Неалкогольная жировая болезнь печени и желчнокаменная болезнь: случайное или закономерное сочетание?
Неалкогольная жировая болезнь печени и желчнокаменная болезнь: случайное или закономерное сочетание?
Черкащенко Н.А., Ливзан М.А., Гаус О.В., Кролевец Т.С. Неалкогольная жировая болезнь печени и желчнокаменная болезнь: случайное или закономерное сочетание? Гастроэнтерология. Хирургия. Интенсивная терапия. Consilium Medicum. 2019; 3: 40–44. DOI: 10.26442/26583739.2019.3.190489
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Cherkashchenko N.A., Livzan M.A., Gaus O.V., Krolevets T.S. Non-alcoholic fatty liver disease and cholelithiasis: a random or regular combination? Gastroenterology. Surgery. Intensive care. Consilium Medicum. 2019; 3: 40–44. DOI: 10.26442/26583739.2019.3.190489
Неалкогольная жировая болезнь печени и желчнокаменная болезнь: случайное или закономерное сочетание?
Черкащенко Н.А., Ливзан М.А., Гаус О.В., Кролевец Т.С. Неалкогольная жировая болезнь печени и желчнокаменная болезнь: случайное или закономерное сочетание? Гастроэнтерология. Хирургия. Интенсивная терапия. Consilium Medicum. 2019; 3: 40–44. DOI: 10.26442/26583739.2019.3.190489
________________________________________________
Cherkashchenko N.A., Livzan M.A., Gaus O.V., Krolevets T.S. Non-alcoholic fatty liver disease and cholelithiasis: a random or regular combination? Gastroenterology. Surgery. Intensive care. Consilium Medicum. 2019; 3: 40–44. DOI: 10.26442/26583739.2019.3.190489
Неалкогольная жировая болезнь печени (НАЖБП) и желчнокаменная болезнь (ЖКБ) широко распространены среди населения в целом. Ввиду общности факторов риска патогенетическая связь НАЖБП и ЖКБ не вызывает сомнения, при этом очевидно, что данная связь является двунаправленной. Спорным остается вопрос, что первично: метаболические нарушения на уровне гепатоцита или холестерин-ассоциированная патология желчного пузыря? В данном обзоре рассмотрены основные факторы риска развития НАЖБП и ЖКБ, также представлены сведения о вкладе холецистэктомии в формирование и прогрессирование НАЖБП.
Non-alcoholic fatty liver disease (NAFLD) and cholelithiasis are widespread among the general population. Due to the common risk factors, the pathogenetic relationship of NAFLD and cholelithiasis is beyond doubt, and it is obvious that this relationship is bidirectional. A controversial question remains: what is primary – metabolic disorders at the level of the hepatocyte or cholesterol-associated pathology of the gallbladder? This review examines the main risk factors for the development of NAFLD and cholelithiasis, also presents information on the contribution of cholecystectomy to the formation and progression of NAFLD.
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[Krolevets T.S., Livzan M.A., Lapteva I.V., Cherkashchenko N.A. Leptinorezistentnost' u patsientov s nealkogol'noi zhirovoi bolezn'iu pecheni, assotsiirovannoi s ozhireniem i izbytochnoi massoi tela. Med. sovet. 2015; 13: 58–62 (in Russian).]
19. Crujeiras AB, Carreira MC, Cabia B et al. Leptin resistance in obesity: An epigenetic landscape. Life Sci 2015; 140: 57–63.
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21. Angulo P, Alba LM, Petrovic LM et al. Leptin, insulin resistance, and liver fibrosis in human nonalcoholic fatty liver disease. J Hepatology 2014; 41: 943–9.
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31. Boursier J, Mueller O, Barret M et al. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology 2016; 63 (3): 764–75.
32. Yuan L, Bambha K. Bile acid receptors and nonalcoholic fatty liver disease. World J Hepatol 2015; 7 (28): 2811–88.
33. Fuchs CD, Traussnigg SA., Trauner M. Nuclear Receptor Modulation for the Treatment of Nonalcoholic Fatty Liver Disease. Semin Liver Dis 2016; 36 (1): 69–86.
34. Zhang DY, Zhu L, Liu HN et al. The protective effect and mechanism of the FXR agonist obeticholic acid via targeting gut microbiota in non-alcoholic fatty liver disease. Drug Des Devel Ther 2019; 13: 2249–70.
35. Brar PC, Kohn B. Use of the microbiome in the management of children with type 2 diabetes mellitus. Curr Opin Pediatr 2019; 31 (4): 524–30.
36. Aron-Wisnewsky J, Clément K, Nieuwdorp M. Fecal Microbiota Transplantation: a Future Therapeutic Option for Obesity/Diabetes? Curr Diab Rep 2019; 19 (8): 51.
