[1] European Association for the Study of the Liver (EASL), European Association for the Study of Diabetes (EASD), European Association for the Study of Obesity (EASO). EASL-EASD-EASO Clinical Practice Guidelines for the management of non-alcoholic fatty liver disease. J Hepatol, 2016, 64: 1388-1402. [2] Yu Y, Cai J, She Z, et al. Insights into the Epidemiology, Pathogenesis, and Therapeutics of Nonalcoholic Fatty Liver Diseases. Adv Sci (Weinh), 2019, 6: 1801585. [3] Wong GL, Wong VW. How many deaths are caused by non-alcoholic fatty liver disease in the Asia-Pacific region? Lancet Gastroenterol Hepatol, 2020, 5: 103-105. [4] Chow MD, Lee YH, Guo GL. The role of bile acids in nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Mol Aspects Med, 2017, 56: 34-44. [5] Wang C, Zhu C, Shao L, et al. Role of Bile Acids in Dysbiosis and Treatment of Nonalcoholic Fatty Liver Disease. Mediators Inflamm, 2019, 2019: 7659509. [6] Gottlieb A, Canbay A. Why Bile Acids Are So Important in Non-Alcoholic Fatty Liver Disease (NAFLD) Progression. Cells, 2019, 8: 1358. [7] 中华医学会肝病学分会脂肪肝和酒精性肝病学组,中国医师协会脂肪性肝病专家委员会.非酒精性脂肪性肝病防治指南(2018更新版). 实用肝脏病杂志,2018,21: 177-186. [8] Safari Z, Gérard P. The links between the gut microbiome and non-alcoholic fatty liver disease (NAFLD). Cell Mol Life Sci, 2019, 76: 1541-1558. [9] Jiao N, Baker SS, Chapa-Rodriguez A, et al. Suppressed hepatic bile acid signalling despite elevated production of primary and secondary bile acids in NAFLD. Gut, 2018, 67: 1881-1891. [10] Rao A, Kosters A, Mells JE, et al. Inhibition of ileal bile acid uptake protects against nonalcoholic fatty liver disease in high-fat diet-fed mice. Sci Transl Med, 2016, 8: 357ra122. [11] Ferro D, Baratta F, Pastori D, et al. New Insights into the Pathogenesis of Non-Alcoholic Fatty Liver Disease: Gut-Derived Lipopolysaccharides and Oxidative Stress. Nutrients, 2020, 12: 2762. [12] Jonas W, Schürmann A. Genetic and epigenetic factors determining NAFLD risk. Mol Metab., 2020: 101111. [13] Rotman Y, Sanyal AJ. Current and upcoming pharmacotherapy for non-alcoholic fatty liver disease. Gut, 2017, 66: 180-190. [14] Perino A, Demagny H, Velazquez-Villegas LA, et al. Molecular Physiology of Bile Acid Signaling in Health, Disease and Aging. Physiol Rev, 2021, 101:683-731. [15] Aranha MM, Cortez-Pinto H, Costa A. Bile acid levels are increased in the liver of patients with steatohepatitis. Eur J Gastroenterol Hepatol, 2008, 20: 519-525. [16] Nimer N, Choucair I, Wang Z, et al. Bile acids profile, histopathological indices and genetic variants for non-alcoholic fatty liver disease progression. Metabolism, 2021, 116:154457. [17] Jahnel J, Z?hrer E, Alisi A, et al. Serum Bile Acid Levels in Children With Nonalcoholic Fatty Liver Disease. J Pediatr Gastroenterol Nutr, 2015, 61: 85-90. [18] Yamada S, Kawaguchi H, Yamada T, et al. Cholic Acid Enhances Visceral Adiposity, Atherosclerosis and Nonalcoholic Fatty Liver Disease in Microminipigs. J Atheroscler Thromb, 2017, 24: 1150-1166. |