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

被引:50
|
作者
Patel, Aniruddh P. [1 ,2 ,3 ,4 ,5 ]
Wang, Minxian [6 ,7 ]
Ruan, Yunfeng [2 ,3 ]
Koyama, Satoshi [3 ,8 ]
Clarke, Shoa L. [9 ,10 ]
Yang, Xiong [6 ,7 ]
Tcheandjieu, Catherine [11 ]
Agrawal, Saaket [2 ,3 ,12 ]
Fahed, Akl C. [2 ,3 ,4 ,5 ]
Ellinor, Patrick T. [1 ,2 ,3 ,4 ,5 ]
Tsao, Philip [9 ,10 ]
Sun, Yan, V [13 ]
Cho, Kelly [8 ]
Wilson, Peter W. F. L. [13 ]
Assimes, Themistocles L. [10 ]
van Heel, David A. [14 ]
Butterworth, Adam S. [15 ,16 ]
Aragam, Krishna G. [1 ,2 ,3 ,4 ,5 ]
Natarajan, Pradeep [1 ,2 ,3 ,4 ,5 ]
Khera, Amit V. [2 ,3 ,4 ,17 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Div Cardiol, Boston, MA USA
[2] Massachusetts Gen Hosp, Ctr Genom Med, Dept Med, Boston, MA USA
[3] Broad Inst MIT & Harvard, Cardiovasc Dis Initiat, Cambridge, MA USA
[4] Harvard Med Sch, Dept Med, Boston, MA USA
[5] Massachusetts Gen Hosp, Cardiovasc Res Ctr, Boston, MA USA
[6] Chinese Acad Sci, Beijing Inst Genom, China Natl Ctr Bioinformat, CAS Key Lab Genome Sci & Informat, Beijing, Peoples R China
[7] China Natl Ctr Bioinformat, Beijing, Peoples R China
[8] Vet Affairs Boston Healthcare Syst, Boston, MA USA
[9] Stanford Univ, Sch Med, Palo Alto, CA USA
[10] Vet Affairs Palo Alto Healthcare Syst, Palo Alto, CA USA
[11] Gladstone Inst, San Francisco, CA USA
[12] Northwestern Univ, Feinberg Sch Med, Chicago, IL USA
[13] Vet Affairs Atlanta Healthcare Syst, Decatur, GA USA
[14] Queen Mary Univ London, Blizard Inst, Barts & London Sch Med & Dent, London, England
[15] Univ Cambridge, British Heart Fdn Cardiovasc Epidemiol Unit, Dept Publ Hlth & Primary Care, Cambridge, England
[16] Univ Cambridge, Ctr Res Excellence, Cambridge, England
[17] Verve Therapeut, Boston, MA USA
基金
英国医学研究理事会; 欧洲研究理事会;
关键词
HEART-DISEASE; GENETIC RISK; CARDIOVASCULAR-DISEASE; GENOMIC RISK; HEALTH; ASSOCIATION; VALIDATION; BIOBANK; VARIANTS; ACCURACY;
D O I
10.1038/s41591-023-02429-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A polygenic risk score for coronary artery disease developed using data from individuals of five different ancestries has increased accuracy across diverse populations. 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(Mult), that incorporates genome-wide association data across five ancestries for CAD (>269,000 cases and >1,178,000 controls) and ten CAD risk factors. GPS(Mult) strongly associated with prevalent CAD (odds ratio per standard deviation 2.14, 95% confidence interval 2.10-2.19, P < 0.001) in UK Biobank participants of European ancestry, identifying 20.0% of the population with 3-fold increased risk and conversely 13.9% with 3-fold decreased risk as compared with those in the middle quintile. GPS(Mult) was also associated with incident CAD events (hazard ratio per standard deviation 1.73, 95% confidence interval 1.70-1.76, P < 0.001), identifying 3% of healthy individuals with risk of future CAD events equivalent to those with existing disease and significantly improving risk discrimination and reclassification. Across multiethnic, external validation datasets inclusive of 33,096, 124,467, 16,433 and 16,874 participants of African, European, Hispanic and South Asian ancestry, respectively, GPS(Mult) demonstrated increased strength of associations across all ancestries and outperformed all available previously published CAD polygenic scores. These data contribute a new GPS(Mult) for CAD to the field and provide a generalizable framework for how large-scale integration of genetic association data for CAD and related traits from diverse populations can meaningfully improve polygenic risk prediction.
引用
收藏
页码:1793 / +
页数:22
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