Effect of CYP2C19 Polymorphisms on the Platelet Response to Clopidogrel and Influence on the Effect of High Versus Standard Dose Clopidogrel in Carotid Artery Stenting

被引:27
|
作者
Gonzalez, A. [1 ]
Moniche, F. [2 ]
Cayuela, A. [3 ]
Garcia-Lozano, J. R. [4 ]
Torrecillas, F. [4 ]
Escudero-Martinez, I. [2 ]
Gonzalez-Marcos, J. R. [2 ]
Mayol, A. [1 ]
Montaner, J. [5 ]
机构
[1] Virgen Rocio Univ Hosp, Dept Radiol, Intervent Neuroradiol, Ave Manuel Siurot S-N, Seville 41013, Spain
[2] Virgen Rocio Univ Hosp, Dept Neurol, Seville, Spain
[3] Hlth Management Area South Seville, Publ Hlth Unit, Seville, Spain
[4] Virgen Rocio Univ Hosp, Dept Immunol, IBiS, Seville, Spain
[5] Virgen Rocio Univ Hosp, Neurovasc Res Grp, Stroke Program, IBiS, Seville, Spain
关键词
CYP2C19; Clopidogrel; Carotid artery stenting; PERCUTANEOUS CORONARY INTERVENTION; GENETIC POLYMORPHISMS; RANDOMIZED-TRIAL; PRASUGREL; GENOTYPE; VARIABILITY; METABOLISM; REACTIVITY; OUTCOMES; THERAPY;
D O I
10.1016/j.ejvs.2015.09.020
中图分类号
R61 [外科手术学];
学科分类号
摘要
Objectives: Genetic background has been identified to be a major predictor of post-clopidogrel platelet inhibition in patients undergoing coronary stenting. However, there is a lack of data on clopidogrel response regarding genotype in patients undergoing carotid artery stenting (CAS). The influence of the most common allelic variants of CYP2C19 phenotypes and genotypes on response to baseline clopidogrel and on the pharmacodynamic effect of dose adjustment (high or standard dose of clopidogrel) in patients with high on-treatment reactivity after CAS was investigated. Methods: Platelet reactivity was assessed before and 30 days after carotid stenting using the VerifyNow P2Y12 assay to obtain P2Y12 reactivity unit (PRU) values. Results: A total of 209 patients (79.4% male, 44.1% currents smokers) were treated by CAS. Smokers improved responsiveness to clopidogrel (p = .034). With respect to CYP2C19 enzymatic function, 61 subjects (29.1%) were ultra-rapid metabolizers, 95 patients (45.5%) were extensive metabolizers, 51 (24.4%) were intermediate metabolizers, and two (0.96%) were poor metabolizers. Baseline PRU was significantly higher among intermediate poor metabolizers compared with ultra-rapid (p = .001) or extensive metabolizers (p = .005). At 30 days follow up, in non-responding patients with the intermediate poor metabolizer phenotype, the PRU value and inhibition percentage were significantly reduced with standard dose (p = .008; p = .0029) and high dose of clopidogrel (p = .00 0; p = .000). However, high dose clopidogrel did not achieve a more intense pharmacodynamic effect at 30 days (p = .994) compared with standard dose. Conclusions: In patients undergoing carotid stenting, those with the CYP2C19*2 allele had increased basal PRU values and in fact clopidogrel non-responders increased significantly among intermediate poor metabolizers. Although high dose and standard dose clopidogrel therapy was effective in lowering the 30 day PRU values in patients with high on-treatment reactivity who are intermediate poor metabolizers, the use of high dose clopidogrel did not result in statistically significantly greater reductions in reactivity compared with the standard dose. (C) 2015 European Society for Vascular Surgery. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:175 / 186
页数:12
相关论文
共 50 条
  • [21] Common polymorphisms of CYP2C19 and CYP2C9 affect the pharmacokinetic and pharmacodynamic response to clopidogrel but not prasugrel
    Brandt, J. T.
    Close, S. L.
    Iturria, S. J.
    Payne, C. D.
    Farid, N. A.
    Ernest, C. S., II
    Lachno, D. R.
    Salazar, D.
