New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-01

AUTHORS

Momoko Horikoshi, Hanieh Yaghootkar, Dennis O Mook-Kanamori, Ulla Sovio, H Rob Taal, Branwen J Hennig, Jonathan P Bradfield, Beate St Pourcain, David M Evans, Pimphen Charoen, Marika Kaakinen, Diana L Cousminer, Terho Lehtimäki, Eskil Kreiner-Møller, Nicole M Warrington, Mariona Bustamante, Bjarke Feenstra, Diane J Berry, Elisabeth Thiering, Thiemo Pfab, Sheila J Barton, Beverley M Shields, Marjan Kerkhof, Elisabeth M van Leeuwen, Anthony J Fulford, Zoltán Kutalik, Jing Hua Zhao, Marcel den Hoed, Anubha Mahajan, Virpi Lindi, Liang-Kee Goh, Jouke-Jan Hottenga, Ying Wu, Olli T Raitakari, Marie N Harder, Aline Meirhaeghe, Ioanna Ntalla, Rany M Salem, Karen A Jameson, Kaixin Zhou, Dorota M Monies, Vasiliki Lagou, Mirna Kirin, Jani Heikkinen, Linda S Adair, Fowzan S Alkuraya, Ali Al-Odaib, Philippe Amouyel, Ehm Astrid Andersson, Amanda J Bennett, Alexandra I F Blakemore, Jessica L Buxton, Jean Dallongeville, Shikta Das, Eco J C de Geus, Xavier Estivill, Claudia Flexeder, Philippe Froguel, Frank Geller, Keith M Godfrey, Frédéric Gottrand, Christopher J Groves, Torben Hansen, Joel N Hirschhorn, Albert Hofman, Mads V Hollegaard, David M Hougaard, Elina Hyppönen, Hazel M Inskip, Aaron Isaacs, Torben Jørgensen, Christina Kanaka-Gantenbein, John P Kemp, Wieland Kiess, Tuomas O Kilpeläinen, Norman Klopp, Bridget A Knight, Christopher W Kuzawa, George McMahon, John P Newnham, Harri Niinikoski, Ben A Oostra, Louise Pedersen, Dirkje S Postma, Susan M Ring, Fernando Rivadeneira, Neil R Robertson, Sylvain Sebert, Olli Simell, Torsten Slowinski, Carla M T Tiesler, Anke Tönjes, Allan Vaag, Jorma S Viikari, Jacqueline M Vink, Nadja Hawwa Vissing, Nicholas J Wareham, Gonneke Willemsen, Daniel R Witte, Haitao Zhang, Jianhua Zhao, The Meta-Analyses of Glucose- and Insulin-related traits Consortium, Early Growth Genetics Consortium, James F Wilson, Michael Stumvoll, Andrew M Prentice, Brian F Meyer, Ewan R Pearson, Colin A G Boreham, Cyrus Cooper, Matthew W Gillman, George V Dedoussis, Luis A Moreno, Oluf Pedersen, Maiju Saarinen, Karen L Mohlke, Dorret I Boomsma, Seang-Mei Saw, Timo A Lakka, Antje Körner, Ruth J F Loos, Ken K Ong, Peter Vollenweider, Cornelia M van Duijn, Gerard H Koppelman, Andrew T Hattersley, John W Holloway, Berthold Hocher, Joachim Heinrich, Chris Power, Mads Melbye, Mònica Guxens, Craig E Pennell, Klaus Bønnelykke, Hans Bisgaard, Johan G Eriksson, Elisabeth Widén, Hakon Hakonarson, André G Uitterlinden, Anneli Pouta, Debbie A Lawlor, George Davey Smith, Timothy M Frayling, Mark I McCarthy, Struan F A Grant, Vincent W V Jaddoe, Marjo-Riitta Jarvelin, Nicholas J Timpson, Inga Prokopenko, Rachel M Freathy