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1.Ivashkin V.T., Drapkina O.M., Maev I.V. et al. Rasprostranennost' nealkogol'noi zhirovoi bolezni pecheni u patsientov ambulatorno-poliklinicheskoi praktiki v Rossiiskoi Federatsii: rezul'taty issledovaniia DIREG 2. Ros. zhurn. gastroenterologii, gepatologii, koloproktologii. 2015; 25 (6): 31–41 (in Russian).
2. Jaruvongvanich V, Sanguankeo A, Upala S. Signtificant Association Between Gallstone Disease and Nonalcoholic Fatty Liver Disease: A systematic Review and Meta-Analisys. Dig Dis Sci 2016; 61 (8): 2389–96.
3. Reddy SK, Zhan M, Alexander HR, El-Kamary SS. Nonalcoholic fatty liver disease is associated with benign gastrointestinal disorders. World J Gastroenterol 2013; 19 (45): 8301–11.
4. McQuillian GM, McLean JE, Chiappa M et al. National Health and Nutrition Examination Survey Biospecimen Program: NHANES III (1988-1994) and NHANES 1999-2014. Vital Health Stat 2. 2015; 170: 1–14.
5. Fracanzani AL, Valenti L, Russello M et al. Gallstone Disease Is Associated with More Severe Liver Damage in Patients with Non- Alcoholic Fatty Liver Disease. PLoS ONE 2012; 7 (7): e41183.
6. Komova A.G., Maevskaia M.V., Ivashkin V.T. Printsipy effektivnoi diagnostiki diffuznykh zabolevanii pecheni na ambulatornom etape. Ros. zhurn. gastroenterologii, gepatologii i koloproktologii. 2014; 24 (5): 36–41 (in Russian).
7. Ivashkin V.T., Maevskaia M.V., Pavlov Ch.S. et al. Klinicheskie rekomendatsii po diagnostike i lecheniiu nealkogol'noi zhirovoi bolezni pecheni Rossiiskogo obshchestva po izucheniiu pecheni i Rossiiskoi gastroenterologicheskoi assotsiatsii. Ros. zhurn. gastroenterologii, gepatologii i koloproktologii. 2016; 26 (2): 24–42 (in Russian).
8. EASL. Clinical Practice Guidelines on the prevention, diagnosis and treatment of gallstones. J Hepatol 2016; 65 (1): 146–81.
9. Livzan M.A. et al. Gormony zhirovoi tkani i nealkogol'naia zhirovaia bolezn' pecheni pri metabolicheskom sindrome. Dnevnik kazanskoi meditsinskoi shkoly. 2014; 1 (4): 44–8 (in Russian).
10. Gaus O.V., Akhmedov V.A. Immunologicheskie paralleli v techenii metabolicheskogo sindroma, assotsiirovannogo s zhelchnokamennoi bolezn'iu . Fundamental'nye issledovaniia. 2013; 7: 51–4 (in Russian).
11.Gaus O.V., Akhmedov V.A. Kliniko-biokhimicheskie i immunologicheskie osobennosti zhelchnokamennoi bolezni, assotsiirovannoi s metabolicheskim sindromom. Vestn. NGU. Seriia: Biologiia, klinicheskaia meditsina. 2013; 10 (3): 125–9 (in Russian).
12. Livzan M.A., Krolevets T.S., Lapteva I.V. Nealkogol'naia zhirovaia bolezn' pecheni u lits s abdominal'nym tipom ozhireniia. Dokazatel'naia gastroenterologiia. 2014; 3 (4): 8–14 (in Russian).
13. Neuschwander-Tetri BA. Non-alcoholic fatty liver disease. BMC Med 2017; 14 (1): 45.
14. Wree A, Kahraman A, Gerken G, Canbay A. Obesity affects the liver – the link between adipocytes and hepatocytes. Digestion 2011; 83 (1–2): 124–33.
15. Dongiovanni P, Valenti L, Rametta R et al. Genetic variants regulating insulin receptor signalling are associated with the severity of liver damage in patients with non-alcoholic fatty liver disease. Gut 2010; 59: 267–73.
16. Romeo S, Kozlitina J, Xing C et al. Genetic variation in PNPLA3 confers susceptibility to nonalcoholic fatty liver disease. Nat Genet 2008; 40: 1461–5.
17. Livzan M.A., Lapteva I.V., Miller T.S. Rol' leptina i leptinorezistentnosti v formirovanii nealkogol'noi zhirovoi bolezni pecheni u lits s ozhireniem i izbytochnoi massoi tela. Eksperim. i klin. gastroenterologiia. 2014; 8 (108): 27–33 (in Russian).
