通过全基因组关联研究调查肠道微生物群与神经系统疾病之间的因果关系。

IF 4.6 2区 医学 Q1 NEUROSCIENCES
Molecular Neurobiology Pub Date : 2025-07-01 Epub Date: 2025-03-12 DOI:10.1007/s12035-025-04770-3
Qingchen Jiang, Laiqiang Wu, Xiaochen Wang, Zhe Gao, Xiaorui Liu, Wen Zhang, Li Xue, Juan Yang, Teng Chen, Yanjiong Chen, Biao Wang
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引用次数: 0

摘要

许多报告都强调了肠道微生物群在神经系统疾病的发生、进展和结果中的作用。然而,目前的报道有些混乱,特别是关于肠道微生物群是否对各种神经系统疾病有因果关系。此外,在这些神经系统疾病中是否存在涉及肠道微生物群落的共同机制尚未揭示。在这项研究中,我们利用了MiBioGen联盟最大规模的全基因组关联研究(GWAS)的数据,其中包括来自24个队列的18,340个个体的遗传和微生物组成数据。我们利用与肠道微生物组相关的单核苷酸多态性(snp)作为孟德尔随机化(MR)分析的工具变量(IVs)。这些iv是根据其全基因组和全基因座的重要性严格选择的,以确保可靠的因果推断。我们的研究使用mr建立了特定肠道微生物群与各种神经系统疾病之间的强大关联。我们系统地描述了所有疾病中具有因果关系的细菌,涵盖门,纲,目,科和属的水平。我们确定了34种细菌在疾病中具有重要的风险或保护因素,包括两个主要门,如厚壁菌门(22种)和变形菌门(8种),以及拟杆菌门(2种),放线菌门(1种)和Verrucomicrobiota(1种)。在细菌科水平上,我们发现Lachnospiraceae和Ruminococcaceae与这11种疾病的关系最为密切,它们在同一种疾病中可能发挥不同的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Investigating Causal Links Between Gut Microbiota and Neurological Disorders via Genome-Wide Association Studies.

Many reports have highlighted the involvement of the gut microbiome in the occurrence, progression, and outcomes of neurological disorders. However, current reports are somewhat chaotic, especially concerning whether the gut microbiota has a causal effect on various neurological diseases. Furthermore, whether there is a common mechanism involving gut microbial communities in these neurological disorders has not to be revealed. In this study, we leveraged data from the largest-scale genome-wide association study (GWAS) by the MiBioGen consortium, which includes genetic and microbial composition data from 18,340 individuals spanning 24 cohorts. We utilized single-nucleotide polymorphisms (SNPs) associated with the gut microbiome as instrumental variables (IVs) in Mendelian randomization (MR) analyses. These IVs were rigorously selected based on their genome-wide and locus-wide significance to ensure robust causal inference. Our study established robust associations between specific gut microbiota and various neurological disorders using MR. We systematically depicted the bacteria with causal relationships in all diseases, covering the levels of phylum, class, order, family, and genus. We identified 34 bacterial species as significant risk or protective factors across disorders, including two main phylum levels such as Firmicutes (22 species) and Proteobacteria (8 species), as well as Bacteroidetes (2 species), Actinobacteria (1 species), and Verrucomicrobiota (1 species). At the family level of bacteria, we found that Lachnospiraceae and Ruminococcaceae are the most related to these 11 diseases and they may play different roles in the same disease.

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来源期刊
Molecular Neurobiology
Molecular Neurobiology 医学-神经科学
CiteScore
9.00
自引率
2.00%
发文量
480
审稿时长
1 months
期刊介绍: Molecular Neurobiology is an exciting journal for neuroscientists needing to stay in close touch with progress at the forefront of molecular brain research today. It is an especially important periodical for graduate students and "postdocs," specifically designed to synthesize and critically assess research trends for all neuroscientists hoping to stay active at the cutting edge of this dramatically developing area. This journal has proven to be crucial in departmental libraries, serving as essential reading for every committed neuroscientist who is striving to keep abreast of all rapid developments in a forefront field. Most recent significant advances in experimental and clinical neuroscience have been occurring at the molecular level. Until now, there has been no journal devoted to looking closely at this fragmented literature in a critical, coherent fashion. Each submission is thoroughly analyzed by scientists and clinicians internationally renowned for their special competence in the areas treated.
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