Noble E P, Paredes A
Alcohol Research Center, University of California, Los Angeles 90024.
Recent Dev Alcohol. 1993;11:345-62.
Following our initial observation that the A1 allele of the D2 dopamine receptor (DRD2) gene was associated with alcoholism, a number of studies, both in the United States and abroad, have attempted to replicate and extend this finding in different Caucasian populations. In nine independent studies containing a total of 491 heterogeneous alcoholics (less severe and severe) and 495 heterogeneous controls (assessed and unassessed for alcoholism), the prevalence of the A1 allele was 43.0% in the former group compared with 25.7% in the latter groups (odds ratio = 2.18, p < 10(-6). The prevalence of the A1 allele increased to 56.3% in a more homogeneous sample of 158 severe alcoholics (odds ratio = 3.32, p < 10(-8)). Moreover, the B1 allele of the DRD2 gene was also found to be significantly associated with severe alcoholism. Additional data are accruing which also implicate the DRD2 A1 and B1 alleles in substance use disorders other than alcoholism. If further studies continue to support the results currently available, they would indicate that the DRD2 gene is the most prominent single gene determinant of susceptibility to severe substance abuse. However, the larger role still appears to be played by a combination of environmental factors and as yet unidentified genes.
在我们最初观察到D2多巴胺受体(DRD2)基因的A1等位基因与酒精中毒有关之后,美国和国外的一些研究试图在不同的白种人群体中重复并扩展这一发现。在9项独立研究中,共有491名异质性酗酒者(轻度和重度)和495名异质性对照者(对酒精中毒进行了评估和未评估),前一组中A1等位基因的患病率为43.0%,而后一组为25.7%(优势比=2.18,p<10^(-6))。在158名重度酗酒者组成的更同质样本中,A1等位基因的患病率增至56.3%(优势比=3.32,p<10^(-8))。此外,还发现DRD2基因的B1等位基因与重度酒精中毒显著相关。更多的数据正在积累,这些数据也表明DRD2的A1和B1等位基因与除酒精中毒之外的物质使用障碍有关。如果进一步的研究继续支持目前已有的结果,将表明DRD2基因是严重药物滥用易感性最突出的单基因决定因素。然而,更大的作用似乎仍然由环境因素和尚未确定的基因共同发挥。