Микробиом кишечника и неалкогольная жировая болезнь печени: перспективы лекарственной терапии
https://doi.org/10.31146/1682-8658-ecg-230-10-178-187
Аннотация
Об авторах
Д. А. ТеплюкРоссия
О. Н. Левина
Россия
Ч. С. Павлов
Россия
С. М. Сороколетов
Россия
Е. Ю. Пашкова
Россия
А. С. Аметов
Россия
С. А. Большаков
Россия
Е. В. Шутов
Россия
Список литературы
1. Younossi Z.M., Koenig A.B., Abdelatif D., Fazel Y., Henry L., Wymer M. Global epidemiology of nonalcoholic fatty liver disease - Meta-analytic assessment of prevalence, incidence, and outcomes. Hepatology 2016;64:73-84. doi: 10.1002/hep.28431.
2. Drapkina O.M., Ivashkin V.T. Epidemiologic features of non-alcoholic fatty liver disease in Russia. (Results of open multicenter prospective observational study DIREG L 01903).Russian Journal of Gastroenterology, Hepatology, Proctology. 2014;24:32-8. (in Russ.)@@ Драпкина О.М., Ивашкин В.Т. Эпидемиологические особенности неалкогольной жировой болезни печени в россии (результаты открытого многоцентрового проспективного исследования-наблюдения DIREG L 01903). Российский Журнал Гастроэнтерологии, Гепатологии, Колопроктологии 2014;24:32-8.
3. Ivashkin V.T., Drapkina O.M., Maev I.V. et al. Prevalence of non-alcoholic fatty liver disease in out-patients of the Russian Federation: DIREG 2 study results.Russian Journal of Gastroenterology, Hepatology, Coloproctology. 2015;24:31-8. (in Russ.)@@ Ивашкин В.Т., Драпкина О.М., Маев И.В. и др. Распространенность неалкогольной жировой болезни печени у пациентов амбулаторно-поликлинической практики в Российской Федерации: результаты исследования DIREG 2. Российский Журнал Гастроэнтерологии, Гепатологии, Колопроктологии 2015;24:31-8.
4. Younossi Z.M., Marchesini G., Pinto-Cortez H., Petta S. Epidemiology of Nonalcoholic Fatty Liver Disease and Nonalcoholic Steatohepatitis: Implications for Liver Transplantation. Transplantation. 2019;103:22-7. doi: 10.1097/TP.0000000000002484.
5. Ballestri S., Zona S., Targher G., Romagnoli D., Baldelli E., Nascimbeni F., et al. Nonalcoholic fatty liver disease is associated with an almost twofold increased risk of incident type 2 diabetes and metabolic syndrome. Evidence from a systematic review and meta-analysis. J of Gastro and Hepatol. 2016;31:936-44. doi: 10.1111/jgh.13264.
6. Lu F.B., Hu E.D., Xu L.M. et al. The relationship between obesity and the severity of non-alcoholic fatty liver disease: systematic review and meta-analysis. Expert Rev Gastroenterol Hepatol. 2018;12:491-502. doi: 10.1080/17474124.2018.1460202.
7. Fouad Y., Waked I., Bollipo S., Gomaa A., Ajlouni Y., Attia D. What’s in a name? Renaming ‘NAFLD’ to ‘MAFLD.’ Liver International. 2020;40:1254-61. doi: 10.1111/liv.14478.
8. New MASLD Nomenclature n. d. Available at: https://www.aasld.org/new-masld-nomenclature (accessed June 11, 2024).
9. Younes R., Bugianesi E. NASH in Lean Individuals. Semin Liver Dis. 2019;39:86-95. doi: 10.1055/s-0038-1677517.
10. Abdelmalek M.F., Suzuki A., Guy C., Unalp-Arida A., Colvin R., Johnson R.J., et al. Increased fructose consumption is associated with fibrosis severity in patients with nonalcoholic fatty liver disease. Hepatology. 2010;51:1961-71. doi: 10.1002/hep.23535.
11. Softic S., Cohen D.E., Kahn C.R. Role of Dietary Fructose and Hepatic De Novo Lipogenesis in Fatty Liver Disease. Dig Dis Sci. 2016;61:1282-93. doi: 10.1007/s10620-016-4054-0.
