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Сочетание неалкогольной жировой болезни печени и желчнокаменной болезни: патофизиологические и клинические взаимосвязи, особенности терапии
Сочетание неалкогольной жировой болезни печени и желчнокаменной болезни: патофизиологические и клинические взаимосвязи, особенности терапии
Топчий Т.Б., Ардатская М.Д., Масловский Л.В., Минушкин О.Н. Сочетание неалкогольной жировой болезни печени и желчнокаменной болезни: патофизиологические и клинические взаимосвязи, особенности терапии. Consilium Medicum. 2025;27(12):754–761. DOI: 10.26442/20751753.2025.12.203514
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Аннотация
Неалкогольная жировая болезнь печени (НАЖБП) и желчнокаменная болезнь (ЖКБ) являются широко распространенными заболеваниями во всем мире. Сочетание НАЖБП и ЖКБ – частая клиническая ситуация. ЖКБ и НАЖБП имеют общие факторы риска и тесно ассоциированы с такими сопутствующими заболеваниями, как ожирение, дислипидемия, нарушение углеводного обмена. Многочисленные исследования в разных популяциях показали, что НАЖБП является независимым фактором риска ЖКБ, а ЖКБ представляет собой независимый фактор риска НАЖБП. В настоящее время в качестве ключевого фактора, обеспечивающего связь между НАЖБП и развитием холестеринового холелитиаза, рассматривается инсулинорезистентность. Кроме этого, большую роль играет изменение экспрессии транскрипционных факторов: печеночного Х-рецептора, фарнезоидного Х-рецептора и мембранных рецепторов желчных кислот. В итоге это приводит к повышенному липогенезу в печени, перенасыщению желчи холестерином, способствуя образованию как желчных камней, так и жировой дистрофии печени. Не менее важную роль в патогенезе обоих заболеваний играет нарушение функции желчного пузыря, являющейся важным звеном связи печени и кишечника в печеночно-пузырно-кишечной оси и поддерживающей метаболический гомеостаз холестерина, триглицеридов и желчных кислот. Это подтверждается данными, согласно которым холецистэктомия увеличивает риск НАЖБП, способствует усилению инсулинорезистентности и накопления жира в печени. Выбор лекарственной терапии у пациентов с сочетанием НАЖБП и ЖКБ основывается на знаниях общих патофизиологических процессов, характерных для обоих заболеваний. Лекарственные препараты должны соответствовать принципам многоцелевой монотерапии, воздействуя на максимальное число терапевтических мишеней, а сочетание их фармакологических эффектов – потенцировать действие друг друга. Лечение пациентов с сочетанием НАЖБП и ЖКБ основывается в первую очередь на снижении массы тела с помощью физических нагрузок и средиземноморского типа питания, усиленного лекарственными препаратами псиллиума и масляной кислотой, являющейся ключевым медиатором позитивных эффектов средиземноморской диеты. Препаратом выбора у пациентов с сочетанием НАЖБП и ЖКБ является урсодезоксихолевая кислота, позволяющая патогенетически воздействовать на оба заболевания.
Ключевые слова: неалкогольная жировая болезнь печени, желчнокаменная болезнь, урсодезоксихолевая кислота, псиллиум, масляная кислота
Keywords: non-alcoholic fatty liver disease, cholelithiasis, ursodeoxycholic acid, psyllium, butyric acid
Ключевые слова: неалкогольная жировая болезнь печени, желчнокаменная болезнь, урсодезоксихолевая кислота, псиллиум, масляная кислота
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Keywords: non-alcoholic fatty liver disease, cholelithiasis, ursodeoxycholic acid, psyllium, butyric acid
Полный текст
Список литературы
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17. Biddinger SB, Haas JT, Yu BB, et al. Hepatic insulin resistance directly promotes formation of cholesterol gallstones. Nat Med. 2008;14(7):778-82. DOI:10.1038/nm1785
18. Rosso C, Mezzabotta L, Gaggini M, et al. Peripheral insulin resistance predicts liver damage in nondiabetic subjects with nonalcoholic fatty liver disease. Hepatology. 2016;63(1):107-16. DOI:10.1002/hep.28287
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20. Li S, Brown MS, Goldstein JL. Bifurcation of insulin signaling pathway in rat liver: mTORC1 required for stimulation of lipogenesis, but not inhibition of gluconeogenesis. Proc Natl Acad Sci USA. 2010;107:3441-6. DOI:10.1073/pnas.0914798107
21. Tanaka N, Aoyama T, Kimura S, Gonzalez FJ. Targeting nuclear receptors for the treatment of fatty liver disease. Pharmacol Ther. 2017;179:142-57. DOI:10.1016/j.pharmthera.2017.05.011
22. Ruhl CE, Everhart JE. Association of diabetes, serum insulin, and C-peptide with gallbladder disease. Hepatology. 2000;31:299-303.
