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GWAS Study

Genome-wide association uncovers shared genetic effects among personality traits and mood states.

Luciano M, Huffman JE, Arias-Vásquez A et al.

22628180 PubMed ID
GWAS Study Type
15512 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

LM
Luciano M
HJ
Huffman JE
AA
Arias-Vásquez A
VA
Vinkhuyzen AA
MC
Middeldorp CM
GI
Giegling I
PA
Payton A
DG
Davies G
ZL
Zgaga L
JJ
Janzing J
KX
Ke X
GT
Galesloot T
HA
Hartmann AM
OW
Ollier W
TA
Tenesa A
HC
Hayward C
VM
Verhagen M
MG
Montgomery GW
HJ
Hottenga JJ
KB
Konte B
SJ
Starr JM
VV
Vitart V
VP
Vos PE
MP
Madden PA
WG
Willemsen G
KH
Konnerth H
HM
Horan MA
PD
Porteous DJ
CH
Campbell H
VS
Vermeulen SH
HA
Heath AC
WA
Wright A
PO
Polasek O
KS
Kovacevic SB
HN
Hastie ND
FB
Franke B
BD
Boomsma DI
MN
Martin NG
RD
Rujescu D
WJ
Wilson JF
BJ
Buitelaar J
PN
Pendleton N
RI
Rudan I
DI
Deary IJ
Chapter II

Abstract

Summary of the research findings

Measures of personality and psychological distress are correlated and exhibit genetic covariance. We conducted univariate genome-wide SNP (~2.5 million) and gene-based association analyses of these traits and examined the overlap in results across traits, including a prediction analysis of mood states using genetic polygenic scores for personality. Measures of neuroticism, extraversion, and symptoms of anxiety, depression, and general psychological distress were collected in eight European cohorts (n ranged 546-1,338; maximum total n = 6,268) whose mean age ranged from 55 to 79 years. Meta-analysis of the cohort results was performed, with follow-up associations of the top SNPs and genes investigated in independent cohorts (n = 527-6,032). Suggestive association (P = 8 × 10(-8)) of rs1079196 in the FHIT gene was observed with symptoms of anxiety. Other notable associations (P < 6.09 × 10(-6)) included SNPs in five genes for neuroticism (LCE3C, POLR3A, LMAN1L, ULK3, SCAMP2), KIAA0802 for extraversion, and NOS1 for general psychological distress. An association between symptoms of depression and rs7582472 (near to MGAT5 and NCKAP5) was replicated in two independent samples, but other replication findings were less consistent. Gene-based tests identified a significant locus on chromosome 15 (spanning five genes) associated with neuroticism which replicated (P < 0.05) in an independent cohort. Support for common genetic effects among personality and mood (particularly neuroticism and depressive symptoms) was found in terms of SNP association overlap and polygenic score prediction. The variance explained by individual SNPs was very small (up to 1%) confirming that there are no moderate/large effects of common SNPs on personality and related traits.

6,268 European ancestry individuals

Chapter III

Study Statistics

Key metrics and study information

15512
Total Participants
GWAS
Study Type
Yes
Replicated
9,244 European ancestry individuals
Replication Participants
European
Ancestry
Australia, Netherlands, U.K., Croatia
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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Analysis In Progress

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