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Gut microbiota and human NAFLD: disentangling microbial signatures from metabolic disorders

失调 微生物群 脂肪肝 脂肪性肝炎 肠道菌群 疾病 基因组 医学 混淆 胰岛素抵抗 生物信息学 2型糖尿病 糖尿病 肥胖 代谢综合征 生物 生理学 免疫学 内科学 遗传学 内分泌学 基因
作者
Judith Aron‐Wisnewsky,Chloé Vigliotti,Julia J. Witjes,Phuong Thi Le,Adriaan G. Holleboom,Joanne Verheij,Max Nieuwdorp,Karine Clément
出处
期刊:Nature Reviews Gastroenterology & Hepatology [Nature Portfolio]
卷期号:17 (5): 279-297 被引量:737
标识
DOI:10.1038/s41575-020-0269-9
摘要

Gut microbiota dysbiosis has been repeatedly observed in obesity and type 2 diabetes mellitus, two metabolic diseases strongly intertwined with non-alcoholic fatty liver disease (NAFLD). Animal studies have demonstrated a potential causal role of gut microbiota in NAFLD. Human studies have started to describe microbiota alterations in NAFLD and have found a few consistent microbiome signatures discriminating healthy individuals from those with NAFLD, non-alcoholic steatohepatitis or cirrhosis. However, patients with NAFLD often present with obesity and/or insulin resistance and type 2 diabetes mellitus, and these metabolic confounding factors for dysbiosis have not always been considered. Patients with different NAFLD severity stages often present with heterogeneous lesions and variable demographic characteristics (including age, sex and ethnicity), which are known to affect the gut microbiome and have been overlooked in most studies. Finally, multiple gut microbiome sequencing tools and NAFLD diagnostic methods have been used across studies that could account for discrepant microbiome signatures. This Review provides a broad insight into microbiome signatures for human NAFLD and explores issues with disentangling these signatures from underlying metabolic disorders. More advanced metagenomics and multi-omics studies using system biology approaches are needed to improve microbiome biomarkers. The gut microbiota has been linked to non-alcoholic fatty liver disease (NAFLD), but metabolic confounding factors, such as obesity and diabetes, complicate analysis. This Review provides a broad insight into microbiome signatures for human NAFLD and explores issues with disentangling them from underlying metabolic disorders.
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