Li Yipao, Chen Lu, Lin Shaokai, An Wei, Miao Linfeng, Wan Minghui, Zhang Binjun
National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou, China.
State Key Laboratory of Ophthalmology, Optometry and Vision Science, Eye Hospital, Wenzhou Medical University, Wenzhou, China.
Transl Vis Sci Technol. 2025 Jun 2;14(6):34. doi: 10.1167/tvst.14.6.34.
This study investigates the causal relationship between gut microbiota (GM) and Graves' ophthalmopathy (GO) and explores the mediating role of circulating inflammatory proteins (IPs) in this association.
A two-step, two-sample Mendelian randomization (MR) analysis was performed using GM data from MiBioGen (N = 18,340), GO data from the FinnGen Research Project (691 cases, 411,490 controls), and IP data from a genome-wide association study (N = 14,824). The primary MR analysis utilized the inverse variance-weighted approach, supplemented by MR Egger, weighted median, maximum likelihood, and MR robust adjusted profile score methods. Mediation MR was used to assess the mediating role of IPs.
We identified 26 GM taxa causally associated with GO. Notably, the genus Parabacteroides exhibited a protective effect on GO (odds ratio = 0.29; 95% confidence interval, 0.16-0.51; P < 0.001). Additionally, five circulating IPs demonstrated protective effects, while three IPs (CXCL10, CXCL11, EN-RAGE) were associated with increased GO risk. Mediation MR showed that CXCL10 mediated the pathway from Parabacteroides to GO (mediation effect = -0.07), accounting for 5.27% of the total effect.
This study supports a causal link between GM and GO, mediated by circulating IPs. These findings offer new insights into GO pathogenesis and potential targets for clinical intervention.
Our findings reveal how gut microbiota influences Graves' ophthalmopathy through inflammatory proteins, providing potential therapeutic targets for disease prevention and treatment.
本研究调查肠道微生物群(GM)与格雷夫斯眼病(GO)之间的因果关系,并探讨循环炎症蛋白(IPs)在这种关联中的中介作用。
采用两步两样本孟德尔随机化(MR)分析,使用来自MiBioGen的GM数据(N = 18,340)、来自芬兰基因研究项目的GO数据(691例病例,411,490例对照)以及来自全基因组关联研究的IP数据(N = 14,824)。主要的MR分析采用逆方差加权法,并辅以MR Egger、加权中位数、最大似然法和MR稳健调整轮廓得分法。中介MR用于评估IPs的中介作用。
我们确定了26种与GO有因果关系的GM分类群。值得注意的是,副拟杆菌属对GO具有保护作用(优势比 = 0.29;95%置信区间,0.16 - 0.51;P < 0.001)。此外,五种循环IPs显示出保护作用,而三种IPs(CXCL10、CXCL11、EN-RAGE)与GO风险增加有关。中介MR表明,CXCL10介导了从副拟杆菌到GO的通路(中介效应 = -0.07),占总效应的5.27%。
本研究支持GM与GO之间存在由循环IPs介导的因果联系。这些发现为GO的发病机制和临床干预的潜在靶点提供了新的见解。
我们的研究结果揭示了肠道微生物群如何通过炎症蛋白影响格雷夫斯眼病,为疾病的预防和治疗提供了潜在的治疗靶点。