墨西哥药物遗传学研究现状与展望。

Patricia Cuautle-Rodríguez, Adrián Llerena, Juan Molina-Guarneros
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引用次数: 16

摘要

药品费用占该国卫生支出的24%,有13 000种注册药物正在开处方。糖尿病是该国死亡的主要原因,目前85%以上的糖尿病患者正在接受药物治疗。因此,了解墨西哥人群药物代谢的个体间差异的重要性是显而易见的。本文的目的是提供墨西哥药物遗传研究的现状,重点是药物代谢酶,以及为墨西哥人群开发一种表型鸡尾酒的可能性。到目前为止,已经发表了21篇关于墨西哥人群样本(梅斯蒂索人和美洲印第安人)的药物遗传学研究。这些研究通过细胞色素的表型分型和/或基因分型报道了个体间的差异:CYP2D6、2C19、2C9、2E1和II期酶UGT和NAT2。一些具有重要临床意义的细胞色素尚未在墨西哥人群中表型化。开发一种适合它们的鸡尾酒可能会对以更低的价格和更短的时间获得更多关于药物反应变异性的知识做出重大贡献。有一些经过验证的表型鸡尾酒具有一些实际优势,它们是有价值的、安全的、廉价的药物代谢表征工具,只需要一次实验就可以提供几种细胞色素活性的信息。
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Present status and perspective of pharmacogenetics in Mexico.

Drug costs account for up to 24% of the country's health expenditure and there are 13,000 registered drugs being prescribed. Diabetes is the main cause of death in the country, with over 85% of diabetic patients currently under drug treatment. The importance of knowing interindividual variability in drug metabolism on Mexican populations is thus evident. The purpose of this article is to provide an overlook of the current situation of pharmacogenetic research in Mexico, focusing on drug-metabolizing enzymes, and the possibility of developing a phenotyping cocktail for Mexican populations. So far, 21 pharmacogenetic studies on Mexican population samples (Mestizos and Amerindian) have been published. These have reported interindividual variability through phenotyping and/or genotyping cytochromes: CYP2D6, 2C19, 2C9, 2E1, and phase II enzymes UGT and NAT2. Some cytochromes with important clinical implications have not yet been phenotyped in Mexican populations. The development of a cocktail adapted to them could be a significant contribution to a larger knowledge on drug response variability at a lower price and shorter time. There are validated phenotyping cocktails that present several practical advantages, being valuable, safe, and inexpensive tools in drug metabolism characterization, which require only a single experiment to provide information on several cytochrome activities.

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