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

    1. Kazan State Medical Academy — Branch Campus of the Federal State Budgetary Educational Institution of Further Professional Education “Russian Medical Academy of Continuous Professional Education” of the Ministry of Healthcare of the Russian Federation, 420012, Kazan, Russia
    2. Federal State Budgetary Educational Institution of Higher Education “Kazan Medical University” of the Ministry of Healthcare of the Russian Federation, 420012, Kazan, Russia
    3. State autonomous health care institution “Republican Clinical Hospital Department of Health of the Republic of Tatarstan”, 420064, Kazan, Russia

    Keywords: infl ammatory bowel disease, ulcerative colitis, Crohn’s disease, fecal β-glucuronidase

    Abstract:The aim of research: to investigate the activity of β-glucuronidase in coprofi ltrates (OR feces) in patients with infl ammatory bowel diseases — UC and CD at diff erent severity levels (form of disease- mild, middle, severe) and to determine the signifi cance as a laboratory criterion in the diagnosis, treatment and prognosis of IBD. Materials and methods. In research was prospectively studied 105 patients — 82 patients with IBD (29 patients with CD, 53 patients with UC) and 23 healthy volunteers without clinical laboratory indicators of infl ammatory processes in the organism and diseases of the colon as the comparison group. The activity of β-glucuronidase in feces was determined using phenolphthalein glucuronide as a substrate. Results. The activity of β-glucuronidase in feces in patients with IBD did not diff er from the healthy group (comparison group): in patients with IBD — 86.81 ± 8.4 μM / g / hr, and in norm, healthy group (comparison group) 76.04 ± 10.13 μM / g / hr (p> 0.05). Also we did not fi nd signifi cant diff erences in the activity of β-glucuronidase in patients with CD and UC, in comparison with the norm (healthy group), or between groups of patients with IBD (CD and UC). In both forms of IBD, we did not fi nd signifi cant diff erences in the activity of β-glucuronidase in patients with severe, mild or middle severity level of disease, as in comparison with healthy group so as between group of severity level. Conclusion. We have established that the activity of fecal β-glucuronidase in patients with diff erent severity levels CD and UC did not diff er from in patients of healthy group. Determination of the activity of fecal β-glucuronidasecan not use as objective laboratory criteria for determining the severity of IBD and predicting the course of the disease and, apparently, does not have essential value in the pathogenesis of IBD.

      1. Bien J. Th e intestinal microbiotadysbiosis and Clostridium diffi cile infection: is there a relationship with infl ammatory bowel disease? / J. Bien, V. Palagani, P. Bozko // Th erapAdvGastroenterol. – 2013. – № 6. – P. 53–68.
      2. Monaghan T. M. Pathogenesis of Clostridium diffi cile Infection and Its Potential Role in Infl ammatory Bowel Disease / T. M. Monaghan, A. Cockayne, Y. R. Mahida // Infl amm Bowel Dis. – 2015. – № 21 (8). – Р. 1957–1966.
      3. Mroczyńska M, Galecka M, Szachta P, Kamoda D, Libudzisz Z, Roszak D. Beta-glucuronidase and Beta-glucosidase activity in stool specimens of children with infl ammatory bowel disease.// Pol J Microbiol. 013;62(3):319–25.
      4. Samuel J. Pellock and Matthew R. Redinbo. Glucuronides in the gut: Sugar-driven symbioses between microbe and host// J. Biol. Chem. (2017) 292(21) 8569–8576
      5. McBain A. J., Macfarlane G. T. (1998) Ecological and physiological studies on large intestinal bacteria in relation to production of hydrolytic and reductive enzymes involved in formation of genotoxic metabolites. J Med Microbiol 47: 407–416
      6. Shiau S. Y., Chang G. W. (1983) Eff ects of dietary fi ber on fecal mucinase and β-glucuronidase activity in rats. J Nutr 113: 138–144
      7. Kim DH, JinYH (2001) Intestinal bacterial β-glucuronidase activity of patients with colon cancer. Arch Pharm Res 24: 564–567
      8. Ivashkin V. T., Shely`ginYu.A., Abdulganieva D. I. i dr. Proekt klinicheskix rekomendacij po diagnostike i lecheniy u vzrosly`x pacientov s yazvenny`m kolitom [Draft clinical guidelines for the diagnosis and treatment of adult patients with ulcerative colitis]. Koloproktologiya – [Coloproctology], 2013, no. 3(45), – pp. 2–21.
      9. Ivashkin V. T., Shely`gin Yu. A., Abdulganieva D. I. i dr. Proekt klinicheskix rekomendacij podiagnostike i lecheniy u vzrosly`x pacientov s yazvenny`m kolitom [Draft clinical guidelines for the diagnosis and treatment of adult patients with ulcerative colitis]. Koloproktologiya – [Coloproctology], 2013, no. 3(45), – pp. 22–38.
      10. James D. Lewis Use of the Non-invasive Components of the Mayo Score to Assess Clinical Response in Ulcerative Colitis / James D. Lewis, ShaokunChuai, Lisa Nessel et al. // Infl amm Bowel Dis. – 2008. – № 14(12). – Р. 1660–1666.
      11. Best W. R. Rederived values of the eight coeffi cients of the Crohn’s disease activity index (CDAI) / W. R. Best, J. M. Becktel, J. W. Singleton // Gastroenterology. – 1979. – № 77. – Р. 843–846.
      12. Qin X. Etiology of infl ammatory bowel disease: a unifi ed hypothesis./ Qin X// World J Gastroenterol. 2012 Apr 21; 18(15): 1708–1722.
      13. Qin XF. Impaired inactivation of digestive proteases by deconjugated bilirubin: the possible mechanism for infl ammatory bowel disease. Med Hypotheses 2002; 59: 159–163 [PMID: 12208202DOI: 10.1016/S0306– 9877(02)00243–8]
      14. McIntosh FM, Maison N, Holtrop G, Young P, Stevens VJ, Ince J, et al. Phylogenetic distribution of genes encoding beta-glucuronidase activity in human colonic bacteria and the impact of diet on faecal glycosidase activities. // Environ Microbiol. 2012
     


    Full text is published :
    Zinkevich O. D., Safi na N. A., Abdulganieva D. I., Korovina M. O., Mukhametova D. D., Odintsova A. Kh., Zimaleeva D. Е. Activity of fecal β-glucuronidase in patients with infl ammatory bowel diseases. Experimental and Clinical Gastroenterology. 2019;162(2): 14–18. (In Russ.) DOI: 10.31146/1682-8658-ecg162-2-14-18
    Read & Download full text

    1. Azerbaijan State Advanced Training Institute for doctors named after A.ALIYEV, Baku AZ1012, Azerbaijan
    2. National Center of Oncology, department of invasive diagnostics and treatments, Baku AZ1122, Azerbaijan

    Keywords: ulcerative colitis, Crohn’s disease, infl ammatory bowel disease, endothelial dysfunction, severity

    Abstract:Aim: to create a system for monitoring the condition of patients with infl ammatory bowel disease (IBD). Subjects and methods: In the period from August 2015 to December 2018, 246 patients with IBD were examined at the clinical base of the Department of Therapy Azerbaijan State Advanced Training Institute for doctors named after A.ALIYEV, the Department of Invasive Diagnostics and Treatment of the National Center of Oncology, Memorial Klinika Medical Center. The content of homocysteine, highly sensitive C-reactive protein (h/s CRP), vitamin D and the level of platelets in the blood, albumin in the urine, and calprotectin in the feces were determined in all subjects. Patients were retested if necessary (426 in total) Results: In the general group of patients with IBD, of the 426 studies conducted in 369 (86.6%) cases, there was an increased content of homocysteine i n the blood, in 405 (95.0%) — the level of h/s CRP, in 322 (75.5%) — thrombocytosis, in 411 (96.4%) — a decrease in the content of vitamin D, in 308 (72.3%) albumin was detected in the urine, and in 411 (96.4%) — an increased content of calprotectin was detected in the feces. When analyzing the identifi cation of each of these indicators separately in the UC and CD groups, no diff erence was found (p > 0.05). A correlation was found between some indicators of endothelial dysfunction and the severity of the clinical course in patients with infl ammatory bowel diseases. The proposed new approach to assessing the clinical status of patients with IBD, with the established diagnosis, does not resort to repeated costly studies and obtain real-time results that make it possible to assess the severity of the patient’s condition.

