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GWAS Study

The International SSRI Pharmacogenomics Consortium (ISPC): a genome-wide association study of antidepressant treatment response.

Biernacka JM, Sangkuhl K, Jenkins G et al.

25897834 PubMed ID
GWAS Study Type
2394 Participants
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

BJ
Biernacka JM
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
BB
Baune BT
KM
Kato M
LY
Liu YL
PV
Praphanphoj V
SJ
Stingl JC
TS
Tsai SJ
KM
Kubo M
KT
Klein TE
WR
Weinshilboum R
Chapter II

Abstract

Summary of the research findings

Response to treatment with selective serotonin reuptake inhibitors (SSRIs) varies considerably between patients. The International SSRI Pharmacogenomics Consortium (ISPC) was formed with the primary goal of identifying genetic variation that may contribute to response to SSRI treatment of major depressive disorder. A genome-wide association study of 4-week treatment outcomes, measured using the 17-item Hamilton Rating Scale for Depression (HRSD-17), was performed using data from 865 subjects from seven sites. The primary outcomes were percent change in HRSD-17 score and response, defined as at least 50% reduction in HRSD-17. Data from two prior studies, the Pharmacogenomics Research Network Antidepressant Medication Pharmacogenomics Study (PGRN-AMPS) and the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) study, were used for replication, and a meta-analysis of the three studies was performed (N=2394). Although many top association signals in the ISPC analysis map to interesting candidate genes, none were significant at the genome-wide level and the associations were not replicated using PGRN-AMPS and STAR*D data. The top association result in the meta-analysis of response represents SNPs 5′ upstream of the neuregulin-1 gene, NRG1 (P = 1.20E - 06). NRG1 is involved in many aspects of brain development, including neuronal maturation and variations in this gene have been shown to be associated with increased risk for mental disorders, particularly schizophrenia. Replication and functional studies of these findings are warranted.

298 European ancestry cases, 567 Asian ancestry cases, 1529 European and other ancestry cases

Chapter III

Study Statistics

Key metrics and study information

2394
Total Participants
GWAS
Study Type
No
Replicated
NR, European, European, Asian unspecified
Ancestry
U.S., Germany, China, Thailand, Japan
Recruitment Country
Chapter IV

Analysis

Comprehensive review of health and genetic findings

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