肠道菌群
生物
疾病
脂肪肝
胆汁酸
调解
失调
肠道微生物群
遗传学
胃肠道
微生物群
生物信息学
免疫学
计算生物学
肝病
分类单元
转录组
炎症性肠病
脂肪酸
共生
微生物学
作者
X. H. Yi,Hao Xue Zhu,Meng Yu He,Shu Gao,Ming Li
出处
期刊:PubMed
[National Institutes of Health]
日期:2026-02-20
卷期号:39 (2): 202-214
摘要
Objective: Previous Mendelian randomization (MR) studies have suggested an association between the gut microbiome and metabolic-associated fatty liver disease (MAFLD). However, the reliance on 16S rRNA sequencing data has led to inconsistent findings and limited species-level insights. To address this, we conducted a de novo MR analysis using species-level shotgun metagenomic data, combined it with a meta-analysis to consolidate the existing evidence, and explored metabolite-mediated pathways. Methods: Bidirectional MR analyses were performed between 883 gut microbiota taxa (derived from shotgun metagenomic genome-wide association study) and MAFLD. Published MR studies (up to December 1, 2024) were identified using PubMed, Embase, Web of Science, and the Cochrane Library for meta-analysis. Multivariable MR (MVMR) and mediation analyses were applied to assess the mediating effects of 1,400 blood metabolites. Results: on MAFLD risk (22.06% mediation proportion). Conclusion: This study elucidated the connections between species-level gut microbiota and MAFLD, highlighting the interplay between microbiota, metabolites, and disease pathogenesis. These findings provide novel insights into the potential therapeutic targets for MAFLD.
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