Suppr超能文献

影响氯吡格雷治疗效果的药物基因组学变异在西班牙裔社区健康研究/拉丁裔研究队列中的流行率。

Prevalence of pharmacogenomic variants affecting the efficacy of clopidogrel therapy in the Hispanic Community Health Study/Study of Latinos cohort.

机构信息

Department of Pharmacy Practice, School of Pharmacy, University of Puerto Rico Medical Sciences Campus, San Juan, PR 00936, USA.

Department of Epidemiology & Population Health, Albert Einstein College of Medicine, Bronx, NY 10461, USA.

出版信息

Pharmacogenomics. 2019 Jan;20(2):75-83. doi: 10.2217/pgs-2018-0148. Epub 2018 Dec 6.

Abstract

PURPOSE

Although clopidogrel is the most widely used oral P2Y12 receptor antagonist, up to 10% of acute coronary syndrome patients treated with clopidogrel will experience a recurrent myocardial infarction and 2-3% will experience stent thrombosis within 1 year. The purpose of this research is to describe the prevalence of pharmacogene variants associated with clopidogrel responsiveness (CYP2C19, B4GALT2, ABCB1, PON1, CES1 and P2RY12) in Hispanic/Latino patients of diverse backgrounds.

METHODS

Minor allele frequencies of nine variants from participants of Hispanic Community Health Study/Study of Latinos were compared between subpopulations as well as to continental ancestry references using z-test for independent proportions.

RESULTS

MAFs for six out of nine variants differed between Caribbean and Mainland subpopulations (p < 0.05). Compared with European reference group, MAFs of ABCB1, CES1 and PON1 were higher in Hispanic Community Health Study/Study of Latinos, whereas B4GALT2 and CYP2C19*2 and *17 were lower.

CONCLUSION

Significant differences in the prevalence of most pharmacogenomic variants related to clopidogrel response provide a foundation to better inform ongoing and future clinical studies of clopidogrel pharmacogenetics in the US Hispanic/Latino populations.

摘要

目的

虽然氯吡格雷是最广泛使用的口服 P2Y12 受体拮抗剂,但接受氯吡格雷治疗的急性冠脉综合征患者中,多达 10%会再次发生心肌梗死,2-3%会在 1 年内发生支架血栓形成。本研究旨在描述与氯吡格雷反应性相关的药物基因变异(CYP2C19、B4GALT2、ABCB1、PON1、CES1 和 P2RY12)在不同背景的西班牙裔/拉丁裔患者中的流行情况。

方法

使用独立比例 z 检验,比较西班牙裔社区健康研究/拉丁裔研究参与者中九个变体的次要等位基因频率在亚群之间以及与大陆祖先参考之间的差异。

结果

九个变体中的六个在加勒比和大陆亚群之间的 MAF 不同(p<0.05)。与欧洲参考组相比,西班牙裔社区健康研究/拉丁裔研究中的 ABCB1、CES1 和 PON1 的 MAF 较高,而 B4GALT2 和 CYP2C19*2 和 *17 则较低。

结论

与氯吡格雷反应相关的大多数药物基因组变异的流行率存在显著差异,为更好地为美国西班牙裔/拉丁裔人群中氯吡格雷药物遗传学的正在进行和未来的临床研究提供了依据。

相似文献

引用本文的文献

本文引用的文献

3
A global reference for human genetic variation.人类遗传变异的全球参考。
Nature. 2015 Oct 1;526(7571):68-74. doi: 10.1038/nature15393.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验