      1. Ng SC, Shi HY, Kaplan GG et al. Worldwide incidence and prevalence of infl ammatory bowel disease in the 21st century: a systematic review of population-based studies. Lancet.2018 Dec 23;390(10114):2769–2778.doi: 10.1016/S0140–6736(17)32448–0.
      2. Th ird European Evidence-based Consensus on Diagnosis and Management of Ulcerative Colitis. Part1/2. J Crohns Colitis jjx008.DOI: https://doi.org/10.1093/ecco-jcc/jjx008
      3. 3rd European Evidence-based Consensus on the Diagnosis and Management of Crohn’s Disease 2016: Part 1: Diagnosis and Medical Management. J Crohns Colitis (2017) 11 (1): 3–25.DOI: https://doi.org/10.1093/ecco-jcc/jjw168
      4. Edward L. Barnes et al. New Biomarkers for Diagnosing Infl ammatory Bowel Disease and Assessing Treatment Outcomes. Infl amm Bowel Dis. 2016 Dec; 22(12): 2956– 2965.doi: 10.1097/MIB.0000000000000903
      5. Norouzinia M., Chaleshi V. et al. Biomarkers in infl ammatory bowel diseases: insight into diagnosis, prognosis and treatment. Gastroenterol Hepatol Bed Bench. 2017 Summer; 10(3): 155–167. PMID: 29118930
      6. Derkacz A. et al. Diagnostic Markers for Nonspecifi c Infl ammatory Bowel Diseases. Disease Markers Volume 2018, Article ID7451946, 16 p. https://doi.org / 10.1155/2018/7451946
      7. Babayeva G. H., Babayev Z. M. Chastota viyavleniya nekotorix markerov endotelialnoy disfunksii u bolnix s vospalitelnimi zabolevaniyami kishechnika. Terapevticheskiy arxiv. 2018, no.4, pp.12–16. (In Russ.)
      8. Babayeva G. H., Samedova T. A., Babayev Z. M., Huseynova F. R. O roli defi sita vitamina D pri nekotorix patologicheskix sostoyaniyax.[About some vitamin D defi ciencies in certain pathological conditions]. Saglamliq. 2018, no. 2, pp.23–32. (In Russ.)
     


    Full text is published :
    Babayeva G. H., Babayev Z. M. New approach to the estimation of a clinical fl ow in patients with ulceratıve colitis and Crohn's disease. Experimental and Clinical Gastroenterology. 2019;162(2): 19–23. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-19-23
    Read & Download full text

    1. State Medical University, 644099, Omsk, Russia
    2. Regional Clinical Hospital, 644111, Omsk, Russia n

    Keywords: ulcerative colitis, nutritional factors, sugar, diet

    Abstract:The aim was to аssess the eff ect of nutritional factors on the risk of developing ulcerative colitis based on an analysis of food consumed. Assess the importance of consumption of certain nutrients in its development among the population of Western Siberia. Materials and methods: A survey of 81 patients with ulcerative colitis and 39 healthy volunteers was conducted. The profi le of the eating habits of patients with ulcerative colitis (before diagnosis) in relation to healthy respondents was investigated. Results. The diet of patients with ulcerative colitis before the fi rst signs of the disease is distinguished by the rare consumption of fresh and cooked vegetables and fruits in small portions, the consumption of more sugar with tea and / or coff ee compared to healthy ones. Also, patients poorly tolerated milk and dairy products before the debut of the disease. Conclusion. Our study confi rms the possible eff ect of a lack of dietary fi ber and excessive sugar intake on the onset of ulcerative colitis.

      1. Molodecky N. A., Soon I. S., Rabi D. M. et al. Increasing incidence and prevalence of the infl ammatory bowel diseases with time, based on systematic review // Gastroenterology. – 2012. – № 142. Р. 46–54.
      2. Ordás I., Eckmann L., Talamini M. et al. Ulcerative colitis // Lancet. – 2012. – № 380. – Р.1606–1619.
      3. Geerling B. J., Dagnelie P. C., Badart-Smook A. et al. Diet as a risk factor for the development of ulcerative colitis // Am J Gastroenterol. – 2000. – № 95. – Р.1008–1013.
      4. Sakamoto N., Kono S., Wakai K. et al. Epidemiology Group of the Research Committee on Infl ammatory Bowel Disease in Japan. Dietary risk factors for infl ammatory bowel disease: a multicenter case-control study in Japan // Infl amm Bowel Dis. – 2005. – № 11. – Р.154–163.
      5. Li F., Liu X., Wang W., Zhang D. Consumption of vegetables and fruit and the risk of infl ammatory bowel disease: a meta-analysis // Eur J Gastroenterol Hepatol. –2015. – № 27. – Р.623–633.
      6. Galvez J., Rodriguez-Cabezas M.E., Zarzuelo A. Eff ects of dietary fi ber on infl ammatory bowel disease // Mol Nutr Food Res. 2005, № 49, pp. 601–608.
      7. Chan S. S., Luben R., van Schaik F. et al. Carbohydrate intake in the etiology of Crohn’s disease and ulcerative colitis // Infl amm Bowel Dis. 2014, № 20, pp.2013–2021.
      8. John S., Luben R., Shrestha S. S. et al. Dietary n-3 polyunsaturated fatty acids and the aetiology of ulcerative colitis: a UK prospective cohort study // Eur J Gastroenterol Hepatol. – 2010. – № 22. – Р. 602–606.
      9. Ananthakrishnan A. N., Khalili H., Konijeti G. G. et al. Long-term intake of dietary fat and risk of ulcerative colitis and Crohn’s disease // Gut. – 2014. – № 63. – Р.776–784.
      10. Ivashkin V. T., Shelygin Yu.A., Khalif I. L., Belousova E. A., et al. Clinical guide of russian association of gastroenterology and russian association of coloproctology on diagnostics and treatment of ulcerative colitis. Koloproktologia. 2017;1:6–30.
      11. CINDI dietary guide, Copenhagen, WHO Regional Offi ce for Europe, 2003. – 42 p. (document EUR/00/5018028, E70041R).
     


    Full text is published :
    Bikbavova G. R., Livzan M. A., Sovalkin V. I., Turchaninov D. V., Tretyakova T. V., Lopatina O. E., Panova T. Yu. The effect of nutritional factors on the development of ulcerative colitis. Experimental and Clinical Gastroenterology. 2019;162(2): 24–27. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-24-27
    Read & Download full text

    1. Clinical Hospital № 122 L. G. Sokolova, St. Petersburg, Russia
    2. St. Petersburg State Healthcare Institution Children’s City Hospital № 2 Holy Mary of Magdalene, St. Petersburg, Russia
    3. St. Petersburg State Pediatric Medical University, Ministry of Health of the Russian Federation, St. Petersburg, Russia
    4. Pirogov Russian National Research Medical University, Ministry of Health of the Russian Federation, Moscow, Russia

    Keywords: diet for ulcerative colitis, prevention of exacerbations of ulcerative colitis, specifi c diet, food sensitization, ulcerative colitis, new methods of selection of the diet

    Abstract:There is a new principle of preparing diet for a patient with ulcerative colitis (UC). Within 4 years, we observed and comprehensively examined 60 patients UC who received standard treatment. In group 1(n=30) was used as a dietary therapy specifi c individual elimination hypoallergenic diet (ISEH diet), picked up in vitro and composed by exclusion from the diet of those products, which can be a source of food sensitization. To identify the immunopathological reactions I, III and IY types of food allergens used a range of methods — ELISA (IgE-specifi c) and the reaction of inhibition migration of leukocytes(RIML), modifi ed by NN Matyshevа and LS Kositskаyа. Group 2(n = 30) received a standard mechanically and chemically sparing diet. Patients with UC showed a high degree of sensitization to food antigens. Usage of the ISEН diet promoted a more rapid onset and prolonged maintenance of clinical and endoscopic remission, more than in the standard diet group, without the use of corticosteroids and thiopurins, as well as a signifi cant decrease in the number of disease relapses. Diet of patients with UC should be hypoallergenic. The best results are observed in the preparation of a diet based on a comprehensive individual screening-testing of food allergens using laboratory diagnostic methods based on cell-type reactions and methods for detecting specifi c antibodies to food antigens. Results of a 4- year follow-up for patients with UC show high effi cacy ISEH diet in the treatment and maintaining remission of these patients.

