Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster ( CHRNA5–CHRNA3–CHRNB4 ) interacts with maternal self-reported smoking status during pregnancy to influence birth weight

Author: Tyrrell Jessica   Huikari Ville   Christie Jennifer T.   Cavadino Alana   Bakker Rachel   Brion Marie-Jo A.   Geller Frank   Paternoster Lavinia   Myhre Ronny   Potter Catherine   Johnson Paul C.D.   Ebrahim Shah   Feenstra Bjarke   Hartikainen Anna-Liisa   Hattersley Andrew T.   Hofman Albert   Kaakinen Marika   Lowe Lynn P.   Magnus Per   McConnachie Alex   Melbye Mads   Ng Jane W.Y.   Nohr Ellen A.   Power Chris   Ring Susan M.   Sebert Sylvain P.   Sengpiel Verena   Taal H. Rob   Watt Graham C.M.   Sattar Naveed   Relton Caroline L.   Jacobsson Bo   Frayling Timothy M.   Sørensen Thorkild I.A.   Murray Jeffrey C.   Lawlor Debbie A.   Pennell Craig E.   Jaddoe Vincent W.V.   Hypponen Elina   Lowe William L.   Jarvelin Marjo-Riitta   Davey Smith George   Freathy Rachel M.  

Publisher: Oxford University Press

ISSN: 1460-2083

Source: Human Molecular Genetics, Vol.21, Iss.24, 2012-12, pp. : 5344-5358

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Abstract

Maternal smoking during pregnancy is associated with low birth weight. Common variation at rs1051730 is robustly associated with smoking quantity and was recently shown to influence smoking cessation during pregnancy, but its influence on birth weight is not clear. We aimed to investigate the association between this variant and birth weight of term, singleton offspring in a well-powered meta-analysis. We stratified 26 241 European origin study participants by smoking status (women who smoked during pregnancy versus women who did not smoke during pregnancy) and, in each stratum, analysed the association between maternal rs1051730 genotype and offspring birth weight. There was evidence of interaction between genotype and smoking (P = 0.007). In women who smoked during pregnancy, each additional smoking-related T-allele was associated with a 20 g [95% confidence interval (95% CI): 4–36 g] lower birth weight (P = 0.014). However, in women who did not smoke during pregnancy, the effect size estimate was 5 g per T-allele (95% CI: −4 to 14 g; P = 0.268). To conclude, smoking status during pregnancy modifies the association between maternal rs1051730 genotype and offspring birth weight. This strengthens the evidence that smoking during pregnancy is causally related to lower offspring birth weight and suggests that population interventions that effectively reduce smoking in pregnant women would result in a reduced prevalence of low birth weight.

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