Authors

Yingchang Lu, Icahn School of Medicine at Mount Sinai
Felix R. Day, School of Clinical Medicine
Stefan Gustafsson, Uppsala Universitet
Martin L. Buchkovich, UNC School of Medicine
Jianbo Na, Icahn School of Medicine at Mount Sinai
Veronique Bataille, West Hertfordshire Hospitals NHS Trust
Diana L. Cousminer, Helsingin Yliopisto
Zari Dastani, Institut Lady Davis de Recherches Médicales
Alexander W. Drong, The Wellcome Centre for Human Genetics
Toñu Esko, Tartu Ülikooli Genoomika Instituut
David M. Evans, The University of Queensland
Mario Falchi, King's College London
Mary F. Feitosa, Washington University School of Medicine in St. Louis
Teresa Ferreira, The Wellcome Centre for Human Genetics
Åsa K. Hedman, Uppsala Universitet
Robin Haring, Universitätsmedizin Greifswald
Pirro G. Hysi, King's College London
Mark M. Iles, University of Leeds, School of Medicine
Anne E. Justice, UNC Gillings School of Global Public Health
Stavroula Kanoni, Barts and The London School of Medicine and Dentistry
Vasiliki Lagou, The Wellcome Centre for Human Genetics
Rui Li, Institut Lady Davis de Recherches Médicales
Xin Li, Harvard T.H. Chan School of Public Health
Adam Locke, University of Michigan, Ann Arbor
Chen Lu, Boston University
Reedik Mägi, The Wellcome Centre for Human Genetics
John R.B. Perry, School of Clinical Medicine
Tune H. Pers, The Wellcome Centre for Human Genetics
Qibin Qi, Albert Einstein College of Medicine
Marianna Sanna, King's College London
Ellen M. Schmidt, University of Michigan Medical School
William R. Scott, Imperial College London
Dmitry Shungin, Skånes Universitetssjukhus

Document Type

Article

Publication Date

2-1-2016

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 (Po5108), 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.

Publication Source (Journal or Book title)

Nature Communications

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