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GWAS Study

Meta-analysis of genome-wide association data identifies novel susceptibility loci for obesity.

Pei YF, Zhang L, Liu Y et al.

24064335 PubMed ID
GWAS Study Type
28632 Participants
264 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PY
Pei YF
ZL
Zhang L
LY
Liu Y
LJ
Li J
SH
Shen H
LY
Liu YZ
TQ
Tian Q
HH
He H
WS
Wu S
RS
Ran S
HY
Han Y
HR
Hai R
LY
Lin Y
ZJ
Zhu J
ZX
Zhu XZ
PC
Papasian CJ
DH
Deng HW
Chapter II

Abstract

Summary of the research findings

Obesity is a major public health problem with strong genetic determination. Multiple genetic variants have been implicated for obesity by conducting genome-wide association (GWA) studies, primarily focused on body mass index (BMI). Fat body mass (FBM) is phenotypically more homogeneous than BMI and is more appropriate for obesity research; however, relatively few studies have been conducted on FBM. Aiming to identify variants associated with obesity, we carried out meta-analyses of seven GWA studies for BMI-related traits including FBM, and followed these analyses by de novo replication. The discovery cohorts consisted of 21 969 individuals from diverse ethnic populations and a total of over 4 million genotyped or imputed SNPs. The de novo replication cohorts consisted of 6663 subjects from two independent samples. To complement individual SNP-based association analyses, we also carried out gene-based GWA analyses in which all variations within a gene were considered jointly. Individual SNP-based association analyses identified a novel locus 1q21 [rs2230061, CTSS (Cathepsin S)] that was associated with FBM after the adjustment of lean body mass (LBM) (P = 3.57 × 10(-8)) at the genome-wide significance level. Gene-based association analyses identified a novel gene NLK (nemo-like kinase) in 17q11 that was significantly associated with FBM adjusted by LBM. In addition, we confirmed three previously reported obesity susceptibility loci: 16q12 [rs62033400, P = 1.97 × 10(-14), FTO (fat mass and obesity associated)], 18q22 [rs6567160, P = 8.09 × 10(-19), MC4R (melanocortin 4 receptor)] and 2p25 [rs939583, P = 1.07 × 10(-7), TMEM18 (transmembrane protein 18)]. We also found that rs6567160 may exert pleiotropic effects to both FBM and LBM. Our results provide additional insights into the molecular genetic basis of obesity and may provide future targets for effective prevention and therapeutic intervention.

8,463 European ancestry individuals, 7,478 African American individuals, 3,348 Hispanic individuals, 1,624 Han Chinese ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

28632
Total Participants
GWAS
Study Type
Yes
Replicated
4,979 European ancestry individuals, 2,740 Han Chinese ancestry individuals
Replication Participants
Hispanic or Latin American, East Asian, African American or Afro-Caribbean, European
Ancestry
U.S.
Recruitment Country
Chapter IV

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