Population and pedigree studies reveal a lack of association between the dopamine D2 receptor gene and alcoholism - PubMed (original) (raw)
. 1990 Dec 26;264(24):3156-60.
Affiliations
- PMID: 1979357
Population and pedigree studies reveal a lack of association between the dopamine D2 receptor gene and alcoholism
A M Bolos et al. JAMA. 1990.
Abstract
Using the dopamine D2 receptor clone lambda hD2G1, Blum et al recently found that the D2/Taq I allele (A1) was present in 69% of 35 deceased alcoholics but in only 20% of an equal number of controls. To assess this association further, we evaluated the D2/Taq I polymorphism and a single-strand conformation polymorphism detected by polymerase chain reaction and nondenaturing gel electrophoresis (PCR-SSCP) of the 3' noncoding region of the D2 receptor gene. We studied 40 unrelated white alcoholics, 127 racially matched controls, and two white pedigrees. The Schedule for Affective Disorders and Schizophrenia-Lifetime Version (SADS-L) clinical diagnostic interviews were rated blindly by two clinicians. The SADS-L interviews and other data were then used to ascertain diagnoses according to the Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition (DSM-III-R) criteria. Alcoholics were subtyped according to age of onset, severity, presence of antisocial personality, and family history. No significant differences in either D2/Taq I or PCR-SSCP allele frequencies were observed between alcoholics, subpopulations of alcoholics, or controls. The PCR-SSCP polymorphism provided independent information against linkage at the D2 receptor locus. Several recombinants between the D2/Taq I locus and alcoholism were observed in two white families with an alcoholic parent who possessed the A1 allele. This study does not support a widespread or consistent association between the D2 receptor gene and alcoholism.
Comment in
- The dopamine D2 receptor gene and alcoholism.
[No authors listed] [No authors listed] JAMA. 1991 May 22-29;265(20):2667-8. JAMA. 1991. PMID: 1827166 No abstract available.
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