensitivity. Gastroenterology 2012; 142:844-854
      4. Stasi C, Bellini M, Bassotti G, Blandizzi C, Milani S. Serotonin receptors and their role in the pathophysiology and therapy of irritable bowel syndrome. Tech Coloproctol. 2014;18(7):613-21
      5. Beattie D. T., Smith J. A. Serotonin pharmacology in the gastrointestinal tract: a review.Naunyn Schmiedebergs. Arch. Pharmacol. 2008; 377, 181-203.
      6. Ladabaum U. Safety, efficacy and costs of pharmacotherapy for functional gastrointestinal disorders: the case of alosetron and its implications. Aliment. Pharmacol. Ther. 2003;17, 1021-1030.
      7. Kim J.J, Khan W.I. 5-HT7 receptor signaling: improved therapeutic strategy in gut disorders. Front Behav Neurosci. 2014;11;8:396
      8. Meuser T., Pietruck C., Gabriel A., Xie G.-X., Lim K.-J., Pierce Palmer P. 5-HT7 receptors are involved in mediating 5-HT-induced activation of rat primary afferent neurons. Life Sci.2002; 71, 2279-2289.
      9. Zou B. C., Dong L., Wang Y., Wang S. H., Cao M. B. Expression and role of 5-HT7 receptor in brain and intestine in rats with irritable bowel syndrome. Chin. Med. J. (Engl) 2007; 120, 2069-2074.
      10. Lychkova A. E. Coordination of the myoelectrical activity of the large and small intestine. Experimental and Clinical Gastroenterology Journal. 2012;3:59–
      11. Lychkova A. E., Puzikov A. M. The digestive tract motility and nutritional support with postgastroresectional syndrome. Experimental and Clinical Gastroenterology Journal. 2015;120(8):25–29.
      12. Mayev I. V., Samsonov A. A., Nikushkin I. N., Ivashkina N. Yu. Irritable bowel syndrome, relevance of problem and issues of modern therapy. 2011;2:18–25
      13. Clarke G, Quigley EM, Cryan JF, et al. Irritable bowel syndrome: towards biomarker identification. Trends Mol Med 2009;15:478-89
      14. Poluektova V. A. Pain in the abdomen with functional bowel disorders. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2001;2:27–33
      15. Ардатская М. Д., Топчий Т. Б. Абдоминальная боль и висцеральная гиперчувствительность пациентов с синдромом раздраженного кишечника. Римские критерии IV и клиническая практика.
     


    Full text is published :
    Lychkova A. E., Ruchkina I. N., Poleva N. I., Puzikov A. M. MOTOR FUNCTION OF THE INTESTINE IN IRRITABLE BOWEL SYNDROME WITH CONSTIPATION. Experimental and Clinical Gastroenterology Journal. 2018;153(05):57-60
    Read & Download full text

    1. Acad. E. A. Wagner Perm State Medical University (Perm, Russian Federation)

    Keywords:S. aureus, C. albicans. colonic biotope, antagonism, microbiota

    Abstract:Intestinal microflora is considered as the main determinant of human health and disease. There is evidence that changes in the relationship between the composition of intestinal microbiota and the human body can be accompanied by the development of allergic and immunopathological conditions, as well as a number of diseases. The aim of the investigation was to assess changes in the lumen of the microbial composition of the large intestine in the case of isolation of S. aureus and C. albicans. Results. In the case of the presence of S. aureus a decrease in the frequency of isolation of typical variants of E. coli. This activity of S. aureus is suppressed by Candida, when the occurrence of E. coli corresponds to the level of the control group. In the presence of C. albicans alone, there is a slight decrease in the allocation of typical E. coli variants. Conclusion. The presence of C. albicans eliminates S. aureus antagonistic relationship with E. coli. On the other hand, the presence of S. aureus and C. albicans both individually and jointly contribute to the development of atypical variants of E. coli. Thus, the studies have shown that the detection of S. aureus and/or C. albicans in the large cell biotope can significantly change the composition of the microbiota, which may affect the functional activity of the colon mucosa and the whole human body.

      1. Bulatova E. M., Bogdanova N. M. Intestinal microflora is one of the factors in the formation of human health. Medical Council. 2013; 1: 30–33.
      2. Simonova E. V., Ponomareva O. A. The role of normal microflora in maintaining human health. The Siberian Medical Journal. 2008; 8: 20–25.
      3. Klaerner H. G., Uknis M. E., Acton R. D., Dahlberg P. S., Carlone-Jambor C., Dunn D. L. Candida albicans and Escherichia coli are Synergistic Pathogens during Experimental Microbial Peritonitis. Journal of Surgical Research. – 1997. – Vol. 70(2). – P. 161–165.
      4. De Brucker K., Tan Y., Vints K., De Cremer K. et al. Fungal β-1,3-glucan increases ofloxacin tolerance of Escherichia coli in a polymicrobial E. coli/Candida albicans biofilm. Antimicrobial Agents and Chemotherapy. – 2015. – Vol. 59(6). – P. 3052–3058.
      5. Morales D. K., Hogan D. A. Candida albicans Interactions with Bacteria in the Context of Human Health and Disease. PLOS Pathogens. – 2010. – № 6 (4). Volume 6 (4). – P. 1–4.
      6. Bandara H. M. H. N., Yau J. Y. Y., Watt R. M. et al. Escherichia coli and its lipopolysaccharide modulate in vitro Candida biofilm formation. Journal of Medical Microbiology. – 2009. – № 12 (58). – P. 1623–1631.
      7. Diebel L. N., Liberati D. M., Diglio C. A. et al. Synergistic effects of Candida and Escherichia coli on gut barrier function. Journal of Trauma and Acute Care Surgery. – 1999. – № 6 (47). – P. 1045–1051.
      8. Chadwick P., Niell M. Transferable antibiotic resistance in E. coli and Klebsiella pneumoniae. Canadian Medical Association Journal. – 1973. – Vol. 109(8). – P. 691–696.
      9. Melo T. A., Dos Santos T. F., De Almeida M. E. et al. Inhibition of Staphylococcus aureus biofilm by Lactobacillus isolated from fine cocoa. BMC Microbiology. – 2016. – Vol. 16. – P. 250–9.
      10. Wang J., Zhang R., Zhou L. et al. Lactobacillus inhibit adhesion of Staphylococcus aureus to HeLa cells. Sheng Wu Gong Cheng Xue Bao. – 2012. – Volume 28 (6). – P. 715–725.
      11. Haileselassie Y., Navis M., Vu N. et al. Lactobacillus reuteri and Staphylococcus aureus differentially influence the generation of monocyte‐derived dendritic cells and subsequent autologous T cell responses. Immunity, Inflammation and Disease. – 2016. 4(3). – P. 315–326.
      12. Karska-Wysocki B., Bazo M., Smoragiewicz W. Antibacterial activity of Lactobacillus acidophilus and Lactobacillus casei against methicillin-resistant Staphylococcus aureus (MRSA). Microbiological Research. – 2010. – № 165 (8). – P. 674–686.
      13. Godovalov A. P., Bykova L. P., Nikulina E. A., Ozhgibesov G. P. Study of the microbial landscape of the large intestine in candidiasis. MIA Medical Bulletin. 2016; 1 (80): 41–43.
      14. Godovalov A. P., Bykova L. P., Nikulina E. A., Ozhgibesov G. P. et al. Identification of Staphylococcus aureus in the course of a change in the microbiocenosis of the colon. Experimental and Clinical Gastroenterology Journal. 2016; 12 (136): 36–38.
      15. Godovalov A. P., Karpunina N. S., Karpunina T. I. Microbiota of the intestine and vagina of women with secondary infertility and diseases of the gastrointestinal tract. Experimental and Clinical Gastroenterology Journal. 2016; 6 (130): 109–113.
     


    Full text is published :
    Godovalov A. P., Antonyan A. A., Gorbunova E. A. PECULIARITIES OF MICROFLORA OF THE COLONIC BIOTOPE COLONIZED BY S. AUREUS AND C. ALBICANS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):61-65
    Read & Download full text

    1. The Nikiforov Russian Center of Emergency and Radiation Medicine, EMERCOM of Russia (Moscow, Russian Federation)

    Keywords:microbiota, gerontology, gas chromatography-mass spectrometry, microbial markers

    Abstract:Purpose of research. To study the characteristics of the wall of the intestinal microbiota of elderly persons with multiple organ pathology. Materials and methods. 94 patients aged from 55 to 65 years with various somatic pathology were examined. Results. The study of mass spectrometry of microbial markers in blood plasma (near-wall microbiota) in elderly compared to young allowed to establish the following: total number of microbial markers reduced by 40%; good microbiota reduced by 46%; the proportion of opportunistic pathogenic bacteria significantly increased (older people 48%, and in young only 34%); the share of anaerobic microorganisms localized mainly in the large intestine has decreased; the relationship between individual representatives of the microflora has changed.

      1. Hawrelak J.A., Myers S. P. The causes of intestinal dysbiosis: a review // Altern. Med. Rev., 2004, vol. 9, pp. 180–197.
      2. Valenkevich, L.N. (1987). Gastroenterologiia v geriatrii. Pishchevaritel’naia Sistema pri pishchevarenii [Gastroenterology in geriatrics. Digestive system for digestion]. Leningrad: Meditsina.
      3. D’Imperio N. et al. Studio morfometrico-funsionaledell, intestine tenue nel soggetto anziano // G. Clin. Med., 1984, № 9–10, pp. 419–425.
      4. Etingen, L.E. (2003). Normal’naia morfologiia starcheskogo vozrasta [Normal morphology of senile age]. Moskva.
      5. Tkachenko, E.I., Suvorova, A.N. (2009). Disbioz kishechnika. Rukovodstvo po diagnostike I lecheniiu [Intestinal dysbiosis. A guide to diagnosis and treatment]. (2nd ed.). Sankt-Peterburg: InformMed.
      6. Nemtsov, V.I. (2010). Narusheniia sostava kishechnoi mikroflory i metabolicheskii sindrom [Disorders in the composition of the intestinal microflora and metabolic syndrome]. Kliniko-laboratornii konsilium, (1), 4–13.
      7. Konev, Yu.V. (2004). Disbioz v pozhilom i starcheskom vozraste [Disbiosis in elderly and senile age]. Consilium Medicum, (12), 906–909. [Online] Available: http://www.disbakterioz.ru/108/.
      8. Samsonova, N.G., Zvenigorodskaia, L.A., Cherkashova, E.A. [et. al.], (2010). Disbioz kishechnika i aterogennaia dislepidemiia [Intestinal disbiosis and atherogenic dyslipidemia]. Eksperimental’naia i klinicheskaia gastroenterologiia, (3), 88–94.
      9. Shilov, A.M., Mar’yanovskii, A.A., Petrukhina, N.B. (2013). Endobiotsenoz kishechnika i metabolicheski-assotsiirovannyye sostoyaniia [Endobiocenosis of the intestine and metabolic associated conditions]. Lechebnoe delo, (2), 67–74.
      10. Albert M.A., Danielson E., Rifai N. Effect of statin therapy on C-reactive protein levels: the pravastatin inflammation/CRP evaluation (PRINCE): a randomized trial and cohort study // JAMA, 2001, 286, pp. 64–70.
      11. Mayanskii, A.N. (1999). Mikrobiologiia dlia vrachei [Microbiology for doctors]. Nizhnii Novgorod: NGMA.
      12. Osipov, G.A., Fedosova, N.F., Liadov, K.V. (2007). Kolichestvennyi in situ mikrobiologicheskii analiz po lipidnim markeram v biologicheskikh zhidkostyakh s ispol’zovaniem metoda gazovoi khromatografii – mass spektrometrii [Quantitative in situ microbiological analysis of lipid markers in biological fluids using Gas Chromatography-Mass Spectrometry]. Zdravookhraneniye i meditsinskiye tekhnologii, (5), 20–23.
      13. Kinross J., von Roon A. C., Penney N. et al. The gut microbiota as a target for improved surgical outcome and improved patient care // Curr. Pharm. Des., 2009, 15(13), pp. 1537–1545.
      14. Fedosova, N.F., Liadov, K.V., Osipov, G.A. (2010). Novyye podkhody k analizu infektsionnykh posleoperatsionnykh i posttravmaticheskikh oslozhnenii [New approaches to the analysis of infectious postoperative and post-traumatic complications]. Infektsii v khirurgii, 8(2), 56–62.
      15. Andreitseva, O.I., Kiselev, V.V., Boiko, N.B. [i soavt.] (2010). Mikroekologicheskii status kandidatov na peresadku pecheni [Microecological status of candidates for liver transplantation]. Transplantologiia, (3).
      16. Luckey T. D. Overview of gastrointestinal microecology // Nahrung, 1987, vol. 31, № 5–6, pp. 359–364.
      17. Suau A., Bonnet R., Sutren M. et al. Direct analysis of genes encoding 16S rRNA from complex communities reveals many novel molecular species within the human gut // Appl. Environ. Microbiol., 1999, vol. 65, № 11 pp. 4799–4807.
      18. Veiant, R., Moss, U., Khollis, D. [i soavt.] (1999). Opredelitel' netrivial'nykh patogennykh gramotritsatel'nykh bakterii [The determinant of non-trivial pathogenic gram-negative bacteria]. Moskva: Mir. 612–783.
      19. Osipov, G.A., Demina, A.M. (1996). Khromato-mass-spektrometricheskoye obnaruzheniye mikroorganizmov v anaerobnykh infektsionnykh protsessakh [Chromato-mass-spectrometric detection of microorganisms in anaerobic infectious processes]. Vestnik RAMN, 13(2), 52–59.
      20. White D. C. Validation of quantitative analysis for microbial biomass, community structure, and metabolic activity // Adv. Limnol., 1988, № 31, pp. 1–18.
      21. Konev, Iu.V. [i soavt.] (2001). [Dysbiosis in elderly and senile age]. Klinicheskaia gerontologiia, (9), 7–12.
      22. Lazebnik, L.B., Drozdov, V.N. (2003). Zabolevaniia organov pishchevareniia u pozhilykh [Diseases of the digestive system in the elderly]. Moskva: Anakharsis.
      23. Shenderov, B.A. (1998). Meditsinskaia mikrobnaia ekologiia i funktsional'noye pitaniye. Sotsial'no-ekologicheskiye i klinicheskiye posledstviia disbalansa mikrobnoi ekologii cheloveka i zhivotnykh [Medical microbial ecology and functional nutrition. socio-ecological and clinical consequences of imbalance of microbial ecology of humans and animals]. Moskva: GRANTIE, 2.
      24. Dubinin, A.V., Babin, V.N. (1991). Troficheskiye, reguliatornyye sviazi kishechnoi mikroflory i makroorganizma [Trophic, regulatory connections of the intestinal microflora and macroorganism]. Klinicheskaia meditsina, (7), 24–31.
     


