Lee E J, Kalow W
Department of Pharmacology, National University of Singapore, Kent Ridge.
Clin Pharmacol Ther. 1993 Jul;54(1):28-33. doi: 10.1038/clpt.1993.105.
Thiopurine S-methyltransferase is a cytosolic enzyme that catalyzes the S-methylation of thiopurine drugs. Although a genetic polymorphism has been recognized for this enzyme in populations of Caucasian descent, there has been scanty information about this polymorphism among Asians. In this study, we measured the erythrocyte thiopurine methyltransferase activity in 119 healthy Chinese subjects by a radiochemical assay. Methyltransferase activity was lower than what might have been expected for a white population. A bimodal frequency distribution was obtained that allowed the identification of four individuals with relatively low methyltransferase activity who may be heterozygotes for thiopurine S-methyltransferase deficiency; if so, the frequency of the mutant allele would be lower in this Chinese population than that observed in a white population (chi 2, p < 0.02). No gender-based differences were observed.
硫嘌呤S-甲基转移酶是一种催化硫嘌呤类药物S-甲基化的胞质酶。虽然在白种人后裔群体中已认识到该酶存在基因多态性,但关于亚洲人群中这种多态性的信息却很少。在本研究中,我们采用放射化学分析法测定了119名健康中国受试者的红细胞硫嘌呤甲基转移酶活性。甲基转移酶活性低于白种人群体中预期的水平。获得了双峰频率分布,从而鉴定出4名甲基转移酶活性相对较低的个体,他们可能是硫嘌呤S-甲基转移酶缺乏症的杂合子;如果是这样,该中国人群体中突变等位基因的频率将低于白种人群体中观察到的频率(卡方检验,p < 0.02)。未观察到基于性别的差异。