| Literature DB >> 30389748 |
Connor A Emdin1,2,3, Amit V Khera1,2,3, Krishna Aragam1,2,3, Mary Haas1,2,3, Mark Chaffin3, Derek Klarin1,3,4, Pradeep Natarajan1,2,3, Alexander Bick1,3, Seyedeh M Zekavat1,3,5, Akihiro Nomura1,2,3, Diego Ardissino6,7, James G Wilson8, Heribert Schunkert9, Ruth McPherson10, Hugh Watkins11,12, Roberto Elosua13,14,15, Matthew J Bown16, Nilesh J Samani16, Usman Baber17, Jeanette Erdmann18,19, Namrata Gupta3, John Danesh20,21,22, Danish Saleheen23,24, Stacey Gabriel3, Sekar Kathiresan25,2,3.
Abstract
A genetic predisposition to higher waist-to-hip ratio adjusted for BMI (WHRadjBMI), a measure of body fat distribution, associates with increased risk for type 2 diabetes. We conducted an exome-wide association study of coding variation in UK Biobank (405,569 individuals) to identify variants that lower WHRadjBMI and protect against type 2 diabetes. We identified four variants in the gene ACVR1C (encoding the activin receptor-like kinase 7 receptor expressed on adipocytes and pancreatic β-cells), which independently associated with reduced WHRadjBMI: Asn150His (-0.09 SD, P = 3.4 × 10-17), Ile195Thr (-0.15 SD, P = 1.0 × 10-9), Ile482Val (-0.019 SD, P = 1.6 × 10-5), and rs72927479 (-0.035 SD, P = 2.6 × 10-12). Carriers of these variants exhibited reduced percent abdominal fat in DEXA imaging. Pooling across all four variants, a 0.2 SD decrease in WHRadjBMI through ACVR1C was associated with a 30% lower risk of type 2 diabetes (odds ratio [OR] 0.70, 95% CI 0.63, 0.77; P = 5.6 × 10-13). In an analysis of exome sequences from 55,516 individuals, carriers of predicted damaging variants in ACVR1C were at 54% lower risk of type 2 diabetes (OR 0.46, 95% CI 0.27, 0.81; P = 0.006). These findings indicate that variants predicted to lead to loss of ACVR1C gene function influence body fat distribution and protect from type 2 diabetes.Entities:
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Year: 2018 PMID: 30389748 PMCID: PMC6302541 DOI: 10.2337/db18-0857
Source DB: PubMed Journal: Diabetes ISSN: 0012-1797 Impact factor: 9.461