Document Detail


Association analysis between polymorphisms in the dopamine D2 receptor (DRD2) and dopamine transporter (DAT1) genes with cocaine dependence.
MedLine Citation:
PMID:  20170711     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
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 TaqI 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.
Authors:
Falk W Lohoff; Paul J Bloch; Rachel Hodge; Aleksandra H Nall; Thomas N Ferraro; Kyle M Kampman; Charles A Dackis; Charles P O'Brien; Helen M Pettinati; David W Oslin
Publication Detail:
Type:  Journal Article; Research Support, N.I.H., Extramural; Research Support, U.S. Gov't, Non-P.H.S.     Date:  2010-02-17
Journal Detail:
Title:  Neuroscience letters     Volume:  473     ISSN:  1872-7972     ISO Abbreviation:  Neurosci. Lett.     Publication Date:  2010 Apr 
Date Detail:
Created Date:  2010-03-24     Completed Date:  2010-04-08     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7600130     Medline TA:  Neurosci Lett     Country:  Ireland    
Other Details:
Languages:  eng     Pagination:  87-91     Citation Subset:  IM    
Affiliation:
Center for Neurobiology and Behavior, Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia, PA, USA. lohoff@mail.med.upenn.edu <lohoff@mail.med.upenn.edu>
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MeSH Terms
Descriptor/Qualifier:
African Americans
Cocaine-Related Disorders / genetics*
Dopamine Plasma Membrane Transport Proteins / genetics*
Female
Genetic Association Studies
Genetic Predisposition to Disease
Humans
Male
Polymorphism, Single Nucleotide
Receptors, Dopamine D2 / genetics*
Tandem Repeat Sequences
Grant Support
ID/Acronym/Agency:
K08MH080372/MH/NIMH NIH HHS; MH059565/MH/NIMH NIH HHS; MH059571/MH/NIMH NIH HHS; MH059588/MH/NIMH NIH HHS; MH060879/MH/NIMH NIH HHS; MH061675/MH/NIMH NIH HHS; MH067257/MH/NIMH NIH HHS; MH59566/MH/NIMH NIH HHS; MH59586/MH/NIMH NIH HHS; MH59587/MH/NIMH NIH HHS; P50-12756//PHS HHS; P60-051186//PHS HHS
Chemical
Reg. No./Substance:
0/Dopamine Plasma Membrane Transport Proteins; 0/Receptors, Dopamine D2; 0/SLC6A3 protein, human

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