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Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males

BACKGROUND: Brain imaging studies and knock-out animal models have derived substantial abetment for dopamine receptor (DR) subtypes as potential candidates in susceptibility to addictive disorders, including alcohol dependence (AD). Various association studies that compared the frequencies of allele...

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Autores principales: Prasad, Pushplata, Ambekar, Atul, Vaswani, Meera
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853477/
https://www.ncbi.nlm.nih.gov/pubmed/24135011
http://dx.doi.org/10.1186/1756-0500-6-418
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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: Brain imaging studies and knock-out animal models have derived substantial abetment for dopamine receptor (DR) subtypes as potential candidates in susceptibility to addictive disorders, including alcohol dependence (AD). Various association studies that compared the frequencies of alleles of the dopamine D1, D2, D3 and D4 receptor genes between alcohol dependent and control subjects have produced suggestive results, though some of them are discordant in nature. In the absence of genetic data from Indian population, we evaluated genetic association of three polymorphisms namely rs4532 in DRD1, rs6280 in DRD3 and 120 bp duplication in 1.2 kb upstream region of DRD4 with AD. METHODS: A total of 90 cases (alcohol dependent males) and 122 age and ethnicity matched healthy male controls were recruited in the study by following DSM-IV criteria. Three polymorphisms, namely rs4532 in DRD1, rs6280 in DRD3 and 120 bp duplication in 1.2 kb upstream region of DRD4 were selected (based on minor allele frequency and available literature) for genotyping by PCR-RFLP/LP method. Allele and genotype frequencies of these genetic markers were compared using Pearson’s χ(2) test followed by risk assessment using odds ratio. Statistical analysis of clinical parameters such as AUDIT scores of case subjects was also performed. RESULTS: Statistically significant associations of polymorphisms in DRD1 and DRD4 with alcoholism were found. CONCLUSIONS: Our results underscore that genetic variations in dopamine receptors D1 and D4 may influence genetic predisposition to alcoholism. Unavailability of comparative data from Indian population and small sample size necessitate replication of results in an independent cohort.
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spelling pubmed-38534772013-12-07 Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males Prasad, Pushplata Ambekar, Atul Vaswani, Meera BMC Res Notes Research Article BACKGROUND: Brain imaging studies and knock-out animal models have derived substantial abetment for dopamine receptor (DR) subtypes as potential candidates in susceptibility to addictive disorders, including alcohol dependence (AD). Various association studies that compared the frequencies of alleles of the dopamine D1, D2, D3 and D4 receptor genes between alcohol dependent and control subjects have produced suggestive results, though some of them are discordant in nature. In the absence of genetic data from Indian population, we evaluated genetic association of three polymorphisms namely rs4532 in DRD1, rs6280 in DRD3 and 120 bp duplication in 1.2 kb upstream region of DRD4 with AD. METHODS: A total of 90 cases (alcohol dependent males) and 122 age and ethnicity matched healthy male controls were recruited in the study by following DSM-IV criteria. Three polymorphisms, namely rs4532 in DRD1, rs6280 in DRD3 and 120 bp duplication in 1.2 kb upstream region of DRD4 were selected (based on minor allele frequency and available literature) for genotyping by PCR-RFLP/LP method. Allele and genotype frequencies of these genetic markers were compared using Pearson’s χ(2) test followed by risk assessment using odds ratio. Statistical analysis of clinical parameters such as AUDIT scores of case subjects was also performed. RESULTS: Statistically significant associations of polymorphisms in DRD1 and DRD4 with alcoholism were found. CONCLUSIONS: Our results underscore that genetic variations in dopamine receptors D1 and D4 may influence genetic predisposition to alcoholism. Unavailability of comparative data from Indian population and small sample size necessitate replication of results in an independent cohort. BioMed Central 2013-10-17 /pmc/articles/PMC3853477/ /pubmed/24135011 http://dx.doi.org/10.1186/1756-0500-6-418 Text en Copyright © 2013 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
Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title_full Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title_fullStr Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title_full_unstemmed Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title_short Case–control association analysis of Dopamine receptor polymorphisms in alcohol dependence: a pilot study in Indian males
title_sort case–control association analysis of dopamine receptor polymorphisms in alcohol dependence: a pilot study in indian males
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3853477/
https://www.ncbi.nlm.nih.gov/pubmed/24135011
http://dx.doi.org/10.1186/1756-0500-6-418
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