18. Krolevets T.S., Livzan M.A., Lapteva I.V., Cherkashchenko N.A. Leptinorezistentnost' u patsientov s nealkogol'noi zhirovoi bolezn'iu pecheni, assotsiirovannoi s ozhireniem i izbytochnoi massoi tela. Med. sovet. 2015; 13: 58–62 (in Russian).
19. Crujeiras AB, Carreira MC, Cabia B et al. Leptin resistance in obesity: An epigenetic landscape. Life Sci 2015; 140: 57–63.
20. Javor ED, Ghany MG, Cochran EK et al. Leptin reverses nonalcoholic steatohepatitis in patients with severe lipodystrophy. Hepatology 2005; 41: 753–60.
21. Angulo P, Alba LM, Petrovic LM et al. Leptin, insulin resistance, and liver fibrosis in human nonalcoholic fatty liver disease. J Hepatology 2014; 41: 943–9.
22. Michelino DR, Malaguarnera, L. Genetic variants in candidate genes influencing NAFLD progression. J Mol Med 2012; 90: 105–18.
23. Ahmed MH, Ali A. Nonalcoholic fatty liver disease and cholesterol gallstones: which comes first? Scand J Gastroenterol 2014; 49 (5): 521–7.
24. Di Ciaula A, Wang DQ, Portincasa P. Cholesterol cholelithiasis: part of a systemic metabolic disease, prone to primary prevention. Exp Rev Gastroenterol Hepatol 2019; 13 (2): 157–71.
25. Akhmedov V.A., Gaus O.V. Porazhenie organov gepatobiliarnoi sistemy i podzheludochnoi zhelezy pri ozhirenii. Therapeutic Archive. 2017; 89 (1): 128–33 (in Russian).
26. Kononov A.V., Livzan M.A. Meditsina, osnovannaia na dokazatel'stvakh, v praktike klinicheskogo patologa. Sibirskii Konsilium. 2002; 2: 18–22 (in Russian).
27. Cong P, Pricolo V, Biancani P, Behar J. Effects of cholesterol on CCK-1 receptors and caveolin-3 proteins recycling in human gallbladder muscle. Am J Physiol Gastrointest Liver Physiol 2010; 299 (3): G742–G750.
28. Makhov V.M., Romasenko L.V., Turko T.V. Komorbidnost' disfunktsional'nykh rasstroistv organov pishchevareniia. Rus. med. zhurn. Bolezni organov pishchevareniia. 2007; 9 (2): 37–42 (in Russian).
29. Prasenjit Manna, Sushil K Jain. Obesity, oxidative stress, adipose tissue dysfunction, and the associated health risks: causes and therapeutic strategies. Metabolic Syndrome and Related Disorders 2015; 13 (10): 423–44.
30. Yu SJ, Kim W, Kim D et al. Visceral obesity predicts significant fibrosis in patients with nonalcoholic fatty liver disease. Medicine (Baltimore) 2015; 94 (48): e2159.
31. Boursier J, Mueller O, Barret M et al. The severity of nonalcoholic fatty liver disease is associated with gut dysbiosis and shift in the metabolic function of the gut microbiota. Hepatology 2016; 63 (3): 764–75.
32. Yuan L, Bambha K. Bile acid receptors and nonalcoholic fatty liver disease. World J Hepatol 2015; 7 (28): 2811–88.
33. Fuchs CD, Traussnigg SA., Trauner M. Nuclear Receptor Modulation for the Treatment of Nonalcoholic Fatty Liver Disease. Semin Liver Dis 2016; 36 (1): 69–86.
34. Zhang DY, Zhu L, Liu HN et al. The protective effect and mechanism of the FXR agonist obeticholic acid via targeting gut microbiota in non-alcoholic fatty liver disease. Drug Des Devel Ther 2019; 13: 2249–70.
35. Brar PC, Kohn B. Use of the microbiome in the management of children with type 2 diabetes mellitus. Curr Opin Pediatr 2019; 31 (4): 524–30.
36. Aron-Wisnewsky J, Clément K, Nieuwdorp M. Fecal Microbiota Transplantation: a Future Therapeutic Option for Obesity/Diabetes? Curr Diab Rep 2019; 19 (8): 51.
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38. Greco EA, Lenzi A, Migliaccio S. Role of Hypovitaminosis D in the Pathogenesis of Obe-sity-Induced Insulin Resistance. Nutrients 2019;11 (7): pii: E1506.
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1. ФГБУЗ «Западно-Сибирский центр ФМБА России», Омск, Россия;
2. ФГБОУ ВО «Омский государственный медицинский университет» Минздрава России, Омск, Россия