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近视与神经退行性疾病之间的双向因果关系:两样本孟德尔随机化分析

Bidirectional Causal Relationship Between Myopia and Neurodegenerative Diseases: Two-Sample Mendelian Randomization Analyses.

作者信息

Fan Yuanyuan, Wang Zhijie, Wu Mengai, Lin Li, Chen Lifeng, Zheng Bin

机构信息

National Clinical Research Center for Ocular Diseases, Eye Hospital, Wenzhou Medical University, Wenzhou, Zhejiang, China.

出版信息

Br J Hosp Med (Lond). 2025 Jun 25;86(6):1-19. doi: 10.12968/hmed.2025.0183. Epub 2025 Jun 18.

Abstract

Myopia is highly prevalent in certain neurodegenerative diseases (NDDs), and both conditions demonstrate genetic susceptibility. This study investigated the potential bidirectional causal relationships between myopia and four NDDs, Parkinson's disease (PD), Alzheimer's disease (AD), multiple sclerosis (MS), and amyotrophic lateral sclerosis (ALS), using Mendelian randomization (MR). We aimed to determine whether myopia contributes to the risk of NDDs and vice versa. We analyzed data from two independent, large-scale genome-wide association study (GWAS) cohorts on myopia, comprising 212,571 participants in the first cohort (finn-b-H7_MYOPIA) and 95,619 in the second (GCST009521). GWAS summary statistics for the four NDDs, encompassing 589,439 samples, were also incorporated. Bidirectional MR was employed to investigate causal relationships between myopia and each of the four NDDs. The inverse variance-weighted (IVW) method served as the primary analytical approach. Sensitivity analyses, including MR-Egger regression, weighted median, weighted mode, and simple mode, were conducted to assess the robustness of the findings. Horizontal pleiotropy was evaluated using the MR-Egger regression intercept test and the Mendelian randomization pleiotropy residual sum and outlier (MR-PRESSO) global test, while heterogeneity was assessed via Cochran's Q test. Leave-one-out analyses were conducted to evaluate the influence of individual single nucleotide polymorphisms (SNPs). Odds ratios (ORs) with 95% confidence intervals (CIs) were reported, and statistical significance was set at < 0.05. MR analyses identified no evidence of a causal relationship between myopia and refractive error and increased risk of any of the four NDDs (all > 0.05). Similarly, none of the NDDs were associated with an increased risk of myopia or refractive error (all > 0.05). Sensitivity analyses revealed no SNPs with significant influence on the causal associations (all > 0.05), supporting the robustness of the findings. This study provides no evidence of a bidirectional causal relationship between myopia and the four NDDs among individuals of European ancestry. Future research should extend beyond direct causal inference to investigate potential mediating biological mechanisms.

摘要

近视在某些神经退行性疾病(NDDs)中高度流行,且这两种情况都表现出遗传易感性。本研究使用孟德尔随机化(MR)方法,调查了近视与四种神经退行性疾病(帕金森病(PD)、阿尔茨海默病(AD)、多发性硬化症(MS)和肌萎缩侧索硬化症(ALS))之间潜在的双向因果关系。我们旨在确定近视是否会增加神经退行性疾病的风险,反之亦然。我们分析了来自两项独立的大规模全基因组关联研究(GWAS)队列中关于近视的数据,第一个队列(finn-b-H7_MYOPIA)有212,571名参与者,第二个队列(GCST009521)有95,619名参与者。还纳入了涵盖589,439个样本的四种神经退行性疾病的GWAS汇总统计数据。采用双向MR方法研究近视与四种神经退行性疾病中每一种之间的因果关系。逆方差加权(IVW)方法作为主要分析方法。进行了敏感性分析,包括MR-Egger回归、加权中位数、加权众数和简单众数分析,以评估研究结果的稳健性。使用MR-Egger回归截距检验和孟德尔随机化多效性残差和异常值(MR-PRESSO)全局检验评估水平多效性,同时通过 Cochr an's Q检验评估异质性。进行了留一法分析,以评估单个单核苷酸多态性(SNP)的影响。报告了具有95%置信区间(CIs)的优势比(ORs),统计学显著性设定为<0.05。MR分析未发现近视和屈光不正与四种神经退行性疾病中任何一种风险增加之间存在因果关系的证据(所有P>0.05)。同样,没有一种神经退行性疾病与近视或屈光不正风险增加相关(所有P>0.05)。敏感性分析未发现对因果关联有显著影响的SNP(所有P>0.05),支持了研究结果的稳健性。本研究没有提供欧洲血统个体中近视与四种神经退行性疾病之间存在双向因果关系的证据。未来的研究应超越直接因果推断,以研究潜在的中介生物学机制。

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