    Full text is published :
    Rodionov G. G., Shantyr I. I., Kolobova E. A., Svetkina E. V. FEATURES OF THE PARIETAL INTESTINAL MICROBIOTA OF THE ELDERLY MEN OF SAINT-PETERSBURG. Experimental and Clinical Gastroenterology Journal. 2018;153(05):66-72
    Read & Download full text

    1. Federal research center “Krasnoyarsk scientific center” Siberian branch of the Russian Academy of Sciences Research Institute of Medical Problems of the North (Krasnoyarsk, Russian Federation)
    2. Krasnoyarsk regional clinical cancer center named. A. I. Kryzhanovsky (Krasnoyarsk, Russian Federation)

    Keywords:neutrophilic granulocytes; chemiluminescence; rectal cancer

    Abstract:The purpose of our work is to study the spontaneous and induced chemiluminescent activity of neutrophilic granulocytes (NG) in patients with rectal cancer in dynamics. Materials and methods. The study included 56 patients with rectal cancer. At the first stage there were 9 people, in the II stage 19 people, on the III 17 and at the IV stage 11 patients. The object of study are neutrophilic granulocytes isolated from venous blood. The control group consisted of 112 healthy blood donors. The intensity of synthesis of active oxygen species of NG was determined by the method of chemiluminescence analysis. Results. The study showed a significant increase in the intensity of spontaneous and induced luminescence and the area under the curve of spontaneous chemiluminescence in the II-IV stages of the disease. When studying zymosan-induced chemiluminescence, the area under the curve is increased in all groups of patients, while in patients at stage IV the total production of reactive oxygen species (ROS) is significantly higher than in stages I and II. On the 7th day after the surgical treatment, the intensity of spontaneous chemiluminescence remains elevated only in patients at the IV stage of the rectal cancer. The intensity of induced chemiluminescence and the area under the curve of spontaneous and induced luminescence are increased at all stages of the disease with respect to control. The activation index was increased in patients at all stages of with rectal cancer both before and after surgery. Сonclusion. As a result of the study, an increase in the intensity of ROS synthesis in patients with rectal cancer was revealed. The total production of reactive oxygen species is higher in the late stage of the disease. An increase in the activation index of neutrophils in all stages of the RPC characterizes the metabolic capabilities of neutrophils to the enhanced synthesis of ROS in functional activation.

      1. Гордеев С.С., Барсуков Ю. А., Ткачёв С. И. и соавт. Местнораспространенный рак прямой кишки (мррРПК): определение, классификация, современные методы лечения // Вестник московского онкологического общества. -2014, -№ 2 -с.2-6.
      2. Балканов А.С., Гуров А. Н., Катунцева Н. А., Белоусова Е. А. Заболеваемость раком прямой кишки населения Московской области в 2010-2014 гг // Альм клин мед. -2016. -№ 44 (5). -С. 599-605.
      3. Райков Н.С., Чупин Р.Н., Попов И. Н. и соавт. Рак прямой кишки // Тюменский медицинский журнал. -2010. -№ 3-4. - С. 75-77.
      4. Нестерова И.В., Ковалева С.В, Чудилова Г. А. и соавт. Двойственная роль нейтрофильных гранулоцитов в реализации противоопухолевой защиты // Иммунология. -2012. -№ 5. - С. 281-285.
      5. Мальцева В.Н., Сафронова В. Г. Неоднозначность роли нейтрофила в генезе опухоли // Цитология. -2009. -Т. 51, № 6. -С. 467-474.
      6. Fridlender Z.G., Albelda S. M. Tumor-associated neutrophils: frend or foe? // Carcinogenesis. -2012. -Vol.33, no. 5. -Р. 949-955.
      7. Finisguerra V., Di Conza G., Di Matteo M. et аl. MET is required for the recruitment of anti-tumoral neutrophils // Nature. -2015. -Vol. 522, no. 7556. -P. 349-353.
      8. Swierczak A., Mouchemore K. A., Hamilton J. A., Anderson R. L. Neutrophils: important contributors to tumor progression and metastasis // Cancer Metastasis Rev. - 2015. -Vol. 34(4), - Р.735-751.
      9. Грачева Т. А. Совершенствование хемилюминесцентного метода исследования функциональной активности фагоцитирующих клеток // Клиническая лабораторная диагностика. -2008. -№ 2. -С. 54-55.
      10. Di Carlo E., Forni G., Lollini P. L., Colomobo M. P. et al. The intriguing role of polymorphonuclear neutrophils in antitumor reactions // Blood. - 2001. -Vol. 97(2): - Р. 339-345.
      11. Кит О. И., Франциянц Е. М., Никипелова Е. А., Комарова Е. Ф. Состояние свободнорадикальных процессов в ткани злокачественной опухоли толстой кишки // Сиб. мед. обозрение. -2014. -№ 1. -С. 30-34
      12. Prestwich R.J., Errington F., Hatfield Р., Roodman D. G. The immune system - is it relevant to саnсеr development, progression and treatment? // Clin. Oncol. -2008. -Vol. 20. -Р. 101-112.
      13. Коленчукова О.А., Савченко А. А., Смирнова С. В. Особенности нейтрофильных гранулоцитов у больных хроническим риносинуситом // Медицинская Иммунология. -2010. -Т. 12, № 4-5. -С.385-390.
      14. Schins R.Р.F., Воrm Р. J.А., Van Schooten F.J Neutropihis and respiratory tract DNA damage and mutagenesis: а review // Mutagenesis. -2006. -Vol. 21. -Р. 225-236.
      15. Смирнова О.В., Манчук В. Т., Агилова Ю. Н. Особенности хемилюминесцентной активности нейтрофильных гранулоцитов у больных миеломной болезнью G-формы в зависимости от стадии заболевания // Медицинская иммунология. -2015. -T.17, № 6. -C. 579-584.
      16. Смирнова O.B., Титова Н. М., Елманова Н. Г. Особенности хемилюминисцентной активности нейтрофильных гранулоцитов больных механической желтухой доброкачественного генеза // Российский иммунологический журнал. -2015. T. 2(1) (18). -C. 313-315.
      17. Смирнова О. В., Манчук В. Т., Агилова Ю. Н. Роль неспецифического иммунитета при прогрессировании миеломной болезни // Современные проблемы науки и образования. -2014. -№ 2. -С.515.
     


    Full text is published :
    Smirnova O. V., Kasparov E. V., Perepechay Ya.I., Versenev A. A., Laletin I. A. THE FEATURES OF NONSPECIFIC IMMUNITY IN THE PROGRESSION OF COLORECTAL CANCER. Experimental and Clinical Gastroenterology Journal. 2018;153(05):73-77
    Read & Download full text

    1. Federal state budgetary institution “national medical and surgical Center. N. And. Pirogov” Ministry of health of the Russian Federation in Moscow (Moscow, Russian Federation)
    2. State budget educational institution of higher professional education “Moscow State medical and dental University. A. I. Evdokimov” (Moscow, Russian Federation)

    Keywords:Yersinia enterocolitica, infliximab, adalimumab, Crohn’s disease, immunosuppressive therapy, mesenchymal stromal bone marrow cells, ulcerative colitis

    Abstract:In patients with ulcerative colitis and Crohn’s disease long-term appointment of biological therapy in combination with GCS/CT increases the frequency of development of yersiniosis infection, which worsens the clinical course of the disease and increases the period of exacerbation. Yersiniosis in inflammatory bowel diseases (IBD), often accompanied by extra-intestinal manifestations of the disease (polyarthritis, erythema nodosa and uveitis). However, the question remains: is yersiniosis a cause of the development of an extra-intestinal manifestation or a sign of reactivation of opportunistic infections against the background of immunosuppressive therapy or an etiological factor of inflammatory bowel diseases? This issue requires further research. According to the literature with inflammatory bowel diseases among the extraintestinal manifestations predominate articular lesions to 42.7% [36]. Although yersiniosis plays a leading role in the pathogenesis of arthritis, clinical and diagnostic studies on yersiniosis were not carried out in IBD. Until now, there are no clear diagnostic and prognostic criteria for the development of adverse outcomes of yersiniosis, in connection with which clinicians do not conduct examinations for the presence of yersiniosis.

      1. Bockemuhl J., Wong J. Yersinia. In Murry P. R., Baron E. J., Jorgansen J. H., Pfaller M. A., Yolken R. H., editors. Manual of clinical microbiology. 8th ed. Wachington (DC): ASMPress; 2003.p.672-83
      2. Дробященко, М. А. Колонизация и размножение YersiniaenterocoliticaО9 в пищевых продуктах, изготовленных в современных технологических условиях / М. А. Дробященко, В. И. Пушкарева, Д. С. Юрьев, В. Ю. Поляков // Эпидемиология и вакцинопрофилактика. - 2010. - № 4 (53). - С. 51-56
      3. Bhaduri, Saumya. Prevalence of pathogenic Yersinia enterocoliticastrains in pigs in the United States / SaumyaBhaduri // Appl. Envirion. Microbiol. - 2005. - № 11 - Р. 7117-7121
      4. Смирнов И. В. Возбудитель иерсиниоза и близкие к нему микроорганизмы // Клин. Микробиолантимикробхимиотер. 2004. Том 6, № 1. С. 10-21.
      5. Иерсиниозы / Н. Д. Ющук, Г. Я. Ценева, Г. Н. Кареткина, Л. Е. Бродов. - М.: Медицина, 2003. - 208 с.
      6. Autenrieth L.B., Firsching R. Penetration of M cells and destruction of Peyer’s patches by Yersinia enterocolitica: an ultrastructural and histological study // J. Med. Microbiol. - 1996. -Vol. 44, № 4. - P.285-294.
      7. Цинзерлинг А. В., Цинзерлинг В. А. Современныеинфекции. Патологическая анатомия и вопросы патогенеза: Рук-во. - СПб: Сотис, 2002. -346 с.
      8. Currie B. Yersinia enterocolitica // Pediatr. Rev. - 1998. - Vol. 19, № 7. - P.250-251.
      9. Бродов Л. Е., Ющук Н. Д., Кареткина Г. Н. и др. Трудности дифференциальной диагностики между рядом инфекционных заболеваний и пищевымитоксикоинфекциями // Клин, медицина. - 1989. - № 7. - С. 131-135
      10. Кареткина Г. Н., Ющук Н. Д., Бродов Л. Е. и др. Клиника и диагностика гастроинтестинальной и абдоминальной формы иерсиниоза // Клин, медицина.-1986.-№ 8. С. 136-139.
      11. Юшук Н. Д., Кузнецов В. Ф., Кареткина Г. Н. и др. Иерсиниоз: Метод, рекомендации. - М.: МЗ РФ, ВНУМЦ,1995. - 20 с.
      12. Кареткина Г. Н., Ющук Н. Д., Бродов Л. Е. и др. Диагностика и лечение генерализованной формы иерсиниоза // Клин, медицина. - 1987. - № 8. -С. 102-105.
      13. Boelaert J. R., van Landuyt H. W., Valcke Y. J. et al. The role of iron overload in Yersinia enterocolitica and Yersinia pseudotuberculosis bacteremia in hemodialysis patients // J. Infect. Dis. - 1987. - Vol.156, № 2. - P. 384-387.
      14. Cauchie P., Vincken W., Peeters O., Charels K. Hemochromatosis and Yersinia enterocolitica septicemia // Dig. Dis. Sci. - 1987. - Vol. 32, № 12. - P. 1438.
      15. Roggencamp A., Ruckdeschel K., Leitritz L. et al. Deletin of amino acids 29 to 81 in adhrsion protein YadA of Yersinia enterocolitica serotype 0:8 results in selective abrogation of adherence to neutrophils // Infect. Immun. - 1996. - Vol. 56.-P. 2506-2514.
      16. Инина Л. И., Иванова М. М., Акимова Р. Т. и др. Клинико-иммунологическая характеристика осложненного и неосложненного иерсиниоза //Вестник АМН CGGP. - 1989. - № 6. - С. 60-65.
      17. Попова О. В. Особенности иммунного ответа при различных формах иерсиниоза: Автореф. дисс… канд. мед.наук. - М., 2006. - 26 с.
      18. Gaston J. S., Lillicrap M. S. Artritis associated with enteric infection //Best Pract. Res. Clin. Rheumatol. - 2003. - Vol. 17. - P. 219-239.
      19. Kvien Т. К., Glennas A., Melby K. et al. Reactive arthritis: incidence, triggering agents and clinical presentation // J. Rheumatol. - 1994. - Vol. 21.-P. 115-122.
      20. Spieper J., Braun J. Reactive arthritis // Curr. Opin.Rheumol. - 1999. -№ 11.-238-243.
      21. Colmegna L, Cuchacovich R., Espinoza L. R. HLA-B27-associated reactive arthritis: Pathogenetic and clinical considerations // Clin. Microbiol.Rev. -2004. - Vol. 17, № 2. - P. 348-369.
      22. Gerard H. C., Branigan P. J., Schumacher H. R., Hudson A. P. Synovial Chlamydia trachomatis in patients with reactive arthritis / Reiters syndrome are viable but show aberrant gene expression // J. Rheumatol. - 1998. - Vol. 25. - P. 734-742.
      23. Granfors K., Merilahti-Palo R., Luukkainen R. et al. Persistence of Yersinia antigens in peripheral blood cells from patients with Yersinia enterocolitica 0:3 infection with or without reactive arthritis. // Arthr. and Rheum. - 1998. - Vol. 41. - P. 855.
      24. Toivanen P. From reactive arthritis to rheumatoid arthritis // J. Autoimmun. -2001. - Vol. 16. - P. 369-371.
      25. Meyer-Bahlburg A., Brinkhoff J., Krenn V. et al: Infection of synovial fibroblasts in culture by Yersinia enterocolitica and Samonella enteric serovarenteritidis: ultrastructural investigation with respect to the pathogenesis of reactive arthritis // Infect. And Immun. - 2001. - Vol. 69. - P. 7015-7921
      26. Ющук Н. Д., Кареткина Г. Н. Иерсиниоз как хирургическая проблема // Хирургия. - М., 1999. - № 1 2. - С. 50-52.
      27. Heesemann J., Gaede K., Autenrieth L.B. Experimental Yersinia enterocolitica infection in rodents: a model for human yersiniosis // APMIS. - 1993. -Vol. 101, № 6. - P. 417-429.
      28. Стебунова Т. К. Дифференциальная диагностика и терапия затяжных рецидивирующих форм псевдотуберкулеза у детей: Автореф. дисс. канд. мед.наук. - СПб, 2003. - 24 с.
      29. Учайкин В. Ф. и др. Иерсиниозы у детей / В. Ф. Учайкин, А. В. Гордец, С. Н. Бениова. - М.: ГЭОТАР-Медиа, 2005. - 144 с.
      30. Ющук Н. Д., Шестакова И. В., Шепелева Г. К., Ценева Г. Я., Андреев И. В. К вопросу о формировании иммунопатологии у больных с хроническим течением иерсиниозной инфекции. Сборник докладов. Тезисы V1 Российского съезда инфекционистов. СПб 2003.
      31. Ющук Н. Д., Шестакова И. В., Балмасова И. П. Клинико-прогностические критерии различных форм и вариантов течения иерсиниозной инфекции. Терарх 2009; 81: 11: 44-48.
      32. O’Connor S.M., Taylor Ch.E., Yughes J. M. Emerging infections determinantsof chronic diseases. EmergInfectDis 2006; 12: 7: 1051-1057.
      33. Сафронова А. Н. Микробиологические и экологические особенности штаммов иерсиний, циркулирующих на территории Якутии // Диссер. на соискание ученой степени к. м. н. 2014 г. стр 123.
      34. Шестакова И. В. Иерсиниоз: расширяя традиционные представления о диагностике, лечении и диспансеризации больных / И. В. Шестакова, Н. Д. Ющук // Лечащий врач. - 2010. - № 10. - С. 26.
      35. Ющук Н. Д. Особенности течения и отдаленные исходы генерализованной и вторично-очаговой формы иерсиниозной инфекции больных / Н. Д. Ющук, И. В. Шестакова // Лечащий врач. - 2009. - № 11. - С. 82-86.
      36. Внекишечные проявления неспецифического язвенного колита / Евдокимова Е. Ю. [и др.] //Бюллетень ВСНЦ СО РАМН. - 2005. - № 4 (42). - С. 71.
     


