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Type: Journal article
Title: Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women
Author: Palmer, L.
Fox, C.S.
Liu, Y.
White, C.C.
Feitosa, M.
Smith, A.V.
Heard-Costa, N.
Lohman, K.
GIANT Consortium
MAGIC Consortium
GLGC Consortium
Johnson, A.D.
Foster, M.C.
Greenawalt, D.M.
Griffin, P.
Ding, J.
Newman, A.B.
Tylavsky, F.
Miljkovic, I.
Kritchevsky, S.B.
et al.
Citation: PLoS Genetics, 2012; 8(5):e1002695-1-e1002695-14
Publisher: Public Library of Science
Issue Date: 2012
ISSN: 1553-7390
Statement of
Caroline S. Fox ... GIANT Consortium, MAGIC Consortium, GLGC Consortium ... et al.
Abstract: Body fat distribution, particularly centralized obesity, is associated with metabolic risk above and beyond total adiposity. We performed genome-wide association of abdominal adipose depots quantified using computed tomography (CT) to uncover novel loci for body fat distribution among participants of European ancestry. Subcutaneous and visceral fat were quantified in 5,560 women and 4,997 men from 4 population-based studies. Genome-wide genotyping was performed using standard arrays and imputed to ~2.5 million Hapmap SNPs. Each study performed a genome-wide association analysis of subcutaneous adipose tissue (SAT), visceral adipose tissue (VAT), VAT adjusted for body mass index, and VAT/SAT ratio (a metric of the propensity to store fat viscerally as compared to subcutaneously) in the overall sample and in women and men separately. A weighted z-score meta-analysis was conducted. For the VAT/SAT ratio, our most significant p-value was rs11118316 at LYPLAL1 gene (p = 3.1×10E-09), previously identified in association with waist–hip ratio. For SAT, the most significant SNP was in the FTO gene (p = 5.9×10E-08). Given the known gender differences in body fat distribution, we performed sex-specific analyses. Our most significant finding was for VAT in women, rs1659258 near THNSL2 (p = 1.6×10-08), but not men (p = 0.75). Validation of this SNP in the GIANT consortium data demonstrated a similar sex-specific pattern, with observed significance in women (p = 0.006) but not men (p = 0.24) for BMI and waist circumference (p = 0.04 [women], p = 0.49 [men]). Finally, we interrogated our data for the 14 recently published loci for body fat distribution (measured by waist–hip ratio adjusted for BMI); associations were observed at 7 of these loci. In contrast, we observed associations at only 7/32 loci previously identified in association with BMI; the majority of overlap was observed with SAT. Genome-wide association for visceral and subcutaneous fat revealed a SNP for VAT in women. More refined phenotypes for body composition and fat distribution can detect new loci not previously uncovered in large-scale GWAS of anthropometric traits.
Keywords: GIANT Consortium; MAGIC Consortium; GLGC Consortium; Humans; Lysophospholipase; Proteins; Body Mass Index; Phenotype; European Continental Ancestry Group; Adult; Aged; Intra-Abdominal Fat; Subcutaneous Fat, Abdominal; Cytokines; Middle Aged; Genome-Wide Association Study; Polymorphism, Single Nucleotide; Sex Characteristics; HapMap Project; Female; Male
Description: MAGIC Consortium member: Lyle Palmer for the University of Adelaide
Rights: This is an open-access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
RMID: 0020137884
DOI: 10.1371/journal.pgen.1002695
Appears in Collections:Translational Health Science publications

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