| Literature DB >> 33955455 |
Jeffrey J Beck1,2, René Pool2, Margot van de Weijer2, Xu Chen3, Eva Krapohl4, Scott D Gordon5, Marianne Nygaard6, Birgit Debrabant6, Teemu Palviainen7, Matthijs D van der Zee2, Bart Baselmans2,8, Casey T Finnicum1, Lu Yi3, Sebastian Lundström9, Toos van Beijsterveldt2, Lene Christiansen6,10, Kauko Heikkilä7, Julie Kittelsrud1, Anu Loukola7, Miina Ollikainen7, Kaare Christensen6, Nicholas G Martin5, Robert Plomin4, Michel Nivard2, Meike Bartels2, Conor Dolan2, Gonneke Willemsen2, Eco de Geus2, Catarina Almqvist3, Patrik K E Magnusson3, Hamdi Mbarek2, Erik A Ehli1, Dorret I Boomsma1,2, Jouke-Jan Hottenga2.
Abstract
Birth weight (BW) is an important predictor of newborn survival and health and has associations with many adult health outcomes, including cardiometabolic disorders, autoimmune diseases and mental health. On average, twins have a lower BW than singletons as a result of a different pattern of fetal growth and shorter gestational duration. Therefore, investigations into the genetics of BW often exclude data from twins, leading to a reduction in sample size and remaining ambiguities concerning the genetic contribution to BW in twins. In this study, we carried out a genome-wide association meta-analysis of BW in 42 212 twin individuals and found a positive correlation of beta values (Pearson's r = 0.66, 95% confidence interval [CI]: 0.47-0.77) with 150 previously reported genome-wide significant variants for singleton BW. We identified strong positive genetic correlations between BW in twins and numerous anthropometric traits, most notably with BW in singletons (genetic correlation [rg] = 0.92, 95% CI: 0.66-1.18). Genetic correlations of BW in twins with a series of health-related traits closely resembled those previously observed for BW in singletons. Polygenic scores constructed from a genome-wide association study on BW in the UK Biobank demonstrated strong predictive power in a target sample of Dutch twins and singletons. Together, our results indicate that a similar genetic architecture underlies BW in twins and singletons and that future genome-wide studies might benefit from including data from large twin registers.Entities:
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Year: 2021 PMID: 33955455 PMCID: PMC8444448 DOI: 10.1093/hmg/ddab121
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150