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

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • 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
  • Hansen, Torben
  • Torben Jørgensen
  • Oskari Kilpeläinen, Tuomas
  • Louise Pedersen
  • Vaag, Allan
  • Nadja Hawwa Vissing
  • Daniel R Witte
  • Pedersen, Oluf Borbye
  • Bønnelykke, Klaus
  • Hans Bisgaard
  • Meta-Analyses of Glucose- and Insulin-related traits Consortium (MAGIC)
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.
OriginalsprogEngelsk
TidsskriftNature Genetics
Vol/bind45
Udgave nummer1
Sider (fra-til)76-82
Antal sider7
ISSN1061-4036
DOI
StatusUdgivet - 2013

ID: 46219418