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PMID: 21750520 Published · ppublish English Journal Article Meta-Analysis Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Implication of European-derived adiposity loci in African Americans.

International journal of obesity (2005) ·Vol. 36 ·No. 3 ·2012-03-00 ·Pages 465-73

Hester JM, Wing MR, Li J, Palmer ND, Xu J, Hicks PJ, Roh BH, Norris JM, Wagenknecht LE, Langefeld CD, Freedman BI, Bowden DW, Ng MC

Abstract

Recent genome-wide association studies (GWAS) have identified multiple novel loci associated with adiposity in European-derived study populations. Limited study of these loci has been reported in African Americans. Here we examined the effects of these previously identified adiposity loci in African Americans. A total of 46 representative single-nucleotide polymorphisms (SNPs) in 19 loci that were previously reported in GWAS in Europeans (including FTO and MC4R) were genotyped in 4992 subjects from six African-American cohorts. These SNPs were tested for association with body mass index (BMI) after adjustment for age, gender, disease status and population structure in each cohort. Meta-analysis was conducted to combine the results. Meta-analysis of 4992 subjects revealed seven SNPs near four loci, including NEGR1, TMEM18, SH2B1 /ATP2A1 and MC4R, showing significant association at 0.005<P<0.05, and had effect sizes between 0.04 and 0.06 s.d. units (or 0.30 to 0.44  g m(-2)) of BMI for each copy of the BMI-increasing allele. The most significantly associated SNPs (rs9424977, rs3101336 and rs2568958) are located in the NEGR1 gene (P=0.005, 0.020 and 0.019, respectively). We replicated the association of variants at four loci in six African-American cohorts that demonstrated a consistent direction of association with previous studies of adiposity in Europeans. These loci are all highly expressed in the brain, consistent with an important role for central nervous system processes in weight regulation. However, further comprehensive examination of these regions may be necessary to fine map and elucidate for possible genetic differences between these two populations.

MeSH Terms
Adaptor Proteins, Signal Transducing/genetics Adiposity/genetics African Americans/genetics Alpha-Ketoglutarate-Dependent Dioxygenase FTO Body Weight/genetics Cell Adhesion Molecules, Neuronal/genetics Diabetes Mellitus, Type 2/epidemiology,genetics Female GPI-Linked Proteins/genetics Genetic Predisposition to Disease Genetic Variation Genome-Wide Association Study Genotype Humans Male Membrane Proteins/genetics Middle Aged Obesity/epidemiology,genetics Polymorphism, Single Nucleotide Proteins/genetics Receptor, Melanocortin, Type 4/genetics Transcription Factors Whites/genetics
Chemicals
Adaptor Proteins, Signal Transducing Cell Adhesion Molecules, Neuronal GPI-Linked Proteins MC4R protein, human Membrane Proteins NEGR1 protein, human Proteins Receptor, Melanocortin, Type 4 SH2B1 protein, human TMEM18 protein, human Transcription Factors Alpha-Ketoglutarate-Dependent Dioxygenase FTO FTO protein, human
Authors & Affiliations
13 authors, click to expand affiliations / ORCID
Hester J M
Center for Diabetes Research, Wake Forest University School of Medicine, Winston-Salem, NC 27157, USA.
Wing M R
Li J
Palmer N D
Xu J
Hicks P J
Roh B H
Norris J M
Wagenknecht L E
Langefeld C D
Freedman B I
Bowden D W
Ng M C Y
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Article Info
Journal
International journal of obesity (2005)
Abbr.
Int J Obes (Lond)
ISSN
1476-5497
Published
2012-03-00
Epub
2011-00-12
Pages
465-73
Language
English
Region
England
NLM ID
101256108
PMCID
PMC3306054
Subset
IM
Grants
NHLBI NIH HHS · R01 HL56266 · United States
NHLBI NIH HHS · R01 HL060944 · United States
NIDDK NIH HHS · R01 DK087914 · United States
NCRR NIH HHS · M01 RR007122 · United States
NCRR NIH HHS · M01 RR07122 · United States
NIDDK NIH HHS · R01 DK053591 · United States
NIDDK NIH HHS · R01 DK070941-01A1 · United States
NHLBI NIH HHS · R01 HL061210 · United States
NIDDK NIH HHS · R01 DK070941 · United States
PHS HHS · HHSC268200782096C · United States
NIDDK NIH HHS · K99 DK081350 · United States
NIDDK NIH HHS · R01 DK066358 · United States
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