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Biol Psychiatry. 2012 Oct 15;72(8):637-44. doi: 10.1016/j.biopsych.2012.02.038. Epub 2012 Apr 19.

Linkage analysis followed by association show NRG1 associated with cannabis dependence in African Americans.

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1
Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut; Veterans Affairs Connecticut Healthcare Center, West Haven, CT 06516, USA.

Abstract

BACKGROUND:

A genetic contribution to cannabis dependence (CaD) has been established but susceptibility genes for CaD remain largely unknown.

METHODS:

We employed a multistage design to identify genetic variants underlying CaD. We first performed a genome-wide linkage scan for CaD in 384 African American (AA) and 354 European American families ascertained for genetic studies of cocaine and opioid dependence. We then conducted association analysis under the linkage peak, first using data from a genome-wide association study from the Study of Addiction: Genetics and Environment, followed by replication studies of prioritized single nucleotide polymorphisms (SNPs) in independent samples.

RESULTS:

We identified the strongest linkage evidence with CaD (logarithm of odds = 2.9) on chromosome 8p21.1 in AAs. In the association analysis of the Study of Addiction: Genetics and Environment sample under the linkage peak, we identified one SNP (rs17664708) associated with CaD in both AAs (odds ratio [OR] = 2.93, p = .0022) and European Americans (OR = 1.38, p = .02). This SNP, located at NRG1, a susceptibility gene for schizophrenia, was prioritized for further study. We replicated the association of rs17664708 with CaD in an independent AAs sample (OR = 2.81, p = .0068). The joint analysis of the two AA samples demonstrated highly significant association between rs17664708 and CaD with adjustment for either global (p = .00044) or local ancestry (p = .00075).

CONCLUSIONS:

Our study shows that NRG1 is probably a susceptibility gene for CaD, based on convergent evidence of linkage and replicated associations in two independent AA samples.

PMID:
22520967
PMCID:
PMC3699339
DOI:
10.1016/j.biopsych.2012.02.038
[Indexed for MEDLINE]
Free PMC Article
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