12. Zhao S., Jang C., Liu J., Uehara K., Gilbert M., Izzo L. et al. Dietary fructose feeds hepatic lipogenesis via microbiota-derived acetate. Nature. 2020;579:586-91. doi: 10.1038/s41586-020-2101-7.
13. Schwenger K.J., Clermont-Dejean N., Allard J.P. The role of the gut microbiome in chronic liver disease: the clinical evidence revised. JHEP Reports. 2019;1:214-26. doi: 10.1016/j.jhepr.2019.04.004.
14. Vajro P., Paolella G., Fasano A. Microbiota and Gut-Liver Axis: Their Influences on Obesity and Obesity-Related Liver Disease. J Pediatr Gastroenterol Nutr. 2013;56:461-8. doi: 10.1097/MPG.0b013e318284abb5.
15. Aron-Wisnewsky J., Gaborit B., Dutour A., Clement K. Gut microbiota and non-alcoholic fatty liver disease: new insights. Clinical Microbiology and Infection. 2013;19:338-48. doi: 10.1111/1469-0691.12140.
16. Yiu J.H.C., Dorweiler B., Woo C.W.Interaction between gut microbiota and toll-like receptor: from immunity to metabolism. J Mol Med. 2017;95:13-20. doi: 10.1007/s00109-016-1474-4.
17. Goodwin B., Jones S.A., Price R.R. et al. A Regulatory Cascade of the Nuclear Receptors FXR, SHP-1, and LRH-1 Represses Bile Acid Biosynthesis. Molecular Cell. 2000;6:517-26. doi: 10.1016/S1097-2765(00)00051-4.
18. Zhu Y., Li F., Guo G.L. Tissue-specific function of farnesoid X receptor in liver and intestine. Pharmacological Research. 2011;63:259-65. doi: 10.1016/j.phrs.2010.12.018.
19. Shaik F.B., Prasad D.V.R., Narala V.R. Role of farnesoid X receptor in inflammation and resolution. Inflamm Res. 2015;64:9-20. doi: 10.1007/s00011-014-0780-y.
20. Inagaki T., Moschetta A., Lee Y.-K., Peng L., Zhao G., Downes M. et al. Regulation of antibacterial defense in the small intestine by the nuclear bile acid receptor. Proc Natl Acad Sci USA. 2006;103:3920-5. doi: 10.1073/pnas.0509592103.
21. Di Ciaula A., Garruti G., Lunardi Baccetto R. et al. Bile Acid Physiology. Annals of Hepatology. 2017;16: S4-14. doi: 10.5604/01.3001.0010.5493.
22. Sayin S.I., Wahlström A., Felin J. et al. Gut Microbiota Regulates Bile Acid Metabolism by Reducing the Levels of Tauro-beta-muricholic Acid, a Naturally Occurring FXR Antagonist. Cell Metabolism. 2013;17:225-35. doi: 10.1016/j.cmet.2013.01.003.
23. Arab J.P., Karpen S.J., Dawson P.A., Arrese M., Trauner M. Bile acids and nonalcoholic fatty liver disease: Molecular insights and therapeutic perspectives. Hepatology. 2017;65:350-62. doi: 10.1002/hep.28709.
24. Shen F., Zheng R.D., Sun X.Q., Ding W.J., Wang X.Y., Fan J.G. Gut microbiota dysbiosis in patients with non-alcoholic fatty liver disease. Hepatobiliary & Pancreatic Diseases International. 2017;16:375-81. doi: 10.1016/S1499-3872(17)60019-5.
25. Hoyles L., Fernández-Real J.-M., Federici M. et al. Molecular phenomics and metagenomics of hepatic steatosis in non-diabetic obese women. Nat Med. 2018;24:1070-80. doi: 10.1038/s41591-018-0061-3.
26. Zhu L., Baker S.S., Gill C. et al. Characterization of gut microbiomes in nonalcoholic steatohepatitis (NASH) patients: A connection between endogenous alcohol and NASH. Hepatology. 2013;57:601-9. doi: 10.1002/hep.26093.
27. Loomba R., Seguritan V., Li W. et al. Gut Microbiome-Based Metagenomic Signature for Non-invasive Detection of Advanced Fibrosis in Human Nonalcoholic Fatty Liver Disease. Cell Metabolism. 2017;25:1054-1062.e5. doi: 10.1016/j.cmet.2017.04.001.
