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Genome-wide approach identifies a novel gene-maternal pre-pregnancy BMI interaction on preterm birth

Preterm birth (PTB) contributes significantly to infant mortality and morbidity with lifelong impact. Few robust genetic factors of PTB have been identified. Such ‘missing heritability' may be partly due to gene × environment interactions (G × E), which is largely unexplored. Here we conduct ge...

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Detalles Bibliográficos
Autores principales: Hong, Xiumei, Hao, Ke, Ji, Hongkai, Peng, Shouneng, Sherwood, Ben, Di Narzo, Antonio, Tsai, Hui-Ju, Liu, Xin, Burd, Irina, Wang, Guoying, Ji, Yuelong, Caruso, Deanna, Mao, Guangyun, Bartell, Tami R., Zhang, Zhongyang, Pearson, Colleen, Heffner, Linda, Cerda, Sandra, Beaty, Terri H., Fallin, M. Daniele, Lee-Parritz, Aviva, Zuckerman, Barry, Weeks, Daniel E., Wang, Xiaobin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5472707/
https://www.ncbi.nlm.nih.gov/pubmed/28598419
http://dx.doi.org/10.1038/ncomms15608
Descripción
Sumario:Preterm birth (PTB) contributes significantly to infant mortality and morbidity with lifelong impact. Few robust genetic factors of PTB have been identified. Such ‘missing heritability' may be partly due to gene × environment interactions (G × E), which is largely unexplored. Here we conduct genome-wide G × E analyses of PTB in 1,733 African-American women (698 mothers of PTB; 1,035 of term birth) from the Boston Birth Cohort. We show that maternal COL24A1 variants have a significant genome-wide interaction with maternal pre-pregnancy overweight/obesity on PTB risk, with rs11161721 (P(G × E)=1.8 × 10(−8); empirical P(G × E)=1.2 × 10(−8)) as the top hit. This interaction is replicated in African-American mothers (P(G × E)=0.01) from an independent cohort and in meta-analysis (P(G × E)=3.6 × 10(−9)), but is not replicated in Caucasians. In adipose tissue, rs11161721 is significantly associated with altered COL24A1 expression. Our findings may provide new insight into the aetiology of PTB and improve our ability to predict and prevent PTB.