23. Shen C, Wu X, Xu C, et al. Association of cholecystectomy with metabolic syndrome in a Chinese population. PloS One. 2014;9(2):e88189. DOI:10.1371/journal.pone.0088189
24. Cortés V, Quezada N, Uribe S, et al. Effect of cholecystectomy on hepatic fat accumulation and insulin resistance in non-obese Hispanic patients: A pilot study. Lipids Health Dis. 2017;16(1):129. DOI:10.1186/s12944-017-0525-3
25. Housset C, Chretien Y, Debray D, Chignard N. Functions of the gallbladder. Comprehens Physiol. 2016;6(3):1549-77. DOI:10.1002/cphy.c150050
26. Chen S, Zheng Y, Cai J, et al. Gallstones after bariatric surgery: Mechanisms and prophylaxis. Front Surg. 2025;12:1506780. DOI:10.3389/fsurg.2025.1506780
27. Lanzini A, Facchinetti D, Pigozzi MG, et al. Best-buy regimen of ursodeoxycholic acid for patients with gallstones. Scand J Gastroenterol. 1991;26(5):551-6. DOI:10.3109/00365529108998579
28. Setchell KD, Galzigna L, O'Connell N, et al. Bioequivalence of a new liquid formulation of ursodeoxycholic acid (Ursofalk suspension) and Ursofalk capsules measured by plasma pharmacokinetics and biliary enrichment. Aliment Pharmacol Ther. 2005;21(6):709-21. DOI:10.1111/j.1365-2036.2005.02385.x
29. Butorova LI, Ardatskaya MD, Osadchuk MA, et al. Comparative effectiveness of ursodeoxycholic acid preparations in the treatment of biliary sludge. Terapevticheskii Arkhiv (Ter. Arkh.). 2020;92(8):60-5 (in Russian). DOI:10.26442/00403660.2020.08.000700
30. Kucheryavyy YA, Cheremushkin SV. Therapeutic efficacy evaluation of the reference drug ursodeoxycholic acid and its analogues in the biliary sludge dissolution: A meta-analysis. Consilium Medicum. 2022;24(12):860-4 (in Russian). DOI:10.26442/20751753.2022.12.201429
31. Nair S, Diehl AM, Wiseman M, et al. Metformin in the treatment of non-alcoholic steatohepatitis: A pilot open label trial. Aliment Pharmacol Ther. 2004;20(1):23-8. DOI:10.1111/j.1365-2036.2004.02025.x
32. Newsome PN, Buchholtz K, Cusi K, et al.; NN9931-4296 Investigators. A placebo-controlled trial of subcutaneous semaglutide in nonalcoholic steatohepatitis. N Engl J Med. 2021;384(12):1113-24. DOI:10.1056/NEJMoa2028395
33. Jalleh RJ, Marathe CS, Rayner CK, et al. Physiology and pharmacology of effects of GLP-1-based therapies on gastric, biliary and intestinal motility. Endocrinology. 2024;166(1):bqae155. DOI:10.1210/endocr/bqae155
34. Drapkina OM, Kontsevaya AV, Kalinina AM, et al. Comorbidity of patients with noncommunicable diseases in general practice. Eurasian guidelines. Cardiovascular Therapy and Prevention. 2024;23(3):3996 (in Russian). DOI:10.15829/1728-8800-2024-3996
35. Oynotkinova OSh, Roitberg GE, Kukharchuk VV, et al. Current issues of clinical lipidology Is the use of statins for the prevention of cholelithiasis justified? Expert consensus opinion of lipidologists, hepatologists, gastroenterologists. Proffesors’ Journal. Series: Medical Sciences. 2025;1-2:35-48 (in Russian). DOI:10.18572/2658-7130-2025-1-2-35-48
36. Сoppola S, Avagliano C, Calignano A, Berni Canani R. The protective role of butyrate against obesity and obesity-related diseases. Molecules. 2021;26(3):682. DOI:10.3390/molecules26030682
37. Gonzalez A, Krieg R, Massey HD, et al. Sodium butyrate ameliorates insulin resistance and renal failure in CKD rats by modulating intestinal permeability and mucin expression. Nephrol Dial Transplant. 2019;34(5):783-94. DOI:10.1093/ndt/gfy238