28. Raman M., Ahmed I., Gillevet P.M. et al. Fecal Microbiome and Volatile Organic Compound Metabolome in Obese Humans With Nonalcoholic Fatty Liver Disease. Clinical Gastroenterology and Hepatology. 2013;11:868-875.e3. doi: 10.1016/j.cgh.2013.02.015.
29. 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;63:764-75. doi: 10.1002/hep.28356.
30. Qin N., Yang F., Li A. et al. Alterations of the human gut microbiome in liver cirrhosis. Nature. 2014;513:59-64. doi: 10.1038/nature13568.
31. Chen Y., Ji F., Guo J., Shi D., Fang D., Li L. Dysbiosis of small intestinal microbiota in liver cirrhosis and its association with etiology. Sci Rep. 2016;6:34055. doi: 10.1038/srep34055.
32. Bajaj J.S., Heuman D.M., Hylemon P.B. et al. Altered profile of human gut microbiome is associated with cirrhosis and its complications. Journal of Hepatology. 2014;60:940-7. doi: 10.1016/j.jhep.2013.12.019.
33. Chen Y., Yang F., Lu H., Wang B. et al. Characterization of fecal microbial communities in patients with liver cirrhosis. Hepatology. 2011;54:562-72. doi: 10.1002/hep.24423.
34. Aron-Wisnewsky J., Prifti E., Belda E. et al. Major microbiota dysbiosis in severe obesity: fate after bariatric surgery. Gut. 2019;68:70-82. doi: 10.1136/gutjnl-2018-316103.
35. MetaHIT consortium, Forslund K., Hildebrand F. et al. Disentangling type 2 diabetes and metformin treatment signatures in the human gut microbiota. Nature. 2015;528:262-6. doi: 10.1038/nature15766.
36. Kakiyama G., Pandak W.M., Gillevet P.M. et al. Modulation of the fecal bile acid profile by gut microbiota in cirrhosis. Journal of Hepatology. 2013;58:949-55. doi: 10.1016/j.jhep.2013.01.003.
37. Chávez-Talavera O., Tailleux A., Lefebvre P., Staels B. Bile Acid Control of Metabolism and Inflammation in Obesity, Type 2 Diabetes, Dyslipidemia, and Nonalcoholic Fatty Liver Disease. Gastroenterology. 2017;152:1679-1694.e3. doi: 10.1053/j.gastro.2017.01.055.
38. Aron-Wisnewsky J., Vigliotti C., Witjes J. et al. Gut microbiota and human NAFLD: disentangling microbial signatures from metabolic disorders. Nat Rev Gastroenterol Hepatol. 2020;17:279-97. doi: 10.1038/s41575-020-0269-9.
39. Larsen N., Vogensen F.K., Van Den Berg F.W.J. et al. Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults. PLoS ONE. 2010;5: e9085. doi: 10.1371/journal.pone.0009085.
40. Karlsson F.H., Tremaroli V., Nookaew I. et al. Gut metagenome in European women with normal, impaired and diabetic glucose control. Nature. 2013;498:99-103. doi: 10.1038/nature12198.
41. Caussy C., Tripathi A., Humphrey G. et al. A gut microbiome signature for cirrhosis due to nonalcoholic fatty liver disease. Nat Commun. 2019;10:1406. doi: 10.1038/s41467-019-09455-9.
42. Mohebali N., Ekat K., Kreikemeyer B., Breitrück A. Barrier Protection and Recovery Effects of Gut Commensal Bacteria on Differentiated Intestinal Epithelial Cells In Vitro. Nutrients. 2020;12:2251. doi: 10.3390/nu12082251.
43. Kim H., Jeong Y., Kang S., You H.J., Ji G.E. Co-Culture with Bifidobacterium catenulatum Improves the Growth, Gut Colonization, and Butyrate Production of Faecalibacterium prausnitzii: In Vitro and In Vivo Studies. Microorganisms. 2020;8:788. doi: 10.3390/microorganisms8050788.
44. Cani P.D., Amar J., Iglesias M.A. et al. Metabolic Endotoxemia Initiates Obesity and Insulin Resistance. Diabetes. 2007;56:1761-72. doi: 10.2337/db06-1491.
