Genetic Polymorphism of CYP2C19 in Pakistani Population

S. Riaz, Sadia Muhammad Din, Muhammad Usman Tareen, F. Tariq, Yusra Latif, S. Siddiqi, Aneesa Sultan, A. Mansoor
{"title":"Genetic Polymorphism of CYP2C19 in Pakistani Population","authors":"S. Riaz, Sadia Muhammad Din, Muhammad Usman Tareen, F. Tariq, Yusra Latif, S. Siddiqi, Aneesa Sultan, A. Mansoor","doi":"10.22037/IJPR.2019.1100644","DOIUrl":null,"url":null,"abstract":"CYP2C19 polymorphism is associated with pretreatment drug response prediction, metabolism, and disposition. Pakistan consists of a population comprising of various ethnic groups residing in different regions of the country each claiming diverse ethnic origins. The identification of CYP450 genotypic composition of these populations is therefore necessary to avoid adverse drug reactions in these individuals. The main objective of the study was to investigate the prevalence of CYP2C19*2 and CYP2C19*17 alleles in these ethnic groups. The study was conducted on one thousand and twenty-eight (n = 1028) healthy volunteers from nine ethnic groups of Pakistan namely Brusho (n = 28), Hazara (n = 102), Kalash (n = 64), Pathan (n = 170), Punjabi (n = 218), Saraiki (n = 59), Brahui (n = 118), Parsi (n = 90), and Sindhi (n = 179). DNA was extracted from leukocytes and analyzed by allele specific amplification polymerase chain reaction (ASA-PCR). Multi allelic polymorphism of CYP2C19 led to four distinct phenotypes identified as extensive metabolizer (EM), poor metabolizer (PM), intermediate metabolizer (IM), and ultra-rapid metabolizer (UM). Over all, the percentage of predicted poor metabolizer allele was 29.0% compared to UM allele (23.70%). Among the studied groups, Saraiki and Brahui showed highest percentage of PM allele (40%, 36%) whereas Parsi and Hazara had highest percentage of UM allele (37% and 30% respectively). In conclusion, the high allele frequency of PM (CYP2C19*2 and *17) in Pakistani population led to the recommendation of a pre-treatment test to monitor drug response and dosage (personalized medicine) to avoid post-treatment adverse drug reactions.","PeriodicalId":416671,"journal":{"name":"Iranian Journal of Pharmaceutical Research : IJPR","volume":"53 211 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2019-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Iranian Journal of Pharmaceutical Research : IJPR","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.22037/IJPR.2019.1100644","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

Abstract

CYP2C19 polymorphism is associated with pretreatment drug response prediction, metabolism, and disposition. Pakistan consists of a population comprising of various ethnic groups residing in different regions of the country each claiming diverse ethnic origins. The identification of CYP450 genotypic composition of these populations is therefore necessary to avoid adverse drug reactions in these individuals. The main objective of the study was to investigate the prevalence of CYP2C19*2 and CYP2C19*17 alleles in these ethnic groups. The study was conducted on one thousand and twenty-eight (n = 1028) healthy volunteers from nine ethnic groups of Pakistan namely Brusho (n = 28), Hazara (n = 102), Kalash (n = 64), Pathan (n = 170), Punjabi (n = 218), Saraiki (n = 59), Brahui (n = 118), Parsi (n = 90), and Sindhi (n = 179). DNA was extracted from leukocytes and analyzed by allele specific amplification polymerase chain reaction (ASA-PCR). Multi allelic polymorphism of CYP2C19 led to four distinct phenotypes identified as extensive metabolizer (EM), poor metabolizer (PM), intermediate metabolizer (IM), and ultra-rapid metabolizer (UM). Over all, the percentage of predicted poor metabolizer allele was 29.0% compared to UM allele (23.70%). Among the studied groups, Saraiki and Brahui showed highest percentage of PM allele (40%, 36%) whereas Parsi and Hazara had highest percentage of UM allele (37% and 30% respectively). In conclusion, the high allele frequency of PM (CYP2C19*2 and *17) in Pakistani population led to the recommendation of a pre-treatment test to monitor drug response and dosage (personalized medicine) to avoid post-treatment adverse drug reactions.
巴基斯坦人群CYP2C19基因多态性研究
CYP2C19多态性与预处理药物反应预测、代谢和处置相关。巴基斯坦的人口由居住在该国不同地区的各种民族组成,每个民族都声称自己有不同的民族血统。因此,确定这些人群的CYP450基因型组成对于避免这些个体的药物不良反应是必要的。本研究的主要目的是调查这些民族中CYP2C19*2和CYP2C19*17等位基因的患病率。该研究对来自巴基斯坦九个民族的1228名(n = 1028)健康志愿者进行了研究,分别是Brusho (n = 28)、Hazara (n = 102)、Kalash (n = 64)、Pathan (n = 170)、Punjabi (n = 218)、Saraiki (n = 59)、Brahui (n = 118)、Parsi (n = 90)和Sindhi (n = 179)。从白细胞中提取DNA,采用等位基因特异性扩增聚合酶链反应(ASA-PCR)进行分析。CYP2C19的多等位基因多态性导致了广泛代谢型(EM)、差代谢型(PM)、中间代谢型(IM)和超快速代谢型(UM) 4种不同的表型。总体而言,预测代谢不良等位基因的比例为29.0%,而UM等位基因的比例为23.70%。在研究群体中,萨拉基族和布拉赫族的PM等位基因比例最高,分别为40%和36%,而帕西族和哈扎拉族的UM等位基因比例最高,分别为37%和30%。综上所述,巴基斯坦人群中PM (CYP2C19*2和*17)等位基因频率较高,建议进行治疗前检测,监测药物反应和剂量(个体化用药),避免治疗后药物不良反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信