38. Seethaler B, Nguyen NK, Basrai M, et al. Short-chain fatty acids are key mediators of the favorable effects of the Mediterranean diet on intestinal barrier integrity: Data from the randomized controlled LIBRE trial. Am J Clin Nutr. 2022;116(4):928-42. DOI:10.1093/ajcn/nqac175
39. Coppola S, Nocerino R, Paparo L, et al. Therapeutic effects of butyrate on pediatric obesity: A randomized clinical trial. JAMA Netw Open. 2022;5(12):e2244912. DOI:10.1001/jamanetworkopen.2022.44912
40. Sun Y, Fan Z, Zhu X, et al. Sodium butyrate activates peroxisome proliferator-activated receptor γ to suppress lithogenic diet-induced cholesterol gallstones in mice. Food Sci Biotechnol. 2024;34(4):1015-26. DOI:10.1007/s10068-024-01721-x
41. Xu H, Wang X, Song S, Zhang L. Efficacy of sodium butyrate in improving nonalcoholic fatty liver disease: A meta-analysis of preclinical studies. Medicine (Baltimore). 2025;104(15):e42101. DOI:10.1097/MD.0000000000042101
42. Fogacci F, Giovannini M, Di Micoli V, et al. Effect of supplementation of a butyrate-based formula in individuals with liver steatosis and metabolic syndrome: A randomized double-blind placebo-controlled clinical trial. Nutrients. 2024;16(15):2454. DOI:10.3390/nu16152454
43. Evropeiskie rekomendatsii po profilaktike serdechno-sosudistykh zabolevanii v klinicheskoi praktike (peresmotr 2012 g.). Russian Journal of Cardiology. 2012;4(96):4-84 (in Russian).
44. Komissarenko IA, Levchenko SV. The use of pleiotropic effects of some gastroenterological drugs in the treatment of patients with nonalcoholic fatty liver disease and cardiovascular diseases: A review. Consilium Medicum. 2024;26(12):868-74 (in Russian). DOI:10.26442/20751753.2024.12.203090
45. Gibb RD, Sloan KJ, McRorie JW Jr. Psyllium is a natural nonfermented gel-forming fiber that is effective for weight loss: A comprehensive review and meta-analysis. J Am Assoc Nurse Pract. 2023;35(8):468-76. DOI:10.1097/JXX.0000000000000882
46. Gibb RD, McRorie JW Jr, Russell DA, et al. Psyllium fiber improves glycemic control proportional to loss of glycemic control: A meta-analysis of data in euglycemic subjects, patients at risk of type 2 diabetes mellitus, and patients being treated for type 2 diabetes mellitus. Am J Clin Nutr. 2015;102(6):1604-14. DOI:10.3945/ajcn.115.106989
47. Jovanovski E, Yashpal S, Komishon A, et al. Effect of psyllium (Plantago ovata) fiber on LDL cholesterol and alternative lipid targets, non-HDL cholesterol and apolipoprotein B: A systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr. 2018;108(5):922-32. DOI:10.1093/ajcn/nqy115
48. Khan K, Jovanovski E, Ho HVT, et al. The effect of viscous soluble fiber on blood pressure: A systematic review and meta-analysis of randomized controlled trials. Nutr Metab Cardiovasc Dis. 2018;28(1):3-13. DOI:10.1016/j.numecd.2017.09.007
49. McRorie JW Jr, Fahey GC Jr, Gibb RD, Chey WD. Laxative effects of wheat bran and psyllium: Resolving enduring misconceptions about fiber in treatment guidelines for chronic idiopathic constipation. J Am Assoc Nurse Pract. 2020;32(1):15-23. DOI:10.1097/JXX.0000000000000346
50. Ford AC, Talley NJ, Spiegel BM, et al. Effect of fibre, antispasmodics, and peppermint oil in the treatment of irritable bowel syndrome: Systematic review and meta-analysis. BMJ. 2008;337:a2313. DOI:10.1136/bmj.a2313. Erratum in: BMJ. 2009;338:b1881.
