The First Genome-Wide Association Study for Type 2 Diabetes in Youth: The Progress in Diabetes Genetics in Youth (ProDiGY) Consortium

Author:

Srinivasan Shylaja1,Chen Ling2,Todd Jennifer3,Divers Jasmin4,Gidding Samuel5,Chernausek Steven6ORCID,Gubitosi-Klug Rose A.7ORCID,Kelsey Megan M.8ORCID,Shah Rachana9,Black Mary Helen10,Wagenknecht Lynne E.11,Manning Alisa212,Flannick Jason1213,Imperatore Giuseppina14,Mercader Josep M.21215,Dabelea Dana16ORCID,Florez Jose C.21215ORCID

Affiliation:

1. Division of Pediatric Endocrinology, University of California, San Francisco, San Francisco, CA

2. Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA

3. Division of Pediatric Endocrinology, University of Vermont, Burlington, VT

4. NYU Langone Health, New York, NY

5. Genomic Medicine Institute, Geisinger, Danville, PA

6. Pediatric Diabetes and Endocrinology Section, University of Oklahoma College of Medicine, Oklahoma City, OK

7. Pediatric Endocrinology, Diabetes, and Metabolism, Case Western Reserve University and Rainbow Babies and Children’s Hospital, Cleveland, OH

8. Pediatric Endocrinology, University of Colorado School of Medicine, Aurora, CO

9. Pediatric Endocrinology and Diabetes, Children’s Hospital of Philadelphia, Philadelphia, PA

10. Janssen Pharmaceuticals, Spring House, PA

11. Public Health Sciences, Wake Forest School of Medicine, Winston-Salem, NC

12. Program in Medical and Population Genetics, Broad Institute of Harvard and Massachusetts Institute of Technology, Cambridge, MA

13. Department of Pediatrics, Boston Children’s Hospital, Boston, MA

14. Centers for Disease Control and Prevention, Atlanta, GA

15. Diabetes Research Center, Diabetes Unit, Department of Medicine, Massachusetts General Hospital, Boston, MA

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

Abstract

The prevalence of type 2 diabetes in youth has increased substantially, yet the genetic underpinnings remain largely unexplored. To identify genetic variants predisposing to youth-onset type 2 diabetes, we formed ProDiGY, a multiethnic collaboration of three studies (TODAY, SEARCH, and T2D-GENES) with 3,006 youth case subjects with type 2 diabetes (mean age 15.1 ± 2.9 years) and 6,061 diabetes-free adult control subjects (mean age 54.2 ± 12.4 years). After stratifying by principal component–clustered ethnicity, we performed association analyses on ∼10 million imputed variants using a generalized linear mixed model incorporating a genetic relationship matrix to account for population structure and adjusting for sex. We identified seven genome-wide significant loci, including the novel locus rs10992863 in PHF2 (P = 3.2 × 10−8; odds ratio [OR] = 1.23). Known loci identified in our analysis include rs7903146 in TCF7L2 (P = 8.0 × 10−20; OR 1.58), rs72982988 near MC4R (P = 4.4 × 10−14; OR 1.53), rs200893788 in CDC123 (P = 1.1 × 10−12; OR 1.32), rs2237892 in KCNQ1 (P = 4.8 × 10−11; OR 1.59), rs937589119 in IGF2BP2 (P = 3.1 × 10−9; OR 1.34), and rs113748381 in SLC16A11 (P = 4.1 × 10−8; OR 1.04). Secondary analysis with 856 diabetes-free youth control subjects uncovered an additional locus in CPEB2 (P = 3.2 × 10−8; OR 2.1) and consistent direction of effect for diabetes risk. In conclusion, we identified both known and novel loci in the first genome-wide association study of youth-onset type 2 diabetes.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

American Diabetes Association

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference27 articles.

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