巴西人群药物代谢酶的药物遗传学研究。

Alvaro Cerda, Mario Hiroyuki Hirata, Rosario Dominguez Crespo Hirata
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引用次数: 7

摘要

I期和II期药物代谢酶(DMEs)在内源性和外源性化合物(包括目前药物治疗中使用的药物)的生物转化中发挥重要作用。此外,DMEs的遗传变异性导致药物和代谢物暴露、药物反应和药物不良反应风险的重要个体差异。我们回顾了药物遗传学/药物基因组学(PGx)研究,这些研究评估了CYPs基因(主要是CYP1、CYP2和CYP3基因家族)和II期基因(TPMT、NAT2、GSTs和UGTs)多态性对巴西队列治疗反应的影响。巴西人的种族混合导致了一个具有独特遗传特征的人口,其中祖先信息标记在种族群体中不断变化。因此,一些PGx生物标志物在巴西人中的分布不同,来自明确族群的PGx数据不适用于巴西人群。为了确定遗传多样性对具有复杂遗传混合物组成的人群对临床相关药物的治疗反应的影响,需要巴西研究中针对I期和II期DMEs的PGx数据。本文对这些研究及其影响进行了讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pharmacogenetics of drug metabolizing enzymes in Brazilian populations.

Phase I and II drug metabolizing enzymes (DMEs) play an important role in biotransformation of endogenous and exogenous compounds including drugs currently used in pharmacoterapy. Moreover, the genetic variability of DMEs causes important interindividual differences in drug and metabolite exposure, drug response, and risk of adverse drug reactions. We reviewed pharmacogenetics/pharmacogenomics (PGx) studies that evaluated the influence of polymorphisms in the CYPs genes - mainly CYP1, CYP2 and CYP3 gene families - and in the phase II genes - TPMT, NAT2, GSTs and UGTs - on therapeutic response in Brazilian cohorts. Ethnic admixture of Brazilians resulted in a population characterized by a unique genetic profile, in which ancestry informative markers change continuously among ethnic groups. Therefore, some of the PGx biomarkers have a different distribution among Brazilians and PGx data from well-defined ethnic groups are not applicable to Brazilian populations. PGx data focused on phase I and phase II DMEs from Brazilian studies are needed in order to establish the influence of the genetic diversity on therapeutic response to clinically relevant drugs in a population with a composition from a complex genetic admixture. These studies and their impact are discussed in this review.

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