Title
Association between copy number variation losses and alcohol dependence across african american and european american ethnic groups
Date Issued
01 January 2014
Access level
open access
Resource Type
journal article
Author(s)
Universidad de Nuevo México
Publisher(s)
Blackwell Publishing Ltd
Abstract
Background: Copy number variations (CNVs) are structural genetic mutations consisting of segmental gains or losses in DNA sequence. Although CNVs contribute substantially to genomic variation, few genetic and imaging studies report association of CNVs with alcohol dependence (AD). Our purpose is to find evidence of this association across ethnic populations and genders. This work is the first AD-CNV study across ethnic groups and the first to include the African American (AA) population. Methods: This study considers 2 CNV data sets, one for discovery (2,345 samples) and the other for validation (239 samples), both including subjects with AD and healthy controls of European and African ancestry. Our analysis assesses the association between AD and CNV losses across ethnic groups and gender by examining the effect of overall losses across the whole genome, collective losses within individual cytogenetic bands, and specific losses in CNV regions. Results: Results from the discovery data set showed an association between CNV losses within 16q12.2 and AD diagnosis (p = 4.53 × 10-3). An overlapping CNV region from the validation data set exhibited the same direction of effect with respect to AD (p = 0.051). This CNV region affects the genes CES1p1 and CES1, which are members of the carboxylesterase (CES) family. The enzyme encoded by CES1 is a major liver enzyme that typically catalyzes the decomposition of ester into alcohol and carboxylic acid and is involved in drug or xenobiotics, fatty acid, and cholesterol metabolisms. In addition, the most significantly associated CNV region was located at 9p21.2 (p = 1.9 × 10-3) in our discovery data set. Although not observed in the validation data set, probably due to small sample size, this result might hold potential connection to AD given its connection with neuronal death. In contrast, we did not find any association between AD and the overall total losses or the collective losses within individual cytogenetic bands. Conclusions: Overall, our study provides evidence that the specific CNVs at 16q12.2 contribute to the development of alcoholism in AA and European American populations. © 2014 by the Research Society on Alcoholism.
Start page
1266
End page
1274
Volume
38
Issue
5
Language
English
OCDE Knowledge area
Genética, Herencia
Epidemiología
Psicología
Subjects
Scopus EID
2-s2.0-84899463394
PubMed ID
Source
Alcoholism: Clinical and Experimental Research
ISSN of the container
0145-6008
Sponsor(s)
National Institutes of Health
National Institute on Drug Abuse R33DA027626 NIDA
Sources of information:
Directorio de Producción Científica
Scopus