45. Mao J.W., Tang H.Y., Zhao T. et al.Intestinal mucosal barrier dysfunction participates in the progress of nonalcoholic fatty liver disease.Int J Clin Exp Pathol. 2015;8:3648-58.
46. Simbirtseva G.D., Petrasheva N.I. [Blast transformation of lymphocytes in lymphogranulomatosis]. Klin Med (Mosk). 1974;52:124-8.
47. Caporaso J.G., Kuczynski J., Stombaugh J. et al. QIIME allows analysis of high-throughput community sequencing data. Nat Methods. 2010;7:335-6. doi: 10.1038/nmeth.f.303.
48. Schloss P.D., Westcott S.L., Ryabin T. et al.Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities. Appl Environ Microbiol. 2009;75:7537-41. doi: 10.1128/AEM.01541-09.
49. Langille M.G.I., Zaneveld J., Caporaso J.G. et al. Predictive functional profiling of microbial communities using 16S rRNA marker gene sequences. Nat Biotechnol. 2013;31:814-21. doi: 10.1038/nbt.2676.
50. Ranjan R., Rani A., Metwally A., McGee H.S., Perkins D.L. Analysis of the microbiome: Advantages of whole genome shotgun versus 16S amplicon sequencing. Biochemical and Biophysical Research Communications. 2016;469:967-77. doi: 10.1016/j.bbrc.2015.12.083.
51. Musazadeh V., Assadian K., Rajabi F. et al. The effect of synbiotics on liver enzymes, obesity indices, blood pressure, lipid profile, and inflammation in patients with non-alcoholic fatty liver: A systematic review and meta-analysis of randomized controlled trials. Pharmacol Res. 2024;208:107398. doi: 10.1016/j.phrs.2024.107398.
52. Pan Y., Yang Y., Wu J., Zhou H., Yang C. Efficacy of probiotics, prebiotics, and synbiotics on liver enzymes, lipid profiles, and inflammation in patients with non-alcoholic fatty liver disease: a systematic review and meta-analysis of randomized controlled trials. BMC Gastroenterol. 2024;24:283. doi: 10.1186/s12876-024-03356-y.
53. Mozaffari S., Aliari M., Emamgholipour S. et al. The effect of probiotic consumption on lipid profile, glycemic index, inflammatory markers, and liver function in NAFLD patients: A systematic review and meta-analysis of randomized controlled trials. J Diabetes Complications. 2024;38:108780. doi: 10.1016/j.jdiacomp.2024.108780.
54. Rong L., Ch’ng D., Jia P., Tsoi K.K.F., Wong S.H., Sung J.J.Y. Use of probiotics, prebiotics, and synbiotics in non-alcoholic fatty liver disease: A systematic review and meta-analysis. J Gastroenterol Hepatol. 2023;38:1682-94. doi: 10.1111/jgh.16256.
55. Zhou X., Wang J., Zhou S., Liao J., Ye Z., Mao L. Efficacy of probiotics on nonalcoholic fatty liver disease: A meta-analysis. Medicine (Baltimore). 2023;102: e32734. doi: 10.1097/MD.0000000000032734.
56. Wang Y., Wang Y., Sun J. The clinical effect of probiotics on patients with non-alcoholic fatty liver disease: a meta-analysis. Bioengineered. 2022;13:14960-73. doi: 10.1080/21655979.2023.2185941.
57. Huang Y., Wang X., Zhang L. et al. Effect of Probiotics Therapy on Nonalcoholic Fatty Liver Disease.Comput Math Methods Med. 2022;2022:7888076. doi: 10.1155/2022/7888076.
58. Xiao M.W., Lin S.X., Shen Z.H., Luo W.W., Wang X.Y. Systematic Review with Meta-Analysis: The Effects of Probiotics in Nonalcoholic Fatty Liver Disease. Gastroenterol Res Pract. 2019;2019:1484598. doi: 10.1155/2019/1484598.
59. Naghipour A., Amini-Salehi E., Orang Gorabzarmakhi M. et al. Effects of gut microbial therapy on lipid profile in individuals with non-alcoholic fatty liver disease: an umbrella meta-analysis study. Syst Rev. 2023;12:144. doi: 10.1186/s13643-023-02299-x.