ABSTRACT

Birth weight within the normal range is associated with a variety of adult-onset diseases, but the mechanisms behind these associations are poorly understood. Previous genome-wide association studies of birth weight identified a variant in the ADCY5 gene associated both with birth weight and type 2 diabetes and a second variant, near CCNL1, with no obvious link to adult traits. In an expanded genome-wide association meta-analysis and follow-up study of birth weight (of up to 69,308 individuals of European descent from 43 studies), we have now extended the number of loci associated at genome-wide significance to 7, accounting for a similar proportion of variance as maternal smoking. Five of the loci are known to be associated with other phenotypes: ADCY5 and CDKAL1 with type 2 diabetes, ADRB1 with adult blood pressure and HMGA2 and LCORL with adult height. Our findings highlight genetic links between fetal growth and postnatal growth and metabolism. More... »

PAGES

76

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  • Journal

    TITLE

    Nature Genetics

    ISSUE

    1

    VOLUME

    45

    Author Affiliations

  • Wellcome Centre for Human Genetics
  • University of Exeter
  • Weill Cornell Medical College in Qatar
  • London School of Hygiene & Tropical Medicine
  • Erasmus University Medical Center
  • Medical Research Council The Gambia Unit
  • Children's Hospital of Philadelphia
  • University of Bristol
  • Mahidol University
  • University of Oulu
  • University of Helsinki
  • Tampere University Hospital
  • University of Copenhagen
  • University of Western Australia
  • Centre for Genomic Regulation
  • Statens Serum Institut
  • University College London
  • University of Potsdam
  • University of Southampton
  • Peninsula College of Medicine and Dentistry
  • Swiss Institute of Bioinformatics
  • University of Eastern Finland
  • Duke NUS Graduate Medical School
  • VU University Amsterdam
  • University of North Carolina at Chapel Hill
  • Turku University Hospital
  • Université Lille 2 Droit et Santé
  • Harokopio University
  • Boston Children's Hospital
  • University of Dundee
  • King Faisal Specialist Hospital & Research Centre
  • University of Edinburgh
  • University of North Carolina System
  • Alfaisal University
  • University of Oxford
  • Imperial College London
  • Pompeu Fabra University
  • University Hospital Southampton NHS Foundation Trust
  • University of Southern Denmark
  • Centre for Medical Systems Biology
  • Leipzig University
  • Hannover Medical School
  • Northwestern University
  • Charité
  • Ludwig Maximilian University of Munich
  • Steno Diabetes Center
  • Western General Hospital
  • University College Dublin
  • University of Zaragoza
  • Novo Nordisk (Denmark)
  • University of Turku
  • Singapore Eye Research Institute
  • Kuopion Liikuntalääketieteen Tutkimuslaitos
  • University of Lausanne
  • Centro de Investigación Biomédica en Red de Epidemiología y Salud Pública
  • National Institute for Health and Welfare
  • University of Pennsylvania
  • Churchill Hospital
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/ng.2477

    DOI

    http://dx.doi.org/10.1038/ng.2477

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1047138202

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/23202124


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    75 schema:description Birth weight within the normal range is associated with a variety of adult-onset diseases, but the mechanisms behind these associations are poorly understood. Previous genome-wide association studies of birth weight identified a variant in the ADCY5 gene associated both with birth weight and type 2 diabetes and a second variant, near CCNL1, with no obvious link to adult traits. In an expanded genome-wide association meta-analysis and follow-up study of birth weight (of up to 69,308 individuals of European descent from 43 studies), we have now extended the number of loci associated at genome-wide significance to 7, accounting for a similar proportion of variance as maternal smoking. Five of the loci are known to be associated with other phenotypes: ADCY5 and CDKAL1 with type 2 diabetes, ADRB1 with adult blood pressure and HMGA2 and LCORL with adult height. Our findings highlight genetic links between fetal growth and postnatal growth and metabolism.
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