Evidence map›Paper›PMID 40196261›Full record

ArticlemedRxiv : the preprint server for health sciences2025

Multi-trait Polygenic Probability Risk Score Enhances Glaucoma Prediction Across Ancestries.

Xiaoyi Raymond Gao

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

Xiaoyi Raymond GaoDepartment of Ophthalmology and Visual Sciences, The Ohio State University, Columbus, OH 43210, USA.

Funding

Mexican American Glaucoma Genetic Study (MAGGS)R01EY022651 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI GAO, XIAOYI RAYMOND · 2012 to 2016
$4.2M
The Ohio State University Vision Sciences Research Core Program (OSU-VSRCP)P30EY032857 · NEI · OHIO STATE UNIVERSITY · PI Sayoko E Moroi · 2022 to 2026
$3.6M
NEI NIH HHS P30 EY032857NEI NIH HHS R01 EY022651
6 · The paper itself

Abstract

Primary open-angle glaucoma (POAG) remains the leading cause of irreversible blindness worldwide, with early detection crucial for preventing vision loss. However, current risk assessment methods have limited predictive power. Here, we present a multi-trait polygenic probability risk score (PPRS) approach that integrates multiple glaucoma-related traits and leverages functional genomic annotations to enhance POAG prediction across diverse ancestries. We constructed PRSs for POAG, intraocular pressure (IOP), vertical cup-to-disc ratio (VCDR), and retinal nerve fiber layer (RNFL) thickness using extensive genomic coverage (>7 million variants) and 96 functional annotations through the SBayesRC method. Validation in the UK Biobank (n=324,713, European ancestry) and Mexican American Glaucoma Genetic Study (MAGGS, n=4,549, Latino ancestry) demonstrated significant improvements in predictive accuracy over conventional approaches. Our multi-trait PPRS achieved area under the curve (AUC) values of 0.814 in Europeans and 0.801 in Latinos, compared to AUC ≤0.79 for single-trait models. We identified ancestry-specific differences in genetic contributions, with IOP demonstrating the strongest association in Europeans (OR=1.63,

Indexed as

genetic predictionglaucomamulti-ancestrypolygenic risk scoreprecision medicine

Identifiers

PMID40196261
PMCPMC11974974

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.