Big Data Laboratory, Joint Shantou International Eye Center of Shantou University and The Chinese University of Hong Kong, Shantou, Guangdong, China.
Department of Anesthesiology, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China.
Int Ophthalmol. 2024 Sep 30;44(1):397. doi: 10.1007/s10792-024-03319-y.
Frailty and age-related eye diseases are common in older people; however, whether there is a causal link remains unknown. We aimed to explore the causal associations between the frailty index (FI) and ophthalmic traits and identify modifiable mediators.
Linkage disequilibrium score regression and two-sample Mendelian randomization were applied to identify genetic correlations and causal associations between FI and ophthalmic traits. Summary data for FI was obtained from a genome-wide association study that included 175,226 individuals of European ancestry. Summary-level statistics for ophthalmic traits were obtained from relative GWASs. Summary-level data for cardiovascular risk factors, inflammatory biomarkers, and the central nervous system were used to identify the possible mediators.
FI had a significant genetic correlation with 10 ophthalmic traits. Per SD increment of FI, the odds ratio was 1.329 (95% CI, 1.123, 1.573; P = 9.5 × 10) for cataracts, 1.825 (95% CI, 1.115, 2.986; P = 0.016) for keratitis, 1.798 (95% CI, 1.039, 3.11; P = 0.036) for disorders of vitreous body and 1.478 (95% CI, 1.005, 2.173; P = 0.046) for disorders of sclera, cornea, iris and ciliary body. The MR effect estimates of FI on ophthalmic traits were attenuated after adjusting for mental disorders, type 2 diabetes, triglyceride, and interleukin-8 (IL-8) levels.
This study reports a genetic correlation and causal association between FI and ophthalmic traits, in which mental disorders, type 2 diabetes, triglycerides, and IL-8 may play a mediating role. These findings highlight a possible method to reduce the risk of FI-related ophthalmic diseases.
虚弱和与年龄相关的眼病在老年人中很常见;然而,两者之间是否存在因果关系尚不清楚。本研究旨在探讨虚弱指数(FI)与眼科特征之间的因果关系,并确定可改变的中介因素。
连锁不平衡评分回归和两样本孟德尔随机化被用于确定 FI 与眼科特征之间的遗传相关性和因果关系。FI 的全基因组关联研究(GWAS)汇总数据纳入了 175226 名欧洲血统个体。眼科特征的汇总水平统计数据来自相关的 GWAS。心血管危险因素、炎症生物标志物和中枢神经系统的汇总水平数据用于确定可能的中介因素。
FI 与 10 种眼科特征存在显著的遗传相关性。FI 每增加一个标准差,患白内障的优势比为 1.329(95%可信区间,1.1231.573;P=9.5×10),患角膜炎的优势比为 1.825(95%可信区间,1.1152.986;P=0.016),患玻璃体病变的优势比为 1.798(95%可信区间,1.0393.11;P=0.036),患巩膜、角膜、虹膜和睫状体病变的优势比为 1.478(95%可信区间,1.0052.173;P=0.046)。调整精神障碍、2 型糖尿病、甘油三酯和白细胞介素-8(IL-8)水平后,FI 对眼科特征的 MR 效应估计值减弱。
本研究报告了 FI 与眼科特征之间存在遗传相关性和因果关系,其中精神障碍、2 型糖尿病、甘油三酯和 IL-8 可能发挥中介作用。这些发现强调了一种降低与 FI 相关的眼科疾病风险的可能方法。