    Full text is published :
    Sagynbaeva V. E., Golovanova E. V., Lazebnik L. B., Fighters S. A. YERSINIOSIS - THE REASON FOR THE DEVELOPMENT OF EXTRAINTESTINAL INFLAMMATORY BOWEL DISEASE, OR SYMPTOM OF REACTIVATION OF OPPORTUNISTIC INFECTIONS AGAINST THE BACKGROUND OF BIOLOGICAL THERAPY?. Experimental and Clinical Gastroenterology Journal. 2018;153(05):78-85
    Read & Download full text

    1. State budgetary institution of high professional education “Moscow State University of Medicine and Dentistry named after A. I. Evdokimov” of the Ministry of Healthcare of the Russian Federation, Department of outpatient therapy (Moscow, Russian Federation)

    Keywords:diverticular disease of the colon conservative therapy, antispasmodics, probiotics, intestinal antiseptics, butyrat

    Abstract:The article presents the results of long-term monitoring of patients diverticular disease of the colon to study the effectiveness of different groups of medicines on the basis of which the proposed rational scheme of treatment according to age of patients, duration of anamnesis of disease and presence of comorbidities. In the period 2003-2016 the study included 396 patients aged 24 to 89 years (mean age 61,4±9.3 years) with instrumental confirmed diverticula of the colon. A big problem in the elderly is polymorbidity and, as a result, forced polypragmasia. In our study of 295 patients over 60 years of age at the time of inclusion in the study had 4.7-5.2 diseases per 1 person. The most common were systemic atherosclerosis, constipation and hyperlipidemia. Constipation was detected in 193 patients (65.4%), hyperlipidemia - in 170 (57.6%). Drugs psillium and lactulose have long been widely known as effective laxatives with prebiotic properties and safe with long-term use. In our study, 120 patients took psyllium and 116-lactulose. For two years, we estimated the number of relapses of NSC (resumption of pain and symptoms of intestinal dyspepsia). It was found that in the psyllium group during the two-year follow-up period the number of recurrences was 20% less than in the lactulose group. Summary. The most effective drug for relief of abdominal pain syndrome in patients with diverticular disease of the colon in all age groups is trimebutin In the treatment of symptomatic diverticular disease of the colon in patients younger than 45 years, it is advisable to prescribe intestinal antiseptics (rifaximin, nifuroxazide) for at least 7 days from the moment of treatment. Patients over 75 years of age need normalization of the stool with the predominant use of laxatives with prebiotic action. When combined with diverticular disease and constipation hyperlipidemia drug of choice is psyllium (mukofalk, vibrolux). At presence at patients of senile age concomitant cardiovascular pathology with the purpose of correction of possible ischemia of the bowel wall at the microscopic level should be provided citoprotected drug of butyric acid.

      1. Kang J.Y., Firwana B., Green A. E. et al. Uncomplicated diverticular disease is not a common cause of colonic symptoms. Aliment.Pham.Ther., 2011, Vol.33(4), P. 487-494
      2. Tursi A, Papa A, Danese S. Review article: the pathophysiology and medical management of diverticulosis and diverticular disease of the colon. Aliment Pharmacol Ther 2015; 42: 664-684
      3. Viniol A, Keunecke C, Biroga T, Stadje R, Dornieden K, Bösner S, Donner-Banzhoff N, Haasenritter J, Becker A Studies of the symptom abdominal pain-a systematic review and meta-analysis. Fam Pract. 2014 Oct;31(5):517-29. doi: 10.1093/fampra/cmu036.
      4. Bevan R, Lee T.J, Nickerson C, Rubin G, Rees C.J; NHS BCSP Evaluation Group. Non-neoplastic findings at colonoscopy after positive faecal occult blood testing: data from the English Bowel Cancer Screening Programme. J Med Screen 2014; 21: 8994.
      5. Kliniko-morfologicheskie varianty divertikulyarnoj bolezni tolstoj kishki. Levchenko S. V., Lazebnik L. B., Potapova V. B., Rogozina V. A. Eksperimental’naya i klinicheskaya gastroehnterologiya 2013 № 3:23–30
      6. Strate L.L, Modi R, Cohen E, Spiegel B.M. Diverticular disease as a chronic illness: evolving epidemiologic and clinical insights. Am J Gastroenterol 2012; 107: 1486-1493
      7. Morris A.M, Regenbogen S.E, Hardiman K.M, Hendren S Sigmoid diverticulitis: a systematic review. JAMA. 2014 Jan 15;311(3):287-97. doi: 10.1001/jama.2013.282025
      8. Spiller R. Is it diverticular disease or is it irritable bowel syndrome? Dig Dis 2012; 30: 64-69
      9. Cuomo R, Barbara G, Andreozzi P, Bassotti G, Casetti T, Grassini M, Ierardi E, Maconi G, Marchi S, Sarnelli G, Savarino V, Usai P, Vozzella L, Annibale B. Symptom patterns can distinguish diverticular disease from irritable bowel syndrome. Eur J Clin Invest 2013; 43: 1147-1155.
      10. Tursi A. Diverticulosis today: unfashionable and still under-researched. Therap Adv Gastroenterol 2016; 9: 213-228
      11. Ford A.C., Talley N. J., Spiegel B. M. et al. Effect of fiber, antispasmodics and peppermint oil in the treatment of irritable bowel syndrome: systematic review and metaanalysis. BMJ, 2008, Now, 337 doi: https://doi.org/10.1136/bmj.a2313
      12. Shepberd N.A Diverticular disease in chronic idiopathic inflammatory bowel disease: associations and masquerades Gut 1996; 38:801-2.
      13. Lamps L.W, Knapple W.L. Diverticular disease-associated segmental colitis. Clin Gastroenterol Hepatol 2007;5:27-31]
      14. Levchenko S. V., Gudkova R. B., Potapova V. B., Lazebnik L. B. Reakciya immunokompetentnyh kletok i strukturnye izmeneniya slizistoj obolochki tolstoj kishki u bol’nyh divertikulyarnoj bolezn’yu // EHksperim. i klinich. gastroehnterol. 2009, – № 5. – S. 17–20
      15. Minushkin O. N., Kruchinina M. A. Sindrom izbytochnogo bakterial’nogo rosta u bol’nyh divertikulyarnoj bolezn’yu tolstoj kishki. Kremlevskaya medicina. 2014,1:99–104
      16. Popova E. V. Narushenie sostava kishechnoj mikroflory v mekhanizmah formirovaniya kliniko-morfologicheskih proyavlenij u bol’nyh divertikulyarnoj bolezn’yu tolstoj kishki. Diss. k. m.n., 2012,121 str
      17. Komissarenko I. A., Levchenko S. V., Gudkova R. B., Sil’vestrova S. Yu. Effekty dlitel’nogo primeneniya psilliuma pri lechenii bol’nyh s divertikulyarnoj bolezn’yu tolstoj kishki. // KPGG, 2014:3: 29–36
      18. Strate L.L., Liu Y. L., Aldoori W. H. et al. Obesity increases the risks of diverticulitis and diverticular bleeding, Gastroenterol., 2009, 136(1), P. 115-22
      19. Kopylov U, Ben-Horin S, Lahat A, Segev S. Obesity, metabolic syndrome and the risk of development of colonic diverticulosis, Digestion 2012;86(3):201-5
      20. Levchenko S. V., Lazebnik L. B., Potapova V. B., Rogozina V. A. Kliniko-morfologicheskie varianty divertikulyarnoj bolezni tolstoj kishki. Eksperimental’naya i klinicheskaya gastroehnterologiya 2013 № 3:23–20
      21. Krokowicz L., Stojcev Z, Kaczmarek B.F, Kociemba W, Kaczmarek E, Walkowiak J, Krokowicz P, Drews M, Banasiewicz T. Microencapsulated sodium butyrate administered to patients with diverticulosis decreases incidence of diverticulitis - a prospective randomized study. Int J Colorectal Dis. 2014 Mar;29(3):387-93. doi: 10.1007/s00384-013-1807-5
     


    Full text is published :
    Boytsov S. A., Lazebnik L. B., Levchenko S. V., Komissarenko I. A. RATIONAL PHARMACOTHERAPY OF THE SYMPTOMATIC UNCOMPLICATED COLON DIVERTICULAR DISEASE. Experimental and Clinical Gastroenterology Journal. 2018;153(05):86-92
    Read & Download full text

    1. Yaroslavl Regional Oncology Hospital (Yaroslavl, Russian Federation)
    2. Yaroslavl State Medical University (Yaroslavl, Russian Federation)

    Keywords:colonoscopy, preparation, mathematical model

    Abstract:The aim. Assess the possibility of successful colon preparation for colonoscopy on the basis of a multidimensional mathematical model with a predictive effect. Materials and methods: 105 patients who were preparing for colonoscopy with PEG in two versions. An assessment of the quality of colon cleansing according to the Boston scale was carried out. Results: Significant factors distinguishing groups with adequate and inadequate preparation of the colon from each other were identified. Realization of the probability of separation of “adequate” and “inadequate preparation” was found only by 10 factors: gender and patient education, which specialist is he directed to research, time between the end the colon preparation and the beginning of a colonoscopy, compliance with recommendations on diet and receive extra fluid in preparation for colonoscopy, patient’s violation of instructions for the administration of PEG; diabetes, constipation and history of abdominal surgery. The predictive power of the model was 83.8%. Four managed factors were established. The sensitivity of the model was 67.9%, specificity 90.5%, confidence interval from 0.76 to 0.90. The area under the curve was 0.84

