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巴基斯坦人群中常见药物代谢酶和 ABC 转运蛋白的遗传变异的影响。

Implications of genetic variation of common Drug Metabolizing Enzymes and ABC Transporters among the Pakistani Population.

机构信息

Jinnah Medical and Dental College, Sohail University, 22-23 Shaheed-e-Millat Road, Karachi, 75400, Pakistan.

Institute of Experimental and Clinical Pharmacology, Christian Albrechts University Kiel, Hospitalstr. 4, Kiel, 24105, Germany.

出版信息

Sci Rep. 2019 May 13;9(1):7323. doi: 10.1038/s41598-019-43736-z.

Abstract

Genetic polymorphism of drug metabolizing enzymes and transporters may influence drug response. The frequency varies substantially between ethnicities thus having implications on appropriate selection and dosage of various drugs in different populations. The distribution of genetic polymorphisms in healthy Pakistanis has so far not been described. In this study, 155 healthy adults (98 females) were included from all districts of Karachi. DNA was extracted from saliva and genotyped for relevant SNVs in CYP1A1, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP3A4 and CYP3A5 as well as ALDH3A1, GSTA1, ABCB1 and ABCC2. About 64% of the participants were born to parents who were unrelated to each other. There was generally a higher prevalence (p < 0.05) of variant alleles of CYP450 1A2, 2B6, 2C19, 3A5, ALDH3A1, GSTM1 as well as ABCB1 and ABCC2 in this study cohort than in other ethnicities reported in the HapMap database. In contrast, the prevalence of variant alleles was lower in GSTA1. Therefore, in the Pakistani population sample from Karachi a significantly different prevalence of variant drug metabolizing enzymes and ABC transporters was observed as compared to other ethnicities, which could have putative clinical consequences on drug efficacy and safety.

摘要

药物代谢酶和转运体的遗传多态性可能影响药物反应。由于种族之间存在很大差异,因此这对不同人群中各种药物的适当选择和剂量有影响。目前尚未描述健康巴基斯坦人的遗传多态性分布。在这项研究中,从卡拉奇的所有地区招募了 155 名健康成年人(98 名女性)。从唾液中提取 DNA,并对 CYP1A1、CYP2B6、CYP2C9、CYP2C19、CYP2D6、CYP3A4 和 CYP3A5 以及 ALDH3A1、GSTA1、ABCB1 和 ABCC2 中的相关 SNV 进行基因分型。大约 64%的参与者的父母彼此没有血缘关系。与 HapMap 数据库中报告的其他种族相比,本研究队列中 CYP450 1A2、2B6、2C19、3A5、ALDH3A1、GSTM1 以及 ABCB1 和 ABCC2 的变体等位基因的普遍患病率(p<0.05)较高。相比之下,GSTA1 中的变体等位基因的患病率较低。因此,与其他种族相比,在卡拉奇的巴基斯坦人群样本中观察到药物代谢酶和 ABC 转运体的变体明显不同的患病率,这可能对药物疗效和安全性产生潜在的临床影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0722/6514210/6628edca4c7d/41598_2019_43736_Fig1_HTML.jpg

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