Authors

Keri L. Monda, Amgen Incorporated
Gary K. Chen, Keck School of Medicine of USC
Kira C. Taylor, UNC Gillings School of Global Public Health
Cameron Palmer, Massachusetts Institute of Technology
Todd L. Edwards, Vanderbilt University
Leslie A. Lange, UNC School of Medicine
Maggie C.Y. Ng, Wake Forest University School of Medicine
Adebowale A. Adeyemo, National Human Genome Research Institute (NHGRI)
Matthew A. Allison, University of California, San Diego
Lawrence F. Bielak, University of Michigan, Ann Arbor
Guanjie Chen, National Human Genome Research Institute (NHGRI)
Mariaelisa Graff, UNC Gillings School of Global Public Health
Marguerite R. Irvin, The University of Alabama at Birmingham
Suhn K. Rhie, Keck School of Medicine of USC
Guo Li, University of Washington School of Medicine
Yongmei Liu, Wake Forest University School of Medicine
Youfang Liu, UNC School of Medicine
Yingchang Lu, Icahn School of Medicine at Mount Sinai
Michael A. Nalls, National Institute on Aging (NIA)
Yan V. Sun, Rollins School of Public Health
Mary K. Wojczynski, Washington University School of Medicine in St. Louis
Lisa R. Yanek, Johns Hopkins University School of Medicine
Melinda C. Aldrich, Vanderbilt University Medical Center
Adeyinka Ademola, University of Ibadan
Christopher I. Amos, The University of Texas MD Anderson Cancer Center
Elisa V. Bandera, Rutgers Cancer Institute of New Jersey
Cathryn H. Bock, Wayne State University
Angela Britton, National Institute on Aging (NIA)
Ulrich Broeckel, Medical College of Wisconsin
Quiyin Cai, Vanderbilt University Medical Center
Neil E. Caporaso, National Cancer Institute (NCI)
Chris S. Carlson, Fred Hutchinson Cancer Center
John Carpten, Translational Genomics Research Institute

Document Type

Article

Publication Date

6-1-2013

Abstract

Genome-wide association studies (GWAS) have identified 36 loci associated with body mass index (BMI), predominantly in populations of European ancestry. We conducted a meta-analysis to examine the association of >3.2 million SNPs with BMI in 39,144 men and women of African ancestry and followed up the most significant associations in an additional 32,268 individuals of African ancestry. We identified one new locus at 5q33 (GALNT10, rs7708584, P = 3.4 × 10-11) and another at 7p15 when we included data from the GIANT consortium (MIR148A-NFE2L3, rs10261878, P = 1.2 × 10-10). We also found suggestive evidence of an association at a third locus at 6q16 in the African-ancestry sample (KLHL32, rs974417, P = 6.9 × 10 -8). Thirty-two of the 36 previously established BMI variants showed directionally consistent effect estimates in our GWAS (binomial P = 9.7 × 10-7), five of which reached genome-wide significance. These findings provide strong support for shared BMI loci across populations, as well as for the utility of studying ancestrally diverse populations. © 2013 Nature America, Inc. All rights reserved.

Publication Source (Journal or Book title)

Nature Genetics

First Page

690

Last Page

696

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