60. Li S., Liu J., Wang Z., Duan F., Jia Z., Chen X., et al. The promising role of probiotics/prebiotics/synbiotics in energy metabolism biomarkers in patients with NAFLD: A systematic review and meta-analysis. Front Public Health. 2022;10:862266. doi: 10.3389/fpubh.2022.862266.
61. Noormohammadi M., Ghorbani Z., Löber U. et al. The effect of probiotic and synbiotic supplementation on appetite-regulating hormones and desire to eat: A systematic review and meta-analysis of clinical trials. Pharmacol Res. 2023;187:106614. doi: 10.1016/j.phrs.2022.106614.
62. Amini-Salehi E., Hassanipour S., Keivanlou M.H. et al. The impact of gut microbiome-targeted therapy on liver enzymes in patients with nonalcoholic fatty liver disease: an umbrella meta-analysis. Nutr Rev. 2024;82:815-30. doi: 10.1093/nutrit/nuad086.
63. Vakilpour A., Amini-Salehi E., Soltani Moghadam A. et al. The effects of gut microbiome manipulation on glycemic indices in patients with non-alcoholic fatty liver disease: a comprehensive umbrella review. Nutr Diabetes. 2024;14:25. doi: 10.1038/s41387-024-00281-7.
64. Kazeminasab F., Miraghajani M., Mokhtari K., Karimi B., Rosenkranz S.K., Santos H.O. The effects of probiotic supplementation and exercise training on liver enzymes and cardiometabolic markers in patients with non-alcoholic fatty liver disease: a systematic review and meta-analysis of randomized clinical trials. Nutr Metab (Lond). 2024;21:59. doi: 10.1186/s12986-024-00826-8.
65. Ahmed L.A., Salem M.B., Seif el-Din S.H. et al. Gut microbiota modulation as a promising therapy with metformin in rats with non-alcoholic steatohepatitis: Role of LPS/TLR4 and autophagy pathways. European Journal of Pharmacology. 2020;887:173461. doi: 10.1016/j.ejphar.2020.173461.
66. Zhang Z., Zhou H., Zhou X. et al. Lactobacillus casei YRL577 ameliorates markers of non-alcoholic fatty liver and alters expression of genes within the intestinal bile acid pathway. Br J Nutr. 2021;125:521-9. doi: 10.1017/S0007114520003001.
67. Okubo H., Sakoda H., Kushiyama A. et al. Lactobacillus casei strain Shirota protects against nonalcoholic steatohepatitis development in a rodent model. American Journal of Physiology-Gastrointestinal and Liver Physiology. 2013;305: G911-8. doi: 10.1152/ajpgi.00225.2013.
68. Wagnerberger S., Spruss A., Kanuri G. et al. Lactobacillus casei Shirota protects from fructose-induced liver steatosis: A mouse model. The Journal of Nutritional Biochemistry. 2013;24:531-8. doi: 10.1016/j.jnutbio.2012.01.014.
69. Naito E., Yoshida Y., Makino K. et al. Beneficial effect of oral administration of Lactobacillus casei strain Shirota on insulin resistance in diet-induced obesity mice: Effect of LcS on insulin resistance. Journal of Applied Microbiology. 2011;110:650-7. doi: 10.1111/j.1365-2672.2010.04922.x.
70. Zhao Z., Chen L., Zhao Y. et al. Lactobacillus plantarum NA136 ameliorates nonalcoholic fatty liver disease by modulating gut microbiota, improving intestinal barrier integrity, and attenuating inflammation. Appl Microbiol Biotechnol. 2020;104:5273-82. doi: 10.1007/s00253-020-10633-9.
71. Wang Y., Xu N., Xi A., Ahmed Z., Zhang B., Bai X. Effects of Lactobacillus plantarum MA2 isolated from Tibet kefir on lipid metabolism and intestinal microflora of rats fed on high-cholesterol diet. Appl Microbiol Biotechnol. 2009;84:341-7. doi: 10.1007/s00253-009-2012-x.
72. Park E.-J., Lee Y.-S., Kim S.M. et al. Beneficial Effects of Lactobacillus plantarum Strains on Non-Alcoholic Fatty Liver Disease in High Fat/High Fructose Diet-Fed Rats. Nutrients. 2020;12:542. doi: 10.3390/nu12020542.