51. Moayyedi P, Quigley EM, Lacy BE, et al. The effect of fiber supplementation on irritable bowel syndrome: A systematic review and meta-analysis. Am J Gastroenterol. 2014;109(9):1367-74. DOI:10.1038/ajg.2014.195
2. Brunt EM, Wong VW, Nobili V, et al. Nonalcoholic fatty liver disease. Nat Rev Dis Primers. 2015;1:15080. DOI:10.1038/nrdp.2015.80
3. Sayiner M, Koenig A, Henry L, Younossi ZM. Epidemiology of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis in the United States and the rest of the world. Clin Liver Dis. 2016;20(2):205-14. DOI:10.1016/j.cld.2015.10.001
4. Евстифеева С.Е., Шальнова С.А., Куценко В.А., и др. Распространенность неалкогольной жировой болезни печени среди населения трудоспособного возраста: ассоциации с социально-демографическими показателями и поведенческими факторами риска (данные ЭССЕ-РФ-2). Кардиоваскулярная терапия и профилактика. 2022;21(9):3356 [Evstifeeva SE, Shalnova SA, Kutsenko VA, et al. Prevalence of non-alcoholic fatty liver disease among the working-age population: associations with socio-demographic indicators and behavioral risk factors (ESSE RF-2 data). Cardiovascular Therapy and Prevention. 2022;21(9):3356 (in Russian)]. DOI:10.15829/1728-8800-2022-3356
5. Adams LA, Lymp JF, St Sauver J, et al. The natural history of nonalcoholic fatty liver disease: A population-based cohort study. Gastroenterology. 2005;129(1):113-21. DOI:10.1053/j.gastro.2005.04.014
6. Lammert F, Gurusamy K, Ko CW, et al. Gallstones. Nat Rev Dis Primers. 2016;2:16024. DOI:10.1038/nrdp.2016.24
7. Portincasa P, Moschetta A, Palasciano G. Cholesterol gallstone disease. Lancet. 2006;368(9531):230-9. DOI:10.1016/S0140-6736(06)69044-2
8. Méndez-Sánchez N, Bahena-Aponte J, Chávez-Tapia NC, et al. Strong association between gallstones and cardiovascular disease. Am J Gastroenterol. 2005;100(4):827-30. DOI:10.1111/j.1572-0241.2005.41214.x
9. Younossi ZM, Koenig AB, Abdelatif D, et al. Global epidemiology of nonalcoholic fatty liver disease – Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016;64(1):73-84. DOI:10.1002/hep.28431
10. Koller T, Kollerova J, Hlavaty T, et al. Cholelithiasis and markers of nonalcoholic fatty liver disease in patients with metabolic risk factors. Scand J Gastroenterol. 2012;47(2):197-203. DOI:10.3109/00365521.2011.643481
11. Qiao QH, Zhu WH, Yu YX, et al. Nonalcoholic fatty liver was associated with asymptomatic gallstones in a Chinese population. Medicine (Baltimore). 2017;96(38):e7853. DOI:10.1097/MD.0000000000007853
12. Fracanzani AL, Valenti L, Russello M, et al. Gallstone disease is associated with more severe liver damage in patients with nonalcoholic fatty liver disease. PloS one. 2012;7(7):e41183. DOI:10.1371/journal.pone.0041183
13. Méndez-Sánchez N, Chavez-Tapia NC, Motola-Kuba D, et al. Metabolic syndrome as a risk factor for gallstone disease. World J Gastroenterol. 2005;1(11):1653-7. DOI:10.3748/wjg.v11.i11.1653
14. Arrese M, Cortés V, Barrera F, Nervi F. Nonalcoholic fatty liver disease, cholesterol gallstones, and cholecystectomy: new insights on a complex relationship. Curr Opin Gastroenterol. 2018;34(2):90-6. DOI:10.1097/MOG.0000000000000416