      1. Kashin S. V., Zav’yalov D.V., Nekhajkova N. V., Sorogin S. A., Belova A. N. Aktual’nye voprosy povysheniya kachestva kolonoskopii, vypolnyaemoj s cel’yu skrininga polipov i kolorektal’nogo raka. Klinicheskaya ehndoskopiya. 2016; 1(47):3–18.
      2. Kashin S. V., Nekhajkova N. V., Vidyaeva N. S., Belova A. N. Osnovnye polozheniya rekomendacij Evropejskogo obshchestva gastrointestinal’noj ehndoskopii po podgotovke tolstoj kishki k skriningovoj kolonoskopii. Dokazatel’naya gastroehnterologiya. 2017;6(3):36–50 DOI: 10.17116/dokgastro20176336–50
      3. Zav’yalov D.V., Kashin S. V. Propushchennye neoplazii tolstoj kishki. Koloproktologiya. 2015; 1 (51):32–37.
      4. Kazarian E.S, Carreira F.S, Toribara N.W, Denberg T. D. Colonoscopy completion in a large safety net health care system. // Clin Gastroenterol Hepatol. 2008 Apr;6(4):438–42. doi: 10.1016/j.cgh.2007.12.003.
      5. Calderwood A.H., Jacobson B. C. Comprehensive validation of the Boston Bowel Preparation Scale. // Gastrointest Endosc. 2011;72:686–692.
      6. Hassan C, Fuccio L, Bruno M. A. Predictive model identifies patients most likely to have inadequate bowel preparation for colonoscopy. // Clin Gastroenterol Hepatol 2012; 10: 501–506. DOI: http://dx.doi.org/10.1016/j.cgh.2011.12.037
      7. Dik V.K, Moons L.M, Huyuk M. Predicting inadequate bowel preparation for colonoscopy in participants receiving split-dose bowel preparation: development and validation of a prediction score. // Gastrointest Endosc 2015; 81: 665-672. DOI 10.1016/j.gie.2014.09.066
      8. Gimeno-García A.Z., Baute J. L., Hernandez G., Morales D, Gonzalez-Pérez C.D., Nicolás-Pérez D., Alarcon-Fernández O, Jiménez A, Hernandez-Guerra M, Romero R, Alonso I, Gonzalez Y, Adrian Z, Carrillo M, Ramos L, Quintero E. Risk factors for inadequate bowel preparation: a validated predictive score. // Endoscopy. 2017 Jun;49(6):536-543. doi: 10.1055/s-0043-101683.
      9. Veselov V. V., Nikiforov P. A., Fedorov E. D. Klinicheskie rekomendacii po podgotovke pacientov k ehndoskopicheskomu issledovaniyu tolstoj kishki. 2017. Moskva. 78 p
      10. Chan W.K, Saravanan A, Manikam J, Goh K.L, Mahadeva S. Appointment waiting times and education level influence the quality of bowel preparation in adult patient undergoing colonoscopy. // BMC Gastroenterol. 2011 Jul 28;11:86. doi: 10.1186/1471–230X-11–86.
     


    Full text is published :
    Zavyalov D.V., Kashin S.V., Vidyaeva N.S., Sorogin S.A., Shubin L.B. PREPARING FOR A COLONOSCOPY AND THE SOLUTION OF PROBLEM ITS INADEQUACY. Experimental and Clinical Gastroenterology Journal. 2018;153(05):93-97
    Read & Download full text

    1. Federal State Budget Scientific Institution “Institute of Experimental Medicine” (St. Petersburg, Russian Federation)

    Keywords:circadian rhythm, regularity, defecation, intestinal habit, constipation

    Abstract:A new chronobiological strategy for the treatment of patients with constipation is presented. There are four main aspects of this strategy: physiological, pathological, general biological and therapeutic. The physiological aspect of the chronobiological strategy is the need for a fundamentally new approach to determining and understanding the natural daily rhythm of defecation. Defecation is one of the fundamental circadian (every day) biorhythms, whose normal frequency is regular and is at least 7 times a week. The pathological aspect presupposes a new definition of constipation as a violation of the circadian rhythm of defecation. Three stages of severity of constipation are suggested: mild - with a stool frequency of 5-6 times a week, moderate - 3-4 times a week, severe - with a stool frequency 1-2 times a week. The regular dependence of the regularity of the rhythm of defecation on the moment of realization of this rhythm is established. Regular bowel movement is associated with the morning bowel movement, and irregular defecation is associated with the absence of the morning phase of defecation. It is emphasized that the main factor in restoring the regularity of the rhythm of defecation is a conscious correction of the way of life to restore the daily bowel habit to morning defecation. The therapeutic aspect of the problem of constipation is based on the personal account of the whole complex of factors that lead to defecation irregularity and the need to use the most effective and safe drugs that have a degree of evidence of 1A.

      1. Lazebnik L. B. Metabolic syndrome and organs digestion / L. B. Lazebnik, L. A. Zvenigorodskaya. – M.: Anaharsis, 2009. – 184 p.
      2. Leung L1, Riutta T, Kotecha J, Rosser W. Chronic constipation: an evidence-based review. J. Am Board Fam Med. 2011 Jul-Aug;24(4):436–51.
      3. Shemerovsky K. A. Constipation is a risk factor of colorectal cancer. Clinical medicine. 2005, No. 2, P. 60–64.
      4. Shemerovsky K. A. From the evidence farmcoterapies through chronomedicine to preventive medicine / K. A. Shemerovsky // New St. Petersburg medical records. – 2008. – No. 1. – P. 29–35.
      5. Maev I. V., Samsonov A. A. Syndrome of chronic constipation – M.: GOU VUNMTS MOH & SD of the Russian Federation, 2005. – 96 p.
      6. Rozen P, Young G. P., Levin B., Spann S. J. Colorectal Cancer in Clinical Practice. Martin Dunitz, 2002, – 136.
      7. Talley N.J., Lasch K.L, Baum C. L. A gap in our understanding: chronic constipation and its comorbid conditions.Clin Gastroenterol Hepatol. 2009 Jan;7(1):9–19.
      8. Honkura K, Tomata Y, Sugiyama K, et al. Defecation frequency and cardiovascular disease mortality in Japan: The Ohsaki cohort study. Atherosclerosis. 2016; 246: 251–256.
      9. Tack J, Muller-Lissner S. Лечение хронического запора: современная медикаментозная терапия и ее перспективы // Клиническая гастроэнтерология и гепатология. Русское издание. – 2009, Т. 2, № 6, С. 438–445.
      10. Ivashkin V. T., S. A. Alekseenko, T. A. Kolesova, N. V. Korochanskaya, E. A. Poluektova, V. I. Simanenkov, A. V. Tkachev, A. S. Trukhmanov, Khlynov I. B., Sheptulin A. A., O. S. Shifrin. Expert-Council resolution devoted to the problems of diagnostics and treatment of functional diseases of the gastrointestinal tract. RJGHC2016; 26(4), P. 129–130.
      11. Bollinger T, Schilber U. Circadian rhythms – from genes to physiology and disease. Swiss Med Wkly. 2014 Jul 24, 144–155.
      12. Zimmerman Ya. S. Clinical gastroenterology. 2009, GEOTAR-Media, 416 p.
      13. Shemerovskii K. A. Chronoenterography: monitoring of circadian rhythm of the intestinal evacuatory function. // Bull Exp Biol Med. 2002 May; 133(5): P. 582–584.
      14. Shemerovsky K. A. The dependence of the quality of health from the regularity of the evacuation function of the intestine // Clinical pathophysiology. – 2007 – № 1–2, P. 64–66.
      15. Shemerovsky K. A., Mithracin V. F., Uspenskaya Yu. K. Dependence of the level of medication on regularity of the circadian rhythm of the intestine // Bulletin of the Russian Military medical Academy. – 2012, № 1(37), P. 112–115.
      16. Ugolev A. M. Evolution of digestion and principles of the evolution of functions. 1985, L. Nauka, P. 223–257.
      17. Halberg F, Watanabe H. Cronobiology and Chronomedicine – Tokyo.; Medical Review, 1992, 297 p.
      18. Рапопорт С.И., Фролов В. А., Хетагурова Л. Г. Хронобиология и хрономедицина. Руководство. М. Медицинское информационное агенство. 2012, 480 с.
      19. Rapoport S. I., Frolov V. A., Khetagurova L. G. Chronobiology and chronomedicine. Guide. M. Medical news Agency. 2012, 480 p.
      20. Shemerovsky K. A., Ovsyannikov V. I., Nguyen H. H, Uspenskaya, Y. K., V. F. Mithracin. Levels of quality of life of medical students with regular and irregularlar rectal rhythm. Pediatrician, 2013. Vol. 4, No. 2, Pp. 65–69.
      21. Drossman DA. Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features and Rome IV. Gastroenterology. 2016 Feb 19. pii: S0016–5085(16)00223–7. doi: 10.1053/j.gastro.2016.02.032. [Epub ahead of print]
      22. Drossman DA, Hasler WL. Rome IV-Functional GI Disorders: Disorders of Gut-Brain Interaction. Gastroenterology. 2016 May;150(6):1257–61.
      23. Schmulson MJ, Drossman DA. What Is New in Rome IV. J Neurogastroenterol Motil. 2017 Apr 30;23(2):151–163.
      24. Shemerovsky K. A. Chronophysiological risk factor of constipation / Shemerovsky K. A. // Russian journal of Gastroenterology, Hepatology, Coloproctology. – 2000. – Vol. 10, No. 3. – P. 84–87.
      25. Shemerovsky K. A. Chronomedical approach to the therapy of constipation. New St. Petersburg medical records. 2012, no. 1, Pp. 92–94.
      26. Ткаченко Е.И., Успенский Ю. П. Питание, микробиоценоз и интеллект человека. Санкт-Петербург, СпецЛит, 2006, 590 с.
      27. Thaiss CA, Zeevi D, Levy M, et al. A day in the life of the meta-organism: diurnal rhythms of the intestinal microbiome and its host. Gut Microbes. 2015;6(2):137–42.
      28. Климов А.Н., Никульчева Н. Г. Липиды, липопротеиды и атеросклероз.Вопросы медицинской химии. 1997. Т. 43. № 1. С. 58.
      29. Клинические рекомендации. Стандарты ведения больных. Выпуск 2. – М.: ГЭОТАР-Медиа, 2008. – 1376 с.
     


    Full text is published :
    Shemerovsky K. A. CHRONOBIOLOGICAL STRATEGY FOR TREATMENT OF PATIENTS WITH CONSTIPATIONS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):98-103
    Read & Download full text

    1. Russian Medical Academy of Continuous Professional Education (Moscow, Russian Federation)
    2. State Scientific Centre of Coloproctology (Moscow, Russian Federation)
    3. NRC Institute of Immunology FMBA of Russia (Moscow, Russian Federation)

    Keywords:ulcerative colitis, Crohn’s disease, microbiome

    Abstract:The review deals modern ideas about state of microbiome in healthy people and its change in inflammatory bowel disease.

