Evidence map›Paper›PMID 40045046›Full record

ArticleCommunications biology2025

Assessment of polygenic risk score performance in East Asian populations for ten common diseases.

Hae-Un Jung, Hyein Jung, Eun Ju Baek, Ji-One Kang, Shin Young Kwon, Jaeyoon You, Ji Eun Lim, Bermseok Oh

Abstract read
In one paragraph

Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Hae-Un Jung *Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Hyein Jung *Department of Biomedical Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Eun Ju BaekMendel Inc, Seoul, Republic of Korea.
Ji-One KangDepartment of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, Republic of Korea.
Shin Young KwonDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea.
Jaeyoon YouMendel Inc, Seoul, Republic of Korea.
Ji Eun LimDepartment of Biochemistry and Molecular Biology, School of Medicine, Kyung Hee University, Seoul, Republic of Korea. jelim@khu.ac.kr.ORCID http://orcid.org/0000-0001-5858-9119
Bermseok OhDepartment of Biomedical Science, Graduate School, Kyung Hee University, Seoul, Republic of Korea. ohbs@khu.ac.kr.ORCID http://orcid.org/0000-0002-4199-0608

Funding

National Research Foundation of Korea (NRF) 2019M3E5D3073365
6 · The paper itself

Abstract

Polygenic risk score (PRS) uses genetic variants to assess disease susceptibility. While PRS performance is well-studied in Europeans, its accuracy in East Asians is less explored. This study evaluated PRSs for ten diseases in the Health Examinees (HEXA) cohort (n = 55,870) in Korea. Single-population PRSs were constructed using PRS-CS, LDpred2, and Lassosum based on East Asian GWAS summary statistics (sample sizes: 51,442-341,204), while cross-population PRSs were developed using PRS-CSx and CT-SLEB by integrating European and East Asian GWAS data. PRS-CS consistently outperformed other single-population methods across key metrics, including the likelihood ratio test (LRT), odds ratio per standard deviation (perSD OR), net reclassification improvement (NRI), and area under the curve (AUC). Cross-population PRSs further improved predictive performance, with average increases of 1.08-fold (LRT), 1.07-fold (perSD OR), and 1.15-fold (NRI) across seven diseases with statistical significance, and a 1.01-fold improvement in AUC. Differences in R² between single- and cross-population PRSs were statistically significant for five diseases, showing an average increase of 1.13%. Cross-population PRSs achieved 87.8% of the predictive performance observed in European PRSs. These findings highlight the benefits of integrating European GWAS data while underscoring the need for larger East Asian datasets to improve prediction accuracy.

Indexed as

East Asian PeopleGenetic Risk ScoreAsia, EasternFemaleGenome-Wide Association StudyHumansMalePolymorphism, Single NucleotideRepublic of KoreaRisk Assessment

Identifiers

PMID40045046
PMCPMC11882803

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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.