73. Dorofeev A.E., Rudenko N.N., Tkach S.M., Dynya Yu.Z.Complex therapy of non-alcoholic fatty liver disease in combination with bacterial overgrowth syndrome. Modern Gastroenterology. 2019;1:77-84.@@ Дорофеев А.Э., Руденко Н.Н., Ткач С.М., Дыня Ю.З. Комплексная терапия неалкогольной жировой болезни печени в сочетании с синдромом избыточного бактериального роста. Современная Гастроэнтерология. 2019;1:77-84.
74. Ritze Y., Bárdos G., Claus A. et al. Lactobacillus rhamnosus GG protects against non-alcoholic fatty liver disease in mice. PLoS One. 2014;9: e80169. doi: 10.1371/journal.pone.0080169.
75. Kim B., Park K.Y., Ji Y., Park S., Holzapfel W., Hyun C.K. Protective effects of Lactobacillus rhamnosus GG against dyslipidemia in high-fat diet-induced obese mice. Biochem Biophys Res Commun. 2016;473:530-6. doi: 10.1016/j.bbrc.2016.03.107.
76. Liu Q., Liu Y., Li F. et al. Probiotic culture supernatant improves metabolic function through FGF21-adiponectin pathway in mice. The Journal of Nutritional Biochemistry. 2020;75:108256. doi: 10.1016/j.jnutbio.2019.108256.
77. Naudin C.R., Maner-Smith K., Owens J.A. et al. Lactococcus lactis Subspecies cremoris Elicits Protection Against Metabolic Changes Induced by a Western-Style Diet. Gastroenterology. 2020;159:639-651.e5. doi: 10.1053/j.gastro.2020.03.010.
78. Mei L., Tang Y., Li M., Yang P. et al. Co-Administration of Cholesterol-Lowering Probiotics and Anthraquinone from Cassia obtusifolia L. Ameliorate Non-Alcoholic Fatty Liver. PLoS ONE. 2015;10: e0138078. doi: 10.1371/journal.pone.0138078.
79. Xue L., He J., Gao N. et al. Probiotics may delay the progression of nonalcoholic fatty liver disease by restoring the gut microbiota structure and improving intestinal endotoxemia. Sci Rep. 2017;7:45176. doi: 10.1038/srep45176.
80. Kim D.H., Kim H., Jeong D. et al. Kefir alleviates obesity and hepatic steatosis in high-fat diet-fed mice by modulation of gut microbiota and mycobiota: targeted and untargeted community analysis with correlation of biomarkers. The Journal of Nutritional Biochemistry. 2017;44:35-43. doi: 10.1016/j.jnutbio.2017.02.014.
81. Jena P.K., Sheng L., Li Y., Wan Y.J.Y. Probiotics VSL#3 are effective in reversing non-alcoholic steatohepatitis in a mouse model. Hepatobiliary Surg Nutr. 2020;9:170-82. doi: 10.21037/hbsn.2019.09.07.
82. Yang Y., Yang L., Wu J. et al. Optimal probiotic combinations for treating nonalcoholic fatty liver disease: A systematic review and network meta-analysis. Clinical Nutrition. 2024;43:1224-39. doi: 10.1016/j.clnu.2024.04.004.
83. Zhu Y., Tan J.K., Liu J., Goon J.A. Roles of Traditional and Next-Generation Probiotics on Non-Alcoholic Fatty Liver Disease (NAFLD) and Non-Alcoholic Steatohepatitis (NASH): A Systematic Review and Network Meta-Analysis. Antioxidants (Basel). 2024;13:329. doi: 10.3390/antiox13030329.
84. Takai A., Kikuchi K., Ichimura M. et al. Fructo-oligosaccharides ameliorate steatohepatitis, visceral adiposity, and associated chronic inflammation via increased production of short-chain fatty acids in a mouse model of non-alcoholic steatohepatitis. BMC Gastroenterol. 2020;20:46. doi: 10.1186/s12876-020-01194-2.
85. Haubert N.J.B.G.B., Marchini J.S., Cunha S.F.C. et al. Choline and Fructooligosaccharide: Non-alcoholic Fatty Liver Disease, Cardiac Fat Deposition, and Oxidative Stress Markers. Nutr Metab Insights. 2015;8: NMI.S24385. doi: 10.4137/NMI.S24385.
