Gelernter J, O'Malley S, Risch N, Kranzler H R, Krystal J, Merikangas K, Kennedy J L, Kidd K K
Department of Psychiatry, Yale University School of Medicine, New Haven, Conn.
JAMA. 1991 Oct 2;266(13):1801-7.
--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.
--We compared allele frequencies at the previously described Taq I restriction fragment length polymorphism system of DRD2 in alcoholics and random population controls.
--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.
--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.
--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.
我们试图复制已报道的DRD2(D2多巴胺受体基因座)的A1等位基因与酒精中毒之间的正向等位基因关联。
我们比较了酒精成瘾者和随机人群对照组中DRD2先前描述的Taq I限制性片段长度多态性系统的等位基因频率。
酒精成瘾者为44名无亲缘关系的白人个体,通过直接结构化访谈诊断为酒精依赖(根据《精神疾病诊断与统计手册》第三版修订版标准)。我们随机人群对照组的研究对象(N = 68)也为白人。
对照组中,DRD2的等位基因频率为0.20(A1)和0.80(A2)。总体酒精成瘾组的等位基因频率为0.23(A1)和0.77(A2)。酒精成瘾者和对照组在DRD2基因座的等位基因频率没有显著差异。两组的等位基因频率与大多数先前描述的对照人群中观察到的频率非常一致。根据是否有酒精中毒家族史、是否有反社会人格障碍、发病年龄、是否有身体戒断症状或近期饮酒量(作为严重程度的衡量指标)对酒精成瘾组进行亚型分析,在任何情况下均未发现等位基因频率有显著差异。
我们未能复制先前报道的结果。我们得出结论,我们的数据不支持DRD2基因座的A1等位基因与酒精中毒之间的等位基因关联。