Service d'Hépato-Gastroentérologie, Cliniques Universitaires Saint-Luc, UCLouvain, 1200 Brussels, Belgium.
Laboratory of Gastroenterology and Hepatology, Institut de Recherche Expérimentale et Clinique, UCLouvain, 1200 Brussels, Belgium.
Cells. 2022 Aug 31;11(17):2718. doi: 10.3390/cells11172718.
Numerous studies show a modification of the gut microbiota in patients with obesity or diabetes. Animal studies have also shown a causal role of gut microbiota in liver metabolic disorders including steatosis whereas the human situation is less clear. Patients with metabolic dysfunction associated fatty liver disease (MAFLD) also have a modification in their gut microbiota composition but the changes are not fully characterized. The absence of consensus on a precise signature is probably due to disease heterogeneity, possible concomitant medications and different selection or evaluation criteria. The most consistent changes were increased relative abundance of Proteobacteria, Enterobacteriaceae and species and decreased abundance of and . Possible mechanisms linking the microbiota and MAFLD are increased intestinal permeability with translocation of microbial products into the portal circulation, but also changes in the bile acids and production of microbial metabolites such as ethanol, short chain fatty acids and amino acid derivatives able to modulate liver metabolism and inflammation. Several interventional studies exist that attempt to modulate liver disease by administering antibiotics, probiotics, prebiotics, synbiotics, postbiotics or fecal transplantation. In conclusion, there are both gaps and hopes concerning the interest of gut microbiome evaluation for diagnosis purposes of MAFLD and for new therapeutic developments that are often tested on small size cohorts.
大量研究表明,肥胖症或糖尿病患者的肠道微生物群会发生改变。动物研究还表明,肠道微生物群在包括脂肪变性在内的肝脏代谢紊乱中起着因果作用,而人类的情况则不太清楚。患有与代谢功能障碍相关的脂肪性肝病(MAFLD)的患者其肠道微生物群组成也发生了改变,但这些变化尚未完全阐明。缺乏对确切特征的共识可能是由于疾病异质性、可能同时存在的药物以及不同的选择或评估标准。最一致的变化是厚壁菌门、肠杆菌科和属的相对丰度增加,和属的丰度降低。微生物群与 MAFLD 之间可能存在联系的机制是肠道通透性增加,导致微生物产物易位到门静脉循环,以及胆汁酸的变化和微生物代谢产物的产生,如乙醇、短链脂肪酸和氨基酸衍生物,这些物质能够调节肝脏代谢和炎症。有一些干预性研究试图通过给予抗生素、益生菌、益生元、合生元、后生元和粪便移植来调节肝脏疾病。总之,关于肠道微生物组评估在 MAFLD 的诊断目的以及新的治疗方法的发展方面,存在着差距和希望,这些新的治疗方法往往在小规模队列中进行测试。