      1. Atlas. Vospalitel’nye zabolevaniya kishechnika: diagnostika i lechenie / pod red. prof. Halifa I. L., chlen-korr. RAN Shelygina YU.A. SPb: Gippokrat. - 2017. - 116 S.
      2. Loranskaya I.D., Boldyreva M. N., Lavrent’eva O. A. Sostav mukoznoj mikroflory zheludochno-kishechnogo trakta pri sindrome razdrazhennogo kishechnika. Eksperimental’naya i klinicheskaya gastroehnterologiya. - 2013. - № 3. - S. 15-22.
      3. Pristenochnaya mikroflora kishechnika // I. D. Loranskaya i dr. - M.: Prima Print, 2015. - 100 S.
      4. Chaplin A.V., Rebrikov D. V., Boldyreva M. N. Mikrobiom cheloveka // VESTNIK RGMU. - 2017. - № 2. - S. 5-13.
      5. Al-Mofarreh M.A., Al-Mofleh I. A. Emerging inflammatory bowel disease in Saudi outpatients: a report of 693 cases // Saudi J Gastroenterol. - 2013. - № 19. - Р.16-22.
      6. Ananthakrishnan A. N. Epidemiology and risk factors for IBD // Nat Rev Gastroenterol Hepatol. - 2015. - № 12. - Р. 205-17.
      7. Biasco G., Zannoni U., Paganelli G. M. et al. Folic acid supplementation and cell kinetics of rectal mucosa in patients with ulcerative colitis // Cancer Epidemiol. Biomarkers Prev. - 1997. - № 6. - Р.469-471.
      8. Cho J.H., Brant S. R. Recent insights into the genetics of inflammatory bowel disease // Gastroenterology. - 2011. - № 140. - Р.1704-12.
      9. Clemente J.C., Ursell L. K., Parfrey L. W. et al. The impact of the gut microbiota on human health: an integrative view // Cell. - 2012. - № 148. - Р. 1258-70.
      10. Darfeuille-Michaud A., Boudeau J., Bulois P. et al. High prevalence of adherent-invasive Escherichia coli associated with ileal mucosa in Crohn’s disease // Gastroenterology. - 2004. - № 127. - Р.412-421.
      11. Devkota S., Wang Y., Musch M. W. et al. Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il10-/- mice // Nature. - 2012. - № 487(7405). - Р.104-8.
      12. Fanaro S., Chierici R., Guerrini P. et al. Intestinal microflora in early infancy: composition and development // Acta pediat. - 2003. - V. 91(441). - P. 48-55.
      13. Flint H.J., Bayer E. A., Rincon M. T. et al. Polysaccharide utilization by gut bacteria: potential for new insights from genomic analysis // Nat. Rev. Microbiol. - 2008. - № 6. - Р.121-131.
      14. Floch M. H. Intestinal microecology in health and wellness // J Clin Gastroenterol. - 2011. - № 45. - Р.108-10.
      15. Frank D.N., Amand A. L. St, Feldman R. A. et al. Molecular-phylogenetic characterization of microbial community imbalances in human inflammatory bowel diseases // Proc. Natl. Acad. Sci. U.S.A. - 2007. - № 104. - P. 13780-13785.
      16. Frick J.S., Autenrieth I. B. The gut microflora and its variety of roles in health and disease // Curr Top Microbiol Immunol. - 2013. - № 358. - Р.273-89.
      17. Garrett W.S., Gallini C. A., Yatsunenko T. et al. Enterobacteriaceae act in concert with the gut microbiota to induce spontaneous and maternally transmitted colitis // Cell Host Microbe. - 2010. - № 8. - Р.292-300.
      18. Geddes K., Rubino S., Streutker C., et al. Nod1 and Nod2 regulation of inflammation in the Salmonella colitis model // Infect. Immun. - 2010. - № 78. - Р.5107-5115.
      19. Hugot J.P., Chamaillard M., Zouali H. et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease // Nature. - 2001. - № 411. - Р.599-603.
      20. Kang S., Denman S. E., Morrison M. et al. Dysbiosis of fecal microbiota in Crohn’s disease patients as revealed by a custom phylogenetic microarray // Inflamm. Bowel Dis. - 2010. - № 16. - P. 2034-2042.
      21. Khor B., Gardet A., Xavier R. J. Genetics and pathogenesis of inflammatory bowel disease // Nature. - 2011. - № 474. - Р. 307-17.
      22. Lopez-Siles M., Khan T. M., Duncan S. H. et al. Cultured representatives of two major phylogroups of human colonic Faecalibacterium prausnitzii can utilize pectin, uronic acids, and host-derived substrates for growth // Appl. Environ. Microbiol. - 2012. - № 78. - Р.420-428.
      23. Machiels K., Joossens M., Sabino J. et al. A decrease of the butyrate-producing species Roseburia hominis and Faecalibacterium prausnitzii defines dysbiosis in patients with ulcerative colitis // Gut. - 2014. - № 63. - Р.1275-1283.
      24. Man S.M., Kaakoush N. O., Leach S. T. et al. Host attachment, invasion, and stimulation of proinflammatory cytokines by Campylobacter concisus and other non-Campylobacter jejuni Campylobacter species // J. Infect. Dis. - 2010. - № 202. - Р.1855-1865.
      25. Martinez-Medina M., Garcia-Gil L. J. Escherichia coli in chronic inflammatory bowel diseases: An update on adherent invasive Escherichia coli pathogenicity // World J Gastrointest Pathophysiol. - 2014. - № 5(3). - Р.213-27.
      26. Mazmanian S. K., Round J. L., Kasper D. L. A microbial symbiosis factor prevents intestinal inflammatory disease // Nature. - 2008. - № 453. - Р.620-625.
      27. Morgan X.C., Tickle T. L., Sokol H. et al. Dysfunction of the intestinal microbiome in inflammatory bowel disease and treatment // Genome Biol. - 2012. - № 13. - R79.
      28. Mukhopadhya I., Hansen R., El-Omar E.M. et al. IBD-what role do Proteobacteria play? // Nat. Rev. Gastroenterol. Hepatol. - 2012. - № 9. - Р.219-230.
      29. Muyzer G., Stams A. J. The ecology and biotechnology of sulphate-reducing bacteria // Nat. Rev. Microbiol. - 2008. - № 6. - Р.441-454.
      30. Nagao-Kitamoto H., Kamada N. Host-microbial Cross-talk in Inflammatory Bowel Disease // Immune Netw. - 2017. - № 17(1). - Р.1-12.
      31. Ogura Y., Bonen D. K., Inohara N. et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn’s disease // Nature. - 2001. - № 411. - Р. 603-6.
      32. Qin J.J., Li R. Q., Raes J. et al. A human gut microbial gene catalogue established by metagenomic sequencing // Nature. - 2010. - № 464. - Р.59-65.
      33. Rehman A., Lepage P., Nolte A. et al. Transcriptional activity of the dominant gut mucosal microbiota in chronic inflammatory bowel disease patients // J. Med. Microbiol. - 2010. - № 59. - Р.1114-1122.
      34. Rowan F., Docherty N. G., Murphy M. et al. Desulfovibrio bacterial species are increased in ulcerative colitis // Dis. Colon Rectum. - 2010. - № 53. - Р.1530-1536.
      35. Ruby T., McLaughlin L., Gopinath S. et al. Salmonella’s long-term relationship with its host // FEMS Microbiol. Rev. - 2012. - № 36. - Р.600-615.
      36. Sender R., Fuchs S., Milo R. Revised estimates for the number of human and bacteria cells in the body // PLoS Biol. - 2016. - 14: e1002533.
      37. Sokol H., Pigneur B., Watterlot L. et al. O. Faecalibacterium prausnitzii is an anti-inflammatory commensal bacterium identified by gut microbiota analysis of Crohn disease patients // Proc. Natl. Acad. Sci. U.S.A. - 2008. - № 105. - Р.16731-16736.
      38. Sokol H., Seksik P., Rigottier-Gois L. et al. Specificities of the fecal microbiota in inflammatory bowel disease // Inflamm. Bowel Dis. - 2006. - № 12. - Р.106-111.
      39. Sonnenburg J.L., Backhed F. Diet-microbiota interactions as moderators of human metabolism // Nature. - 2016. - № 535. - Р.56-64.
      40. Theriot C.M., Koenigsknecht M. J., Carlson P. E. et al. Antibiotic-induced shifts in the mouse gut microbiome and metabolome increase susceptibility to Clostridium difficile infection // Nat. Commun. - 2014. - № 5. - Р.3114.
      41. Wagner J., Short K., Catto-Smith A.G. et al. Identification and characterisation of Pseudomonas 16S ribosomal DNA from ileal biopsies of children with Crohn’s disease // PLoS One. - 2008. - 3: e3578.
      42. Waidmann M., Bechtold O., Frick J. S. et al. Bacteroides vulgatus protects against Escherichia coliinduced colitis in gnotobiotic interleukin-2-deficient mice // Gastroenterology. - 2003. - № 125. - Р.162-177.
      43. Wexler H. M. Bacteroides: the good, the bad, and the nitty-gritty // Clin. Microbiol. Rev. - 2007. - № 20. - Р.593-621.
      44. Wilson J.C., Furlano R. I., Jick S. S. et al. Inflammatory bowel disease and the risk of autoimmune diseases // J Crohns Colitis. - 2016. - № 10. - Р.186-93.
      45. Wong S.H., Ng S. C. What can we learn from inflammatory bowel disease in developing countries? // Curr Gastroenterol Rep. - 2013. - № 15. - Р.313.
      46. Yatsunenko T., Rey F. E., Manary M. J. et al. Human gut microbiome viewed across age and geography // Nature. - 2012. - № 486. - Р.222-7.
     


    Full text is published :
    Loranskaya I.D., Khalif I.L., Boldyreva M.N., Kupaeva V.A. CHARACTERISTIC OF MICROBIOME IN INFLAMMATORY BOWEL DISEASE (REVIEW). Experimental and Clinical Gastroenterology Journal. 2018;153(05):104-111
    Read & Download full text

    1. A. I. Yevdokimov Moscow state university of medicine and dentistry (Moscow, Russian Federation)
    2. Penza state university (Penza, Russian Federation)
    3. Infectious Clinical Hospital № 2 of the Moscow Department of Health care (Moscow, Russian Federation)

    Keywords:HIV-infection, viral hepatitis, remaxol

    Abstract:The aim of the study was to evaluate the effectiveness of remaxol long-term use in HIV-infected patients with chronic viral hepatitis. The results of observation and treatment of 46 HIV-infected patients with diffuse liver damage of a viral etiology (chronic hepatitis C and / or B) were analyzed. Patients were divided into two groups, depending on the treatment regimen. 16 patients of the first group were treated with remaxol (intravenous drip 400 ml daily for 12 days, 2-4 times a year at intervals of 3-6 months) and patients of the second group received standard symptomatic therapy. No specific treatment of HIV was carried out before remaxol prescription. The effectiveness of the therapy was evaluated by clinical, biochemical (liver enzymatic activity) and instrumental (elastography including an assessment of fibrosis levels with METAVIR scale). Inclusion of Remaxol in complex therapy of HIV-infected patients with hepatic damage of viral etiology (CHC and / or CHB) stabilized patients’ general condition. It shows hepatoprotective effect, which is manifested by severity of specific symptoms and enzymatic activity decrease, as well as fibrotic changes in liver tissue. To illustrate this, we describe a clinical case of long-term treatment of a patient using remaxol. The revealed positive effect of remaxol on condition of HIV-infected patients with diffuse liver lesions allows to recommend inclusion of the drug in therapy regimens of these patients.

      1. Zaplutanov V. A. Remaxol: A reference collection of experimental and clinical scientific papers cited in PubMed (a database of medical and biological publications) Zaplutanov V. A., Romantsov M. G., Sukhanov D. S. – SPb, 2012. – 184 s.
      2. Okovityy S. V. Hepatoprotectors/ Okovityy S. V., Bezborodkina N. N., Uleychik S. G., Shulepin S. N.. – M.: GEOTAR-Media, 2010. –112 s.
      3. Remaxol. Solution for infusions: Information about the innovative product for clinicians. – SPb, 2011. – 16 s.
      4. Romancov M.G., Sologub T. V., Goryacheva L.G, Kovalenko S. N., Suhanov D. S. SHul'dyakov A.A., Bondarenko A. N., Kovalenko A. L., Petrov A. Yu. Pathogenetically substantiated, with an assessment of the quality of life, calculation of the risk of the outcome of the disease, therapy for patients with viral hepatitis C Antibiotiki i himioterapiya. 2010; № 3–4: 45–55
      5. Romantsov M. G. Sologub T. V., Goryacheva L. G. Modern approach to adequate therapy of chronic hepatitis. Efficiency of etiotropic and pathogenetic therapy, assessment of quality of life, risk of development of disease outcomes SPb., 2010, – 64 s.
      6. Fedoskina E. A. Treatment of complications of cirrhosis: a method. Rec. For doctors./ Fedoskina E.A Maevskaya M. V., Galimova S. F.; pod red. Ivashkina V. T..; Rossiyskaya gastroenterolog. assots., Rossiyskoye o-vo po izucheniyu pecheni. – M.: 4TE Art, 2009. – 60 s
      7. Yushchuk N. D. Recommendations for the diagnosis and treatment of adult patients with hepatitis B and C. / N. D. Yushchuk [i dr.]. M.: GEOTAR-Media, 2015. 302 s.
      8. Muriel P., Rivera-Espinoza Y. Bentficial drugs for liver diseases J/Appl. Toxicol. 2008; Vol.28 (2): 93–103
      9. Mato J.M., S. C. Lu Role of S-adenosyl-L-methionine in liver health and Hepatology 2007; Vol.45(5): 1306–1312
     


    Full text is published :
    Sundukov A.V., Mel’nikov L.V., Alikeeva G.K., Vdovina E.T., Safiullina N.Kh. HEPATOPROTECTIVE THERAPY FOR DIFFUSION LIVER DISEASES IN HIV-INFECTED PATIENTS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):112-116
    Read & Download full text

    1. FSBI “A. N. Ryzhykh State scientific center of coloproctology” of Ministry of health of Russian Federation
    2. FSBEI FPE RMACPE MOH Russia (Moscow, Russian Federation)
    3. Pirogov Russian National Research Medical University (RNRMU) (Moscow, Russian Federation)

    Keywords: impedance planimetric technique, anal sphincter deficiency, pelvic floor muscles, high resolution anorectal manometry, elasticity, extensibility, intraluminal imaging probe EndoFLIP

    Abstract:The article gives an overview of publications on the use of impedance planimetric method in the study of anorectal function. Anal sphincters normally respond reflexively to the stretching of the rectum by intestinal contents that fill and stretch the rectum. The idea of the method lies in the fact that is artificial stretching of the anal canal with simultaneous recording of pressure and building a virtual geometric shape directly in response to the tension, and calculates a coefficient of elasticity of the anal canal that quantitatively characterize the response of the anal sphincter in tension. For the first time in Russia, it became possible to use this method in coloproctological patients in the State Scietific Centre of Coloproctology. In the article step by step assessed the main uses of the techniques described in the literature: the description of the method and normative values, then - comparison of extensibility of anal sphincters at rest and with voluntary reduction in norm in volunteers and patients with anal incontinence, including patients with scleroderma, then compared the results of this technique with high-resolution 3D manometry. In addition, the use of the Endoflip method as a dynamic control of the treatment of anal sphincter failure by means of sacral stimulation is analyzed.

