Xiaoyi Gao
Introduction Primary open-angle glaucoma (POAG) remains a leading cause of irreversible blindness worldwide, with early detection crucial for preventing vision loss. Current polygenic risk scores (PRS) for POAG, however, demonstrate limited predictive power. Methods Here, we present a multi-trait polygenic probability risk score (PPRS) approach that integrates PRSs of multiple glaucoma-related traits, including POAG, intraocular pressure (IOP), vertical cup-to-disc ratio (VCDR), and retinal nerve fiber layer thickness, while leveraging functional genomic annotations and extensive genomic coverage (>7 million variants) to enhance POAG prediction across diverse ancestries. We evaluated the PPRS in the UK Biobank (n = 324,713, European ancestry) and the Mexican American Glaucoma Genetic Study (MAGGS, n = 4,549, Latino ancestry). Results The PPRS improved prediction compared with conventional approaches, achieving area under the receiver operating characteristic curve (AUC) values of 0.814 in Europeans and 0.802 in Latinos, versus 0.721 and 0.753 for baseline models with age and sex alone. Genetic contributions varied by ancestry: IOP PRS showed the strongest association in Europeans (OR = 1.63, P = 5.37 × 10 −89 ), whereas VCDR PRS predominated in Latinos (OR = 1.64, P = 2.04 × 10 −11 ). Risk stratification was substantial, with the highest PPRS decile showing 74.4-fold and 49.3-fold greater POAG risk compared with the lowest decile in Europeans and Latinos, respectively. Discussion These findings show that integrating multiple disease-relevant PRSs and functional annotations significantly improves genetic prediction of POAG across diverse populations, supporting applications in targeted screening and early intervention.