医学
孟德尔随机化
青光眼
优势比
置信区间
视网膜静脉
全基因组关联研究
内科学
眼科
闭塞
单核苷酸多态性
遗传学
基因型
遗传变异
基因
生物
作者
Zixun Wang,Kaihua Xu,Xiaoling Zhang,Ruihua Wei,Zhiqing Li
标识
DOI:10.1177/03000605241286985
摘要
Objective Retinal vein occlusion (RVO) leads to visual impairment, and risk factors may include glaucoma. Although some studies suggest a relationship between glaucoma and RVO, it is unknown whether this association is causal. We performed Mendelian randomization (MR) analyses to evaluate the causal contribution to RVO of five genetically predicted glaucoma conditions. Methods We conducted two-sample univariable MR analysis using inverse variance weighting, weighted median, and MR-Egger methods. We obtained publicly available datasets of genome-wide association studies (GWAS) meta-analyses for glaucoma as the exposure and a GWAS for RVO in the Finn Gen biobank study as the outcome. Results Genetically predicted glaucoma was causally associated with RVO risk (beta = 0.267, standard error [SE] = 0.052, odds ratio [OR] = 1.306, 95% confidence interval [CI]: 1.181–1.445). This association was supported by sensitivity analyses using weighted median (beta = 0.211, SE = 0.075, OR = 1.235, 95% CI: 1.067–1.429), weighted mode (beta = 0.491, SE = 0.132, OR = 1.633, 95% CI: 1.261–2.116), and MR-Egger (beta = 0.3900, SE = 0.138, OR = 1.476, 95% CI: 1.128–1.933) methods. MR analyses using the validation dataset obtained consistent results. Conclusion Our results indicated that glaucoma is likely causally associated with an increased risk of RVO. The current findings may help in determining the underlying mechanisms via which glaucoma affects the risk of RVO.
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