      1. Шелыгин Ю. А., редактор. Колопроктология/Клинические рекомендации. М.: ГЭОТАР-Медиа; 2015. С. 190-213.
      2. Johanson J. F., Lafferty J. Epidemiology of fecal incontinence: the silent affliction. Am J Gastroenterol. 1996; 91: 33-6.
      3. Фролов С.А., Титов А. Ю., Костарев И. В., Полетов Н. Н., Джанаев Ю. А. Тибиальная нейромодуляция в лечении больных с различными формами недостаточности анального сфинктера. Колопроктология. 2013; 2(44): 37-43.
      4. Whitehead W. E., Borrud L., Goode P. S. et al. Fecal incontinence in US adults: epidemiology and risk factors. Gastroenterology. 2009; 137: 512-7.
      5. Bharucha A. E. Pelvic floor: anatomy and function. Neurogastroenterol Motil. 2006; 18: 507-19.
      6. Sangwan Y. P., Solla J. A. Internal anal sphincter: advances and insights. Dis Colon Rectum. 1998; 41: 1297-311.
      7. Rasmussen O. O., Christiansen J. Physiology and pathophysiology of anal function. Scand J Gastroenterol. Suppl. 1996; 216: 169–74.
      8. Delancey J. O., Toglia M. R., Perucchini D. Internal and external anal sphincter anatomy as it relates to midline obstetric lacerations. Obstet Gynecol. 1997; 90: 924-7.
      9. Bharucha A. E. Anorectal manometry and imaging are necessary in patients with fecal incontinence. Am J Gastroenterol. 2006; 101: 2679-81.
      10. Azpiroz F., Enck P., Whitehead W. E. Anorectal functional testing: review of collective experience. Am J Gastroenterol. 2002; 97: 232-40.
      11. Rao S.S., Hatfield R., Soffer E., Rao S., Beaty J., Conklin J. L. Manometric tests of anorectal function in healthy adults. Am J Gastroenterol. 1999; 94: 773-83.
      12. Eckardt V. F., Kanzler G. How reliable is digital examination for the evaluation of anal sphincter tone? Int J Colorectal Dis. 1993; 8: 95-7.
      13. Harris L. D., Winans C. S., Pope C. E. 2nd. Determination of yield pressures: a method for measuring anal sphincter competence. Gastroenterology. 1966; 50: 754-60.
      14. Kwiatek M. A., Kahrilas P. J., Soper N. J. et al. Esophagogastric junction distensibility after fundoplication assessed with a novel functional luminal imaging probe. J Gastrointest Surg. 2010; 14: 268-76.
      15. Gregersen H., Drewes А. Functional oesophago-gastric junction imaging. World J Gastroenterol. 2006 May 14; 12(18): 2818-2824. www.wjgnet.com World Journal of Gastroenterology ISSN1007-9327
      16. McMahon B., Frøkjær J., Kunwald Р., Liao D., Funch-Jensen Р., Drewes А. et al. The functional lumen imaging probe (FLIP) for evaluation of the esophagogastric junction. Am J Physiol Gastrointest Liver Physiol 292: G377-G384, 2007. First published August 31, 2006; doi:10.1152/ajpgi.00311.2006.
      17. Alqudah M. M., Gregersen H., Drewes A. M., McMahon B. P. Evaluation of anal sphincter resistance and distensibility in healthy controls using EndoFLIP Neurogastroenterol Motil. 2012 Dec; 24(12): 591-9.
      18. Alqudah М., Whelan М., McNamara D., Neary Р., McMahon В. EndoFLIP® to Measure Anal Sphincters Distensibility in Healthy and Faecal Incontinence Gastroenterology. 2014; 146, Issue 5: 715
      19. Luft F., Fynne L., Gregersen H., Lundager F., Buntzen S, Lundby L. et al. Functional luminal imaging probe: a new technique for dynamic evaluation of mechanical properties of the anal canal. Tech Coloproctol. 2012 Aug 31; 16(6): 451-7.
      20. Fynne L., Luft F., Gregersen H., Buntzen S., Lundby L., Lundager F. Distensibility of the anal canal in patients with systemic sclerosis: A study with the Functional Lumen Imaging Probe. Colorectal Dis. 2012 Oct 16. doi: 10.1111/codi.12063.
      21. Gourcerol G., Granier S., Bridoux V., Menard J. F., Ducrotté P., Leroi A. M. Do endoflip assessments of anal sphincter distensibility provide more information on patients with fecal incontinence than high-resolution anal manometry? Neurogastroenterol Motil. 2015 Dec 15. doi: 10.1111/nmo.12740.
      22. Haas S., Liao D., Gregersen H., Lundby L., Laurberg S., Krogh K. Increased yield pressure in the anal canal during sacral nerve stimulation: a pilot study with the functional lumen imaging probe. Neurogastroenterol Motil. 2016 Aug 21; 15: 25-31.
      23. Sorensen G., Liao D., Lundby L., Fynne L., Buntzen S., Gregersen H. et al. Distensibility of the anal canal in patients with idiopathic fecal incontinence: a study with the Functional Lumen Imaging Probe Neurogastroenterol Motil. 2014; 26: 255-263.
      24. Liu J., Guaderrama N., Nager C. W., Pretorius D. H., Master S., Mittal R. K. Functional correlates of anal canal anatomy: puborectalismuscle and anal canal pressure. Am J Gastroenterol. 2006; 101: 1092-1097.
     


    Full text is published :
    Fomenko O.Yu., Shelygin Yu.A., Poryadin G.V., Mudrov A.A. PLANIMETRIC IMPEDANCEOMETRY IN ASSESSMENT OF THE FUNCTIONAL STATE OF ANAL SPHINCATORS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):117-122
    Read & Download full text

    1. Volgograd state medical University (Volgograd, Russian Federation)

    Keywords: whipple’s disease, intestinal lipodystrophy, maladsorption syndrome, maldigestion syndrome, Tropheryma nodes whippeli lumen, polyarthralgia, abdominal pain, polyarthralgia, polyserositis, adrenal insufficiency, endocarditis, antibiotic therapy

    Abstract:This review focuses on the clinical picture, approaches to diagnosis and therapy of Whipple’s disease.

      1. Sparsa L., Fenollar F., Gossec L., Leone J., Pennaforte J. L., Dougados M., Roux C. Whipple disease revealed by anti-TNFα therapy// Rev Med Interne. 2013. Vol. 34 (2). Р. 105-109.
      2. Moos V., Schneider T. Changing paradigms in Whipple’s disease and infection with Tropherymawhipplei // Eur J ClinMicrobiol Infect Dis. 2011. Vol. 30(10).Р.1151-1158.
      3. Lagier J. C., Lepidi H., Raoult D., Fenollar F. Systemic Tropherymawhipplei: clinical presentation of 142 patients with infections diagnosed or confirmed in a reference center // Medicine (Baltimore). 2010. Vol. 89(5).Р.337-345.
      4. Meunier M., Puechal X., Hoppé E., Soubrier M., Dieudé P., Berthelot J. M., Caramaschi P., Gottenberg J. E., Gossec L., Morel J., Maury E., Wipff J., Kahan A., Allanore Y. Rheumatic and musculoskeletal features of Whipple disease: a report of 29 cases // J Rheumatol. 2013. Vol. 40 (12). Р. 2061-2066.
      5. Feurle G. E., Moos V., Schinnerling K., Geelhaar A., Allers K., Biagi F., Bläker H., Moter A., Loddenkemper C., Jansen A., Schneider T. The immune reconstitution inflammatory syndrome in whipple disease: a cohort study // Ann Intern Med. 2010. Vol. 153 (11).Р. 710-717.
      6. Chan V., Wang B., Veinot J. P., Suh K. N., Rose G., Desjardins M., Mesana T. G. Tropherymawhipplei aortic valve endocarditis without systemic Whipple’s disease // Int J Infect Dis. 2011. Vol. 15 (11).Р. 804-806.
      7. Lagier J. C., Fenollar F., Lepidi H., Raoult D. Evidence of lifetime susceptibility to Tropherymawhipplei in patients with Whipple’s disease // J AntimicrobChemother. 2011. Vol. 66 (5). Р. 1188-1189.
      8. Keita A. K., Bassene H., Tall A. et al. Tropherymawhipplei: a common bacterium in rural Senegal. PLoSNegl Trop Dis 2011;5(12): e1403
      9. Bonhomme C. J., Renesto P., Desnues B. et al. Tropherymawhipplei glycosylation in the pathophysiologic profile of Whipple’s disease.J InfectDis 2009;199(7):1043-52.
      10. Parfenov A. I. Bolezni kishechnika: Rukovodstvo dlya vrachej [Diseases of the intestine: A guide for doctors.] - M.: Medicina, 2000. - 613 s.
      11. Maev I. V., Zhilyaev E. V. Bolezn’ Uippla [Whipple’s disease] // Klinicheskaya medicina. 2014. T.18, № 5. S. 2063-2065.
      12. Belov B. S. Bolezn’ Uippla [Whipple’s disease] // Sovremennaya Revmatologiya. 2013. № 1. 12-16 s.
      13. Grebenev A. L., Myagkova L. P. Bolezni kishechnika (sovremennye dostizheniya v diagnostike i terapii) [Bowel diseases (modern advances in diagnosis and therapy)]. - M.: Medicina, 2012. - 130-132 s.
      14. Puéchal X. Whipple’s disease // Ann Rheum Dis. 2013. Vol. 72 (6).Р. 797-803.
      15. Lange U., Teichman J. Whipple arthritis diagnosis by molecular analysis of synovial fluid - current status of diagnosis and therapy // Rheumatology. - 2015. - Vol. 42. - P. 312-313.
      16. Misbah S. A., Mapstone N. P. Whipple’s disease revisited. J. Clin. Pathol. 2014; 53: 750-755.
      17. Geissdörfer W., Moos V., Moter A. et al. High frequency of Tropherymawhipplei in culture-negative endocarditis. J Clin Microbiol 2012; 50(2):216-22.
     


    Full text is published :
    Skvortsov V. V., Tumarenko A. V., Pavlov V. K. DIAGNOSIS AND TREATMENT OF WHIPPLE’S DISEASE. Experimental and Clinical Gastroenterology Journal. 2018;153(05):123-127
    Read & Download full text

    1. North –Western State Medical University named after I. I. Mechnikov (St. Petersburg, Russian Federation)

    Keywords: colon, pathology, mucous membrane

    Abstract:The review contains articles analyzing the structural changes in the epithelium mucous membrane of various parts of the large intestine of humans under normal and some clinical pathology. Analysis of structural changes revealed main characteristics in the dystrophic and regenerative processes developing in epithelium. Changes in the epithelium capture some structures (microvilli, cellular contacts, organelles, nucleus) forming its cells and are nonspecific. They differ in the degree of severity, which depends on the severity of the disease and the individual characteristics of the organism.

      1. Avdeeva TG, Ryabukhin YuV, Parmenova LP, eds. Children's gastroenterology: guide. Moscow, GEOTAR-MEDIA, 2009. 192 p.
      2. Aruin LI, Kapuller LA, Isakov VA Morphological diagnosis of diseases of the stomach and intestines. Moscow, Triada-X, 1998. 496 p.
      3. The report on a condition of health care in Europe in 2009. 2010. 205 p
      4. Ivanova VF, Puzyriov AA, Kostiukevitch SV, Drai RV. Structural changes in rat intestinal wall during starvation. Morfologiia (Saint-Petersburg, Russia), 2009; vol. 136, no. 6, pp. 62–68.
      5. Kvetnoy IM, Yuzhakov VV. Diffusive endocrine system: Guide to histology. SPb, Speclit, 2011. vol. 1, pp 728–750.
      6. Kozlova IV, Osadchuk MA, Kvetnoy IM, eds. Melatonin and serotonin at inflammatory colon diseases and a colorectal cancer. Clinical medicine, 2000; vol. 78, no. 6, pp 32–35.
      7. Komarov FI, Raykhlin NT, Rapoport SI, eds. Syndrome inflammatory bowel diseases. Cliniko-morfologichesky aspects at treatment by Melaksen. Clinical medicine, 2006; vol. 84, no. 11, pp 30–35.
      8. Kostyukevich SV. Differentiation of endocrine epithelial cells of the colon mucosa in humans and some vertebrates. Cytology, 2004; vol. 46, no. 6, pp 506–513.
      9. Kostyukevich SV, Anichkov NM, Ivanova VF, eds. Endocrine cells of rectal epithelium in health, in nonspecific ulcerative colitis and irritable colon syndrome in the treatment with prednisolone and salofalk and in the absence of treatment. Archive of pathology, 2004; vol. 4, pp 23–27.
      10. Kostyukevich SV, Ivanova VF. Colon. Rectum: Guide to histology. SPb, Speclit, 2011. vol. 2, pp 145–152.
      11. Lychkova AE. Serotoninergic regulation of colonic motor function. Therapeutic archive, 2013; vol. 2, pp 89–92.
      12. Makarova M, Rybakova A, Gushchin YA, eds. Anatomical and physiological characteristics of digestive tract in humans and laboratory animals. International bulletin of veterinary science, 2016; vol. 1, pp 82–104.
      13. Markova AA, Kashkina EI. Modern methods of diagnostics and evaluation of the severity of ulcerative colitis. Bulletin of the TGU, 2012; vol. 17, no. 3, pp 915–919.
      14. Osadchuk AM, Osadchuk AM. Morphological and functional upgrading of epithelial cells of the colon and APUD-cells in the pathogenesis and prognosis of ulcerative colitis. Clinical medicine, 2006; vol. 84, no. 12, pp 35–39.
      15. Osadchuk AM, Osadchuk MA, Balashov AV, eds. The role of diffuse endocrine system and cellular renewal of colonocytes in formation of clinical variants of irritable bowel syndrome at persons of young age. Clinical medicine, 2008; vol. 86, no. 3, pp 33–37.
      16. Potekhin PP, Obryadov VP, Lukoyanova GM, eds. The role of morphological research in the diagnosis of ulcerative colitis in children. Clinical medicine, 2010; vol. 2, pp 45–49.
      17. Ham A., Cormac D. Colon: Histology. Moscow, Mir, 1983. vol. 4, pp. 152–158.
      18. Shubnikova EA. Epithelial tissue system. The epithelium of the intestine: Guide to histology. SPb, Speclit, 2011. vol. 1, pp 178–186.
      19. Akiho H., Ihara E., Nakamura K. Low-grade inflammation plays a pivotal role in gastrointestinal dysfunction in irritable bowel syndrome // World Journal Gastrointestinal Pathophysiology. 2010. Vol. 1, № 3. P. 97-105.
      20. Balázs M., Kovács A. Ulcerative colitis: electron microscopic studies with special reference to development of crypt abscesses // Dis. Colon Rectum. 1989. Vol.32, № 4. P. 327-334.
      21. Barrett P., Hobbs R. G., Coats P. J. et al. Endocrine cells of the human gastrointestinal tract have no proliferative capacity // Histochem. J. 1995. Vol. 27. P. 482-486.
      22. Baumgart D.C., Sandborn W. J. Crohn’s disease // The Lancet. 2012. Vol. 380. P. 1590-1605.
      23. Bertrand P.P., Bertrand R. L. Serotonin release and uptake in the gastrointestinal tract //Autonomic Neuroscience: Basic and Clinical. 2010. Vol. 153, № 1-2. P 47-57.
      24. Cheng P., Yao J., Wang C. et al. Molecular and cellular mechanisms of tight junction dysfunction in the irritable bowel syndrome // Molecular Medicine Reports. 2015. Vol. 12, № 3. P. 3257-3264.
      25. Dobbins W.O. 3rd Colonic epithelial cells and polymorphonuclear leukocytes in ulcerative colitis. An electron-microscopic study // Am J. Dig. Dis. 1975. Vol. 20, № 3. P. 236-252.
      26. Dorofeyev A.E., Kiriyan E. A., Vasilenko I. V. et al. Clinical, endoscopical and morphological efficacy of mesalazine in patients with irritable bowel syndrome // Clinical and Experimental Gastroenterology. 2011. Vol. 4. P 141-153.
      27. Dunlop S.P., Jenkins D., Neal K. R., Spiller R. C. Relative importance of enterochromaffin cell hyperplasia, anxiety, and depression in postinfectious IBS // Gastroenterology. 2003. Vol. 125, № 6. P. 1651-1659.
      28. Dvorak A.M., Silen W. Differentiation between Crohn’s disease and other inflammatory conditions by electron microscopy // Ann. Surg. 1985. Vol. 201. P. 53-63.
      29. El-Salhy M., Danielsson A., Stenling R., Grimelius L. Colonic endocrine cells in inflammatory bowel disease // Journal of Internal Medicine. 1997. Vol. 242, № 5. P. 413-419.
      30. Fratila O.C., Craciun C. Ultrastructural evidence of mucosal healing after infliximab in patients with ulcerative colitis // J. Gastrointestin. Liver Dis. 2010. Vol. 19, № 2. P. 147-153
      31. Hsieh S-Y., Shih T. C., Yeh C-Y. et al. Comparative proteomic studies on the pathogenesis of human ulcerative colitis // Proteomics. 2006. Vol. 6, № 19. P. 5322-5331.
      32. Kong W-M., Gong J., Dong L., Chen M-X. Changes in tight junction of intestinal mucosa in patients with irritable bowel syndrome: a study with tracing electron microscope // Nan Fang Yi Ke Da XueXueBao. 2007. Vol. 27, № 8. P. 1167-1170.
      33. Qiao X. T., Ziel J. W., McKimpson W. et al. Prospective identification of a multi-lineage progenitor in murine stomach epithelium // Gastroenterology. 2007. Vol. 133, № 6. P. 1989-1998.
      34. Skinner J. M., Whitehead R., Piris J. Argentaffin cells in ulcerative colitis // Gut. 1971. Vol. 12. P. 636-638.
      35. Solcia E., Greutzfeldt W., Falkmer S. et al. Human gastroenteropancreatic endocrine-paracrine cells: Santa Monica 1980 classification // In: Cellular Basis of Chemical Messengers in the Digestive System, USA, New -York: Academic Press, 1981. Р. 159-165.
      36. Watson A. J., Roy A. D. Paneth cells in the large intestine in ulcerative colitis // J. Path. Bact. 1960. Vol. 80. P. 309-316.
     


