The genetic basis of antiplatelet and anticoagulant therapy: A pharmacogenetic review of newer antiplatelets (clopidogrel, prasugrel and ticagrelor) and anticoagulants (dabigatran, rivaroxaban, apixaban and edoxaban)

被引:31
作者
O'connor, Cormac T. [1 ]
Kiernan, Thomas J. [1 ]
Yan, Bryan P. [2 ]
机构
[1] Univ Hosp Limerick, Cardiol Dept, Limerick, Ireland
[2] Chinese Univ Hong Kong, Prince Wales Hosp, Dept Med & Therapeut, Div Cardiol, Hong Kong, Hong Kong, Peoples R China
关键词
Pharmacogenetics; pharmacogenomics; antiplatelet; anticoagulant; DOAC; CORONARY-ARTERY-DISEASE; GENOME-WIDE ASSOCIATION; IMPLEMENTATION CONSORTIUM GUIDELINES; ACCELERATED PLATELET INHIBITION; ADVERSE CLINICAL-OUTCOMES; FACTOR XA INHIBITOR; CYP2C19; GENOTYPE; CARDIOVASCULAR OUTCOMES; MYOCARDIAL-INFARCTION; ASPIRIN RESISTANCE;
D O I
10.1080/17425255.2017.1338274
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Introduction: 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.
引用
收藏
页码:725 / 739
页数:15
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