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
  • [31] Optimizing clopidogrel dose response: a new clinical algorithm comprising CYP2C19 pharmacogenetics and drug interactions
    Saab, Yolande B.
    Zeenny, Rony
    Ramadan, Wijdan H.
    THERAPEUTICS AND CLINICAL RISK MANAGEMENT, 2015, 11 : 1421 - 1427
  • [32] Effects of CYP2C19 Genetic Polymorphisms on the Pharmacokinetic and Pharmacodynamic Properties of Clopidogrel and Its Active Metabolite in Healthy Chinese Subjects
    Song, Bai-Li
    Wan, Meng
    Tang, Dan
    Sun, Chao
    Zhu, Yu-Bing
    Linda, Nyame
    Fan, Hong-Wei
    Zou, Jian-Jun
    CLINICAL THERAPEUTICS, 2018, 40 (07) : 1170 - 1178
  • [33] Influence of CYP2C19 Phenotype on the Effect of Clopidogrel in Patients Undergoing a Percutaneous Neurointervention Procedure
    Saiz-Rodriguez, Miriam
    Romero-Palacian, Daniel
    Villalobos-Vilda, Carlos
    Luis Caniego, Jose
    Belmonte, Carmen
    Koller, Dora
    Barcena, Eduardo
    Talegon, Maria
    Abad-Santos, Francisco
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2019, 105 (03) : 661 - 671
  • [34] The effect of CYP2C19*17 on platelet response and clinical outcomes in patients taking clopidogrel: a meta-analysis
    Fang, H.
    THERAPEUTIC DRUG MONITORING, 2011, 33 (04) : 479 - 479
  • [35] EFFECT OF CLOPIDOGREL OR TICAGRELOR ON PCI PLATELET INHIBITION RATE IN PATIENTS WITH DIFFERENT CYP2C19 ALLELES
    Jiang, Zhen
    Li, Sai
    Li, Yinjun
    Jin, Xiaoyu
    Bao, Bo
    Wang, Yang
    ACTA MEDICA MEDITERRANEA, 2020, 36 (01): : 299 - 303
  • [36] Differential Impacts of CYP2C19 Gene Polymorphisms on the Antiplatelet Effects of Clopidogrel and Ticlopidine
    Maeda, A.
    Ando, H.
    Asai, T.
    Ishiguro, H.
    Umemoto, N.
    Ohta, M.
    Morishima, M.
    Sumida, A.
    Kobayashi, T.
    Hosohata, K.
    Ushijima, K.
    Fujimura, A.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2011, 89 (02) : 229 - 233
  • [37] High frequency of CYP2C19*2 carriers in PCI-treated patients switched over from clopidogrel to prasugrel based on platelet function monitoring
    Bernlochner, Isabell
    Mayer, Katharina
    Morath, Tanja
    Braun, Siegmund
    Schulz, Stefanie
    Schoemig, Albert
    Koch, Werner
    Kastrati, Adnan
    Sibbing, Dirk
    PLATELETS, 2013, 24 (06) : 500 - 502
  • [38] Inhibition of ADP-induced platelet aggregation by clopidogrel is related to CYP2C19 genetic polymorphisms
    Chen, Bi-Lian
    Zhang, Wei
    Li, Qing
    Li, Ya-Lin
    He, Yi-Jing
    Fan, Lan
    Wang, Lian-Sheng
    Liu, Zhao-Qian
    Zhou, Hong-Hao
    CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2008, 35 (08) : 904 - 908
  • [39] CYP2C19 and Clopidogrel Response: More Than Validation in the Real World
    Shuldiner, A. R.
    CLINICAL PHARMACOLOGY & THERAPEUTICS, 2012, 91 (02) : 170 - 171
  • [40] CYP2C19*2 and other genetic variants affecting platelet response to clopidogrel in patients undergoing percutaneous coronary intervention
    Kassimis, George
    Davlouros, Periklis
    Xanthopoulou, Ioanna
    Stavrou, Eleana F.
    Athanassiadou, Aglaia
    Alexopoulos, Dimitrios
    THROMBOSIS RESEARCH, 2012, 129 (04) : 441 - 446