      1. Tutina O., Fedulova E., Kopeikin V., Fedorova O., Bogomolov A. MEDICAL NUTRITION FOR NON SPECIFIC ULCERATIVE COLITIS AND CROHN'S DISEASE IN CHILDREN. Pediatric pharmacology. 2008;5(5):110–115.
      2. Элина А. А. Клинические проявления и особенности течения неспецифического язвенного колита и болезни Крона // Новости медицины и фармации. Гастроэнтерология. – 2013. – № 2 (451). – С. 14–19.
      3. Avalueva EB, Alexandrov A.I., Bagnenko S.F., et al. European Consensus on the Diagnosis and Treatment of Crohn's Disease. RMJ. 2012, no. 15, pp. 714–747.
      4. Ivashkin V.T., Shelygin Yu.A., Abdulganiyeva D.I., et al. Guidelines of the Russian gastroenterological association and Russian Association of Coloproctology on diagnostics and treatment of ulcerative colitis in adults. Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2015;(1):48–65.
      5. Diet in the pathogenesis and treatment of infl ammatory bowel diseases / D. Lee, L. Albenberg, C. Compher [et al.] // Gastroenterology. – 2015. – Vol. 148 (6). – P. 1087–1106.
      6. Белогурова М.Б., Гончар Н. В., Григович И. Н., Думова Н. Б., Корниенко Е. А., Косенко И. М., Луппова Н. Е., Мельникова И. Ю., Новикова В. П., Приворотский В. Ф., Пронина Е. В., Храмцова Е. Г. Детская гастроэнтерология. Практическое руководство / Под редакцией И. Ю. Мельниковой. Москва, 2018. Сер. Библиотека врача-специалиста
      7. Фролькис. А. В. Заболевания кишечника. – СПб.: ООО «Издательство Фолиант», 2003. – 192 с.
      8. Рот М., Бернхардт В. Воспалительные заболевания кишечника. Практическое руководство / под ред. проф. В. Ю. Голофеевского, С. И. Ситкина. – СПб.: Dr. Falk Pharma, 2007. – 60 с.
      9. Барановский Ю.А., Назаренко Л. И., Райхельсон К. Л. Пищевая непереносимость: учебно-методическое пособие. – СПб.: Издательство «Диалект», 2006. – 136 с
      10. Гурина О.П., Степанова А. А., Дементьева Е. А., Блинов А. Е., Варламова О. Н., Блинов Г. А. Взаимосвязь показателей специфического гуморального иммунитета и показателей аутоагрессии при воспалительных заболеваниях кишечника у детей. В сборнике: Воронцовские чтения. Санкт-Петербург – 2018 материалы XI Российской научно-практической конференции. 2018. С. 17–18.
      11. Гурина О.П., Степанова А. А., Дементьева Е. А., Блинов А. Е., Варламова О. Н., Блинов Г. А. Особенности аутоиммунных реакций при болезни Крона у детей. Клиническая лабораторная диагностика. 2018. Т. 63. № 1. С. 44–50.
      12. Гурина О.П., Дементьева Е. А., Блинов А. Е., Варламова О. Н., Блинов Г. А. Иммунологический профиль у детей с болезнью Крона. Медицинская иммунология. 2017. Т. 19. № S. С. 159.
      13. Reddavide R, Rotolo O, Caruso MG, Stasi E, Notarnicola M, Miraglia C, Nouvenne A, Meschi T, De’ Angelis GL, Di Mario F, Leandro G. Th e role of diet in the prevention and treatment of Infl ammatory Bowel Diseases. Acta Biomed. 2018 Dec 17;89(9-S):60–75. doi: 10.23750/abm. v89i9-S.7952.
      14. Новик Г.А., Ткаченко М. А. Гастроинтестинальные проявления пищевой аллергии у детей // Лечащий врач. – 2012. – № 1. – C. 16–25.
      15. Pearlman M, Akpotaire O. Diet and the Role of Food in Common Gastrointestinal Diseases. Med Clin North Am. 2019 Jan;103(1):101–110. doi: 10.1016/j.mcna.2018.08.008. Review.
      16. DeGeeter C, Guandalini S. Food Sensitivities: Fact Versus Fiction. Gastroenterol Clin North Am. 2018 Dec;47(4):895–908. doi: 10.1016/j.gtc.2018.07.012. Epub 2018 Oct 5. Review.
      17. Новикова В.П., Ревнова М. О., Листопадова А. П. Синдром раздраженной кишки и пищевая аллергия у детей. Педиатр. 2018. Т. 9. № 2. С. 71–77.
      18. Aleksandrova K, Romero-Mosquera B, Hernandez V. Diet, Gut Microbiome and Epigenetics: Emerging Links with Infl ammatory Bowel Diseases and Prospects for Management and Prevention.Nutrients. 2017 Aug 30;9(9). pii: E962. doi: 10.3390/nu9090962. Review.
      19. Матышева Н. Н. Новый способ определения специфической сенсибилизации организма к пищевым аллергенам // Медицинская иммунология. – 2000. – Т. 2, № 2. – С. 113–252.
      20. Халиф И.Л., Лоранская И. Д. Воспалительные заболевания кишечника (неспецифический язвенный колит и болезнь Крона): клиника, диагностика и лечение. – М.: «Миклош», 2004. – 88 с.
      21. Общая аллергология / под ред. Г. Б. Федосеева. – СПб.: Нормед–Издат, 2001. – Т. 1. – С. 501.
      22. Митин Ю. А. Лабораторная диагностика аллергических заболеваний. Методические рекомендации. – СПб., 2010. – 144 с.
      23. Неспецифические воспалительные заболевания кишечника / под ред. Г. И. Воробьева, И. Л. Халифа. – М.: Миклош, 2008 – C. 400.
      24. Lochs H. Disturbed intestinal permeability is a pathogenetic factor for infl ammatory bowel diseasе? // Falk Symp. – 1997. – N98. – P. 65.
     


