Intestinal microbiota and nonalcoholic steatohepatitis

被引:175
作者
Brandl, Katharina [1 ]
Schnabl, Bernd [2 ,3 ]
机构
[1] Univ Calif San Diego, Skaggs Sch Pharm & Pharmaceut Sci, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Med, 9500 Gilman Dr, La Jolla, CA 92093 USA
[3] VA San Diego Healthcare Syst, Dept Med, San Diego, CA USA
关键词
bacterial translocation; dysbiosis; intestinal inflammation; intestinal microbiome; metabolites; FATTY LIVER-DISEASE; GUT MICROBIOTA; INSULIN-RESISTANCE; ACID; DYSBIOSIS; MICE; OBESITY; HUMANS; INFLAMMATION; PROGRESSION;
D O I
10.1097/MOG.0000000000000349
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Purpose of review 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. Recent findings 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. Summary 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.
引用
收藏
页码:128 / 133
页数:6
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