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dc.contributor.authorPulit, SL
dc.contributor.authorStoneman, C
dc.contributor.authorMorris, AP
dc.contributor.authorWood, AR
dc.contributor.authorGlastonbury, CA
dc.contributor.authorTyrrell, J
dc.contributor.authorYengo, L
dc.contributor.authorFerreira, T
dc.contributor.authorMarouli, E
dc.contributor.authorJi, Y
dc.contributor.authorYang, J
dc.contributor.authorJones, S
dc.contributor.authorBeaumont, R
dc.contributor.authorCroteau-Chonka, DC
dc.contributor.authorWinkler, TW
dc.contributor.authorGiant, C
dc.contributor.authorHattersley, AT
dc.contributor.authorLoos, RJF
dc.contributor.authorHirschhorn, JN
dc.contributor.authorVisscher, PM
dc.contributor.authorFrayling, TM
dc.contributor.authorYaghootkar, H
dc.contributor.authorLindgren, CM
dc.date.accessioned2018-11-09T12:39:06Z
dc.date.issued2018-09-14
dc.description.abstractOne in four adults worldwide are either overweight or obese. Epidemiological studies indicate that the location and distribution of excess fat, rather than general adiposity, is most informative for predicting risk of obesity sequellae, including cardiometabolic disease and cancer. We performed a genome-wide association study meta-analysis of body fat distribution, measured by waist-to-hip ratio adjusted for BMI (WHRadjBMI), and identified 463 signals in 346 loci. Heritability and variant effects were generally stronger in women than men, and we found approximately one-third of all signals to be sexually dimorphic. The 5% of individuals carrying the most WHRadjBMI-increasing alleles were 1.62 times more likely than the bottom 5% to have a WHR above the thresholds used for metabolic syndrome. These data, made publicly available, will inform the biology of body fat distribution and its relationship with disease.en_GB
dc.description.sponsorshipThe Li Ka Shing Foundation (to C.M.L.), WT-SSI/John Fell funds; The National Institute for Health Research Biomedical Research Centre, Oxford, by Widenlife (to C.M.L.); National Institutes of Health (CRR00070 CR00.01 to C.M.L.); Veni Fellowship 016.186.071 (ZonMW) from the Dutch Organization for Scientific Research [Nederlandse Organisatie voor Wetenschappelijk Onderzoek (NWO) to S.L.P]; Diabetes UK RD Lawrence fellowship (17/0005594 to H.Y.); The European Research Council (323195:GLUCOSEGENES-FP7-IDEAS-ERC to A.R.W. and T.M.F.); The Wellcome Trust and Royal Society (104150/Z/14/Z to R.B.); European Regional Development Fund (to J.T.); Diabetes Research and Wellness Foundation Fellowship (J.T.); The Medical Research Council (MR/M005070/1 to S.E.J.); Australian National Health and Medical Research Council (1078037 and 1113400 to P.M.V. and J.Y.); The Sylvia & Charles Viertel Charitable Foundation (to J.Y.); The U.S. National Institutes of Health (K01 HL127265 to D.C.C.-C.).en_GB
dc.identifier.citationPublished online 14 September 2018en_GB
dc.identifier.doi10.1093/hmg/ddy327
dc.identifier.urihttp://hdl.handle.net/10871/34689
dc.language.isoenen_GB
dc.publisherOxford University Press (OUP)en_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/30239722en_GB
dc.rights© The Author(s) 2018. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectallelesen_GB
dc.subjectobesityen_GB
dc.subjectphenotypeen_GB
dc.subjectbody mass index procedureen_GB
dc.subjectmetabolic syndrome xen_GB
dc.subjectwaist-hip ratioen_GB
dc.subjectadulten_GB
dc.subjectepidemiologic studiesen_GB
dc.subjectgenomeen_GB
dc.subjectsingle nucleotide polymorphismen_GB
dc.subjectbody fat distributionen_GB
dc.subjectgenome-wide association studyen_GB
dc.subjectoverweighten_GB
dc.subjectbiobanksen_GB
dc.titleMeta-analysis of genome-wide association studies for body fat distribution in 694,649 individuals of European ancestry.en_GB
dc.typeArticleen_GB
dc.date.available2018-11-09T12:39:06Z
exeter.place-of-publicationEnglanden_GB
dc.descriptionThis is the final version. Available on open access from OUP via the DOI in this recorden_GB
dc.identifier.journalHuman Molecular Geneticsen_GB


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