    Full text is published :
    Kryukova O. A., Matysheva N. N., Drygin A. N., Khavkin A. I. Use of a customized hypoallergenic diet in treatment of patients with the infl ammatory bowel diseases. Experimental and Clinical Gastroenterology. 2019;162(2): 28–35. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-28-35
    Read & Download full text

    1. Institute of Osteopathy, 191024, Degt’arnaya str.1A, St. Petersburg, Russian Federation
    2. North-Western State Medical University named after I. I. Mechnikov, Ministry of Health of Russian Federation, 191015, Kirochnay street, 41, Saint-Petersburg, Russian Federation
    3. St. Petersburg State University, 199034, University emb, 7/9, Saint-Petersburg, Russian Federation

    Keywords: osteopathic methods, somatic dysfunction, motor-evacuation functions of the digestive tract, celiac disease

    Abstract:The article presents the results of clinical eff ectiveness of osteopathic correction methods in the treatment of motor-evacuation disorders of the digestive tract in celiac patients based on a comparison of clinical and instrumental data. Materials and methods: 26 patients with celiac disease aged from 18 to 35 years old, in which General clinical, endoscopic and PEGEG studies revealed disorders of motor activity of the digestive tract. The examined patients had been carried out 5 sessions of osteopathic procedures to correct their motor-evacuation disorders of the gastrointestinal tract (GI). Results: the examined patients were observed to have osteopathic disorders, indicating regional somatic dysfunction and combined motility disorders of the upper and lower digestive tract in both phases of the PEGEG. The use of osteopathic correction, aimed at mobilizing the compensatory-adaptive mechanisms of the body, was eff ective for discontinuing gastroenterological symptoms, normalization of propulsive and tonic activity of the gastrointestinal tract. Conclusion: osteopathic correction can be used in the treatment of patients with motility disfunction of the digestive tract.

      1. Berseth CL (1996) Gastrointestinal motility in the neonate. Clin Perinatol. 1996; 23(2):179–90.
      2. Cuomo R, Sarnelli G. Food intake and gastrointestinal motility. A complex interplay. – Nutr Metab Cardiovasc Dis. 2004; 14:173–179
      3. Ugolev A. M. Evoluciya pishevareniya I principi evolucii funkcii [Evolution of digestion and principles of function evolution]. Leningrad, Nauka, 1985. 315 p.
      4. Pokrovskii M. V., Korotko G. F. Fisiologiy cheloveka: uchebnik v 2 tomah [Human fi siology: textbook in 2 toms]. Moscow, Medicina, 2003. 656 p.
      5. Onopriev V. V. Funkcionalnie narusheniy verchnich otdelov pishevaritelnoi sistemi pri rubcovo-yazvennom duodenostase [Functional disorders of the upper digestive system during scar-ulcerative duodenostas]. Kuban scientifi c medical Bulletin. 2006; 7: 93–101.
      6. Shmodt R., Tevs G. Fisiologiy cheloveka: uchebnik v 3 tomah. Tom 3 [Human fi siology: textbook in 3 toms. Tom 3]. Moscow, Mir, 1996. 313 p. ISBN5–03–003577-х.
      7. Mironov A. V., Petuhov V. A., Saveliev V. S., et al. Vliyanie operacii holecistectomii na motoriky organov geludochno-kishechnodo trakta [Th e eff ect of cholecystectomy operation on the motility of the gastrointestinal tract]. Endoscopic surgery. 2007; 3: 32–38.
      8. Avdeev V. G. Klinicheskie proyavleniya, diagnostika I lechenie rasstroistv motornoi funkcii dvenadcatiperstnoi kishki [Clinical manifestations, diagnosis and treatment of disorders of motor function of the duodenum]. Russian journal of Gastroenterology, Hepatology and Coloproctology. 1997; 5: 83–88.
      9. Strods Y. Y., et al. Vosmognosti diagnostiki I korrekcii narushenii duodenalnoi prochodimosti [Possibilities of diagnosis and correction of duodenal patency disorders]. Sovremennie aspekti teoreticheskoi I prakticheskoi gastroenterologii: sbornik statei, 1988, pp. 163–166.
      10. Gaivoronskii I. V., Nechiporuk G. I. Funkcionalnay anatomiy pishevaritelnoy sistemi [Functional anatomi of digestive system]. Saint-Petersburg, Elsbi-SPb, 2008. 71 p.
      11. Sheptulin A. A. Diagnosis and treatment of gastrointestinal motility disorders. Russian Medical journal, 1997, vol. 5, no. 22. Available at: https://www.rmj.ru/ articles/gastroenterologiya/DIAGNOSTIKA_I_lechenie_narusheniy_MOTORIKI_gheludochno-kishechnogo_TRAKTA/ (Accessed 18 November 1997).
      12. Paoletti S. F. Rol tkanei v organizme cheloveka [Role of tissues in human organism]. Saint-Petersburg, Neva Press, 2012. 308 p.
      13. Barral G. P. Visceralnie manipulycii [Visceral manipulation]. Moscow, Mig, 1999. 287 p.
      14. Carolinc Stone, Visceral and Obstetrik Osteopathy. – Elsevier. Ltd, 2007, 349 с.
      15. Mochov D. E., et al. Osteopaticheskay diagnostika somaticheskix disfunkcii. Klinicheskie rekomendacii [Osteopathic diagnosis of somatic dysfunctions. Clinical recommendations]. Saint-Petersburg, Nevskii rakurs, 2015. 90 p.
      16. Skoromec A. A., Egorova I. A., et al. Osteopaticheskie priemi diagnostiki I korrekcii organov geludochno-kishechnogo trakta [Osteopathic methods of diagnosis and correction of the gastrointestinal tract]. Saint-Petersburg, MAPO. Institut osteopaticheskoi medicini, 2010. 16 p.
      17. Mohov D. E., Tregubova E. S., et al. Sovremenniy vzglyd na metodologiu osteopatii [Modern view on the methodology of osteopathy]. Manual Th erapy, 2014; 4 (56): 59–65.
      18. Mohov D. E., Mariyanovich A. T. Osteopatiy kak dokasatelnay medicina [Osteopathy as evidence-based medicine]. Russian osteopathic journal, 2013;1–2(20– 21):138–154.
      19. Mohov D. E. Sovremennay metodologiy osteopatii [Modern methodology of osteopathy]. Moscow, Nevronews. 2015; 1: 8–9.
      20. Lazebnik L. B.1, Tkachenko Ye. I., Oreshko L. S. et al. Guidelines for diagnosis and treatment of celiac disease. Experimental and Clinical Gastroenterology. 2015; 117 (5): 3–12
      21. Stupin V. A. Funkcionalnay gastroenterologiy. Instrumentalnie metodi issledovaniy: posobie dly vrachei [Functional gastroenterology. Instrumental methods of research: a manual for doctors]. Moscow, Medpraktika- M, 2009. 28 p.
      22. Smirnova G. O. Perifericheskay elektrogastroenterografi y v klinicheskoy praktike: posobie dly vrachei [Peripheral electrogastroenterography in clinical practice: a manual for physicians]. Moscow, Medpraktika-M, 2009. 20 p.
     


    Full text is published :
    Оrеshkо A. Yu., Mokhov D. E., Tregubova E. S., Оrеshkо L. S., Seliverstov P. V., Semenova Е. A. Functional disorders of motor activity of the digestive tract and their osteopathic correction in patients with celiac disease. Experimental and Clinical Gastroenterology. 2019;162(2): 36–44. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-36-44
    Read & Download full text

    1. Kemerovo State Medical University, 650056, Kemerovo, Russia
    2. Research Institute for Complex Issues of Cardiovascular Diseases, 650002, Kemerovo, Russia

    Keywords: rectal cancer, TP53, rs1042522, Arg72Pro

    Abstract:The aim was to investigate the prevalence of genetic variants of marker rs1042522 (Arg72Pro) of TP53 among individuals without cancer and patients with colon cancer. Materials and methods. Using allele specifi c PCR we performed genotyping of rs1042522 marker with subsequent comparing of alleles and genotypes frequencies in two studied groups: the comparison group (n=119) and the group of patients with rectal cancer (n=105). Results. Proportion of the minor allele Pro with the expected pathological eff ect in the comparison group was 26,9%, and among patients with rectal cancer — 26,7%. The frequency of the Pro/Pro genotype in the two groups was 6,7% and 5,7%, respectively. The distinction in indicators was not statistically signifi cant.

