Nakamura K, Goto F, Ray W A, McAllister C B, Jacqz E, Wilkinson G R, Branch R A
Clin Pharmacol Ther. 1985 Oct;38(4):402-8. doi: 10.1038/clpt.1985.194.
Interethnic differences in debrisoquin and mephenytoin hydroxylation have been compared between normal white (n = 183) and Japanese (n = 100) subjects with the 8-hour urinary metabolic ratio of debrisoquin and the urinary S/R enantiomeric ratio of mephenytoin to identify extensive (EM) and poor (PM) metabolizers. In white subjects the frequency of PMs was 8.7% and 2.7% for debrisoquin and mephenytoin, respectively. In contrast, in Japanese subjects no PMs of debrisoquin were identified, while the incidence of PMs of mephenytoin was 18%. These substantial differences (P less than 0.001) in polymorphic distributions of oxidative drug metabolizing ability have implications for interethnic efficacy and toxicity of drugs and other xenobiotics that are metabolized by the involved cytochrome P-450 isozymes.
已比较了正常白种人(n = 183)和日本人(n = 100)之间异喹胍和甲妥英羟基化的种族差异,通过异喹胍8小时尿代谢率和甲妥英尿中S/R对映体比例来识别快代谢者(EM)和慢代谢者(PM)。在白种人中,异喹胍和甲妥英的慢代谢者频率分别为8.7%和2.7%。相比之下,在日本受试者中未发现异喹胍慢代谢者,而甲妥英慢代谢者的发生率为18%。氧化药物代谢能力多态性分布的这些显著差异(P小于0.001)对由相关细胞色素P - 450同工酶代谢的药物和其他外源性物质的种族间疗效和毒性具有影响。