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Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study
BACKGROUND: Dopamine is an important neurotransmitter involved in reward mechanism in the brain and thereby influences development and relapse of alcohol dependence. The dopamine D2 receptor (DRD2) gene on chromosome 11 (q22-q23) has been found to be associated with increased alcohol consumption thr...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829542/ https://www.ncbi.nlm.nih.gov/pubmed/20146828 http://dx.doi.org/10.1186/1471-2350-11-24 |
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author | Prasad, Pushplata Ambekar, Atul Vaswani, Meera |
author_facet | Prasad, Pushplata Ambekar, Atul Vaswani, Meera |
author_sort | Prasad, Pushplata |
collection | PubMed |
description | BACKGROUND: Dopamine is an important neurotransmitter involved in reward mechanism in the brain and thereby influences development and relapse of alcohol dependence. The dopamine D2 receptor (DRD2) gene on chromosome 11 (q22-q23) has been found to be associated with increased alcohol consumption through mechanisms involving incentive salience attributions and craving in alcoholic patients. Therefore, we investigated the association of three single nucleotide polymorphisms (SNP) in DRD2 gene with alcohol dependence in the north Indian subjects. METHODS: In a retrospective analysis, genetic association of three polymorphisms from DRD2 gene with alcohol dependence was investigated using a case-control approach. Alcohol dependence was determined by DSM-IV criteria and a total of 90 alcoholics and 60 healthy unrelated age-matched control subjects were recruited. Odds ratio and confidence interval was calculated to determine risk conferred by a predisposing allele/genotype/haplotype. Logistic regression analysis was carried out to correlate various clinical parameters with genotypes, and to study pair-wise interactions between SNPs. RESULTS: The study showed a significant association of -141C Ins allele and a trend of association of TaqI A1 allele of DRD2 with alcohol dependence. Haplotype with the predisposing -141C Ins and TaqI A1 alleles (-141C Ins-A-A1) seems to confer ≈ 2.5 times more risk to develop alcohol dependence. CONCLUSIONS: The study provides preliminary insight into genetic risk to alcohol dependence in Indian males. Two polymorphisms namely, -141C Ins/Del and TaqI A in DRD2 gene may have clinical implications among Indian alcoholic subjects. |
format | Text |
id | pubmed-2829542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-28295422010-02-28 Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study Prasad, Pushplata Ambekar, Atul Vaswani, Meera BMC Med Genet Research Article BACKGROUND: Dopamine is an important neurotransmitter involved in reward mechanism in the brain and thereby influences development and relapse of alcohol dependence. The dopamine D2 receptor (DRD2) gene on chromosome 11 (q22-q23) has been found to be associated with increased alcohol consumption through mechanisms involving incentive salience attributions and craving in alcoholic patients. Therefore, we investigated the association of three single nucleotide polymorphisms (SNP) in DRD2 gene with alcohol dependence in the north Indian subjects. METHODS: In a retrospective analysis, genetic association of three polymorphisms from DRD2 gene with alcohol dependence was investigated using a case-control approach. Alcohol dependence was determined by DSM-IV criteria and a total of 90 alcoholics and 60 healthy unrelated age-matched control subjects were recruited. Odds ratio and confidence interval was calculated to determine risk conferred by a predisposing allele/genotype/haplotype. Logistic regression analysis was carried out to correlate various clinical parameters with genotypes, and to study pair-wise interactions between SNPs. RESULTS: The study showed a significant association of -141C Ins allele and a trend of association of TaqI A1 allele of DRD2 with alcohol dependence. Haplotype with the predisposing -141C Ins and TaqI A1 alleles (-141C Ins-A-A1) seems to confer ≈ 2.5 times more risk to develop alcohol dependence. CONCLUSIONS: The study provides preliminary insight into genetic risk to alcohol dependence in Indian males. Two polymorphisms namely, -141C Ins/Del and TaqI A in DRD2 gene may have clinical implications among Indian alcoholic subjects. BioMed Central 2010-02-11 /pmc/articles/PMC2829542/ /pubmed/20146828 http://dx.doi.org/10.1186/1471-2350-11-24 Text en Copyright ©2010 Prasad et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Prasad, Pushplata Ambekar, Atul Vaswani, Meera Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title | Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title_full | Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title_fullStr | Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title_full_unstemmed | Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title_short | Dopamine D2 receptor polymorphisms and susceptibility to alcohol dependence in Indian males: a preliminary study |
title_sort | dopamine d2 receptor polymorphisms and susceptibility to alcohol dependence in indian males: a preliminary study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2829542/ https://www.ncbi.nlm.nih.gov/pubmed/20146828 http://dx.doi.org/10.1186/1471-2350-11-24 |
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