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中国南方一个大型客家人群 CYP2C19 基因多态性分析。

Analysis of CYP2C19 Genetic Polymorphism in a Large Ethnic Hakka Population in Southern China.

机构信息

Center for Cardiovascular Diseases, Meizhou People's Hospital, Huangtang Hospital, Meizhou Hospital Affiliated to Sun Yat-sen University, Meizhou, Guangdong, China (mainland).

Center for Precision Medicine, Meizhou People's Hospital, Huangtang Hospital, Meizhou Hospital Affiliated to Sun Yat-sen University, Meizhou, Guangdong, China (mainland).

出版信息

Med Sci Monit. 2017 Dec 30;23:6186-6192. doi: 10.12659/msm.905337.

DOI:10.12659/msm.905337
PMID:29288619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5757864/
Abstract

BACKGROUND Cytochrome P450 (CYP) 2C19 is an enzyme involved in the bioactivation of various important therapeutic drugs, from pro-drugs to an active inhibitor of platelet action. Variants in the CYP2C19 gene influence the pharmacokinetics and clinical response to antiplatelet drugs such as clopidogrel; however, there is no available data about the genetic variation of CYP2C19 in the Hakka population in China. MATERIAL AND METHODS A total of 6686 unrelated participants (ages 17-98 years) of self-reported Hakka ancestry admitted at an inpatient department in a hospital in southern China were successfully genotyped by the gene chip platform. RESULTS The identified allele frequencies were CYP2C19*1 (64.33%), *2 (31.06%) and *3 (4.61%). The major prevalent genotype combinations were CYP2C19 *1/*1 (41.73%) and *1/*2 (39.65%). The distribution of CYP2C19 phenotypes was divided into extensive metabolizers (EM) (41.73%), intermediate metabolizers (IM) (45.21%), and poor metabolizers (PM) (13.06%). In the Hakka population, frequencies of the CYP2C19 *2 and *3 variants were observed to be close to those previously identified in Chinese and several other Asian populations. CONCLUSIONS Our study is the first to report on CYP2C19 polymorphisms in the Hakka population, and may help to optimize pharmacotherapy effectiveness by providing personalized medicine to this ethnic group in the near future.

摘要

背景

细胞色素 P450(CYP)2C19 是一种参与多种重要治疗药物生物激活的酶,从前体药物到血小板作用的活性抑制剂。CYP2C19 基因的变异影响抗血小板药物(如氯吡格雷)的药代动力学和临床反应;然而,目前在中国客家人群中尚无 CYP2C19 基因变异的可用数据。

材料与方法

共有 6686 名来自中国南方一家医院住院部的自我报告为客家人的无血缘关系参与者(年龄 17-98 岁)通过基因芯片平台成功进行了基因分型。

结果

鉴定出的等位基因频率为 CYP2C191(64.33%)、2(31.06%)和3(4.61%)。主要的常见基因型组合为 CYP2C191/1(41.73%)和1/2(39.65%)。CYP2C19 表型分布分为广泛代谢者(EM)(41.73%)、中间代谢者(IM)(45.21%)和弱代谢者(PM)(13.06%)。在客家人群中,CYP2C192 和*3 变体的频率与先前在中国和其他几个亚洲人群中确定的频率接近。

结论

我们的研究首次报道了客家人群 CYP2C19 的多态性,这可能有助于通过为该族群提供个性化药物在不久的将来优化药物治疗效果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c2/5757864/2ab1dcb38400/medscimonit-23-6186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c2/5757864/2ab1dcb38400/medscimonit-23-6186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51c2/5757864/2ab1dcb38400/medscimonit-23-6186-g001.jpg

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