Xiong Jiayi, Xu Tiantian, Wang Zheng, Huang Yuanfeng, Zhang Shiyu, Yang Guang, Yang Jiaqi, Gao Shuo, Wang Tianyang, Jian Xingxing, Zhao Guihu, Li Jinchen, Li Bin
Bioinformatics Centre, National Clinical Research Centre for Geriatric Disorders, Department of Geriatrics, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, China.
Comput Struct Biotechnol J. 2025 Jul 16;27:3114-3126. doi: 10.1016/j.csbj.2025.07.029. eCollection 2025.
The gut-brain axis is a key interface between neuropsychiatric and digestive disorders, however, the underlying shared genetic mechanisms and microbial mediators remain poorly understood. Utilizing genome-wide association study (GWAS) data from 18 neuropsychiatric and 24 digestive disorders, along with microbial quantitative trait loci (mbQTL) data encompassing 211 taxa ( = 18,340), we conducted a comprehensive analysis integrating linkage disequilibrium score regression, MAGMA gene-based pleiotropy mapping, and Mendelian randomization. We identified 12 significant genetic correlations between gut-brain disorder pairs, including attention-deficit/hyperactivity disorder (ADHD) and fatty liver disease. In total, 5339 pleiotropic genes were discovered, with MSH5 appearing in 28 disorder pairs. Pathway enrichment analysis implicated immune regulation and synaptic signaling as core biological processes. Novel causal relationships were also uncovered, such as ADHD increasing the risk of irritable bowel syndrome. Co-localization analysis validated three causal associations. Microbiota-focused analyses further demonstrated a protective role of against stroke, resolving previous inconsistencies in the literature. Collectively, these findings highlight the dual role of the gut microbiota-as both modulator and contributor-and provide critical genetic insights that may guide the development of targeted interventions across the gut-brain axis.
肠-脑轴是神经精神疾病和消化系统疾病之间的关键界面,然而,其潜在的共享遗传机制和微生物介质仍知之甚少。利用来自18种神经精神疾病和24种消化系统疾病的全基因组关联研究(GWAS)数据,以及包含211个分类群(=18340)的微生物数量性状位点(mbQTL)数据,我们进行了一项综合分析,整合了连锁不平衡评分回归、基于MAGMA基因的多效性图谱分析和孟德尔随机化分析。我们确定了肠-脑疾病对之间的12种显著遗传相关性,包括注意力缺陷多动障碍(ADHD)和脂肪肝疾病。总共发现了5339个多效性基因,其中MSH5出现在28对疾病中。通路富集分析表明免疫调节和突触信号传导是核心生物学过程。还发现了新的因果关系,如ADHD增加肠易激综合征的风险。共定位分析验证了三种因果关联。以微生物群为重点的分析进一步证明了 对中风的保护作用,解决了文献中先前的不一致之处。总体而言,这些发现突出了肠道微生物群作为调节者和促成者的双重作用,并提供了关键的遗传见解,可能指导跨肠-脑轴的靶向干预措施的开发。