      1. Kopnin B. P., Kopnin P. B., Khromova N. V., Agapova L. S. Multifaced р53: variety of forms, functions, tumor-suppressive and oncogenic activities. Clinical oncohematology. 2008; 1(1): 2–9.
      2. Horn H.F., Vousden K. H. Coping with stress: multiple ways to activate p53. Oncogene, 2007, vol. 26, no. 9, pp. 1306–1316.
      3. Wilson J. M. Gendicine: the fi rst commercial gene therapy product. Hum Gene Th er., 2005, vol. 16, pp. 1014–1015.
      4. Olivier M., Hollstein M., Hainaut P. TP53 mutations in human cancers: origins, consequences, and clinical use. Cold Spring Harb Perspect Biol., 2010, vol. 2, pp. 1–17.
      5. Lyubchenko L. N., Semyanikhina A. V., Fu R. G., Prozorenko E. V. et al. Li-Fraumeni syndrome: TP53-associated multiple primary malignant tumors. Journal of N. N. Blokhin Russian Cancer Research Center RAMS. 2012; 23(2): 52–58.
      6. Aizat A.A., Shahpudin S. N., Mustapha M. A., Zakaria Z. et al. Association of Arg72Pro of P53 polymorphism with colorectal cancer susceptibility risk in Malaysian population. Asian Pacifi c J Cancer Prev., 2011, vol. 12, pp. 2909–2913.
      7. Koushik A., Tranah G. J., Ma J., Stampfer M. J. et al. P53 Arg72Pro polymorphism and risk of colorectal adenoma and cancer. Int. J. Cancer, 2006, vol. 119, pp. 1863–1868.
      8. Song H., Kweon S., Kim H. N. P53 codon 72 polymorphism in patients with gastric and colorectal cancer in a Korean population. Gastric Cancer, 2011, vol. 14, pp. 242–247.
      9. Bland J.M., Altman D. G. Statistics notes: Th e odds ratio. B.M.J., 2000, vol. 320, p. 1468.
      10. Csejtei A., Tibold A., Varga Z. GSTM, GSTT and p53 polymorphisms as modifi ers of clinical outcome in colorectal cancer. Anticancer Research, 2008, vol. 28, pp. 1917–1922.
      11. Stepanov V. A. Genoms, populations, diseases: ethnogenomics and personify medicine. Acta Naturae. 2010; 2(4): 15–30.
      12. Brevik А., Amit D., Onland-Moret N. Polymorphisms in base excision repair genes as colorectal cancer risk factors and modifi ers of the eff ect of diets high in red meat. Cancer Epidemiol Biomarkers Prev., 2010, vol. 19, pp. 3167–3173.
     


    Full text is published :
    Volkov A. N., Padukova A. D., Zinchuk P. V., Kutikhin A. G. Polymorphysm of tumor supressor gene tp53 among healthy donors and patients with rectal cancer. Experimental and Clinical Gastroenterology. 2019;162(2): 45–49. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-45-49
    Read & Download full text

    1. Federal State Funded Edication Institution of Higher Education “Khakass State University named after N. F. Katanov”, 655000, Abakan, Russian Federation
    2. Federal state autonomous educational institution of higher education “Crimean Federal University named after V. I. Vernadsky” Medical Academy named after S. I. Georgievsky, 295051, Simferopol, Crimea, Russian Federation

    Keywords: colorectal cancer, anamnesis of life, factors risk

    Abstract:Aim to study the frequency, expression and simultaneity of risk factors for colorectal cancer in hospital patients. Materials and methods. The statistics of 1690 colorectal cancer (CRC) patients were retrospectively studied. Clinical signs were assessed according to the case histories of 180 patients with colorectal cancer, selected by random sampling and systematic sampling (every tenth of the total population of all patients with CRC). Questioning patients with CRC, based on their informed consent, studied risk factors in 80 people (random sample; every second of the average annual number of patients with CRC). Results. The share of women was 52.5%, men — 47.5%. The average age of patients is 69 (61–77) years. Before the manifestation of colorectal cancer, patients had an overweight in 40.9% of cases, obesity in 39.4% of cases. Women with colorectal cancer more often than men had type 2 diabetes mellitus 4 times (p = 0.015), cholecystectomy 2.5 times (p = 0.09), combined pathology 3 times (p = 0.24) and prolonged history of IBD 5 times (p <0.05). In men with colorectal cancer, hypodynamia (5 times, p = 0.003) and smoking (2 times, p = 0.23) occurred more often than in women. Conclusion. Risk factors for colorectal cancer were, 55 years of age, overweight or obesity, type 2 diabetes.

      1. Clinical guidelines for the diagnosis and treatment of patients with rectal cancer (2014). Available at: http:// oncology-association.ru/docs/recomend/dec2015/41vzrek.pdf (accessed 8 December 2016).
      2. Practice Guidelines the World Gastroenterology Society and the International Union for the prevention of digestive system cancer: Screening for colorectal cancer (2008). Available at: http://www.worldgastroenterology. org/UserFiles/fi le/guidelines/colorectal-cancer-screening-russian-2008.pdf. (accessed 8 December 2016).
      3. Fedorov V. E., Podelyakin K. A. Epidemiologicheskie aspektyi kolorektalnogo raka [Epidemiological aspects of colorectal cancer]. Medicinskij al’manah, 2017, no.4(49), pp.145–148.
      4. Kushi L. H., Doyle C., McCullough M., Rock C. L. American Cancer Society guidelines on nutrition and physical activity for cancer prevention: reducing the risk of cancer with healthy food choices and physical activity. CA Cancer J Clin. 2012; vol.62, no.1, pp.30–67. doi:10.3322/caac.20140
      5. World Cancer Research Fund. Food, nutrition, physical activity, and the prevention of cancer: a global perspective. Washington, DC: World Cancer Research Fund/American Institute of Cancer Research (2007). Available at: https://www.wcrf.org/sites/default/fi les/ english.pdf (accessed 8 December 2016).
      6. Akinyemiju T., Wiener H., Pisu M. Cancer-related risk factors and incidence of major cancers by race, gender and region; analysis of the NIH-AARP diet and health study. BMC Cancer. 2017, vol. 17, pp. 597.
      7. Zhunusova G. S. Razrabotka panelej geneticheskih markerov dlya skrininga semejnyh i sporadicheskih sluchaev kolorektal’nogo raka v kazahstanskih populyaciyah Diss. dokt. fi losof. nauk. [Th e development of genetic markers for screening panels familial and sporadic cases of colorectal cancer in the population of Kazakhstan. Doct. Diss.] Astana, 2014. 125 p.
      8. Zhivotovskiy A. S., Kuthin A. G., Brusina E. B., Tsitko E. A. Epidemiologiya kolorektalnogo raka: obzor faktorov riska [Colorectal Cancer Epidemiology: Review of Risk Factors]. Epidemiologiya i vakcinoprofi laktika, 2013, no.1 (68), pp.58–64.
     


