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Genome-wide association study of offspring birth weight in 86,577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

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  • Robin N Beaumont
  • Nicole M Warrington
  • Alana Cavadino
  • Jessica Tyrrell
  • Michael Nodzenski
  • Momoko Horikoshi
  • Frank Geller
  • Ronny Myhre
  • Rebecca C Richmond
  • Lavinia Paternoster
  • Jonathan P Bradfield
  • Eskil Kreiner-Møller
  • Ville Huikari
  • Sarah Metrustry
  • Kathryn L Lunetta
  • Jodie N Painter
  • Jouke-Jan Hottenga
  • Catherine Allard
  • Sheila J Barton
  • Ana Espinosa
  • Julie A Marsh
  • Catherine Potter
  • Ge Zhang
  • Wei Ang
  • Diane J Berry
  • Luigi Bouchard
  • Shikta Das
  • Hakon Hakonarson
  • Jani Heikkinen
  • Øyvind Helgeland
  • Berthold Hocher
  • Albert Hofman
  • Hazel M Inskip
  • Samuel E Jones
  • Manolis Kogevinas
  • Penelope A Lind
  • Letizia Marullo
  • Sarah E Medland
  • Anna Murray
  • Jeffrey C Murray
  • Pål R Njølstad
  • Ellen A Nohr
  • Christoph Reichetzeder
  • Susan M Ring
  • Katherine S Ruth
  • Loreto Santa-Marina
  • Denise M Scholtens
  • Sylvain Sebert
  • Hans Bisgaard
  • Thorkild Ia Sørensen
  • Early Growth Genetics (EGG) Consortium
Vis graf over relationer

Genome-wide association studies (GWAS) of birth weight have focused on fetal genetics, while relatively little is known about the role of maternal genetic variation. We aimed to identify maternal genetic variants associated with birth weight that could highlight potentially relevant maternal determinants of fetal growth. We meta-analysed data on up to 8.7 million SNPs in up to 86,577 women of European descent from the Early Growth Genetics (EGG) Consortium and the UK Biobank. We used structural equation modelling (SEM) and analyses of mother-child pairs to quantify the separate maternal and fetal genetic effects. Maternal SNPs at 10 loci (MTNR1B, HMGA2, SH2B3, KCNAB1, L3MBTL3, GCK, EBF1, TCF7L2, ACTL9, CYP3A7) were associated with offspring birth weight at P<5x10-8. In SEM analyses, at least 7 of the 10 associations were consistent with effects of the maternal genotype acting via the intrauterine environment, rather than via effects of shared alleles with the fetus. Variants, or correlated proxies, at many of the loci had been previously associated with adult traits, including fasting glucose (MTNR1B, GCK and TCF7L2) and sex hormone levels (CYP3A7), and one (EBF1) with gestational duration. The identified associations indicate genetic effects on maternal glucose, cytochrome P450 activity and gestational duration, and potentially on maternal blood pressure and immune function, are relevant for fetal growth. Further characterization of these associations in mechanistic and causal analyses will enhance understanding of the potentially modifiable maternal determinants of fetal growth, with the goal of reducing the morbidity and mortality associated with low and high birth weights.

OriginalsprogEngelsk
TidsskriftHuman Molecular Genetics
Vol/bind27
Udgave nummer4
Sider (fra-til)742-756
Antal sider15
ISSN0964-6906
DOI
StatusUdgivet - feb. 2018

ID: 52650420