首页> 外文期刊>British Journal of Clinical Pharmacology >Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes.
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Frequencies of CYP2D6 mutant alleles in a normal Japanese population and metabolic activity of dextromethorphan O-demethylation in different CYP2D6 genotypes.

机译:正常日本人群中CYP2D6突变等位基因的频率以及不同CYP2D6基因型的右美沙芬O-去甲基化的代谢活性。

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AIMS: To determine the frequencies of 11 CYP2D6 mutant alleles (CYP2D6*2, *3, *4, *5, *8, *10, *11, *12, *14, *17 and *18), and their relation to the metabolic capacity of CYP2D6 in Japanese subjects. METHODS: One hundred and sixty-two unrelated healthy Japanese subjects were genotyped with the polymerase chain reaction amplification method and 35 subjects were phenotyped with dextromethorphan. RESULTS: The frequencies of CYP2D6*2,*5, *10 and *14 were 12.9, 6.2, 38.6 and 2.2% in our Japanese subjects, respectively. CYP2D6*3, *4, *8, *11, *12, *17 and *18 were not detected. The mean log metabolic ratio of dextromethorphan in subjects with genotypes predicting intermediate metabolizers was significantly greater than that of heterozygotes for functional and defective alleles. CONCLUSIONS: CYP2D6*5 and CYP2D6*14 are the major defective alleles found in Japanese subjects. In addition, CYP2D6*10 may play a more important role than previously thought for the treatment of Japanese patients with drugs metabolized by CYP2D6.
机译:目的:确定11个CYP2D6突变等位基因(CYP2D6 * 2,* 3,* 4,* 5,* 8,* 10,* 11,* 12,* 14,* 17和* 18)的频率及其关系CYP2D6在日本受试者中的代谢能力下降。方法:采用聚合酶链反应扩增方法对162名健康日本人进行基因分型,对35名受试者进行右美沙芬表型分析。结果:在我们的日本受试者中,CYP2D6 * 2,* 5,* 10和* 14的频率分别为12.9%,6.2%,38.6%和2.2%。未检测到CYP2D6 * 3,* 4,* 8,* 11,* 12,* 17和* 18。具有预测中间代谢者基因型的受试者中右美沙芬的平均对数代谢率显着高于功能和缺陷等位基因的杂合子。结论:CYP2D6 * 5和CYP2D6 * 14是在日本受试者中发现的主要缺陷等位基因。另外,CYP2D6 * 10可能比以前认为的更重要的作用对于日本患者中被CYP2D6代谢的药物的治疗。

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