Evidence map›Paper›PMID 41255996›Full record

ArticleResearch square2025

Multi-trait polygenic risk scores improve genomic prediction of atrial fibrillation across diverse ancestries.

Sean Jurgens, Poeya Haydarlou, Daria Kramarenko, Marre Corver, Nobuyuki Enzan, Dominic Zimmerman, Patrick Ellinor, Connie Bezzina

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In one paragraph

Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Sean JurgensAmsterdam UMC.ORCID 0000-0002-1605-9782
Poeya HaydarlouAmsterdam UMC.ORCID 0009-0000-3938-3377
Daria KramarenkoAmsterdam UMC.
Marre CorverAmsterdam UMC.
Nobuyuki EnzanBroad Institute of MIT and Harvard.ORCID 0000-0002-3899-4405
Dominic ZimmermanAmsterdam UMC.
Patrick EllinorBroad institute.
Connie BezzinaHeart Center, Department of Clinical and Experimental Cardiology, Amsterdam UMC, location AMC.ORCID 0000-0002-0633-3514

Funding

IDENTIFICATION OF COMMON GENETIC VARIANTS FOR ATRIAL FIBRILLATION AND PR INTERVALR01HL092577 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI BENJAMIN, EMELIA J., ELLINOR, PATRICK THOMAS · 2009 to 2025
$20.6M
Using Electrocardiogram Genetics to Inform Arrhythmia RiskR01HL157635 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS, MIRSHAHI, TOORAJ · 2022 to 2025
$2.9M
Mentoring in Arrhythmia ResearchK24HL105780 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS · 2011 to 2020
$1.2M
NHLBI NIH HHS K24 HL105780NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL157635
6 · The paper itself

Abstract

Polygenic scores (PGSs) can improve atrial fibrillation (AF) risk prediction, both alone and alongside clinical scores, offering potential for guiding targeted screening. However, their limited accuracy and cross-ancestry transferability remain major barriers to clinical translation. Here, we explored several multi-PGS approaches to generate ancestry-optimized PGSs for AF, and tested these in independent samples from the All of Us Research Program. Our ancestry-specific multi-trait approach, which leverages correlated traits, in particular outperformed the current gold-standard PGS among Asian (OR/SD = 1.76 [1.56-1.99]; AUROC = 0.637; AUPRC = 0.055), Admixed American (1.45 [1.38-1.53]; 0.595; 0.054) and African ancestry groups (1.39 [1.32-1.45]; 0.573; 0.064). Although predictive accuracy remained highest among Europeans (1.89 [1.85-1.93]; 0.646; 0.157) - in whom our PGS explained ~ 50% of SNP-heritability - our multi-trait approach yielded relatively larger gains in non-European populations. Improved risk stratification was also observed at PGS extremes, identifying a substantial proportion of European individuals with risk comparable to rare

Identifiers

PMID41255996
PMCPMC12622184

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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.