O'connor Cormac T, Kiernan Thomas J, Yan Bryan P
a Cardiology Department , University Hospital Limerick , Limerick , Ireland.
b Division of Cardiology, Department of Medicine and Therapeutics , The Chinese University of Hong Kong, Prince of Wales Hospital , Hong Kong SAR , China.
Expert Opin Drug Metab Toxicol. 2017 Jul;13(7):725-739. doi: 10.1080/17425255.2017.1338274. Epub 2017 Jun 13.
The study of pharmacogenomics presents the possibility of individualised optimisation of drug therapy tailored to each patients' unique physiological traits. Both antiplatelet and anticoagulant drugs play a key role in the management of cardiovascular disease. Despite their importance, there is a substantial volume of literature to suggest marked person-to-person variability in their effect. Areas covered: This article reviews the data available for the genetic cause for this inter-patient variability of antiplatelet and anticoagulant drugs. The genetic basis for traditional antiplatelets (i.e. aspirin) is compared with the newly available antiplatelet medicines (clopidogrel, prasugrel and ticagrelor). Similarly, the pharmacogenetics of warfarin is compared with the newer direct oral anticoagulants (DOACs) in detail. Expert Opinion: We identify strengths and weaknesses in the research thus far; including shortcomings in trial design and a review of newer analytical techniques. The direction of this research and its real-world implications are discussed.
药物基因组学研究为根据每个患者独特的生理特征进行个体化药物治疗优化提供了可能性。抗血小板药物和抗凝药物在心血管疾病管理中都起着关键作用。尽管它们很重要,但大量文献表明其效果存在显著的个体差异。涵盖领域:本文回顾了有关抗血小板和抗凝药物患者间差异的遗传原因的现有数据。将传统抗血小板药物(即阿司匹林)的遗传基础与新出现的抗血小板药物(氯吡格雷、普拉格雷和替格瑞洛)进行了比较。同样,对华法林的药物遗传学与更新的直接口服抗凝剂(DOACs)进行了详细比较。专家意见:我们确定了迄今为止研究中的优势和劣势;包括试验设计的缺点以及对更新分析技术的综述。讨论了该研究的方向及其实际意义。