    Full text is published :
    Shtygasheva O. V., Ageeva E. S., Guzar Ya. R. Anamnestic predictors of colorectal cancer. Experimental and Clinical Gastroenterology. 2019;162(2): 50–54. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-50-54
    Read & Download full text

    1. GBUZ Moscow Clinical Research Center named after A. S. Loginov DZM, 111123, Moscow, Russia
    2. Federal State Budgetary Educational lnstitution of Further Professional Education «Russian Medical Academy of Postgraduatc Educatioп» of the Ministry of Healthcare of the Russian Federation, Moscow, Russia
    3. Pirogov Russian National Research Medical University, Moscow, Russia
    4. Moscow State University of Medicine and Dentistry named after A. I. Evdokimov, 127473, Moscow, Russia

    Keywords: nutritional drugs

    Abstract:In the literature there is little information about the occurrence of dielectrolytes with inadequately selected parenteral-enteral correction. This fully applies to the correction of iron defi ciency in colorectal cancer (CRC). Material and methods. On examination were 51 patients with CRC (T3N1M0 and T4N0M1) and iron defi ciency of various severity. Nutritional status was assessed by the parameters of a known alimentary-volemic diagnosis (AED). Iron defi ciencies resulting from chronic blood loss were assessed by the content of serum iron, ferritin, transferrin, the level of Hb and Ht, the number and average volume of red blood cells, and the average content of Hb in the red blood cell. The control group consisted of 10 patients with iron-defi cient anemia. Results. One of the components of the AVD is the determination of electrolyte defi ciencies, including gland. With a defi cit of free iron in plasma up to 11%, a decrease in hemoglobin level and Ht, a slight decrease in the number of erythrocytes and normal parameters of ferritin, the average volume of erythrocyte and the content of Hb in it were suffi cient nutritive correction mixtures containing 3.0–3.5 mg of iron in 100 g dry product. With a higher iron defi ciency, additional parenteral administration of its drugs was required: as part of the nutritional correction, as a pharmacological supplement, supplements were injected with non-sorbed or sorbed iron on a special matrix (ironMatrix), which guaranteed the stability of the iron complex and its controlled release in the body. At the same time, sorbed iron provided a higher safety (no complications were observed in any of the studies. with the administration of non-sorbed iron in 2 cases, there were unpleasant sensations in the heart area, in the right hypochondrium, resembling signs of iron overload (ferritin could increase to 1340 mg), stopped, however, only by the administration of a hepatoprotector and 0.9% of the sodium chloride solution without the additional use of an antidote. Conclusion. For the sake of safety of iron defi ciency correction (prevention of toxic-metabolic complications) when conducting a comprehensive nutritional correction in patients with CRC complicated by mild chronic anemia with iron defi ciency not more than 11%, it is advisable to use drugs containing iron (3–3.5 mg per 100 g of dry product), and in case of a pronounced shortage of it, supplement the nutritional support with parenteral preparations of sorbed iron under the control of the parameters of iron metabolism.

      1. OA Rukavitsyn Anemias. Moscow, Geotar-Media, 2018.-165 p.
      2. I. Ye. Hatkov, L. N. Kostyuchenko. Nutritiology in oncology of the digestive tract. Moscow., 2018. – 346 p.
      3. J. Meyerhardt, M. Sanders / Colon cancer. Moscow., 2009.183 p.
      4. V. J. Marshall. Clinical biochemistry. – M., 2015, p. 343–346.
      5. Perevodchicova NI, Guidelines for the chemotherapy of tumor diseases. 4th ed. M., Practical medicine, 2018, p. 208–223.
      6. Vartanian A. A. Iron metabolism, ferroptosis and cancer. – Russian journal of biotherapy. 2017; vol. 16:14–20. –6
      7. Fonseca-Nunes A., Jakszyn P., Agudo A. Iron and cancer risk – a systematic review and meta-analysis of the epidemiological evidence. Cancer Epidemiol Biomarkers Prev2014;23:12–31. PMID: 24243555. –7
      8. Bregman, D. et al. Hepcidin levels predict non-responsiveness to oral iron therapy in patients with iron defi ciency anaemia. Am J Hematol 2013 Feb;88(2):97–10–8
      9. Ludwig H. et al. Iron metabolism and iron supplementation in cancer patients. Wiener klinische Wochenschrift 127.23–24 (2015): 907–919–9
      10. Gozzelino R., Arosio P. Iron Homeostasis in Health and Disease. Int J Mol Sci 2016;115. –10
      11. Kew M. C. Hepatic iron overload and hepatocellular carcinoma. Liver Cancer. 2014;3(1.:31–40. DOI: 10.1159/00034–11
      12. Cao J. Y., Dixon S. J. Mechanisms of ferroptosis. Cell Mol Life Sci 2016;73:2195–209. DOI: 10.1007/s00018–016–2194. PMID: 27048822. –12
      13. Kaminski M. M. et al. Inhibition of constitutively activated NF-κB induces ROS- and iron dependent cell death in cutaneous T cell lymphoma. Cancer Res 2009;69(6.:2365–74. DOI: 10.1158/0008–5472. PMID: 19258503–13
      14. Snegovoy A. V., Aargo M., et al. Malignant tumors.-2016.-№ 4. – p. 368–377.
      15. Malignant tumors. Practical recommendations of the Russian Society of Clinical Oncology. M..2018, p. 494–502 and 289–325.
      16. Ludwig H., Aapro M., Bokemeyer C. et al. Treatment patterns and outcomes in the management of anaemia in cancer patients in Europe: fi ndings from the Anaemia Cancer Treatment (ACT) study. Eur. J. Cancer 2009; 45: 1603–15–16
      17. Wang J., Pantopoulos K. Regulation of cellular iron metabolism // Biochem J. 2011; 434(Pt 3): 365–381–18
     


    Full text is published :
    Kostyuchenko L. N., Mikhaylyants G. S., Danilov M. A., Atroshchenko A. O., Kruglov A. D., Kuzmina T. N., Noskova K. K., Kostyuchenko M. V., Zhu-kova L. D., Lychkova A. E., Govaleshko A.Yu. Management of Iron defi ciency syndromes and their correction with nutritional drugs Experimental and Clinical Gastroenterology. 2019;162(2): 55–67. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-55-67
    Read & Download full text

    1. Saratov State Medical University n. a. V. I. Razumovsky of the Ministry of Healthcare of the Russian Federation, Saratov, Russia
    2. “Мedical Di center” LLC, Saratov, Russia

    Keywords: Irritable bowel syndrome, refractoriness to treatment, genetic polymorphism, psychological factors.

    Abstract:Purpose of the study. Тo determine predictors of refractory course of irritable bowel syndrome with consideration for genetic markers and psychological peculiarities of patients. Materials and methods. 101 patients with irritable bowel syndrome (73 with refractory form of irritable bowel syndrome, 28 with non-refractory form of the same) have been examined. We analyzed the triggers of the disease, assessed the levels of distress, depression, anxiety, somatization, and aggression, and we have determined polymorphic variants of genes COMT Val158Met, TLR9 G2848A, TLR9 T-1237C. Results. Refractory variant of irritable bowel syndrome is associated with the onset at an earlier age, social and psychological triggers, extraintestinal manifestations and non-gastroenterological symptoms, high levels of distress, depression, anxiety, somatization, and aggression. We have revealed that refractoriness and some clinical forms of irritable bowel syndrome are associated with polymorphic variants of certain genes. Conclusion. Refractory variant of irritable bowel syndrome is associated with certain genetic and psychological factors.

