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GWAS Study

Common body mass index-associated variants confer risk of extreme obesity.

Cotsapas C, Speliotes EK, Hatoum IJ et al.

19553259 PubMed ID
GWAS Study Type
3972 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

CC
Cotsapas C
SE
Speliotes EK
HI
Hatoum IJ
GD
Greenawalt DM
DR
Dobrin R
LP
Lum PY
SC
Suver C
CE
Chudin E
KD
Kemp D
RM
Reitman M
VB
Voight BF
NB
Neale BM
SE
Schadt EE
HJ
Hirschhorn JN
KL
Kaplan LM
DM
Daly MJ
Chapter II

Abstract

Summary of the research findings

To investigate the genetic architecture of severe obesity, we performed a genome-wide association study of 775 cases and 3197 unascertained controls at approximately 550,000 markers across the autosomal genome. We found convincing association to the previously described locus including the FTO gene. We also found evidence of association at a further six of 12 other loci previously reported to influence body mass index (BMI) in the general population and one of three associations to severe childhood and adult obesity and that cases have a higher proportion of risk-conferring alleles than controls. We found no evidence of homozygosity at any locus due to identity-by-descent associating with phenotype which would be indicative of rare, penetrant alleles, nor was there excess genome-wide homozygosity in cases relative to controls. Our results suggest that variants influencing BMI also contribute to severe obesity, a condition at the extreme of the phenotypic spectrum rather than a distinct condition.

775 European ancestry cases, 3,197 European ancestry controls

Chapter III

Study Statistics

Key metrics and study information

3972
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
U.S.
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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