Nonalcoholic Fatty Liver Disease: Modulating Gut Microbiota to Improve Severity?

非酒精性脂肪肝 肠道菌群 益生元 内科学 医学 肝病 脂肪肝 生理学 疾病 生物信息学 生物 免疫学 生物化学
作者
Judith Aron‐Wisnewsky,Moritz V. Warmbrunn,Max Nieuwdorp,Karine Clément
出处
期刊:Gastroenterology [Elsevier]
卷期号:158 (7): 1881-1898 被引量:109
标识
DOI:10.1053/j.gastro.2020.01.049
摘要

Gut microbiota plays a role in the pathophysiology of metabolic diseases, which include nonalcoholic fatty liver diseases, through the gut–liver axis. To date, clinical guidelines recommend a weight loss goal of 7%–10% to improve features of nonalcoholic fatty liver diseases. Because this target is not easily achieved by all patients, alternative therapeutic options are currently being evaluated. This review focuses on therapeutics that aim to modulate the gut microbiota and the gut–liver axis. We discuss how probiotics, prebiotics, synbiotic, fecal microbiota transfer, polyphenols, specific diets, and exercise interventions have been found to modify gut microbiota signatures; improve nonalcoholic fatty liver disease outcomes; and detail, when available, the different mechanisms by which these beneficial outcomes might occur. Apart from probiotics that have already been tested in human randomized controlled trials, most of these potential therapeutics have been studied in animals. Their efficacy still warrants confirmation in humans using appropriate design. Gut microbiota plays a role in the pathophysiology of metabolic diseases, which include nonalcoholic fatty liver diseases, through the gut–liver axis. To date, clinical guidelines recommend a weight loss goal of 7%–10% to improve features of nonalcoholic fatty liver diseases. Because this target is not easily achieved by all patients, alternative therapeutic options are currently being evaluated. This review focuses on therapeutics that aim to modulate the gut microbiota and the gut–liver axis. We discuss how probiotics, prebiotics, synbiotic, fecal microbiota transfer, polyphenols, specific diets, and exercise interventions have been found to modify gut microbiota signatures; improve nonalcoholic fatty liver disease outcomes; and detail, when available, the different mechanisms by which these beneficial outcomes might occur. Apart from probiotics that have already been tested in human randomized controlled trials, most of these potential therapeutics have been studied in animals. Their efficacy still warrants confirmation in humans using appropriate design.
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