New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
- PMID: 26833246
- PMCID: PMC4740398
- DOI: 10.1038/ncomms10495
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk
Abstract
To increase our understanding of the genetic basis of adiposity and its links to cardiometabolic disease risk, we conducted a genome-wide association meta-analysis of body fat percentage (BF%) in up to 100,716 individuals. Twelve loci reached genome-wide significance (P<5 × 10(-8)), of which eight were previously associated with increased overall adiposity (BMI, BF%) and four (in or near COBLL1/GRB14, IGF2BP1, PLA2G6, CRTC1) were novel associations with BF%. Seven loci showed a larger effect on BF% than on BMI, suggestive of a primary association with adiposity, while five loci showed larger effects on BMI than on BF%, suggesting association with both fat and lean mass. In particular, the loci more strongly associated with BF% showed distinct cross-phenotype association signatures with a range of cardiometabolic traits revealing new insights in the link between adiposity and disease risk.
Conflict of interest statement
R.E. received honoraria for lectures from the following companies (within the past 2 years): MSD Sharp&Dohme and Pfizer. J.M.J. disclosed Trinity Partners, Inc., Osteoarthritis Research Society International, Chronic Osteoarthritis Management Initiative of US Bone and Joint Initiative, Samumed, Interleukin Genetics, Inc. and Algynomics, Inc. K.S. is a full-time employee of GlaxoSmithKline. D.S. received honoraria for lectures from the following companies (within the past 2 years): MSD Sharp&Dohme. E.S.-T. received honoraria for lectures, research grants and consultancy fees from the following companies (within the past 2 years): Aegerion, Fresenius, MSD Sharp&Dohme, Pfizer and Sanofi. Peter Vollenweider received an unrestricted grant from GSK to build the CoLaus study.
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