15. Ahn DW, Jeong JB, Kang J, et al. Fatty liver is an independent risk factor for gallbladder polyps. World J Gastroenterol. 2020;26(44):6979-92. DOI:10.3748/wjg.v26.i44.6979
16. Park JH, Hong JY, Kwon M, et al. Association between non-alcoholic fatty liver disease and the risk of biliary tract cancers: A South Korean nationwide cohort study. Eur J Cancer. 2021;150:73-82. DOI:10.1016/j.ejca.2021.03.024
17. Biddinger SB, Haas JT, Yu BB, et al. Hepatic insulin resistance directly promotes formation of cholesterol gallstones. Nat Med. 2008;14(7):778-82. DOI:10.1038/nm1785
18. Rosso C, Mezzabotta L, Gaggini M, et al. Peripheral insulin resistance predicts liver damage in nondiabetic subjects with nonalcoholic fatty liver disease. Hepatology. 2016;63(1):107-16. DOI:10.1002/hep.28287
19. Nakeeb A, Comuzzie AG, Al-Azzawi H, et al. Insulin resistance causes human gallbladder dysmotility. J Gastrointest Surg. 2006;10:940-8; discussion 8-9. DOI:10.1016/j.gassur.2006.04.005
20. Li S, Brown MS, Goldstein JL. Bifurcation of insulin signaling pathway in rat liver: mTORC1 required for stimulation of lipogenesis, but not inhibition of gluconeogenesis. Proc Natl Acad Sci USA. 2010;107:3441-6. DOI:10.1073/pnas.0914798107
21. Tanaka N, Aoyama T, Kimura S, Gonzalez FJ. Targeting nuclear receptors for the treatment of fatty liver disease. Pharmacol Ther. 2017;179:142-57. DOI:10.1016/j.pharmthera.2017.05.011
22. Ruhl CE, Everhart JE. Association of diabetes, serum insulin, and C-peptide with gallbladder disease. Hepatology. 2000;31:299-303.
23. Shen C, Wu X, Xu C, et al. Association of cholecystectomy with metabolic syndrome in a Chinese population. PloS One. 2014;9(2):e88189. DOI:10.1371/journal.pone.0088189
24. Cortés V, Quezada N, Uribe S, et al. Effect of cholecystectomy on hepatic fat accumulation and insulin resistance in non-obese Hispanic patients: A pilot study. Lipids Health Dis. 2017;16(1):129. DOI:10.1186/s12944-017-0525-3
25. Housset C, Chretien Y, Debray D, Chignard N. Functions of the gallbladder. Comprehens Physiol. 2016;6(3):1549-77. DOI:10.1002/cphy.c150050
26. Chen S, Zheng Y, Cai J, et al. Gallstones after bariatric surgery: Mechanisms and prophylaxis. Front Surg. 2025;12:1506780. DOI:10.3389/fsurg.2025.1506780
27. Lanzini A, Facchinetti D, Pigozzi MG, et al. Best-buy regimen of ursodeoxycholic acid for patients with gallstones. Scand J Gastroenterol. 1991;26(5):551-6. DOI:10.3109/00365529108998579
28. Setchell KD, Galzigna L, O'Connell N, et al. Bioequivalence of a new liquid formulation of ursodeoxycholic acid (Ursofalk suspension) and Ursofalk capsules measured by plasma pharmacokinetics and biliary enrichment. Aliment Pharmacol Ther. 2005;21(6):709-21. DOI:10.1111/j.1365-2036.2005.02385.x
29. Буторова Л.И., Ардатская М.Д., Осадчук М.А., и др. Сравнительная эффективность препаратов урсодезоксихолевой кислоты в лечении билиарного сладжа. Терапевтический архив. 2020;92(8):60-5 [Butorova LI, Ardatskaya MD, Osadchuk MA, et al. Comparative effectiveness of ursodeoxycholic acid preparations in the treatment of biliary sludge. Terapevticheskii Arkhiv (Ter. Arkh.). 2020;92(8):60-5 (in Russian)]. DOI:10.26442/00403660.2020.08.000700
