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GWAS Study

A genome-wide approach to children's aggressive behavior: The EAGLE consortium.

Pappa I, St Pourcain B, Benke K et al.

26087016 PubMed ID
GWAS Study Type
15668 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

PI
Pappa I
SP
St Pourcain B
BK
Benke K
CA
Cavadino A
HC
Hakulinen C
NM
Nivard MG
NI
Nolte IM
TC
Tiesler CM
BM
Bakermans-Kranenburg MJ
DG
Davies GE
ED
Evans DM
GM
Geoffroy MC
GH
Grallert H
GM
Groen-Blokhuis MM
HJ
Hudziak JJ
KJ
Kemp JP
KL
Keltikangas-Järvinen L
MG
McMahon G
MV
Mileva-Seitz VR
ME
Motazedi E
PC
Power C
RO
Raitakari OT
RS
Ring SM
RF
Rivadeneira F
RA
Rodriguez A
SP
Scheet PA
SI
Seppälä I
SH
Snieder H
SM
Standl M
TE
Thiering E
TN
Timpson NJ
VR
Veenstra R
VF
Velders FP
WA
Whitehouse AJ
SG
Smith GD
HJ
Heinrich J
HE
Hypponen E
LT
Lehtimäki T
MC
Middeldorp CM
OA
Oldehinkel AJ
PC
Pennell CE
BD
Boomsma DI
TH
Tiemeier H
Chapter II

Abstract

Summary of the research findings

Individual differences in aggressive behavior emerge in early childhood and predict persisting behavioral problems and disorders. Studies of antisocial and severe aggression in adulthood indicate substantial underlying biology. However, little attention has been given to genome-wide approaches of aggressive behavior in children. We analyzed data from nine population-based studies and assessed aggressive behavior using well-validated parent-reported questionnaires. This is the largest sample exploring children's aggressive behavior to date (N = 18,988), with measures in two developmental stages (N = 15,668 early childhood and N = 16,311 middle childhood/early adolescence). First, we estimated the additive genetic variance of children's aggressive behavior based on genome-wide SNP information, using genome-wide complex trait analysis (GCTA). Second, genetic associations within each study were assessed using a quasi-Poisson regression approach, capturing the highly right-skewed distribution of aggressive behavior. Third, we performed meta-analyses of genome-wide associations for both the total age-mixed sample and the two developmental stages. Finally, we performed a gene-based test using the summary statistics of the total sample. GCTA quantified variance tagged by common SNPs (10-54%). The meta-analysis of the total sample identified one region in chromosome 2 (2p12) at near genome-wide significance (top SNP rs11126630, P = 5.30 × 10(-8) ). The separate meta-analyses of the two developmental stages revealed suggestive evidence of association at the same locus. The gene-based analysis indicated association of variation within AVPR1A with aggressive behavior. We conclude that common variants at 2p12 show suggestive evidence for association with childhood aggression. Replication of these initial findings is needed, and further studies should clarify its biological meaning. © 2015 Wiley Periodicals, Inc.

15,668 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

15668
Total Participants
GWAS
Study Type
No
Replicated
European
Ancestry
Finland, Australia, Netherlands, U.K., Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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