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

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 bo...

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Détails bibliographiques
Auteurs principaux: Horikoshi, M, Yaghootkar, H, Mook-Kanamori, DO, Sovio, U, Taal, H, Hennig, B, Bradfield, J, St Pourcain, B, Evans, D, Charoen, P, Kaakinen, M, Cousminer, D, Lehtimäki, T, Kreiner-Møller, E, Warrington, N, Bustamante, M, Feenstra, B, Berry, D, Thiering, E, Pfab, T, Barton, S, Shields, B, Kerkhof, M, van Leeuwen, E, Fulford, A
Format: Journal article
Langue:English
Publié: 2013
Description
Résumé: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.