Ren Shao-Jie, Liu Ting, Xu Man-Hong, Shi Wei, Li Xiao-Rong
Tianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin 300384, China.
Dingzhou Maternal and Child Health Hospital, Dingzhou 073000, Hebei Province, China.
Int J Ophthalmol. 2024 Nov 18;17(11):2100-2108. doi: 10.18240/ijo.2024.11.17. eCollection 2024.
To investigate the causal effect of inflammatory bowel disease (IBD) on ocular inflammation using Mendelian randomization (MR) analysis.
Genetic instruments associated with inflammatory bowel disease (IBD), ulcerative colitis (UC), and Crohn's disease (CD) were derived from the largest genome-wide association studies (GWAS) published to date. The FinnGen research project was utilized to identify genetic risk variants associated with conjunctivitis, keratitis, iridocyclitis, chorioretinitis, episcleritis, and optic neuritis. All participants were of European ancestry. Three methods which included inverse variance weighting (IVW), weighted median (WM), and MR-Egger regression were performed to estimate the causal association in this study. IVW took the inverse variance of each study as the weight to calculate the weighted average of effect sizes, to summarize the effect sizes of multiple independent studies, which could provide the most precise estimated results. IVW was used as the primary outcome, while WM and MR-Egger were used to improve the estimation of IVW.
A nominal causal effect of genetically predicted IBD on risk of non-infectious conjunctivitis, keratitis, iridocyclitis, and optic neuritis, but not on chorioretinitis or episcleritis. After Bonferroni correction, the results showed that genetically predicted UC was significantly associated with an increased risk of iridocyclitis (IVW: OR, 1.17; 95%CI, 1.10-1.24, =2.54×10). CD was significantly associated with conjunctivitis (IVW: OR, 1.05; 95%CI, 1.03-1.08, =3.20×10), keratitis (IVW: OR, 1.06; 95%CI, 1.02-1.09; =1.13×10), and iridocyclitis (IVW: OR, 1.09; 95%CI, 1.04-1.14; =1.43×10).
IBD causally poses a risk of inflammation of conjunctiva, cornea, Iris-ciliary body complex, and optic neuritis. CD is more closely associated with the eye inflammation than UC. These impliy that the relationship of IBD and different parts of the eye structure are different, and provide novel evidence linking based on the association of the gut-eye axis.
采用孟德尔随机化(MR)分析研究炎症性肠病(IBD)对眼部炎症的因果效应。
与炎症性肠病(IBD)、溃疡性结肠炎(UC)和克罗恩病(CD)相关的基因工具来自于迄今为止发表的最大规模全基因组关联研究(GWAS)。利用芬兰基因研究项目确定与结膜炎、角膜炎、虹膜睫状体炎、脉络膜视网膜炎、巩膜炎和视神经炎相关的遗传风险变异。所有参与者均为欧洲血统。本研究采用了三种方法,包括逆方差加权(IVW)、加权中位数(WM)和MR-Egger回归来估计因果关联。IVW将每项研究的逆方差作为权重,计算效应量的加权平均值,以汇总多个独立研究的效应量,从而提供最精确的估计结果。IVW被用作主要结果,而WM和MR-Egger则用于改进IVW的估计。
基因预测的IBD对非感染性结膜炎、角膜炎、虹膜睫状体炎和视神经炎的风险具有名义上的因果效应,但对脉络膜视网膜炎或巩膜炎没有因果效应。经过Bonferroni校正后,结果显示基因预测的UC与虹膜睫状体炎风险增加显著相关(IVW:比值比,1.17;95%可信区间,1.10-1.24,P=2.54×10)。CD与结膜炎(IVW:比值比,1.05;95%可信区间,1.03-1.08,P=3.20×10)、角膜炎(IVW:比值比,1.06;95%可信区间,1.02-1.09;P=1.13×10)和虹膜睫状体炎(IVW:比值比,1.09;95%可信区间,1.04-1.14;P=1.43×10)显著相关。
IBD因果性地导致结膜、角膜、虹膜-睫状体复合体和视神经炎的风险。CD比UC与眼部炎症的关联更密切。这些表明IBD与眼部结构不同部位的关系不同,并基于肠-眼轴的关联提供了新的证据。