    Full text is published :
    Churkova M.L., Kostyukevich S.V. THE EPITHELIUM MUCOSAL OF COLON IN NORMAL AND IN FUNCTIONAL AND INFLAMMATORY BOWEL DISEASES. Experimental and Clinical Gastroenterology Journal. 2018;153(05):128-132
    Read & Download full text

    1. Federal State Budget Educational Institution of Higher Education “Samara State Medical University” of the Ministry of Health of the Russian Federation (Samara, Russian Federation)

    Keywords: Microbiota, non-alcoholic fatty liver disease, non-alcoholic fatty disease of the pancreas, inflammatory bowel disease, irritable bowel syndrome

    Abstract:Aim of the review. Present at the modern level of the development of medicine information on the role of the microbiota of the gastrointestinal tract in the formation of pathology of internal organs and the prospects for correcting the disturbed microbial balance. It is shown that a change in the gastrointestinal microbiota can be associated with various diseases of the internal organs. The most complex issue that needs to be addressed is to determine the coefficient of participation of the bacterial overgrowth factor and the role of individual microbiota in the development of non-alcoholic fatty liver disease, non-alcoholic pancreatic fatty disease, metabolic syndrome, type 2 diabetes mellitus, which is due to the current insufficiency evidence base. It is necessary to conduct large randomized controlled trials on the role of normal gastrointestinal microbiota in the prevention and treatment of these diseases. It seems promising to improve and introduce new methods for restoring the microbiota of the gastrointestinal tract by creating preparations containing bacteriocines aimed at eradication of the target microorganism and vaccines capable of preventing the infection with pathogenic microorganisms.

      1. Qin J., Li R., Raes J., Arumugam M. et al. A human gut microbial gene catalogue established by metagenomic sequencing. Nature. 2010; 464: 59–65.
      2. Guinane С.M., Cotter P. D. Role of the gut microbiota in health and chronic gastrointestinal disease: understanding a hidden metabolic organ. Therap Adv Gastroenterol. 2013; 6(4): 295–308.
      3. Gumayunova N. G. Detection of excessive growth bacteria syndrome in small intestine with psoriasis disease. Aspirantskij vestnik Povolzh'ja. 2009; № 3–4: 162–4.
      4. Osadchuk A.M., Davydkin I. L., Gricenko T. A., et al. Esophagitis in persons receiving cytostatic and antitumor therapy. The current state of the problem. Izvestiya of the Samara Scientific Center of the Russian Academy of Sciences. 2015. 17 (2–3): 603–610.
      5. Yang I., Woltemate S., Piazuelo M. B. et al. Different gastric microbiota compositions in two human populations with high and low gastric cancer risk in Colombia. Sci Rep. 2016; 6: 18594.
      6. Laniro G., Molina-Infante J., Gasbarrini A. Gastric microbiota. Helicobacter. 2015; 20 (Suppl 1): 68–71.
      7. Dicksved J., Linberg M., Rosenquist M., et al. Molecular characterization of the stomach microbiota in patients with gastric cancer and in controls. J. Med. Microbiol. 2009; 58 (Pt 4): 509–16.
      8. Aviles-Jimenes F., Varquez-Jimenes F., Medrano-Guzman R. et al. Stomach microbiota composition varies between patients with non-atrophic gastritis and patients with intestinal type of gastric cancer. Sci Rep. 2014; 4: 4202.
      9. Xiao M., Gao Y., Wang Y. Helicobacter species infection may be associated with cholangiocarcinoma. Int J Clin Pract. 2014; 68: 262–70.
      10. Malfertheiner P., Megraud F., O. Morain C.A. et al. Management of Helicobacter pylori infection – the Maastricht V/Florence Consensus Report. Gut. 2016; 0: 1–25.
      11. Corte C.D., Ferrari F., Villani A., Nobili V. Epidemiology and natural history of NAFLD. J. Med. Biochem. 2015; 34: 13–7.
      12. Romero-Gomez M., Zelber-Sagi S., Trenell M. Treatment of NAFLD with diet, physical activity and exercise. J. Hepatol. 2017; 67(4): 829–846.
      13. Leung C., Rivera L., Furness J. B., Angus PW. The role of the gut microbiota in NAFLD. Nat Rev Gastroenterol Hepatol. 2016; 13(7): 412–25.
      14. Hoy-Schulz Y.E., Jannat K., Roberts T. et al. Safety and acceptability of Lactobacillus reuteri DSM 17938 and Bifidobacterium longum subspecies infantis 35624 in Bangladeshi infants: a phase I randomized clinical trial. BMC Complement Altern Med. 2016; 16:44.
      15. Yilmaz Y., Eren F. Nonalcoholic steatohepatitis and gut microbiota: Future perspectives on probiotics in metabolic liver diseases. Turk J. Gastroenterol. 2017; 28: 327–8.
      16. de Medeiros I. C., de Lima J. G. Nonalcoholic fatty pancreas disease as an endogenous alcoholic fatty pancreas disease. Gastroenterol Hepatol Endosk. 2016; 1(2): 32–39.
      17. Golubeva T.I., Troshina I. A., Medvedeva I. V. Non-alcoholic fatty pancreatic disease in patients with obesity and metabolic syndrome. Universitetskaja medicina Urala. 2017; 2 (9): 50–52.
      18. Simerzin V. V. Fatenkov O. V. Gagloeva I. V., et al. Innovations in the diagnosis and treatment of patients with hypertriglyceridemia. Nauka i innovacii v medicine. 2017; 1(5): 43–51.
      19. Osadchuk A.M., Osadchuk M. A., Kvetnoj I. M. Irritable Bowel Syndrome. 2007; 85(3): 46–50.
      20. Osadchuk M.A., Osadchuk M. M. Irritable Bowel Syndrome and Microbiota: Ways to Optimize Therapy. Vrach. 2015; 56 47–51.
      21. Ghoshal U.C., Shukla R., Ghoshal U. et al. The gut microbiota and irritable bowel syndrome: friend or foe? Int J Inflam. 2012; 2012:151085.
      22. Stojanovic-Stojanovic M., Biagi E., Heilig H. et al. Global and deep molecular analysis of microbiota signatures in fecal samples from patients with irritable bowel syndrome. Gastroenterology. 2011; 141: 1792–1801.
      23. Saulnier D., Riehle K., Mistretta T. et al. Gastrointestinal microbiome signatures of pediatric patients with irritable bowel syndrome. Gastroenterology. 2011. 141: 1782–1791.
      24. Komarov F.I., Osadchuk A. M., Osadchuk M. A., Kvetnoj I. M. Nonspecific ulcerative colitis. – М.: МИА. – 2008. – 256 с.
      25. Davydova O.E., Katorkin S. E., Ljamin A. V., Andreev P. S. Improving the results of treatment of patients with ulcerative colitis using individual schemes of eradication therapy of opportunistic microflora based on microbiological monitoring. Vrach-aspirant. 2016; 77(4); 49–55.
      26. Li Q., Wang C., Tang C., Li N., Li J. Molecular-phylogenetic characterization of the microbiota in ulcerated and non-ulcerated regions in the patients with Crohn’s disease. PLoS One. 2012; 7: e34939.
      27. Barbut F. Managing antibiotic associated diarrhea. BMJ. 2002; 324 (7350): 1345–1346.
      28. McCoy A., Araujo-Perez F., Azcarate-Peril A. et al. Fusobacterium is associated with colorectal adenomas. PLoS One. 2013; 8(1): e53653.
      29. Arthur J., Perez-Chanona E., Muhlbauer M. et al. Intestinal inflammation targets cancer-inducing activity of the microbiota. Science. 2012; 338: 120–123.
      30. Turnbaugh P., Ridaura V., Faith J. et al. The effect of diet on the human gut microbiome: a metagenomic analysis in humanized gnotobiotic mice. Sci Transl Med. 2009; Nov 11; 1(6): 6ra14.
      31. Qin J., Li Y., Cai Z. et al. A metagenome-wide association study of gut microbiota in type 2 diabetes. Nature. 2012; 490: 55–60.
      32. Andreasen A., Larsen N., Pedersen-Skovsgaard T. et al. Effects of Lactobacillus acidophilus NCFM on insulin sensitivity and the systemic inflammatory response in human subjects. Br J Nutr. 2010; Dec; 104(12):1831–8.
      33. Murphy E., Cotter P., Hogan A. et al. Divergent metabolic outcomes arising from targeted manipulation of the gut microbiota in diet-induced obesity. Gut. 2013; Feb; 62(2):220–6.
      34. Kadooka Y., Sato M., Imaizumi K. et al. Regulation of abdominal adiposity by probiotics (Lactobacillus gasseri SBT2055) in adults with obese tendencies in a randomized controlled trial. Eur J Clin Nutr. 2010; 64: 636–643.
      35. Skvorcov V. V. Dysbiosis of the intestine and antibiotic-associated diarrhea, diagnosis and treatment. Lechashhij vrach. 2008; 2: 43–47.
      36. Kinnear C.L., Strugnell R. A. Vaccination Method Affects Immune Response and Bacterial Growth but Not Protection in the Salmonella Typhimurium Animal Model of Typhoid. PLoS One. 2015; 10(10): e0141356.
      37. Zeng M., Mao X. H., Li J. X. et al. Efficacy, safety, and immunogenicity of an oral recombinant Helicobacter pylori vaccine in children in China: a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2015 Oct 10; 386(10002): 1457–64.
     


    Full text is published :
    Osadchuk A. M., Davydkin I. L., Gricenko T. A., Lebedeva E. A., Petrushin A. E. THE ROLE OF THE MICROBIOTA OF THE GASTROINTESTINAL TRACT IN THE DEVELOPMENT OF DISEASES OF INTERNAL ORGANS. Experimental and Clinical Gastroenterology Journal. 2018;153(05):133-139
    Read & Download full text

    1. Military Medical Academy named after S. M. Kirov (St. Petersburg, Russian Federation)

    Keywords: inflammatory bowel diseases (IBD), Crohn’s disease (CD), ulcerative colitis (UC), pathogenesis of IBD, imun, genome, exposome, NOD2/CARD15 gene, IL-23R gene, autophagy, T-cell, microbiome, intestinal microbiota, rebiosis

    Abstract:The relevance of inflammatory bowel disease (IBD) is caused by the growth of primary morbidity, as well as the lack of identity of the mechanisms of their pathogenesis. The purpose of this review - to consider the basic and most fundamental laws of genome changes, the immune system, the role and participation of intestinal microflora in the pathogenesis of these diseases. The report is a synthesis of the accumulated information about the relationship of genetic, immunological and exposomes concept, their role and influence on the development of IBD. Results. It is concluded that the pathogenetic cascade of inflammation in IBD begins with changes in microbiota and the appearance of unknown antigens in the intestine, which, in certain genetically determined defects of the immune system, initiate a cascade of inflammatory reactions that form a clinical picture of Crohn’s disease (CD) or ulcerative colitis (UC). The pathogenesis of IBD is unambiguously linked to changes in environmental factors. Conclusion. The most promising targets for therapeutic intervention in the near future to reduce inflammatory reactions will be intestinal microflora and diet.

