Thomasson H R, Edenberg H J, Crabb D W, Mai X L, Jerome R E, Li T K, Wang S P, Lin Y T, Lu R B, Yin S J
Department of Medicine, Indiana University School of Medicine, Indianapolis 46202-5121.
Am J Hum Genet. 1991 Apr;48(4):677-81.
The liver enzymes alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH), which are responsible for the oxidative metabolism of ethanol, are polymorphic in humans. An allele encoding an inactive form of the mitochondrial ALDH2 is known to reduce the likelihood of alcoholism in Japanese. We hypothesized that the polymorphisms of both ALDH and ADH modify the predisposition to development of alcoholism. Therefore, we determined the genotypes of the ADH2, ADH3, and ALDH2 loci of alcoholic and nonalcoholic Chinese men living in Taiwan, using leukocyte DNA amplified by the PCR and allele-specific oligonucleotides. The alcoholics had significantly lower frequencies of the ADH22, ADH31, and ALDH2*2 alleles than did the nonalcoholics, suggesting that genetic variation in both ADH and ALDH, by modulating the rate of metabolism of ethanol and acetaldehyde, influences drinking behavior and the risk of developing alcoholism.
负责乙醇氧化代谢的肝脏酶——乙醇脱氢酶(ADH)和乙醛脱氢酶(ALDH)在人类中具有多态性。已知一种编码线粒体ALDH2无活性形式的等位基因会降低日本人患酒精中毒的可能性。我们推测,ALDH和ADH的多态性都会改变酒精中毒易感性。因此,我们利用聚合酶链反应(PCR)扩增的白细胞DNA和等位基因特异性寡核苷酸,测定了居住在台湾的酗酒和不酗酒中国男性的ADH2、ADH3和ALDH2基因座的基因型。酗酒者中ADH22、ADH31和ALDH2*2等位基因的频率显著低于不酗酒者,这表明ADH和ALDH的基因变异通过调节乙醇和乙醛的代谢速率,影响饮酒行为和患酒精中毒的风险。