Evidence map›Paper›PMID 22589738›Full record

SynthesisPLoS genetics2012

Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women.

Caroline S Fox, Yongmei Liu, Charles C White, Mary Feitosa, Albert V Smith, Nancy Heard-Costa, Kurt Lohman, GIANT Consortium, MAGIC Consortium, GLGC Consortium and 17 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in PLoS genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 179 papers, 17 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
179citing papers in PubMed, 17 pooled it
16.7field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

179 citing papers in PubMed, 17 syntheses or guidelines pooled it, 277 citations in OpenAlex.

  1. Pooled it
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  5. Epigenome-wide meta-analysis of DNA methylation and childhood asthma.The Journal of allergy and clinical immunology · 2019
    Pooled it
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  14. Pleiotropic genes for metabolic syndrome and inflammation.Molecular genetics and metabolism · 2014
    Pooled it
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  18. Schizophrenia gene expression profile reverted to normal levels by antipsychotics.The international journal of neuropsychopharmacology · 2014
    Trial
  19. Article
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119 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

27 authors at 12 institutions in 2 countries.

Caroline S FoxFramingham Heart Study, National Heart, Lung, and Blood Institute, National Institutes of Health, Framingham, Massachusetts, United States of America. foxca@nhlbi.nih.gov
Yongmei Liu
Charles C White
Mary Feitosa
Albert V Smith
Nancy Heard-Costa
Kurt Lohman
GIANT Consortium
MAGIC Consortium
GLGC Consortium
Andrew D Johnson
Meredith C Foster
Danielle M Greenawalt
Paula Griffin
Jinghong Ding
Anne B Newman
Fran Tylavsky
Iva Miljkovic
Stephen B Kritchevsky
Lenore Launer
Melissa Garcia
Gudny Eiriksdottir
J Jeffrey Carr
Vilmunder Gudnason
Tamara B Harris
L Adrienne Cupples
Ingrid B Borecki
Wake Forest University · USNational Institutes of Health · USFramingham Heart Study · USIcelandic Heart Association · ISNational Heart Lung and Blood Institute · USUniversity of Pittsburgh · USWashington University in St. Louis · USBoston University · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USNational Institute on Aging · USUniversity of Iceland · ISUniversity of Tennessee Health Science Center · US

Funding

UCLA Clinical and Translational Science InstituteUL1TR000124 · NCATS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI DUBINETT, STEVEN M. · 2012 to 2015
$57.0M
Transgenic & Knock-out MouseP30DK063491 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PETER J TONTONOZ · 2003 to 2026
$40.4M
Cardiovascular Genomics and Bioinformatics projectsZIAHL006170 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI JOHNSON, ANDREW · 2013 to 2025
$25.3M
Research BaseP30DK072488 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI MITCHELL, BRAXTON D, TAYLOR, SIMEON I. · 2005 to 2019
$17.3M
CHARGE Consortium: Omics Discovery for CVD and Aging PhenotypesR01HL105756 · NHLBI · UNIVERSITY OF WASHINGTON · PI Bruce M Psaty, NICHOLAS L SMITH · 2011 to 2026
$9.5M
Framingham Heart Study/FoxZIAHL006094 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI FOX, CAROLINE · 2010 to 2015
$6.9M
CLINICAL PROJECT: Age, Gene/Environment Susceptibility Study on the Multi-omics of Aging: A clinical epidemiologic prospective studyZIAAG007380 · NIA · NATIONAL INSTITUTE ON AGING · PI LAUNER, LENORE J · 2009 to 2025
$6.1M
Aging-related Traits and Disease Risk Factors in a Sardinian Population CohortZIAAG000675 · NIA · NATIONAL INSTITUTE ON AGING · PI GOROSPE, MYRIAM · 2009 to 2021
$5.7M
Health, Aging and Body Composition StudyZIAAG007390 · NIA · NATIONAL INSTITUTE ON AGING · PI LAUNER, LENORE J · 2009 to 2024
$4.0M
Genetic Determinants of Visceral AdiposityR01AG032098 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI LIU, YONGMEI · 2009 to 2013
$3.4M
Genetic Markers of Brain AgingZIAAG007270 · NIA · NATIONAL INSTITUTE ON AGING · PI LAUNER, LENORE J · 2009 to 2025
$2.7M
Genetic Epidemiology of Metabolic Diseases of ObesityR01DK075681 · NIDDK · WASHINGTON UNIVERSITY · PI BORECKI, INGRID BERNADETTE · 2008 to 2011
$2.1M
British Heart Foundation RG/07/008/23674Intramural NIH HHSMedical Research Council G0100222Medical Research Council G0600717Medical Research Council G0701863Medical Research Council G0801056Medical Research Council G0902037Medical Research Council G19/35Medical Research Council G8802774Medical Research Council MC_PC_U127561128Medical Research Council MC_U106179471Medical Research Council MC_U127561128Medical Research Council MC_U137686857Medical Research Council MC_U147585824Medical Research Council MC_UP_A100_1003Medical Research Council MC_UP_A620_1014Medical Research Council MC_UP_A620_1015NCATS NIH HHS UL1 TR000124NHGRI NIH HHS HHSN268200782096CNHLBI NIH HHS F32 HL008770NHLBI NIH HHS N01 HC025195NHLBI NIH HHS N01-HC-25195NHLBI NIH HHS N02-HL-6-4278NHLBI NIH HHS R01 HL105756NIA NIH HHS 1R01AG032098-01A1NIA NIH HHS N01 AG062101NIA NIH HHS N01 AG062103NIA NIH HHS N01 AG062106NIA NIH HHS N01-AG-1-2100NIA NIH HHS R01 AG028288NIA NIH HHS R01 AG032098NIDDK NIH HHS 5R01DK075681NIDDK NIH HHS P30 DK063491NIDDK NIH HHS P30 DK072488NIDDK NIH HHS R01 DK075681Wellcome Trust 090532
6 · The paper itself

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.

Indexed as

Intra-Abdominal FatSex CharacteristicsSubcutaneous Fat, AbdominalAdultAgedAlpha-Ketoglutarate-Dependent Dioxygenase FTOBody Mass IndexCytokinesFemaleGenome-Wide Association StudyHapMap ProjectHumansLysophospholipaseMaleMiddle AgedPhenotypeAlpha-Ketoglutarate-Dependent Dioxygenase FTOCytokinesFTO protein, humanLYPLAL1 protein, humanLysophospholipaseProteinsTHNSL2 protein, human

Identifiers

PMID22589738
PMCPMC3349734
OpenAlexW2162377647

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.