Wei Feiran, Zhao Meng, Sun Xiaohui, Ma Hongfei, Yin Huimin, Shen Xiaobing
Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, Jiangsu, China.
Department of Epidemiology and Health Statistics, School of Public Health, Southeast University, Nanjing, Jiangsu, China.
Medicine (Baltimore). 2025 May 30;104(22):e42596. doi: 10.1097/MD.0000000000042596.
The gut microbiota has been implicated in the development of rheumatoid arthritis (RA), but whether these associations reflect causal relationships remains unclear. We conducted a two-sample Mendelian randomization analysis to investigate the potential causal effects of gut microbial taxa on RA risk. Summary-level data from the MiBioGen consortium (n = 13,266) and a large RA genome-wide association study (n = 97,173) were used. Multiple Mendelian randomization methods and sensitivity analyses were applied to ensure robustness. Four microbial taxa showed nominal associations with RA. Increased abundance of Catenibacterium, Desulfovibrio, and Ruminiclostridium 6 was associated with a higher risk of RA, while Lachnospiraceae (UCG008) appeared to have a protective effect. Although these associations did not meet Bonferroni-corrected significance, results were consistent across analytical methods with no evidence of pleiotropy or heterogeneity. This study provides genetic evidence supporting a potential causal link between specific gut microbes and RA risk. The findings highlight host immune modulation as a possible pathway connecting the gut microbiome to RA and identify candidate taxa for future mechanistic and therapeutic research.
肠道微生物群已被认为与类风湿性关节炎(RA)的发病有关,但这些关联是否反映因果关系仍不清楚。我们进行了一项两样本孟德尔随机化分析,以研究肠道微生物分类群对RA风险的潜在因果效应。使用了来自MiBioGen联盟的汇总数据(n = 13266)和一项大型RA全基因组关联研究的数据(n = 97173)。应用了多种孟德尔随机化方法和敏感性分析以确保结果的稳健性。四种微生物分类群与RA存在名义上的关联。加氏菌属、脱硫弧菌属和瘤胃梭菌属6丰度增加与RA风险较高相关,而毛螺菌科(UCG008)似乎具有保护作用。尽管这些关联未达到Bonferroni校正后的显著性水平,但分析方法之间的结果一致,没有多效性或异质性的证据。本研究提供了遗传证据,支持特定肠道微生物与RA风险之间存在潜在因果联系。这些发现突出了宿主免疫调节作为连接肠道微生物群与RA的可能途径,并确定了未来进行机制和治疗研究的候选分类群。