NO ASSOCIATION BETWEEN AN ALLELE AT THE D2-DOPAMINE RECEPTOR GENE (DRD2) AND ALCOHOLISM

被引:220
作者
GELERNTER, J
OMALLEY, S
RISCH, N
KRANZLER, HR
KRYSTAL, J
MERIKANGAS, K
KENNEDY, JL
KIDD, KK
机构
[1] YALE UNIV,SCH MED,DEPT PSYCHIAT,NEW HAVEN,CT 06510
[2] YALE UNIV,SCH MED,DEPT EPIDEMIOL & PUBL HLTH,NEW HAVEN,CT 06510
[3] UNIV CONNECTICUT,SCH MED,FARMINGTON,CT 06032
[4] YALE UNIV,SCH MED,DEPT HUMAN GENET,NEW HAVEN,CT 06510
来源
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 1991年 / 266卷 / 13期
关键词
D O I
10.1001/jama.266.13.1801
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. - We attempted to replicate a positive allelic association between the A1 allele of DRD2 (the D2 dopamine receptor locus) and alcoholism that has been reported. Design. - We compared allele frequencies at the previously described Taq I restriction fragment length polymorphism system of DRD2 in alcoholics and random population controls. Subjects. - The alcoholic subjects were 44 unrelated white individuals, diagnosed by direct structured interview to have alcohol dependence (by the Diagnostic and Statistical Manual of Mental Disorders, Revised Third Edition, criteria). The subjects in our random population control group (N = 68) were also white. Results. - For the control group, allele frequencies at DRD2 were 0.20 (A1) and 0.80 (A2). For the alcoholic group overall, allele frequencies were 0.23 (A1) and 0.77 (A2). There were no significant differences in allele frequencies at the DRD2 locus between alcoholics and controls. The allele frequencies in both groups agreed closely with those observed in most previously described control populations. Subtyping the alcoholic group according to presence or absence of family history of alcoholism, presence or absence of antisocial personality disorder, age of onset, presence or absence of physical withdrawal symptoms, or recent alcohol consumption (as a measure of severity) did not in any case reveal significant differences in allele frequencies. Conclusion. - We were not able to replicate the results previously reported. We conclude that our data do not support an allelic association between the A1 allele at DRD2 and alcoholism.
引用
收藏
页码:1801 / 1807
页数:7
相关论文
共 42 条
[1]  
[Anonymous], EPIDEMIOLOGIC FIELD
[2]   ALLELIC ASSOCIATION OF HUMAN DOPAMINE-D2 RECEPTOR GENE IN ALCOHOLISM [J].
BLUM, K ;
NOBLE, EP ;
SHERIDAN, PJ ;
MONTGOMERY, A ;
RITCHIE, T ;
JAGADEESWARAN, P ;
NOGAMI, H ;
BRIGGS, AH ;
COHN, JB .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1990, 263 (15) :2055-2060
[3]  
BOLOS AM, 1990, JAMA-J AM MED ASSOC, V264, P3156
[4]  
Bowcock A M, 1987, Gene Geogr, V1, P47
[5]   DRIFT, ADMIXTURE, AND SELECTION IN HUMAN-EVOLUTION - A STUDY WITH DNA POLYMORPHISMS [J].
BOWCOCK, AM ;
KIDD, JR ;
MOUNTAIN, JL ;
HEBERT, JM ;
CAROTENUTO, L ;
KIDD, KK ;
CAVALLISFORZA, LL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (03) :839-843
[6]  
BREG WR, 1980, TRISOMY 21 DOWN SYND, P205
[7]   NEUROGENETIC ADAPTIVE-MECHANISMS IN ALCOHOLISM [J].
CLONINGER, CR .
SCIENCE, 1987, 236 (4800) :410-416
[8]  
COMINGS DE, 1990, AM J HUM GENET S, V47, P52
[9]  
CONNEALLY PM, 1991, ARCH GEN PSYCHIAT, V48, P664
[10]   INCREASED FREQUENCY OF HETEROZYGOTES FOR ALPHA-1 ANTITRYPSIN VARIANTS IN INDIVIDUALS WITH EITHER SEX-CHROMOSOME MOSAICISM OR TRISOMY-21 [J].
FINEMAN, RM ;
KIDD, KK ;
JOHNSON, AM ;
BREG, WR .
NATURE, 1976, 260 (5549) :320-321