30. Кучерявый Ю.А., Черемушкин С.В. Оценка терапевтической эффективности референтного препарата урсодезоксихолевой кислоты и его аналогов в растворении билиарного сладжа: метаанализ. Consilium Medicum. 2022;24(12):860-4 [Kucheryavyy YA, Cheremushkin SV. Therapeutic efficacy evaluation of the reference drug ursodeoxycholic acid and its analogues in the biliary sludge dissolution: A meta-analysis. Consilium Medicum. 2022;24(12):860-4 (in Russian)]. DOI:10.26442/20751753.2022.12.201429
31. Nair S, Diehl AM, Wiseman M, et al. Metformin in the treatment of non-alcoholic steatohepatitis: A pilot open label trial. Aliment Pharmacol Ther. 2004;20(1):23-8. DOI:10.1111/j.1365-2036.2004.02025.x
32. Newsome PN, Buchholtz K, Cusi K, et al.; NN9931-4296 Investigators. A placebo-controlled trial of subcutaneous semaglutide in nonalcoholic steatohepatitis. N Engl J Med. 2021;384(12):1113-24. DOI:10.1056/NEJMoa2028395
33. Jalleh RJ, Marathe CS, Rayner CK, et al. Physiology and pharmacology of effects of GLP-1-based therapies on gastric, biliary and intestinal motility. Endocrinology. 2024;166(1):bqae155. DOI:10.1210/endocr/bqae155
34. Драпкина О.М., Концевая А.В., Калинина А.М., и др. Коморбидность пациентов с хроническими неинфекционными заболеваниями в практике врача-терапевта. Евразийское руководство. Кардиоваскулярная терапия и профилактика. 2024;23(3):3996 [Drapkina OM, Kontsevaya AV, Kalinina AM, et al. Comorbidity of patients with noncommunicable diseases in general practice. Eurasian guidelines. Cardiovascular Therapy and Prevention. 2024;23(3):3996 (in Russian)]. DOI:10.15829/1728-8800-2024-3996
35. Ойноткинова О.Ш., Ройтберг Г.Е., Кухарчук В.В., и др. Оправдано ли применение статинов для профилактики желчнокаменной болезни. Экспертное консенсусное мнение липидологов, гепатологов, гастроэнтерологов. Профессорский журнал. Серия: медицинские науки. 2025;1-2:35-48 [Oynotkinova OSh, Roitberg GE, Kukharchuk VV, et al. Current issues of clinical lipidology Is the use of statins for the prevention of cholelithiasis justified? Expert consensus opinion of lipidologists, hepatologists, gastroenterologists. Proffesors’ Journal. Series: Medical Sciences. 2025;1-2:35-48 (in Russian)]. DOI:10.18572/2658-7130-2025-1-2-35-48
36. Сoppola S, Avagliano C, Calignano A, Berni Canani R. The protective role of butyrate against obesity and obesity-related diseases. Molecules. 2021;26(3):682. DOI:10.3390/molecules26030682
37. Gonzalez A, Krieg R, Massey HD, et al. Sodium butyrate ameliorates insulin resistance and renal failure in CKD rats by modulating intestinal permeability and mucin expression. Nephrol Dial Transplant. 2019;34(5):783-94. DOI:10.1093/ndt/gfy238
38. Seethaler B, Nguyen NK, Basrai M, et al. Short-chain fatty acids are key mediators of the favorable effects of the Mediterranean diet on intestinal barrier integrity: Data from the randomized controlled LIBRE trial. Am J Clin Nutr. 2022;116(4):928-42. DOI:10.1093/ajcn/nqac175
39. Coppola S, Nocerino R, Paparo L, et al. Therapeutic effects of butyrate on pediatric obesity: A randomized clinical trial. JAMA Netw Open. 2022;5(12):e2244912. DOI:10.1001/jamanetworkopen.2022.44912
40. Sun Y, Fan Z, Zhu X, et al. Sodium butyrate activates peroxisome proliferator-activated receptor γ to suppress lithogenic diet-induced cholesterol gallstones in mice. Food Sci Biotechnol. 2024;34(4):1015-26. DOI:10.1007/s10068-024-01721-x
