Department of Internal Medicine, St. Vincent's Hospital, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Department of Biostatistics, Epidemiology and Informatics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
J Transl Med. 2024 Apr 15;22(1):355. doi: 10.1186/s12967-024-05152-4.
Glaucoma is a leading cause of worldwide irreversible blindness. Considerable uncertainty remains regarding the association between a variety of phenotypes and the genetic risk of glaucoma, as well as the impact they exert on the glaucoma development.
We investigated the associations of genetic liability for primary open angle glaucoma (POAG) with a wide range of potential risk factors and to assess its impact on the risk of incident glaucoma. The phenome-wide association study (PheWAS) approach was applied to determine the association of POAG polygenic risk score (PRS) with a wide range of phenotypes in 377, 852 participants from the UK Biobank study and 43,623 participants from the Penn Medicine Biobank study, all of European ancestry. Participants were stratified into four risk tiers: low, intermediate, high, and very high-risk. Cox proportional hazard models assessed the relationship of POAG PRS and ocular factors with new glaucoma events.
In both discovery and replication set in the PheWAS, a higher genetic predisposition to POAG was specifically correlated with ocular disease phenotypes. The POAG PRS exhibited correlations with low corneal hysteresis, refractive error, and ocular hypertension, demonstrating a strong association with the onset of glaucoma. Individuals carrying a high genetic burden exhibited a 9.20-fold, 11.88-fold, and 28.85-fold increase in glaucoma incidence when associated with low corneal hysteresis, high myopia, and elevated intraocular pressure, respectively.
Genetic susceptibility to POAG primarily influences ocular conditions, with limited systemic associations. Notably, the baseline polygenic risk for POAG robustly associates with new glaucoma events, revealing a large combined effect of genetic and ocular risk factors on glaucoma incidents.
青光眼是全球范围内导致不可逆性失明的主要原因之一。目前,对于各种表型与青光眼遗传风险之间的关联,以及它们对青光眼发展的影响,仍存在很大的不确定性。
我们研究了原发性开角型青光眼(POAG)的遗传易感性与广泛的潜在危险因素之间的关联,并评估其对新发青光眼风险的影响。采用表型全基因组关联研究(PheWAS)方法,在 UK Biobank 研究的 377852 名和 Penn Medicine Biobank 研究的 43623 名欧洲血统参与者中,确定 POAG 多基因风险评分(PRS)与广泛表型之间的关联。参与者分为低、中、高和极高风险四个风险分层。Cox 比例风险模型评估了 POAG PRS 和眼部因素与新发青光眼事件的关系。
在 PheWAS 的发现和复制队列中,POAG 的遗传易感性越高,与眼部疾病表型的相关性越强。POAG PRS 与低角膜滞后、屈光不正和眼压升高相关,与青光眼的发生有很强的关联。携带高遗传负担的个体与低角膜滞后、高度近视和眼压升高相关的青光眼发病率分别增加了 9.20 倍、11.88 倍和 28.85 倍。
POAG 的遗传易感性主要影响眼部状况,与系统关联有限。值得注意的是,POAG 的基线多基因风险与新发青光眼事件密切相关,揭示了遗传和眼部风险因素对青光眼事件的综合影响。