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GWAS Study

Association of substance dependence phenotypes in the COGA sample.

Wetherill L, Agrawal A, Kapoor M et al.

24832863 PubMed ID
GWAS Study Type
4969 Participants
53 Views
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Chapter I

Publication Details

Comprehensive information about this research publication

Authors

WL
Wetherill L
AA
Agrawal A
KM
Kapoor M
BS
Bertelsen S
BL
Bierut LJ
BA
Brooks A
DD
Dick D
HM
Hesselbrock M
HV
Hesselbrock V
KD
Koller DL
LN
Le N
NJ
Nurnberger JI
SJ
Salvatore JE
SM
Schuckit M
TJ
Tischfield JA
WJ
Wang JC
XX
Xuei X
EH
Edenberg HJ
PB
Porjesz B
BK
Bucholz K
GA
Goate AM
FT
Foroud T
Chapter II

Abstract

Summary of the research findings

Alcohol and drug use disorders are individually heritable (50%). Twin studies indicate that alcohol and substance use disorders share common genetic influences, and therefore may represent a more heritable form of addiction and thus be more powerful for genetic studies. This study utilized data from 2322 subjects from 118 European-American families in the Collaborative Study on the Genetics of Alcoholism sample to conduct genome-wide association analysis of a binary and a continuous index of general substance dependence liability. The binary phenotype (ANYDEP) was based on meeting lifetime criteria for any DSM-IV dependence on alcohol, cannabis, cocaine or opioids. The quantitative trait (QUANTDEP) was constructed from factor analysis based on endorsement across the seven DSM-IV criteria for each of the four substances. Heritability was estimated to be 54% for ANYDEP and 86% for QUANTDEP. One single-nucleotide polymorphism (SNP), rs2952621 in the uncharacterized gene LOC151121 on chromosome 2, was associated with ANYDEP (P = 1.8 × 10(-8) ), with support from surrounding imputed SNPs and replication in an independent sample [Study of Addiction: Genetics and Environment (SAGE); P = 0.02]. One SNP, rs2567261 in ARHGAP28 (Rho GTPase-activating protein 28), was associated with QUANTDEP (P = 3.8 × 10(-8) ), and supported by imputed SNPs in the region, but did not replicate in an independent sample (SAGE; P = 0.29). The results of this study provide evidence that there are common variants that contribute to the risk for a general liability to substance dependence.

up to 2,322 European ancestry individuals from 118 families

Chapter III

Study Statistics

Key metrics and study information

4969
Total Participants
GWAS
Study Type
Yes
Replicated
2,647 European ancestry individuals
Replication Participants
European
Ancestry
U.S.
Recruitment Country
Chapter IV

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