41. Xu H, Wang X, Song S, Zhang L. Efficacy of sodium butyrate in improving nonalcoholic fatty liver disease: A meta-analysis of preclinical studies. Medicine (Baltimore). 2025;104(15):e42101. DOI:10.1097/MD.0000000000042101
42. Fogacci F, Giovannini M, Di Micoli V, et al. Effect of supplementation of a butyrate-based formula in individuals with liver steatosis and metabolic syndrome: A randomized double-blind placebo-controlled clinical trial. Nutrients. 2024;16(15):2454. DOI:10.3390/nu16152454
43. Европейские рекомендации по профилактике сердечно-сосудистых заболеваний в клинической практике (пересмотр 2012 г.). Российский кардиологический журнал. 2012;4(96):4-84 [Evropeiskie rekomendatsii po profilaktike serdechno-sosudistykh zabolevanii v klinicheskoi praktike (peresmotr 2012 g.). Russian Journal of Cardiology. 2012;4(96):4-84 (in Russian)].
44. Комиссаренко И.А., Левченко С.В. Использование плейотропных эффектов некоторых гастроэнтерологических препаратов при лечении пациентов с неалкогольной жировой болезнью печени и заболеваниями сердечно-сосудистой системы. Consilium Medicum. 2024;26(12):868-74 [Komissarenko IA, Levchenko SV. The use of pleiotropic effects of some gastroenterological drugs in the treatment of patients with nonalcoholic fatty liver disease and cardiovascular diseases: A review. Consilium Medicum. 2024;26(12):868-74 (in Russian)]. DOI:10.26442/20751753.2024.12.203090
45. Gibb RD, Sloan KJ, McRorie JW Jr. Psyllium is a natural nonfermented gel-forming fiber that is effective for weight loss: A comprehensive review and meta-analysis. J Am Assoc Nurse Pract. 2023;35(8):468-76. DOI:10.1097/JXX.0000000000000882
46. Gibb RD, McRorie JW Jr, Russell DA, et al. Psyllium fiber improves glycemic control proportional to loss of glycemic control: A meta-analysis of data in euglycemic subjects, patients at risk of type 2 diabetes mellitus, and patients being treated for type 2 diabetes mellitus. Am J Clin Nutr. 2015;102(6):1604-14. DOI:10.3945/ajcn.115.106989
47. Jovanovski E, Yashpal S, Komishon A, et al. Effect of psyllium (Plantago ovata) fiber on LDL cholesterol and alternative lipid targets, non-HDL cholesterol and apolipoprotein B: A systematic review and meta-analysis of randomized controlled trials. Am J Clin Nutr. 2018;108(5):922-32. DOI:10.1093/ajcn/nqy115
48. Khan K, Jovanovski E, Ho HVT, et al. The effect of viscous soluble fiber on blood pressure: A systematic review and meta-analysis of randomized controlled trials. Nutr Metab Cardiovasc Dis. 2018;28(1):3-13. DOI:10.1016/j.numecd.2017.09.007
49. McRorie JW Jr, Fahey GC Jr, Gibb RD, Chey WD. Laxative effects of wheat bran and psyllium: Resolving enduring misconceptions about fiber in treatment guidelines for chronic idiopathic constipation. J Am Assoc Nurse Pract. 2020;32(1):15-23. DOI:10.1097/JXX.0000000000000346
50. Ford AC, Talley NJ, Spiegel BM, et al. Effect of fibre, antispasmodics, and peppermint oil in the treatment of irritable bowel syndrome: Systematic review and meta-analysis. BMJ. 2008;337:a2313. DOI:10.1136/bmj.a2313. Erratum in: BMJ. 2009;338:b1881.