86. Weitkunat K., Schumann S., Petzke K.J., Blaut M., Loh G., Klaus S. Effects of dietary inulin on bacterial growth, short-chain fatty acid production and hepatic lipid metabolism in gnotobiotic mice. J Nutr Biochem. 2015;26:929-37. doi: 10.1016/j.jnutbio.2015.03.010.
87. Bao T., Wang Z., Zhu L. et al. [Inulin increases the proportion of monocytic myeloid-derived suppressor cells in peripheral blood, liver, spleen and regulates the secretion of plasma inflammatory cytokines in mice with non-alcoholic fatty liver disease]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi. 2020;36:228-35.
88. Reshef N., Gophna U., Reshef L. et al. Prebiotic Treatment in Patients with Nonalcoholic Fatty Liver Disease (NAFLD)-A Randomized Pilot Trial. Nutrients. 2024;16:1571. doi: 10.3390/nu16111571.
89. Chong C.Y.L., Orr D., Plank L.D., Vatanen T., O’Sullivan J.M., Murphy R. Randomised Double-Blind Placebo-Controlled Trial of Inulin with Metronidazole in Non-Alcoholic Fatty Liver Disease (NAFLD). Nutrients. 2020;12:937. doi: 10.3390/nu12040937.
90. Singh V., Yeoh B.S., Chassaing B., Xiao X., Saha P., Aguilera Olvera R., et al. Dysregulated Microbial Fermentation of Soluble Fiber Induces Cholestatic Liver Cancer. Cell. 2018;175:679-694.e22. doi: 10.1016/j.cell.2018.09.004.
91. Wen W., Schwabe R.F. Soluble Fibers Improve Metabolic Syndrome but May Cause Liver Disease and Hepatocellular Carcinoma. Hepatology. 2019;70:739-41. doi: 10.1002/hep.30565.
92. Ni Y., Qian L., Siliceo S.L. et al. Resistant starch decreases intrahepatic triglycerides in patients with NAFLD via gut microbiome alterations. Cell Metab. 2023;35:1530-1547.e8. doi: 10.1016/j.cmet.2023.08.002.
93. Liu L., Li P., Liu Y., Zhang Y. Efficacy of Probiotics and Synbiotics in Patients with Nonalcoholic Fatty Liver Disease: A Meta-Analysis. Dig Dis Sci. 2019;64:3402-12. doi: 10.1007/s10620-019-05699-z.
94. Rivero-Gutiérrez B., Gámez-Belmonte R., Suárez M.D. et al. A synbiotic composed of Lactobacillus fermentum CECT5716 and FOS prevents the development of fatty acid liver and glycemic alterations in rats fed a high fructose diet associated with changes in the microbiota. Molecular Nutrition Food Res. 2017;61:1600622. doi: 10.1002/mnfr.201600622.
95. Yao F., Jia R., Huang H. et al. Effect of Lactobacillus paracasei N1115 and fructooligosaccharides in nonalcoholic fatty liver disease. Aoms. 2019;15:1336-44. doi: 10.5114/aoms.2019.86611.
96. Alves C.C., Waitzberg D.L., De Andrade L.S. et al. Prebiotic and Synbiotic Modifications of Beta Oxidation and Lipogenic Gene Expression after Experimental Hypercholesterolemia in Rat Liver. Front Microbiol. 2017;8:2010. doi: 10.3389/fmicb.2017.02010.
97. Malaguarnera M., Vacante M., Antic T. et al. Bifidobacterium longum with fructo-oligosaccharides in patients with non alcoholic steatohepatitis. Dig Dis Sci. 2012;57:545-53. doi: 10.1007/s10620-011-1887-4.
98. Scorletti E., Afolabi P.R., Miles E.A. et al. Synbiotics Alter Fecal Microbiomes, But Not Liver Fat or Fibrosis, in a Randomized Trial of Patients With Nonalcoholic Fatty Liver Disease. Gastroenterology. 2020;158:1597-1610.e7. doi: 10.1053/j.gastro.2020.01.031.
