Association analysis between polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes with cocaine dependence

被引:23
作者
Lohoff, Falk W. [1 ]
Bloch, Paul J.
Hodge, Rachel
Nall, Aleksandra H.
Ferraro, Thomas N.
Kampman, Kyle M. [2 ]
Dackis, Charles A. [2 ]
O'Brien, Charles P. [2 ]
Pettinati, Helen M. [2 ]
Oslin, David W. [2 ]
机构
[1] Univ Penn, Sch Med, Dept Psychiat, Ctr Neurobiol & Behav,Translat Res Labs, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Psychiat, Treatment Res Ctr, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
Addiction; Association study; Cocaine; Dopamine receptor; Dopamine transporter; Genetics; Substance abuse; DEFICIT HYPERACTIVITY DISORDER; POPULATION-BASED SAMPLE; NUCLEUS-ACCUMBENS; AFRICAN-AMERICANS; VENTRAL PALLIDUM; LINKAGE DISEQUILIBRIUM; ADMIXED POPULATIONS; ALCOHOL-DEPENDENCE; ADMIXTURE DYNAMICS; HEROIN DEPENDENCE;
D O I
10.1016/j.neulet.2010.02.021
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Genetic research on cocaine dependence (CD) may help clarify our understanding of the disorder as well as provide novel insights for effective treatment. Since dopamine neurotransmission has been shown to be involved in drug reward, related genes are plausible candidates for susceptibility to CD. The dopamine receptor D(2) (DRD2) protein and dopamine transporter (DAT1) protein play regulatory roles in dopamine neurotransmission. The Taql A single-nucleotide polymorphism (SNP) in the DRD2 gene and the 3' variable number tandem repeat (VNTR) polymorphism in the DAT1, gene have been implicated in psychiatric disorders and drug addictions. In this study, we hypothesize that these polymorphisms contribute to increased risk for CD. Cocaine-dependent individuals (n = 347) and unaffected controls (n = 257) of African descent were genotyped for the polymorphisms in the DRD2 and DAT1 genes. We observed no statistically significant differences or trends in allele or genotype frequencies between cases and controls for either of the tested polymorphisms. Our study suggests that there is no association between the DRD2 and DAT1 polymorphisms and CD. However, additional studies using larger sample sizes and clinically homogenous populations are necessary before confidently excluding these variants as contributing genetic risk factors for CD. (C) 2010 Published by Elsevier Ireland Ltd.
引用
收藏
页码:87 / 91
页数:5
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