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GWAS Study

Meta-analysis of genome-wide association studies for personality.

de Moor MH, Costa PT, Terracciano A et al.

21173776 PubMed ID
GWAS Study Type
20669 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

DM
de Moor MH
CP
Costa PT
TA
Terracciano A
KR
Krueger RF
DG
de Geus EJ
TT
Toshiko T
PB
Penninx BW
ET
Esko T
MP
Madden PA
DJ
Derringer J
AN
Amin N
WG
Willemsen G
HJ
Hottenga JJ
DM
Distel MA
UM
Uda M
SS
Sanna S
SP
Spinhoven P
HC
Hartman CA
SP
Sullivan P
RA
Realo A
AJ
Allik J
HA
Heath AC
PM
Pergadia ML
AA
Agrawal A
LP
Lin P
GR
Grucza R
NT
Nutile T
CM
Ciullo M
RD
Rujescu D
GI
Giegling I
KB
Konte B
WE
Widen E
CD
Cousminer DL
EJ
Eriksson JG
PA
Palotie A
PL
Peltonen L
LM
Luciano M
TA
Tenesa A
DG
Davies G
LL
Lopez LM
HN
Hansell NK
MS
Medland SE
FL
Ferrucci L
SD
Schlessinger D
MG
Montgomery GW
WM
Wright MJ
AY
Aulchenko YS
JA
Janssens AC
OB
Oostra BA
MA
Metspalu A
AG
Abecasis GR
DI
Deary IJ
RK
Räikkönen K
BL
Bierut LJ
MN
Martin NG
VD
van Duijn CM
BD
Boomsma DI
Chapter II

Abstract

Summary of the research findings

Personality can be thought of as a set of characteristics that influence people's thoughts, feelings and behavior across a variety of settings. Variation in personality is predictive of many outcomes in life, including mental health. Here we report on a meta-analysis of genome-wide association (GWA) data for personality in 10 discovery samples (17,375 adults) and five in silico replication samples (3294 adults). All participants were of European ancestry. Personality scores for Neuroticism, Extraversion, Openness to Experience, Agreeableness and Conscientiousness were based on the NEO Five-Factor Inventory. Genotype data of ≈ 2.4M single-nucleotide polymorphisms (SNPs; directly typed and imputed using HapMap data) were available. In the discovery samples, classical association analyses were performed under an additive model followed by meta-analysis using the weighted inverse variance method. Results showed genome-wide significance for Openness to Experience near the RASA1 gene on 5q14.3 (rs1477268 and rs2032794, P=2.8 × 10(-8) and 3.1 × 10(-8)) and for Conscientiousness in the brain-expressed KATNAL2 gene on 18q21.1 (rs2576037, P=4.9 × 10(-8)). We further conducted a gene-based test that confirmed the association of KATNAL2 to Conscientiousness. In silico replication did not, however, show significant associations of the top SNPs with Openness and Conscientiousness, although the direction of effect of the KATNAL2 SNP on Conscientiousness was consistent in all replication samples. Larger scale GWA studies and alternative approaches are required for confirmation of KATNAL2 as a novel gene affecting Conscientiousness.

17,375 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

20669
Total Participants
GWAS
Study Type
Yes
Replicated
3,294 European ancestry individuals
Replication Participants
European
Ancestry
Finland, U.S., Australia, Italy, Netherlands, U.K., Estonia, Germany
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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