Brandl Katharina, Schnabl Bernd
aSkaggs School of Pharmacy and Pharmaceutical Sciences, University of California San Diego bDepartment of Medicine, University of California San Diego, La Jolla, California, USA cDepartment of Medicine, VA San Diego Healthcare System, San Diego, California, USA.
Curr Opin Gastroenterol. 2017 May;33(3):128-133. doi: 10.1097/MOG.0000000000000349.
Nonalcoholic fatty liver disease (NAFLD) is a liver disease with high prevalence in western countries. Progression from NAFLD to nonalcoholic steatohepatitis (NASH) occurs in 10-20%. NASH pathogenesis is multifactorial including genetic and environmental factors. The gut microbiota is involved in disease progression and its role is complex.
NASH is associated with changes in the intestinal microbiota, although findings in recent studies are inconsistent. Dysbiosis can trigger intestinal inflammation and impair the gut barrier. Microbial products can now reach the liver, induce hepatic inflammation and contribute to NAFLD and NASH progression. As the gut microbiota is also involved in the regulation of metabolic pathways, metabolomic approaches identified unique metabolomic profiles in patients with NASH. Altered metabolite patterns can serve as biomarkers, whereas specific metabolites (such as ethanol) have been linked with disease progression. Modifying metabolic profiles might serve as new therapeutic microbiome-based approaches.
In this review, we will highlight findings from the recent literature important to the gut-liver axis. We will predominantly focus on human studies with NASH.
非酒精性脂肪性肝病(NAFLD)是一种在西方国家中患病率很高的肝脏疾病。10%-20%的NAFLD患者会进展为非酒精性脂肪性肝炎(NASH)。NASH的发病机制是多因素的,包括遗传和环境因素。肠道微生物群参与疾病进展,其作用较为复杂。
NASH与肠道微生物群的变化有关,尽管近期研究结果并不一致。生态失调可引发肠道炎症并损害肠道屏障。微生物产物现在能够到达肝脏,诱发肝脏炎症,并促进NAFLD和NASH的进展。由于肠道微生物群还参与代谢途径的调节,代谢组学方法在NASH患者中识别出了独特的代谢组学特征。代谢产物模式的改变可作为生物标志物,而特定代谢产物(如乙醇)与疾病进展有关。改变代谢谱可能成为基于微生物群的新治疗方法。
在本综述中,我们将重点介绍近期文献中对肠-肝轴重要的研究发现。我们将主要关注NASH的人体研究。