Zhang Jikang, Hu Yiqi, Xu Jin, Shao Hua, Zhu Qingping, Si Hao
General Surgery Department, The Second Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Digestive Endoscopic Treatment Center, The Second Affiliated Hospital of Nanjing University of Chinese Medicine, Nanjing, China.
Front Microbiol. 2024 Dec 16;15:1442506. doi: 10.3389/fmicb.2024.1442506. eCollection 2024.
Increasing evidence suggests an association between gut microbiota and Autoimmune Liver Diseases (AILDs). However, causal inference remains controversial due to confounding bias in observational studies. Additionally, there is currently no clear evidence indicating that immune cells act as intermediate phenotypes in the pathogenesis of AILDs. This study utilizes the Mendelian Randomization (MR) method to investigate the causal relationships among gut microbiota, immune cells, and AILDs.
Initially, we conducted a two-sample MR analysis to predict the causal relationships among 412 gut microbiota, 731 immune phenotypes, and AILDs. Subsequently, a series of sensitivity analyses were performed to validate the initial MR results and reverse MR analysis was conducted to exclude reverse causality. Finally, a two-step MR analysis was utilized to quantify the proportion of the impact of gut microbiota on AILDs mediated by immune cells.
Following rigorous MR analysis, our findings indicate that increased involvement of the gut microbiome in the is positively associated with an elevated risk of Autoimmune Hepatitis (AIH). The effect is partially mediated by the , which accounts for 17.47% of the total effect. Moreover, the appears to mediate the development of Primary Sclerosing Cholangitis (PSC) through , contributing to 32.47% of the total observed effect.
Our study highlights the potential mediating mechanisms of immune cells in the causal relationship between the gut microbiome and AILDs. These insights provide a foundation for developing preventive strategies for AILDs in clinical practice.
越来越多的证据表明肠道微生物群与自身免疫性肝病(AILDs)之间存在关联。然而,由于观察性研究中存在混杂偏倚,因果推断仍存在争议。此外,目前尚无明确证据表明免疫细胞在AILDs发病机制中作为中间表型起作用。本研究采用孟德尔随机化(MR)方法来研究肠道微生物群、免疫细胞和AILDs之间的因果关系。
首先,我们进行了两样本MR分析,以预测412种肠道微生物群、731种免疫表型和AILDs之间的因果关系。随后,进行了一系列敏感性分析以验证初始MR结果,并进行了反向MR分析以排除反向因果关系。最后,采用两步MR分析来量化肠道微生物群对AILDs的影响中由免疫细胞介导的比例。
经过严格的MR分析,我们的研究结果表明肠道微生物群参与度增加与自身免疫性肝炎(AIH)风险升高呈正相关。这种效应部分由[具体内容缺失]介导,其占总效应的17.47%。此外,[具体内容缺失]似乎通过[具体内容缺失]介导原发性硬化性胆管炎(PSC)的发展,占总观察效应的32.47%。
我们的研究突出了免疫细胞在肠道微生物群与AILDs因果关系中的潜在介导机制。这些见解为临床实践中制定AILDs的预防策略提供了基础。