51. Moayyedi P, Quigley EM, Lacy BE, et al. The effect of fiber supplementation on irritable bowel syndrome: A systematic review and meta-analysis. Am J Gastroenterol. 2014;109(9):1367-74. DOI:10.1038/ajg.2014.195
________________________________________________
2. Brunt EM, Wong VW, Nobili V, et al. Nonalcoholic fatty liver disease. Nat Rev Dis Primers. 2015;1:15080. DOI:10.1038/nrdp.2015.80
3. Sayiner M, Koenig A, Henry L, Younossi ZM. Epidemiology of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis in the United States and the rest of the world. Clin Liver Dis. 2016;20(2):205-14. DOI:10.1016/j.cld.2015.10.001
4. Evstifeeva SE, Shalnova SA, Kutsenko VA, et al. Prevalence of non-alcoholic fatty liver disease among the working-age population: associations with socio-demographic indicators and behavioral risk factors (ESSE RF-2 data). Cardiovascular Therapy and Prevention. 2022;21(9):3356 (in Russian). DOI:10.15829/1728-8800-2022-3356
5. Adams LA, Lymp JF, St Sauver J, et al. The natural history of nonalcoholic fatty liver disease: A population-based cohort study. Gastroenterology. 2005;129(1):113-21. DOI:10.1053/j.gastro.2005.04.014
6. Lammert F, Gurusamy K, Ko CW, et al. Gallstones. Nat Rev Dis Primers. 2016;2:16024. DOI:10.1038/nrdp.2016.24
7. Portincasa P, Moschetta A, Palasciano G. Cholesterol gallstone disease. Lancet. 2006;368(9531):230-9. DOI:10.1016/S0140-6736(06)69044-2
8. Méndez-Sánchez N, Bahena-Aponte J, Chávez-Tapia NC, et al. Strong association between gallstones and cardiovascular disease. Am J Gastroenterol. 2005;100(4):827-30. DOI:10.1111/j.1572-0241.2005.41214.x
9. Younossi ZM, Koenig AB, Abdelatif D, et al. Global epidemiology of nonalcoholic fatty liver disease – Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology. 2016;64(1):73-84. DOI:10.1002/hep.28431
10. Koller T, Kollerova J, Hlavaty T, et al. Cholelithiasis and markers of nonalcoholic fatty liver disease in patients with metabolic risk factors. Scand J Gastroenterol. 2012;47(2):197-203. DOI:10.3109/00365521.2011.643481
11. Qiao QH, Zhu WH, Yu YX, et al. Nonalcoholic fatty liver was associated with asymptomatic gallstones in a Chinese population. Medicine (Baltimore). 2017;96(38):e7853. DOI:10.1097/MD.0000000000007853
12. Fracanzani AL, Valenti L, Russello M, et al. Gallstone disease is associated with more severe liver damage in patients with nonalcoholic fatty liver disease. PloS one. 2012;7(7):e41183. DOI:10.1371/journal.pone.0041183
13. Méndez-Sánchez N, Chavez-Tapia NC, Motola-Kuba D, et al. Metabolic syndrome as a risk factor for gallstone disease. World J Gastroenterol. 2005;1(11):1653-7. DOI:10.3748/wjg.v11.i11.1653
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Авторы
Т.Б. Топчий*, М.Д. Ардатская, Л.В. Масловский, О.Н. Минушкин
ФГБУ ДПО «Центральная государственная медицинская академия» Управления делами Президента РФ, Москва, Российская Федерация
*tantop@mail.ru
Central State Medical Academy of the President of the Russian Federation, Moscow, Russian Federation
*tantop@mail.ru
ФГБУ ДПО «Центральная государственная медицинская академия» Управления делами Президента РФ, Москва, Российская Федерация
*tantop@mail.ru
________________________________________________
Central State Medical Academy of the President of the Russian Federation, Moscow, Russian Federation
*tantop@mail.ru
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