Trans‐ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study

Author:

Qu Hui‐Qi1ORCID,Connolly John J1,Kraft Peter2,Long Jirong3,Pereira Alexandre24,Flatley Christopher5,Turman Constance2,Prins Bram6,Mentch Frank1,Lotufo Paulo A78,Magnus Per910,Stampfer Meir J21112,Tamimi Rulla2,Eliassen A Heather2,Zheng Wei3,Knudsen Gun Peggy Stromstad5,Helgeland Oyvind5,Butterworth Adam S.6131415,Hakonarson Hakon116171819ORCID,Sleiman Patrick M.11617,

Affiliation:

1. The Center for Applied Genomics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

2. Department of Epidemiology Harvard T.H. Chan School of Public Health Boston Massachusetts USA

3. Division of Epidemiology, Department of Medicine Vanderbilt University Medical Center Nashville Tennessee USA

4. Department of Population Health Sciences Weill Cornell Medicine New York New York USA

5. Division of Health Data and Digitalization, Department of Genetics and Bioinformatics Norwegian Institute of Public Health Oslo Norway

6. British Heart Foundation Cardiovascular Epidemiology Unit, Department of Public Health and Primary Care University of Cambridge Cambridge UK

7. Faculdade de Medicina da Universidade de São Paulo São Paulo Brazil

8. Centro de Pesquisas Clínicas e Epidemiológicas, Hospital Universitário Universidade de São Paulo São Paulo Brazil

9. University of Oslo Oslo Norway

10. Center for Fertility and Health Norwegian Institute of Public Health Oslo Norway

11. Department of Nutrition, Harvard T.H. Chan School of Public Health Boston Massachusetts USA

12. Channing Division of Network Medicine Department of Medicine Harvard Medical School Boston Massachusetts USA

13. The National Institute for Health Research Blood and Transplant Research Unit (NIHR BTRU) in Donor Health and Genomics, Department of Public Health and Primary Care University of Cambridge Cambridge UK

14. British Heart Foundation Centre of Research Excellence University of Cambridge Cambridge UK

15. Health Data Research UK Cambridge Wellcome Genome Campus and University of Cambridge Cambridge UK

16. Department of Pediatrics, The Perelman School of Medicine University of Pennsylvania Philadelphia Pennsylvania USA

17. Division of Human Genetics Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

18. Division of Pulmonary Medicine Children's Hospital of Philadelphia Philadelphia Pennsylvania USA

19. Faculty of Medicine University of Iceland Reykjavik Iceland

Abstract

AbstractBackgroundWhile polygenic risk scores hold significant promise in estimating an individual's risk of developing a complex trait such as obesity, their application in the clinic has, to date, been limited by a lack of data from non‐European populations. As a collaboration model of the International Hundred K+ Cohorts Consortium (IHCC), we endeavored to develop a globally applicable trans‐ethnic PRS for body mass index (BMI) through this relatively new international effort.MethodsThe polygenic risk score (PRS) model was developed, trained and tested at the Center for Applied Genomics (CAG) of The Children's Hospital of Philadelphia (CHOP) based on a BMI meta‐analysis from the GIANT consortium. The validated PRS models were subsequently disseminated to the participating sites. Scores were generated by each site locally on their cohorts and summary statistics returned to CAG for final analysis.ResultsWe show that in the absence of a well powered trans‐ethnic GWAS from which to derive marker SNPs and effect estimates for PRS, trans‐ethnic scores can be generated from European ancestry GWAS using Bayesian approaches such as LDpred, by adjusting the summary statistics using trans‐ethnic linkage disequilibrium reference panels. The ported trans‐ethnic scores outperform population specific‐PRS across all non‐European ancestry populations investigated including East Asians and three‐way admixed Brazilian cohort.ConclusionsHere we show that for a truly polygenic trait such as BMI adjusting the summary statistics of a well powered European ancestry study using trans‐ethnic LD reference results in a score that is predictive across a range of ancestries including East Asians and three‐way admixed Brazilians.

Funder

National Institutes of Health

Norges Forskningsråd

NIHR BioResource

British Heart Foundation

Economic and Social Research Council

Publisher

Wiley

Subject

Molecular Medicine,Medicine (miscellaneous)

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