Tolosa-Tort Paulina, DeWan Andrew T
Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Center for Perinatal, Pediatric and Environmental Epidemiology, Yale School of Public Health, New Haven, CT, USA.
Mol Neurobiol. 2025 May 24. doi: 10.1007/s12035-025-05074-2.
Primary open-angle glaucoma is the most common form of glaucoma worldwide and one of the leading causes of irreversible blindness. Current therapies focus on intraocular pressure control despite substantial evidence on the importance of additional pathogenic mechanisms involved in neuronal repair and regeneration. Some of these mechanisms may be shared with and across other neurodegenerative disorders, such as Alzheimer's disease. Joint analyses that address this pathogenic overlap can be leveraged to identify suspected neurodegenerative and neuroprotective pathways. In this study, we derived gene-level summary statistics from available genome-wide association studies for primary open-angle glaucoma and Alzheimer's Disease and employed a multivariate analysis to identify genes with an effect on both neurodegenerative diseases. We assessed the influence of the prioritized genes using Mendelian randomization to obtain the effect of retina- and brain cortex-specific gene expression on primary open-angle glaucoma risk. We identified ten genes with evidence of a pleiotropic effect on primary open-angle glaucoma and Alzheimer's disease: TMCO1, ANXA11, ARHGAP27, PLEKHM1, CRHR1, KANSL1, LRRC37A, ARL17A, LRRC37A2, and CBY1. Additionally, gene expression in either the retina or brain cortex of TMCO1, ANXA11, ARHGAP27, PLEKHM1, KANSL1, LRRC37A, ARL17A, LRRC37A2, and CBY1 influenced POAG risk. These genes have known roles in neurodegeneration-associated pathways. Our analysis uncovered evidence of pleiotropy and gene expression as a mechanism impacting disease risk. Further investigation into these genes may yield valuable insights into their involvement in neurodegenerative pathways potentially informing new approaches for early detection, classification, and treatment strategies.
原发性开角型青光眼是全球最常见的青光眼类型,也是不可逆性失明的主要原因之一。尽管有大量证据表明神经元修复和再生涉及的其他致病机制很重要,但目前的治疗方法主要集中在眼压控制上。其中一些机制可能与其他神经退行性疾病(如阿尔茨海默病)共有且相互关联。针对这种致病重叠的联合分析可用于识别可疑的神经退行性和神经保护途径。在本研究中,我们从现有的原发性开角型青光眼和阿尔茨海默病全基因组关联研究中获得基因水平的汇总统计数据,并采用多变量分析来识别对这两种神经退行性疾病均有影响的基因。我们使用孟德尔随机化评估了优先基因的影响,以获得视网膜和大脑皮层特异性基因表达对原发性开角型青光眼风险的作用。我们鉴定出了十个对原发性开角型青光眼和阿尔茨海默病具有多效性作用证据的基因:TMCO1、ANXA11、ARHGAP27、PLEKHM1、CRHR1、KANSL1、LRRC37A、ARL17A、LRRC37A2和CBY1。此外,TMCO1、ANXA11、ARHGAP27、PLEKHM1、KANSL1、LRRC37A、ARL17A、LRRC37A2和CBY1在视网膜或大脑皮层中的基因表达影响原发性开角型青光眼风险。这些基因在神经退行性相关途径中具有已知作用。我们的分析揭示了多效性和基因表达作为影响疾病风险机制的证据。对这些基因的进一步研究可能会为它们参与神经退行性途径提供有价值的见解,从而可能为早期检测、分类和治疗策略提供新方法。