99. Asgharian A., Askari G., Esmailzade A., Feizi A., Mohammadi V. The effect of symbiotic supplementation on liver enzymes, c-reactive protein and ultrasound findings in patients with non-alcoholic fatty liver disease: A clinical trial.Int J Prev Med. 2016;7:59. doi: 10.4103/2008-7802.178533.
100. Mitrović M., Dobrosavljević A., Odanović O. et al. The effects of synbiotics on the liver steatosis, inflammation, and gut microbiome of metabolic dysfunction-associated liver disease patients-randomized trial. Rom J Intern Med. 2024;62:184-93. doi: 10.2478/rjim-2024-0004.
101. Leila Javadi, Manouchehr Khoshbaten, Abdolrasoul Safaiyan, Mostafa Ghavami, Mehran Mesgari Abbasi, Bahram Pourghassem Gargari. Pro- and prebiotic effects on oxidative stress and inflammatory markers in non-alcoholic fatty liver disease. Asia Pacific Journal of Clinical Nutrition. 2018;27. doi: 10.6133/apjcn.042018.05.
102. Escouto G.S., Port G.Z., Tovo C.V. et al. Probiotic Supplementation, Hepatic Fibrosis, and the Microbiota Profile in Patients with Nonalcoholic Steatohepatitis: A Randomized Controlled Trial. J Nutr. 2023;153:1984-93. doi: 10.1016/j.tjnut.2023.05.019.
103. Kelly C.R., Kahn S., Kashyap P. et al. Update on Fecal Microbiota Transplantation 2015: Indications, Methodologies, Mechanisms, and Outlook. Gastroenterology. 2015;149:223-37. doi: 10.1053/j.gastro.2015.05.008.
104. Eiseman B., Silen W., Bascom G.S., Kauvar A.J. Fecal enema as an adjunct in the treatment of pseudomembranous enterocolitis. Surgery. 1958;44:854-9.
105. Zhou D., Pan Q., Shen F. et al. Total fecal microbiota transplantation alleviates high-fat diet-induced steatohepatitis in mice via beneficial regulation of gut microbiota. Sci Rep. 2017;7:1529. doi: 10.1038/s41598-017-01751-y.
106. Vrieze A., Van Nood E., Holleman F. et al. Transfer of Intestinal Microbiota From Lean Donors Increases Insulin Sensitivity in Individuals With Metabolic Syndrome. Gastroenterology. 2012;143:913-916.e7. doi: 10.1053/j.gastro.2012.06.031.
107. Kootte R.S., Levin E., Salojärvi J. et al. Improvement of Insulin Sensitivity after Lean Donor Feces in Metabolic Syndrome Is Driven by Baseline Intestinal Microbiota Composition. Cell Metabolism. 2017;26:611-619.e6. doi: 10.1016/j.cmet.2017.09.008.
108. Craven L., Rahman A., Nair Parvathy S. et al. Allogenic Fecal Microbiota Transplantation in Patients With Nonalcoholic Fatty Liver Disease Improves Abnormal Small Intestinal Permeability: A Randomized Control Trial. Am J Gastroenterol. 2020;115:1055-65. doi: 10.14309/ajg.0000000000000661.
109. Xue L., Deng Z., Luo W., He X., Chen Y. Effect of Fecal Microbiota Transplantation on Non-Alcoholic Fatty Liver Disease: A Randomized Clinical Trial. Front Cell Infect Microbiol. 2022;12:759306. doi: 10.3389/fcimb.2022.759306.
Рецензия
Для цитирования:
Теплюк Д.А., Левина О.Н., Павлов Ч.С., Сороколетов С.М., Пашкова Е.Ю., Аметов А.С., Большаков С.А., Шутов Е.В. Микробиом кишечника и неалкогольная жировая болезнь печени: перспективы лекарственной терапии. Экспериментальная и клиническая гастроэнтерология. 2024;(10):178-187. https://doi.org/10.31146/1682-8658-ecg-230-10-178-187
For citation:
Teplyuk D.A., Levina O.N., Pavlov Ch.S., Sorokoletov S.M., Pashkova E.Yu., Ametov A.S., Bolshakov S.A., Shutov E.V. The gut microbiome and nonalcoholic fatty liver disease: prospects for drug therapy. Experimental and Clinical Gastroenterology. 2024;(10):178-187. (In Russ.) https://doi.org/10.31146/1682-8658-ecg-230-10-178-187