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Genetic variability of CYP3A4 in a heterogeneous Brazilian population from Maranh?o

机译:CYP3A4在Maranh?o异种巴西种群中的遗传变异

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Inter-individual variability in drug metabolism may result in adverse drug responses. Pharmacogenetic studies have shown that polymorphisms in drug metabolizing enzymes may contribute to this variability. Among these enzymes, CYP3A4 is responsible for metabolizing over 50% of the clinically used drugs. The Brazilian population is composed of people with Native American, European, and African ancestries, and is therefore considered as one of the most intermixed populations in the world. A thorough knowledge of the genetic frequencies of CYP3A4 allelic variants is useful for the establishment of better pharmacological therapies; therefore, the aim of this study was to describe the polymorphic frequencies for CYP3A4 -392AG (rs2740574) in a sample population from Maranh?o, Brazil. Our results showed that 75.1, 21.9, and 3.0% of the individuals expressed the -392AA, -392AG, and -392GG genotypes, respectively. The -392A and -392G alleles were observed in 86.1 and 13.9% of the population, respectively. Our results reiterate the need for a better understanding of the variations in the genotype and allele frequencies of CYP3A4 -392AG polymorphisms in various Brazilian regions, in order to elucidate the variability in drug response.
机译:药物代谢的个体差异可能导致药物不良反应。药物遗传学研究表明,药物代谢酶中的多态性可能导致这种变异。在这些酶中,CYP3A4负责代谢超过50%的临床使用药物。巴西人口由具有美洲原住民,欧洲和非洲祖先的人组成,因此被认为是世界上最混杂的人口之一。全面了解CYP3A4等位基因变异的遗传频率可用于建立更好的药理学治疗方法;因此,本研究的目的是描述一个来自巴西Maranh?o的样本人群中CYP3A4 -392A> G(rs2740574)的多态性频率。我们的结果表明,分别有75.1、21.9和3.0%的个体表达-392AA,-392AG和-392GG基因型。在人口的86.1和13.9%中分别观察到-392A和-392G等位基因。我们的结果重申,需要更好地了解各个巴西地区CYP3A4 -392A> G多态性的基因型和等位基因频率的变化,以便阐明药物反应的变异性。

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