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GWAS Study

Association of the Polygenic Scores for Personality Traits and Response to Selective Serotonin Reuptake Inhibitors in Patients with Major Depressive Disorder.

Amare AT, Schubert KO, Tekola-Ayele F et al.

29559929 PubMed ID
GWAS Study Type
261726 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

AA
Amare AT
SK
Schubert KO
TF
Tekola-Ayele F
HY
Hsu YH
SK
Sangkuhl K
JG
Jenkins G
WR
Whaley RM
BP
Barman P
BA
Batzler A
AR
Altman RB
AV
Arolt V
BJ
Brockmöller J
CC
Chen CH
DK
Domschke K
HD
Hall-Flavin DK
HC
Hong CJ
IA
Illi A
JY
Ji Y
KO
Kampman O
KT
Kinoshita T
LE
Leinonen E
LY
Liou YJ
MT
Mushiroda T
NS
Nonen S
SM
Skime MK
WL
Wang L
KM
Kato M
LY
Liu YL
PV
Praphanphoj V
SJ
Stingl JC
BW
Bobo WV
TS
Tsai SJ
KM
Kubo M
KT
Klein TE
WR
Weinshilboum RM
BJ
Biernacka JM
BB
Baune BT
Chapter II

Abstract

Summary of the research findings

Studies reported a strong genetic correlation between the Big Five personality traits and major depressive disorder (MDD). Moreover, personality traits are thought to be associated with response to antidepressants treatment that might partly be mediated by genetic factors. In this study, we examined whether polygenic scores (PGSs) derived from the Big Five personality traits predict treatment response and remission in patients with MDD who were prescribed selective serotonin reuptake inhibitors (SSRIs). In addition, we performed meta-analyses of genome-wide association studies (GWASs) on these traits to identify genetic variants underpinning the cross-trait polygenic association. The PGS analysis was performed using data from two cohorts: the Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomic Study (PGRN-AMPS, n = 529) and the International SSRI Pharmacogenomics Consortium (ISPC, n = 865). The cross-trait GWAS meta-analyses were conducted by combining GWAS summary statistics on SSRIs treatment outcome and on the personality traits. The results showed that the PGS for openness and neuroticism were associated with SSRIs treatment outcomes at p < 0.05 across PT thresholds in both cohorts. A significant association was also found between the PGS for conscientiousness and SSRIs treatment response in the PGRN-AMPS sample. In the cross-trait GWAS meta-analyses, we identified eight loci associated with (a) SSRIs response and conscientiousness near YEATS4 gene and (b) SSRI remission and neuroticism eight loci near PRAG1, MSRA, XKR6, ELAVL2, PLXNC1, PLEKHM1, and BRUNOL4 genes. An assessment of a polygenic load for personality traits may assist in conjunction with clinical data to predict whether MDD patients might respond favorably to SSRIs.

865 individuals with SSRI response data, 260,861 individuals with personality trait data

Chapter III

Study Statistics

Key metrics and study information

261726
Total Participants
GWAS
Study Type
No
Replicated
U.S., Germany, Japan, Thailand, Taiwan
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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