Drug metabolising enzyme polymorphisms in Middle- and Eastern-European Slavic populations.

Jaroslav A Hubacek
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引用次数: 15

Abstract

Inter-individual differences in genes for drug metabolising enzymes and drug transporters are important for understanding efficacy in drug therapy. These differences are important both for the timely estimation of the dosage that should be prescribed to a patient and for the detection of individuals who are prone to side effects from the drug at normal doses. This review summarises the literature concerning the gene variants within nine major drug metabolising enzymes and drug transporters (i.e., CYP1A2, CYP2A6, CYP2C9, CYP2C19, CYP2D6, CYP2E1, CYP3A4, CYP3A5, and MDR-1) in the Middle European region. Notably, published data are not extensive, and most studies were performed on relatively low numbers of individuals. No country has a complete coverage of all genes. Two variants (C2677T/A and C3435T) within the multidrug resistance-1 (MDR-1) gene and variants within the CYP2C9 gene were analysed within most Slavic populations. Nevertheless, even from this incomplete coverage (where unexpectedly high variability was at times seen both between and within populations), it could be extrapolated that the variants within the drug metabolising enzyme genes are present in roughly the same frequencies as in neighbouring countries.

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中欧和东欧斯拉夫人群的药物代谢酶多态性。
药物代谢酶和药物转运体基因的个体间差异对于了解药物治疗的疗效非常重要。这些差异对于及时估计应该给病人开的剂量和检测在正常剂量下容易产生药物副作用的个体都很重要。本文综述了有关中欧地区九种主要药物代谢酶和药物转运体(CYP1A2、CYP2A6、CYP2C9、CYP2C19、CYP2D6、CYP2E1、CYP3A4、CYP3A5和MDR-1)基因变异的文献。值得注意的是,已发表的数据并不广泛,大多数研究都是在相对较少的个体上进行的。没有一个国家能够完全覆盖所有基因。在大多数斯拉夫人群中分析了多药耐药-1 (MDR-1)基因的两个变异(C2677T/A和C3435T)和CYP2C9基因的变异。然而,即使从这种不完整的覆盖(在人群之间和人群内部有时会出现意外的高变异性),也可以推断出药物代谢酶基因内的变异与邻国的频率大致相同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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