    Winters, K. J.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2007, 5 (12) : 2429 - 2436
  • [22] Evaluation of CYP2C19, P2Y12, and ABCB1 polymorphisms and phenotypic response to clopidogrel in healthy Indian adults
    Sridharan, Kannan
    Kataria, Rachna
    Tolani, Drishti
    Bendkhale, Shital
    Gogtay, Nithya J.
    Thatte, Urmila M.
    INDIAN JOURNAL OF PHARMACOLOGY, 2016, 48 (04) : 350 - 354
  • [23] Genetic polymorphisms of CYP2C19 influences the response to clopidogrel in ischemic heart disease patients in the South Indian Tamilian population
    Subraja, K.
    Dkhar, S. A.
    Priyadharsini, R.
    Ravindra, B. K.
    Shewade, D. G.
    Satheesh, S.
    Sridhar, M. G.
    Narayan, S. K.
    Adithan, C.
    EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 2013, 69 (03) : 415 - 422
  • [24] CYP2C19*17 increases clopidogrel-mediated platelet inhibition but does not alter the pharmacokinetics of the active metabolite of clopidogrel
    Pedersen, Rasmus Steen
    Nielsen, Flemming
    Stage, Tore Bjerregaard
    Vinholt, Pernille Just
    el Achwah, Alaa Bilal
    Damkier, Per
    Brosen, Kim
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2014, 41 (11) : 870 - 878
  • [25] Dosing Clopidogrel Based on CYP2C19 Genotype and the Effect on Platelet Reactivity in Patients With Stable Cardiovascular Disease
    Mega, Jessica L.
    Hochholzer, Willibald
    Frelinger, Andrew L., III
    Kluk, Michael J.
    Angiolillo, Dominick J.
    Kereiakes, Dean J.
    Isserman, Steven
    Rogers, William J.
    Ruff, Christian T.
    Contant, Charles
    Pencina, Michael J.
    Scirica, Benjamin M.
    Longtine, Janina A.
    Michelson, Alan D.
    Sabatine, Marc S.
    JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2011, 306 (20): : 2221 - 2228
  • [26] Isolated and interactive impact of common CYP2C19 genetic variants on the antiplatelet effect of chronic clopidogrel therapy
    Sibbing, D.
    Gebhard, D.
    Koch, W.
    Braun, S.
    Stegherr, J.
    Morath, T.
    Von Beckerath, N.
    Mehilli, J.
    Schoemig, A.
    Schuster, T.
    Kastrati, A.
    JOURNAL OF THROMBOSIS AND HAEMOSTASIS, 2010, 8 (08) : 1685 - 1693
  • [27] Effect of CYP2C19*2 and *3 on clinical outcome in ischemic stroke patients treated with clopidogrel
    Wang, Yingting
    Cai, Huan
    Zhou, Guoqing
    Zhang, Zhizhong
    Liu, Xinfeng
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2016, 369 : 216 - 219
  • [28] Effectiveness of Clopidogrel Dose Escalation to Normalize Active Metabolite Exposure and Antiplatelet Effects in CYP2C19 Poor Metabolizers
    Horenstein, Richard B.
    Madabushi, Rajnikanth
    Zineh, Issam
    Yerges-Armstrong, Laura M.
    Peer, Cody J.
    Schuck, Robert N.
    Figg, William Douglas
    Shuldiner, Alan R.
    Pacanowski, Michael A.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2014, 54 (08) : 865 - 873
  • [29] The influence of the CYP2C19*10 allele on clopidogrel activation and CYP2C19☆2 genotyping
    Langaee, Taimour Y.
    Zhu, Hao-Jie
    Wang, Xinwen
    El Rouby, Nihal
    Markowitz, John S.
    Goldstein, Joyce A.
    Johnson, Julie A.
    PHARMACOGENETICS AND GENOMICS, 2014, 24 (08) : 381 - 386
  • [30] Impact of the proton pump inhibitors and CYP2C19*2 polymorphism on platelet response to clopidogrel as assessed by four platelet function assays
    Tsantes, Argirios E.
    Ikonomidis, Ignatios
    Papadakis, Ioannis
    Bonovas, Stefanos
    Gialeraki, Argiri
    Kottaridi, Christine
    Kyriakou, Elias
    Kokori, Styliani
    Douramani, Panagiota
    Kopterides, Petros
    Karakitsos, Petros
    Lekakis, John
    Kapsimali, Violetta
    THROMBOSIS RESEARCH, 2013, 132 (02) : E105 - E111