      1. Sheptulin A. A., Vize-Hripunova M. A. Review of RomeIV criteria for the irritable bowel syndrome: are there any basic changes? Rossijskij zhurnal gastroehnterologii, gepatologii, koloproktologii. 2016; 26(5): 99–103
      2. Drossman DA. Functional Gastrointestinal Disorders: History, Pathophysiology, Clinical Features, and Rome IV. Gastroenterology 2016; 150 (6): 1262–79
      3. Mayev IV, Cheromushkin SV, Kucheryavy YUA. Irritable bowel syndrome. Roman criteria IV. On the role of visceral hypersensitivity and methods of its correction. Мoscow: Prima Print, 2016; 64p.
      4. Tikhonova TA, Kozlova IV. Irritable bowel syndrome: epidemiological and pathogenetic aspects (review). Saratov Journal of Medical Scientifi c Research 2018; 14 (1): 53–60.
      5. Loranskaya I.D, Kozlova YU. A. Search for new treatment options for irritable bowel syndrome with a refractory course. Pharmateka 2013; 2: 73–78
      6. Osadchuk M. A., Burdina V. O. Irritable bowel syndrome with extraintestinal manifestations from a position of neuroendocrine pathology. Ehksperimental’naya i klinicheskaya gastroehnterologiya 2015; 2 (114): 29–34.
      7. Butorova LI, Tokmulina GM, Plavnik T E et al. Roman criteria for the IV of irritable bowel syndrome: the evolution of views on pathogenesis, diagnosis and treatment. Lechashchiy vrach 2017; (3).
      8. Lackner JM, Jaccard J, Keefer L et al. Improvement in Gastrointestinal Symptoms Aft er Cognitive Behavior Th erapy for Refractory Irritable Bowel Syndrome. Gastroenterology 2018;155 (1): 47–57.
      9. Kozlova I. V., Myalina Yu.N., Badieva O. E. et al. Clinical and laboratory criteria in treatment effi ciency estimation for patients with irritable bowel syndrome. Lechashchiy vrach 2016; (4): 125–129.
      10. Kozlova I.V, Lekareva L. I., Tikhonova T. A. et al. Psychological features of patients with functional and infl ammatory bowel diseases. Saratov Journal of Medical Scientifi c Research 2014; 10(1): 80–85.
      11. Poluehktova E. A., SHeptulin A.A., Ivashkin V. T. et al. Possibilities of improving the results of treatment of patients with irritable bowel syndrome. Clinical prospects of gastroenterology, hepatology 2006; 3: 16–27.
      12. Semenova YeV, Ivanov AV. Th e role of single nucleotide polymorphisms of a number of genes of innate immunity in the development of irritable bowel syndrome. Gastroenterologiya Sankt- Peterburga 2017; (1): 30–41.
      13. Sharova IA, Stashkevich DS, Evdokimov AV, Ivanova EL. Polymorphism of the genes of the main cytokines and the toll-like receptor 4 and the variability of irritable bowel syndrome in the Russian Chelyabinsk region. Nauchno-metodicheskiy elektronnyy zhurnal «Kontsept» 2017; (39): 3241–3245.
      14. Camilleri М, Katzka DA. Irritable Bowel Syndrome: Methods, Mechanisms, and Pathophysiology. Genetic epidemiology and pharmacogenetics in irritable bowel syndrome. American Journal of Physiology 2012; 302 (10): G1075-G1084.
      15. Spiller R, Lam C. An Update on Post-infectious Irritable Bowel Syndrome: Role of Genetics, Immune Activation, Serotonin and Altered Microbiome. J Neurogastroenterol Motil 2012; 18(3): 258–268.
      16. Morisky DE, Green LW, Levine DM. Concurrent and predictive validity of a self-reported measure of medication adherence. Med Care 1986; 24(1): 67–74.
      17. Blake MR, Raker JM, Whelan K. Validity and reliability of the Bristol Stool Form Scale in healthy adults and patients with diarrhoea‐predominant irritable bowel syndrome. Alimentary Pharmacology and Th erapeutics 2016; 44(7): 693–703
      18. Smulevich A. B., Yakhno N. N., Terluin B. et al. The Four-Dimensional Symptom Questionnaire (4DSQ) to Assess Distress, Depression, Anxiety and Somatization in Autonomic and Borderline Psychosomatic Disorders Zhurnal nevrologii i psihiatrii 2014;11:60–66.
      19. Buss AH, Durkee A. An inventory for assessing diff erent kinds of hostility. Journal of Consulting Psychology 1957; 21(4): 343–349.
      20. Arias В, Serretti А, Lorenzi С et al. Analysis of COMT gene (Val 158 Met polymorphism) in the clinical response to SSRIs in depressive patients of European origin. Journal of Aff ective Disorders 2006; 90 (2–3): 251–256
      21. Khan А, Khan Z, Warnakulasuriya S. Cancer-associated toll-like receptor modulation and insinuation in infection susceptibility: association or coincidence? Annals of Oncology 2016; 27 (6): 984–997.
      22. Carvalho А, Cunha С, Carotti А et al. Polymorphisms in Toll-like receptor genes and susceptibility to infections in allogeneic stem cell transplantation. Experimental Hematology 2009; 37 (9): 1022–1029.
      23. Вaune ВТ, Hohoff С, Berger К et al. Association of the COMT val158met Variant with Antidepressant Treatment Response in Major Depression. Neuropsychopharmacology 2008; 33: 924–932.
      24. Valverde-Villegas JM, Santos BP, Machado MB et al. G2848A and T-1237C polymorphisms of the TLR9 gene and susceptibility to infl ammatory bowel disease in patients from southern Brazil. John Wiley & Sons Ltd Tissue Antigens 2014; (83): 190–192.
      25. Cynthia KY, Cheung J, Wu CY. Genetic polymorphism in pathogenesis of irritable bowel syndrome. World J Gastroenterol 2014; 20(47): 17693–17698.
      26. Kovsh E. M. Ermakov P. N. Vorob’eva E. V. Th e Association of the Polymorphic Marker Val158Met of Gene COMT with the Level of Aggressiveness and Strategies of Behavior in Confl ict among Girls 18–24 Years Old. Severo-Kavkazskij psihologicheskij vestnik 2015; 13 (3): 15–21
      27. Pontus Karling, Ake Danielsson, Mikael Wikgren et al. Th e Relationship between the Val158Met Catechol-oMethyltransferase (COMT) Polymorphism and Irritable Bowel Syndrome. PLoS ONE2011; 6(3): 1–5
      28. Agafonova NA. Post-infectious irritable bowel syndrome. Мoscow: Forte print, 2013; 52р.
      29. Kovalchuk L. V., Svitich O. A., Gankovskaya L. V. et al. Th e role of Toll-like receptors in pathogenesis of human infection. Kurskii nauchno-prakticheskii vestnik “Chelovek i ego zdorov’e” 2012; 2: 147–153
     


    Full text is published :
    Tikhonova T. A., Kozlova I. V., Fedotov E. A. Genetic and psychological prerequisites for development of refractory variant of irritable bowel syndrome. Experimental and Clinical Gastroenterology. 2019;162(2): 68–74. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-68-74
    Read & Download full text

    1. GBUZ Moscow Clinical Research Center named after A. S. Loginov DZM, 111123, Moscow, Russia

    Keywords: irritable bowel syndrome, constipation, intestinal motility

    Abstract:Irritable Bowel Syndrome (IBS) is a functional bowel disease in which relapsing abdominal pain is associated with bowel movements or bowel movements. Despite the numerous works devoted to the investigation of the mechanisms of IBS development, the intestinal motility in this disease has not been studied enough. The aim is to reveal the features of the motor function of the large and small intestine in irritable bowel syndrome with constipation (IBS-C) and in the case of dolichosigma. Material and methods. 84 patients with IBS-C by electromyography in comparison with a group of 25 patients with dolichosigma and a group of 35 patients with functional constipation were examined. The frequency of slow waves of the small and large intestine (patients with functional constipation) and the left parts of the colon (patients with IBS-3 and dolichosigma) by the Conan-M hardware and software complex were measured Results and discussion. IBS-C is characterized by hypomotor dyskinesia of the left divisions with pronounced spastic contractions of the smooth muscles of the circulatory layer of the gut, possibly due to the activity of stimulating serotonergic eff ects on the spastic activity of the circular muscle layer or inhibitory adrenergic neurons of the intermuscular (Auerbach) nerve plexus. With dolichosigma, hypomotor dyskinesia of the left parts of the colon was revealed due to stretching of the mechanoreceptors of the aff erent neurons of the intramural refl ex arcs.

