Using Pharmacogenetic Testing to Tailor Warfarin Therapy: The Singapore Experience and What the Future Holds.

IF 3.2 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
European Cardiology Review Pub Date : 2020-06-29 eCollection Date: 2020-02-01 DOI:10.15420/ecr.2019.12
Grace Shu-Wen Chang, Doreen Su-Yin Tan
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引用次数: 1

Abstract

Genetic polymorphisms significantly affect individual responses to warfarin, contributing to unpredictability and challenges in managing anticoagulation. Although numerous studies have demonstrated that pharmacogenetic testing improves anticoagulation-related outcomes in the Caucasian population, its effect in the Asian population has not been well studied. This article discusses controversies surrounding tailoring warfarin therapy using pharmacogenetic testing and its role in clinical practice, with a focus on the Asian context. Using the Singapore experience as an example, the authors propose how pharmacogenetic testing can be a means to reduce dose titrations in select patient populations, and how it may be positioned as an enabler to reduce healthcare resources needed for anticoagulation management.

使用药物遗传学测试来定制华法林治疗:新加坡的经验和未来。
遗传多态性显著影响个体对华法林的反应,有助于抗凝治疗的不可预测性和挑战。尽管大量研究表明,药物遗传学检测可以改善高加索人群的抗凝相关结果,但其在亚洲人群中的效果尚未得到很好的研究。本文讨论了围绕使用药物遗传学检测定制华法林治疗及其在临床实践中的作用的争议,重点是亚洲背景。以新加坡的经验为例,作者提出了药物遗传学检测如何在特定患者群体中成为减少剂量滴定的一种手段,以及如何将其定位为减少抗凝治疗所需的医疗资源的推动者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Cardiology Review
European Cardiology Review CARDIAC & CARDIOVASCULAR SYSTEMS-
CiteScore
5.40
自引率
0.00%
发文量
23
审稿时长
12 weeks
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