Polygenic Risk for Type 2 Diabetes in African Americans

Author:

Irvin Marguerite R.1ORCID,Ge Tian2345,Patki Amit6,Srinivasasainagendra Vinodh6,Armstrong Nicole D.1,Davis Brittney7,Jones Alana C.1,Perez Emma89,Stalbow Lauren10,Lebo Matthew5911,Kenny Eimear1213,Loos Ruth J.F.1014,Ng Maggie C.Y.15ORCID,Smoller Jordan W.2345,Meigs James B.51617,Lange Leslie A.18,Karlson Elizabeth W.89,Limdi Nita A.7,Tiwari Hemant K.6

Affiliation:

1. 1Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL

2. 2Psychiatric and Neurodevelopmental Genetics Unit, Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA

3. 3Center for Precision Psychiatry, Massachusetts General Hospital, Boston, MA

4. 4Department of Psychiatry, Massachusetts General Hospital, Boston, MA

5. 5Stanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Cambridge, MA

6. 6Department of Biostatistics, School of Public Health, University of Alabama at Birmingham, Birmingham, AL

7. 7Department of Neurology, School of Medicine, University of Alabama at Birmingham, Birmingham, AL

8. 8Department of Medicine, Brigham and Women's Hospital, Boston, MA

9. 9Mass General Brigham Personalized Medicine, Boston, MA

10. 10The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY

11. 11Department of Pathology, Brigham and Women's Hospital, Boston, MA

12. 12Institute for Genomic Health, Icahn School of Medicine at Mount Sinai, New York, NY

13. 13Division of Genomic Medicine, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY

14. 14The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medicine, University of Copenhagen, Copenhagen, Denmark

15. 15Vanderbilt Genetics Institute, Division of Genetic Medicine, Vanderbilt University Medical Center, Nashville, TN

16. 16Department of Medicine, Massachusetts General Hospital, Boston, MA

17. 17Division of General Internal Medicine, Massachusetts General Hospital, Boston, MA

18. 18Department of Epidemiology, University of Colorado School of Public Health, Aurora, CO

Abstract

African Americans (AAs) have been underrepresented in polygenic risk score (PRS) studies. Here, we integrated genome-wide data from multiple observational studies on type 2 diabetes (T2D), encompassing a total of 101,987 AAs, to train and optimize an AA-focused T2D PRS (PRSAA), using a Bayesian polygenic modeling method. We further tested the score in three independent studies with a total of 7,275 AAs and compared the PRSAA with other published scores. Results show that a 1-SD increase in the PRSAA was associated with 40–60% increase in the odds of T2D (odds ratio [OR] 1.60, 95% CI 1.37–1.88; OR 1.40, 95% CI 1.16–1.70; and OR 1.45, 95% CI 1.30–1.62) across three testing cohorts. These models captured 1.0–2.6% of the variance (R2) in T2D on the liability scale. The positive predictive values for three calculated score thresholds (the top 2%, 5%, and 10%) ranged from 14 to 35%. The PRSAA, in general, performed similarly to existing T2D PRS. The need remains for larger data sets to continue to evaluate the utility of within-ancestry scores in the AA population. Article Highlights

Funder

National Heart and Lung Institute

National Human Genome Research Institute

Publisher

American Diabetes Association

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