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GWAS Study

Genetic Meta-Analysis of Twin Birth Weight Shows High Genetic Correlation with Singleton Birth Weight.

Beck JJ, Pool R, van de Weijer M et al.

33955455 PubMed ID
GWAS Study Type
42212 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BJ
Beck JJ
PR
Pool R
VD
van de Weijer M
CX
Chen X
KE
Krapohl E
GS
Gordon SD
NM
Nygaard M
DB
Debrabant B
PT
Palviainen T
VD
van der Zee MD
BB
Baselmans B
FC
Finnicum CT
YL
Yi L
LS
Lundström S
VB
van Beijsterveldt T
CL
Christiansen L
HK
Heikkilä K
KJ
Kittelsrud J
LA
Loukola A
OM
Ollikainen M
CK
Christensen K
MN
Martin NG
PR
Plomin R
NM
Nivard M
BM
Bartels M
DC
Dolan C
WG
Willemsen G
DG
de Geus E
AC
Almqvist C
MP
Magnusson PKE
MH
Mbarek H
EE
Ehli EA
BD
Boomsma DI
HJ
Hottenga JJ
Chapter II

Abstract

Summary of the research findings

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.

42,212 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

42212
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Sweden, Netherlands, U.S., Finland, Denmark, U.K., Australia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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