Evidence map›Paper›PMID 37414900›Full record

ArticleNature medicine2023

A multi-ancestry polygenic risk score improves risk prediction for coronary artery disease.

Aniruddh P Patel, Minxian Wang, Yunfeng Ruan, Satoshi Koyama, Shoa L Clarke, Xiong Yang, Catherine Tcheandjieu, Saaket Agrawal, Akl C Fahed, Patrick T Ellinor and 11 more

Abstract read
In one paragraph

Article in Nature medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 193 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
193citing papers in PubMed, 6 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

193 citing papers in PubMed, 6 syntheses or guidelines pooled it.

  1. Pooled it
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  3. Pooled it
  4. Pooled it
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  6. Pooled it
  7. Trial
  8. Polygenic risk, aspirin, and primary prevention of coronary artery disease.European heart journal. Cardiovascular pharmacotherapy · 2025
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  20. Evaluating the Role ofDiagnostics (Basel, Switzerland) · 2026
    Article

133 more citing papers are in PubMed but not listed here.

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

21 authors.

Aniruddh P Patel *Division of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Minxian Wang *CAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, China. wangmx@big.ac.cn.ORCID http://orcid.org/0000-0002-3753-508X
Yunfeng RuanCenter for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Satoshi KoyamaCenter for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Shoa L ClarkeStanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0002-6592-1172
Xiong YangCAS Key Laboratory of Genome Sciences and Information, Beijing Institute of Genomics, Chinese Academy of Sciences and China National Center for Bioinformation, Beijing, China.
Catherine TcheandjieuGladstone Institutes, San Francisco, CA, USA.ORCID http://orcid.org/0000-0001-9559-4339
Saaket AgrawalCenter for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Akl C FahedDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Patrick T EllinorDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0002-2067-0533
Genes & Health Research Team; the Million Veteran Program
Philip S TsaoStanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0001-7274-9318
Yan V SunVeteran Affairs Atlanta Healthcare System, Decatur, GA, USA.ORCID http://orcid.org/0000-0002-2838-1824
Kelly ChoVeteran Affairs Boston Healthcare System, Boston, MA, USA.
Peter W F WilsonVeteran Affairs Atlanta Healthcare System, Decatur, GA, USA.
Themistocles L AssimesStanford University School of Medicine, Palo Alto, CA, USA.ORCID http://orcid.org/0000-0003-2349-0009
David A van HeelBlizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.ORCID http://orcid.org/0000-0002-0637-2265
Adam S ButterworthBritish Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care, and Centre of Research Excellence, University of Cambridge, Cambridge, UK.ORCID http://orcid.org/0000-0002-6915-9015
Krishna G AragamDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Pradeep NatarajanDivision of Cardiology, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8402-7435
Amit V KheraCenter for Genomic Medicine, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA. avkhera@mgh.harvard.edu.ORCID http://orcid.org/0000-0001-6535-5839

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
Institutional Career Development Core (KL2)KL2TR003143 · NCATS · STANFORD UNIVERSITY · PI ASCH, STEVEN M. · 2019 to 2023
$8.7M
Clonal hematopoiesis in the Womens Health Initiative Memory StudyR01HL148565 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI ALEXANDER P REINER, Eric A. Whitsel · 2019 to 2026
$5.9M
Clonal hematopoiesis in humans: determinants of development and progressionR01HL148050 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI BALLANTYNE, CHRISTIE MITCHELL, NATARAJAN, PRADEEP · 2019 to 2022
$5.9M
Enabling improved applicability and transferability of polygenic scores across populationsU01HG011719 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI Alicia Martin · 2021 to 2026
$5.5M
New methods for constructing and evaluating polygenic scoresR01HG011432 · NHGRI · STANFORD UNIVERSITY · PI PRITCHARD, JONATHAN K · 2020 to 2023
$3.3M
Using Electrocardiogram Genetics to Inform Arrhythmia RiskR01HL157635 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ELLINOR, PATRICK THOMAS, MIRSHAHI, TOORAJ · 2022 to 2025
$2.9M
Polygenic prediction of common, complex diseasesK08HG010155 · NHGRI · MASSACHUSETTS GENERAL HOSPITAL · PI KHERA, AMIT VIKRAM · 2018 to 2021
$1.1M
Population Assessments of Aggregate Genetic Risk for DilatedýCardiomyopathyK08HL153937 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI ARAGAM, KRISHNA G · 2021 to 2025
$846k
Integrating genomic and nongenomic risk for coronary artery diseaseK08HL161448 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI Akl C Fahed · 2022 to 2026
$751k
Genetics of Cardiometabolic Diseases in the VA PopulationI01BX003362 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI Kyong-Mi Chang, Philip S Tsao · 2017 to 2026
–
Cardiovascular Disease Risk Factors, Cardiovascular Disease Risk Prediction, and Genetics in the Million Veteran ProgramI01BX004821 · VA · VETERANS HEALTH ADMINISTRATION · PI PETER WYMAN WILSON · 2020 to 2026
–
BLRD VA I01 BX003362BLRD VA I01 BX004821British Heart Foundation CH/12/2/29428British Heart Foundation RG/18/13/33946Medical Research Council M009017Medical Research Council MR/X009777/1Medical Research Council MR/X009920/1NCATS NIH HHS KL2 TR003143NHGRI NIH HHS K08 HG010155NHGRI NIH HHS R01 HG011432NHGRI NIH HHS U01 HG011719NHLBI NIH HHS K08 HL153937NHLBI NIH HHS K08 HL161448NHLBI NIH HHS R01 HL092577NHLBI NIH HHS R01 HL148050NHLBI NIH HHS R01 HL148565NHLBI NIH HHS R01 HL157635Wellcome Trust 210561/Z/18/ZWellcome Trust WT102627Wellcome Trust WT210561
6 · The paper itself

Abstract

Identification of individuals at highest risk of coronary artery disease (CAD)-ideally before onset-remains an important public health need. Prior studies have developed genome-wide polygenic scores to enable risk stratification, reflecting the substantial inherited component to CAD risk. Here we develop a new and significantly improved polygenic score for CAD, termed GPS

Indexed as

Coronary Artery DiseaseGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPhenotypeRisk Factors

Identifiers

PMID37414900
PMCPMC10353935

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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.