      1. Belousova EA. Ulcerative colitis and Crohn's disease. – Tver: Publishing House "Triada", 2002. – p.128.
      2. Jonkers D., D. Renders, Masks, A., Pierik M. Probiotics in the treatment of inflammatory bowel disease (a systematic review of intervention studies among adult patients). Gastroenterology and Hepatology, 2013, No. 2, pp. 28–48.
      3. Maev I. V., Andreev D. N., Dichev, D. T., E. V. Giants Crohn's Disease: etiopathogenesis, diagnosis and conservative treatment.//Manual for doctors. – Moscow, 2016. – p.67.
      4. Kirsner JB, Spencer JA. Family occurrences of ulcerative colitis, regional enteritis, and ileocolitis. // Ann. Intern. Med. – 1963. – vol. 59. – pp.133–144.
      5. Hugot J-P, Laurent-Puig P, Gower-Rousseau C et al. Mapping of a susceptibility locus for Crohn’s disease on chromosome 16. Nature, 1996, vol. 379, pp. 821–823.
      6. Cooney R., Baker J., Brain O et al. Nod2 stimulation induces autophagy in dendritic cells influencing bacterial handling and antigen presention. Nat. Med, 2010, vol.16, pp.90–97.
      7. Hooper K., Barlou P., Stevens C., Henderson P. Inflammatory bowel disease drugs: a focus on autophagy. Jornal of Crohn’s and Colitis, 2017, vol.11, № 1, pp. 118–127.
      8. Ogura Y., Bonen D. K., Inohara N. et al. A frameshift mutation in Nod2 associated with susceptibility to Crohn’s desease. Nature, 2001, vol.411, pp. 603–606.
      9. Hugot J-P, Chamaiilard M., Zouali H. et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature, 2001, vol.411, pp. 599–603.
      10. Сhassaing B., Vijay-Kumar M., Gewitz A. T. How diet can impact gut microbiota to promote or endanger health. Curr. Opin.Gastroenterolog, 2017, vol.33, № 6, pp. 417–421.
      11. Duerr R. H., Taylor K. D., Brant S. R. et al. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science, 2006, vol. 314, pp. 1461–1463.
      12. Kitahora T, Utsunomiya T, Yokota A. Epidemiological study of ulcerative colitis in Japan: incidence and familial occurrence. The Epidemiology Group of the Research Committee of Inflammatory Bowel Disease in Japan. J. Gastroentero, 1995, vol. 30 (Suppl. 8), pp. 5–8.
      13. Fiocchi С. Inflammatory bowel disease pathogenesis: Where are we? J. Gastroenter. Hepatol, 2015, vol. 30 (Suppl. 1), pp. 12–18.
      14. Brown A., Rampertab C., Mullin G. E. Existing Dietary Guidelines for Crohn’s Disease and Ulcerative Colitis. Expert Rev. Gastroenterol. Hepatol, 2011, vol.5, № 3, pp. 411–425.
      15. Wu G. D., Chen J., Hoffmann C. et al. Linking long-term dietary patterns with gut microbial enterotypes. Science, 2011, vol. 334, pp. 105–108.
      16. Desai M.S, Seekatz A.M, Koropatkin N. M., et al. A dietary fiber-deprived gut microbiota degrades the colonic mucus barrier and enhances pathogen susceptibility. Cell, 2016, vol, 167, pp.1339–1353.
      17. Hamer H. M., Jonkers D., Venema K. et al. Review article: the role of butyrate on colonic function. Aliment. Pharmacol.Ther, 2008, vol.27, pp. 833–839.
      18. Park J, Kim M, Kang SG, et al. Short-chain fatty acids induce both effector and regulatory T cells by suppression of histone deacetylases and regulation of the mTOR-S6K pathway. Mucosal Immunol, 2015, vol.8, pp.80–93.
      19. Rambaud Y.C, Buts Y. P., Corthier G., Flourie B. Gut microflora. Digestive physiology and pathology. – Paris, 2006.
      20. Maev I. V., Andreev D. N., Dichev, D. T., E. V. Giants Crohn's Disease: etiopathogenesis, diagnosis and conservative treatment.//Manual for doctors. – Moscow, 2016. – p.67.
      21. Salazar N., Dewulf E. M., Neyrinck A. M., et al. Inulin-type fructans modulate intestinal bifidobacterium species populations and decrease fecal short-chain fatty acids in obese women. ClinNutr, 2015, vol.34, pp. 501–507.
      22. Swidsinski A., Ung V., Sydora BC, et al. Bacterial overgrowth and inflammation of small intestine after carboxymethylcellulose ingestion in genetically susceptible mice. Inflamm. Bowel Dis, 2009, vol.15, pp.359–364.
      23. Chassaing B., Van de Wiele T., De Bodt J., et al. Dietary emulsifiers directly alter human microbiota composition and gene expression ex vivo potentiating intestinal inflammation. Gut, 2017, vol. 66, pp. 1414–1427.
      24. Roberts C. L., Keita A. V., Duncan S. H., et al. Translocation of Crohn›s disease Escherichia coliacross M-cells: contrasting effects of soluble plant fibres and emulsifiers. Gut, 2010, vol. 59, pp.1331–1339.
      25. Chassaing B., Koren O., Goodrich J. K., et al. Dietary emulsifiers impact the mouse gut microbiota promoting colitis and metabolic syndrome. Nature, 2015, vol. 519, pp.92–96.
      26. Yan X., Huang Y., Wang H. et al. Maternal obesity induces sustained inflammation in both fetal and offspring large intestine of sheep. Inflamm. Bowel Dis, 2011, vol. 17, pp. 1513–22.
      27. Gonzalez-Correa C.A., Mulett-Vásquez E., Miranda D. A., et al. The colon revisited or the key to wellness, health and disease. Medical Hypotheses, 2017, Vol. 108, p.133.
      28. Chassaing B., Koren O., Carvalho F. A., et al. AIEC pathobiont instigates chronic colitis in susceptible hosts by altering microbiota composition. Gut, 2013, vol. 63, pp.1069–1080.
      29. Chassaing B., Raja S. M., Lewis J. D., et al. Colonic microbiota encroachment correlates with dysglycemia in humans. Cell MolGastroenterolHepatol, 2017, vol. 4, pp. 205–221.
      30. Faith J. J., Guruge J. L., Charbonneau M., et al. The long-term stability of the human gut microbiota. Science, 2013, vol. 341, p.1237439.
      31. Human Microbiome Project Collaboration Structure, function and diversity of the healthy human microbiome. Nature, 2012, vol. 486, pp.207–214.
      32. Kostic A. D., Gevers D., Siljander H., et al. The dynamics of the human infant gut microbiome in development and in progression toward type 1 diabetes. Cell Host Microbe, 2015, vol.17, pp.260–273.
      33. Lloyd-Price J, Abu-Ali G, Huttenhower C. The healthy human microbiome. Genome Med, 2016, vol. 8, p.51.
      34. Qin J, Li R, Raes J, et al. A human gut microbial gene catalogue established bymetagenomic sequencing. Nature, 2010, vol. 464, pp.59–65.
      35. Butto LF, Haller D. Dysbiosis in intestinal inflammation: cause or consequence. Int. J. Med. Microbiol, 2016, vol. 306, pp. 302–309.
      36. Wu GD, Compher C, Chen EZ, et al. Comparative metabolomics in vegans and omnivores reveal constraints on diet-dependent gut microbiota metabolite production. Gut, 2014, vol. 65, pp.63–72.
      37. Hildebrandt MA, Hoffmann C, Sherrill-Mix SA, et al. High-fat diet determines the composition of the murine gut microbiome independently of obesity. Gastroenterology, 2009, vol.137, pp.1716–1724.
      38. Filippo C, Cavalieri D, Di Paola M et al. Impact of diet in shaping gut microbiota revealed by a comparative study in children from Europe and rural Africa. Proc. Natl Acad. Sci, 2010, vol.107, pp. 14691–14696.
      39. Devkota S, Wang Y, Musch MW et al. Dietary-fat-induced taurocholic acid promotes pathobiont expansion and colitis in Il 10- mice. Nature, 2012, vol. 487, pp. 104–108.
      40. Chen Y., Blaser M. J. Helicobacter pylori colonization is inversely assosiated with childhood asthma. J. Infect. Dis, 2008, vol. 198, pp.553–560.
      41. Luther J., Dave M., Higgins R. et al. Association between Helicobacter pillory and inflammatory bowel disease: a meta- analysis and systematic review of the literature. Inflam. Bow.Dis, 2010, vol.16, pp.1077–1084.
      42. Luther J., Stephanie Y., Owyang Y. et al. Helicobacter pylori DNA decreases pro-inflammotory cytokine production by dendritic cells and attenuates dextran sulphate-induced cjlitis. Gut, 2011, vol.60, № 11, pp.1479–1486.
      43. Jonkers D., D. Renders, Masks, A., Pierik M. Probiotics in the treatment of inflammatory bowel disease (a systematic review of intervention studies among adult patients). Gastroenterology and Hepatology, 2013, № 2, pp. 28–48.
      44. Borchers A. T., SelmiC., Meyers F. J. et al. Probiotics and immunity. Gastroenterol, 2009, vol. 44, № 1, pp. 26–46.
      45. Pilipenko V. I. Probiotics as signal molecules: Saccharomyces boulardii. Clinical gastroenterology and Hepatology, 2008, vol. 1, № 6, pp. 456–462
      46. Oeschlaeger T. A. Mechanisms of probiotic actions: a review. Int. J. Med. Microbiol, 2010, vol.300, № 1, pp. 57–62.
      47. Karczewski J., Troost F. J., Konings I. et al. Regulation of human epithelial tight junction proteins by Lactobacillus plantarum in vivo and protective effects on the epithelial barrier. Am. J. Physiol. Gastrointest, 2010, vol.298, № 6, pp. G851-G859.
      48. Mattar A. F., Teitelbaum D. H., Drongowski R. A. et al. Probiotics up-regulate MUC-2 mucin gene expression in a Caco-2 cell-culture model. Pediatr. Surg. Int, 2002, vol.18, № 7, pp. 586–590.
      49. Claes I. J., Keersmaecker S. C., Vanderleyden J. et al. Lessons from probiotic-host interaction stadies in murine models of experimental colitis. Mol. Nutr.Food Res, 2011, vol.55, № 10, pp. 1441–1453.
      50. Guslandi M., Mezzi G., Testoni P. A. Saccaromycesboulardimaitenanse treatment of Crohnsdesease. Dig. Dis. Sci, 2000, vol.11, pp.1462–1464.
      51. Khalili H., Granath F., Smedby K. E. et al. Association Between Long-term Oral Contraceptive Use and Risk of Crohn’s Disease Complications in a Nationwide Study. Gastroenterology, 2016, vol.150, № 7, pp. 1561–1567.
      52. Moayyedi P. Fecal Transplantation: Any Real Hope for Inflammatory Bowel Disease? Curr. Opin.Gastroenterol, 2016, vol. 32, № 4. – pp. 282–286.
     


    Full text is published :
    Pershko A. M., Grinevich V. B., Solovyov I. A., Shotik A. V., Kurilo D. P. PRIVATE THE PATHOGENESIS OF INFLAMMATORY BOWEL DISEASES. Experimental and Clinical Gastroenterology Journal. 2018;153(05):140-149
    Read & Download full text

    1. V. I. Vernadsky Crimean Federal University (Simferopol, Russian Federation)
    2. Kazan Federal University (Kazan, Russian Federation)
    3. Kazan State Medical University (Kazan, Russian Federation)

    Abstract:In different years ileocecal valve was named in honor of Gabriele Fallopio (1523-1562), Costanzo Varolio (1543-1575), Caspar Bauhin (1560-1624), Nicolas Tulp (1593-1674), and, perhaps, Alexander Macalister (1844-1919). It’s most detailed description is found in N. Tulp’s work. Article provides its Russian translation. Biography of N. Tulp and his contribution to medicine is briefly set out.

      1. Goncharov N. I. Illyustrirovannyj slovar' ehponimov v morfologii. Volgograd: Izdatel', 2009. – 504s.
      2. Stedman Th. L. Stedman’s medical eponyms. Baltimore: Lippincott Williams & Wilkins, 2005. – 899p.
      3. Van Hoof H. Dictionnaire des éponymes médicaux: français-anglais. Louvain: Peeters Publishers, 1993. – 405p.
      4. Reuter P. Wörterbuch der Humanbiologie / Dictionary of Human Biology: Deutsch-Englisch / Englisch-Deutsch. English-German / German-English. Basel: Birkhäuser, 2000. – 992p.
      5. Tulp N. Observationum medicarum. Amstelredami: Ludovicum Elzevirium, 1641. – 279p.
      6. Kutia S. A., Shaymardanova L. R. Pieter Pauw (1564–1617) // Russian Open Medical Journal. – 2017. – Vol.6, № 3. – e0309. DOI: 10.15275/rusomj.2017.0309
      7. Mellick S. A. Dr. Nicolaes Tulp of Amsterdam, 1593–1674: anatomist and doctor of medicine // ANZ J Surg. – 2007. – Vol.77, № 12. – Р. 1102–1109. DOI: 10.1111/j.1445-2197.2007.04328.x
      8. Simpson D. Nicolaes Tulp and the golden age of the Dutch republic // ANZ J Surg. –2007. – Vol.77, № 12. – Р. 1095–1101. DOI: 10.1111/j.1445-2197.2007.04327.x
     


    Full text is published :
    Kutia S.A., Nikolaeva N.G., Moroz G.A., Pikaliuk V.S., Polishchuk E. A. NICOLAS TULP’S DESCRIPTION OF THE ILEOCECAL VALVE. Experimental and Clinical Gastroenterology Journal. 2018;153(05):150-153
    Read & Download full text

    1. FGBOU VO RyazGMU in the Russian Federation Ministry of Health (Ryazan, Russian Federation)

    Abstract:The article is devoted to the main life milestones of the Veteran of the Great Patriotic War, famous Soviet practicing physician gastroenterologist, professor of the Ryazan Medical University Alexander Mikhailovich Nogaller.

     
     


    Full text is published :
    Butov M.A. THANK YOU, VETERANS!. Experimental and Clinical Gastroenterology Journal. 2018;153(05):154-155
    Read & Download full text