      1. Tokmulina G. M., i dr. Rimskie kriterii IV sindroma razdrazhennogo kishechnika: evolyutsiya vzglyadov na patogenez, diagnostiku i lechenie. [Roman criteria for irritable bowel syndrome IV: evolution of views on pathogenesis, diagnosis and treatment. Attending Doctor 2017; 3: 61–67].
      2. Gershon MD, Tack J. Th e serotonin signaling system: from basic understanding to drug development for functional GI disorders. Gastroenterology. 2007;132:397–414.
      3. Hoff man J. M., Tyler K., MacEachern S.J. 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. et al. 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, effi cacy and costs of pharmacotherapy for functional gastrointestinal disorders: the case of alosetron and its implications. Aliment. Pharmacol. Th er. 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. et al. 5-HT7 receptors are involved in mediating 5-HT-induced activation of rat primary aff erent neurons. Life Sci.2002; 71, 2279–2289.
      9. Zou B. C., Dong L., Wang Y. et al. 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. Koordinatsiya mioelektricheskoy aktivnosti tonkoy i tolstoy kishki. [Coordination of myoelectric activity of the small and large intestine]. Experimental and clinical gastroenterology. 2012;3:59–61.
      11. Lychkova A. E., Puzikov A. M. EHlektricheskaya aktivnost’ pishchevaritel’nogo trakta i ee ehnteral’naya korrekciya [Electrical activity of the digestive tract and its enteric correction]. Experimental and clinical gastroenterology. 2015; 120 (8): 25–29,
      12. Maev I. V., Samsonov A. A., Nikushkina I. N., Ivashkina N. Yu. Sindrom razdrazhennogo kishechnika, aktual’nost’ problemy i voprosy sovremennoy terapii. [Irritable bowel syndrome, the relevance of the problem and issues of modern therapy]. Farmateka. 2011;2:214.
      13. Maev I. V., Samsonov A. A., Nikushkina I. N., Ivashkina N. Yu. Sindrom razdrazhennogo kishechnika, aktual’nost’ problemy i voprosy sovremennoy terapii. [Irritable bowel syndrome, the relevance of the problem and issues of modern therapy]. Farmateka. 2011;2:214.
      14. Poluektova V. A. Bol’ v zhivote pri funktsional’nykh rasstroystvakh kishechnika. [Abdominal pain with functional bowel disorders. Clinical perspectives in gastroenterology, hepatology. 2001; 2: 27–33.
      15. Ardatskaya M. D., Topchiy T. B. Abdominal’naya bol’ i vistseral’naya giperchuvstvitel’nost’ patsientov s sindromom razdrazhennogo kishechnika. Rimskie kriterii IV i klinicheskaya praktika. [Abdominal pain and visceral hypersensitivity of patients with irritable bowel syndrome. Rome IV criteria and clinical practice]. Moscow, 2017, 63 p.
     


    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. 2019;162(2): 75–78. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-75-78
    Read & Download full text

    1. Bashkir state medical University of the Ministry of health of Russia, 450008, Ufa, Lenin street, 3, Russia

    Keywords: personality-oriented educational program, biliary pathology, young age, psychosomatic examination

    Abstract:Purpose of the study. Show the eff ectiveness of training for young people with chronic non-calculous cholecystitis on the example of a personality oriented educational program. Materials and methods. A total of 64 patients with chronic non-calculous cholecystitis in the remission phase were examined. They determined the levels of anxiety, indicators of quality of life, types of attitudes towards the disease. The obtained data were compared before and after training in a person-centered program. Results. In the course of dynamic management of patients with biliary pathology, a decrease in high anxiety levels, an increase in persons with a low level of anxiety, an increase in ergopathic, mixed types of attitudes towards the disease, a decrease in anxiety and hypochondriacal types was noted. In terms of quality of life, an increase in self-satisfaction along with a scale of health status was reliably detected. Positive changes in the behavior of patients in terms of adherence to the implementation of the recommendations of the doctor according to the person-oriented program are identifi ed. Individual approach, familiarity of patients with the basics of the disease, risk factors, self-help, mutual aid, non-drug, urgent measures contribute to the primary and secondary prevention of the disease. Conclusion. In the course of this study, positive results were obtained in the psychosomatic status of patients. Due to the development of this trend now, increasing the level of education of certain groups of the population, individual approach to each patient, resolving issues together with the doctor in class, discussing emerging issues, getting advice — all this allows you to increase the patient’s participation in resolving issues of self-, mutual assistance, control the state of the main indicators of the level of health, monitor the levels of anxiety, depression and promptly contact specialists; therefore, this technique is relevant to and Use at the outpatient stage for people of all ages.

      1. Russell Jesse. Cholecystitis. Moscow, 2012. 106
      2. Volevach L. V., Demidova N. A., Gabbasova L. V., Guryev R. D. Biliary pathology and obesity: risk factors, clinical and functional features. Tambov, Consulting company Ucom Publ,. 2018. 108 p.
      3. Sarsenbaeva A. S. Outgoing plenum scientifi c society of gastroenterology “classical and interdisciplinary gastroenterology. Current issues regional pathology” (the city of chelyabinsk, 27 – november 28, 2014). Experimental and clinical gastroenterology. 2014;12(112):107–108.
      4. Volevach L. V., Osmaeva V. V., Bashirova, E. S. Evaluation of eff ectiveness of personal-oriented educational programs among young patients suff ering from disorders of the biliary system. Kazan medical journal, 2012, vol. 93, no. 4, pp. 637–641.
      5. Volevach L. V., Demidova N. A., Kamalova A. A. et al. Interconnection of psycho-emotional status and biochemical composition of bile in young patients with biliary diseases. Modern problems of science and education. 2018, no. 6, on-line: http://www.scienceeducation.ru/ru/ article/view?id=28314.
      6. Cotton P. B., Elta G. H., Carter C. R., Pasricha P. J. et al. Rome IV. Gallbladder and Sphincter of Oddi Disorders. Gastroenterology. 2016. (DOI: 10.1053/j.gastro.2016.02.033).
      7. Goussous N., Kowdley G. C., Sardana N., Spiegler E. et al. Gallbladder dysfunction: how much longer will it be controversial? Digestion. 2014. vol.90.no.3.P.47–54.4.
      8. Lazebnik L. B., Shcherbakov, P. L. (ed) Gastroenterology. Diseases of adults. Moscow, 2011. 479 p.
      9. Lazebnik L. B., Tkachenko E. I., Abdulkhakov R. A. et al. Standards of diagnosis and treatment of acid-dependent and Helicobacter pylori-associated diseases. Chronic gastritis. Bulletin of the practical doctor. Special issue, 2013, no. 3, pp. 12–14.
      10. Lee Y. S., Kang B. K., Hwang I. K., Kim J. et al. Long-term outcomes of symptomatic gallbladder sludge. Journal of clinical gastroenterology. 2015. vol. 49. no.7. Р.594–598.
      11. Slattery S. A., Niaz O., Aziz Q., Ford A. C., Farmer A. D. Systematic review with meta-analysis: the prevalence of bile acid malabsorption in the irritable bowel syndrome with diarrhoea. Aliment Pharmacol Th er 2015;42(1):3–11. DOI:10.1111/apt.13227.
      12. Wanjura V., Sandblom G. How Do Quality-of-Life and Gastrointestinal Symptoms Differ Between Postcholecystectomy Patients and the Background Population? World J Surg 2016;40(1):81–8. DOI:10.1007/ s00268–015–3240–0.
      13. Cotton P. B., Pauls Q., Keith J., Th ornhill A., Drossman D., Williams A. et al. Th e EPISOD study: long-term outcomes. Gastrointestinal Endoscopy 2017. DOI:10.1016/j. gie.2017.04.015.
      14. Lemeshko Z. A. Endless possibilities for diagnosing biliary tract today. Gastroenterology SYLLABUS. Panorama of modern gastroenterology. (Moscow, September 27–29, 2013). Moscow, 2013, pp. 333–339.
     


    Full text is published :
    Volevach L. V., Sarsenbaeva A. S., Gabbasova L. V., Demidovа N. A., Garipova R. A., Guriyev R. D., Kamalova A. A. The personal oriented educational program in the management of patients with biliary pathology. Experimental and Clinical Gastroenterology. 2019;162(2): 79–83. (In Russ.) DOI: 10.31146/1682-8658-ecg-162-2-79-83
    Read & Download full text