CYP2C19 and PON1 polymorphisms regulating clopidogrel bioactivation in Chinese, Malay and Indian subjects

被引:4
|
作者
Chan, Mark Y. [1 ,2 ]
Tan, Karen [3 ]
Tan, Huay-Cheem [1 ]
Huan, Pei-Tee [3 ]
Li, Bei
Phua, Qian-Hui [2 ]
Lee, Hong-Kai [2 ,3 ]
Lee, Chi-Hang [1 ,2 ]
Low, Adrian [1 ,2 ]
Becker, Richard C. [4 ]
Ong, Wen-Chong [2 ]
Richards, Mark A. [2 ]
Salim, Agus [2 ]
Tai, E-Shyong [2 ,3 ]
Koay, Evelyn [2 ,3 ]
机构
[1] Natl Univ Heart Ctr, Singapore 119228, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore 117595, Singapore
[3] Natl Univ Hlth Syst, Singapore, Singapore
[4] Duke Clin Res Inst, Durham, NC USA
基金
英国医学研究理事会;
关键词
Asian clopidogrel; CYP2C19; metabolism; pharmacogenetics; PON1; CORONARY STENT PLACEMENT; OF-FUNCTION POLYMORPHISM; PLATELET REACTIVITY; GENETIC POLYMORPHISMS; MYOCARDIAL-INFARCTION; ANTIPLATELET THERAPY; CLINICAL-OUTCOMES; MAJOR DETERMINANT; PARAOXONASE-1; POPULATION;
D O I
10.2217/PGS.12.24
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Aim, materials & methods: We investigated the functional significance of CYP2C19*2, *3, *17 and PON1 Q192R SNPs in 89 consecutive Asian patients on clopidogrel treatment and the prevalence of functionally significant polymorphisms among 300 Chinese, Malays and Asian Indians. Results: Both CYP2C19 loss-of-function alleles (*2 or *3) were associated with higher platelet reactivity while the CYP2C19 gain-of-function allele (*17) had lower platelet reactivity. For PON1, the median PRI was not significantly different between the QQ, QR and RR groups. The allele frequencies of CYP2C19*2, CYP2C19*3 and CYP2C19*17 were 0.280, 0.065 and 0.010 (rare) for Chinese, 0.310, 0.050 and 0.025 for Malays, and 0.375, 0.010 (rare) and 0.165 for Indians, respectively. Conclusion: Our data suggest that genotyping studies to investigate clopidogrel response should include CYP2C19*2 and *3 but not *17 polymorphisms in Chinese, and CYP2C19*2 and *17 polymorphisms but not *3 in Indians. All three polymorphisms should preferably be genotyped in Malays.
引用
收藏
页码:533 / 542
页数:10
相关论文
共 50 条
  • [31] 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
  • [32] Influence of CYP2C19 Polymorphisms on the Pharmacokinetics of Omeprazole in Elderly Subjects
    Na, Joo Young
    Jeon, Inseung
    Yoon, Jangsoo
    Choi, Yewon
    Yoon, Seo Hyun
    Yu, Kyung-Sang
    Chung, Jae-Yong
    CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2021, 10 (12): : 1469 - 1477
  • [33] Influence of CYP2C19, ABCB1 and PON1 genotypes on the plasma concentrations of clopidogrel metabolite and platelet aggregation in patients after coronary stenting (PCI)
    Barbara Gawrońska-Szklarz
    Anna Czerkawska
    Urszula Adamiak-Giera
    Szymon Olędzki
    Mateusz Kurzawski
    Maria Jastrzębska
    Krzysztof Safranow
    Zdzisława Kornacewicz-Jach
    Pharmacological Reports, 2013, 65 (Suppl 1) : 46 - 46
  • [34] CYP2C19*2 polymorphism and clopidogrel resistance
    Joob, Beuy
    Wiwanitkit, Viroj
    ARCHIVOS DE CARDIOLOGIA DE MEXICO, 2020, 90 (04): : 505 - 505
  • [35] CYP2C19 polymorphism and antiplatelet effects of clopidogrel in Chinese stroke patients
    Yang Jie
    Zhao Hong-Dong
    Tan Jie
    Ding Yun-Long
    Zou Jian-Jun
    PHARMAZIE, 2013, 68 (03): : 183 - 186
  • [36] Both CYP2C19 and PON1 Q192R Genotypes Influence Platelet Response to Clopidogrel by Thrombelastography in Patients with Acute Coronary Syndrome
    Peng, Wenxing
    Shi, Xiujin
    Xu, Xiaoyu
    Lin, Yang
    CARDIOVASCULAR THERAPEUTICS, 2019, 2019
  • [37] Different Influences of CYP2C19 Gene Polymorphisms on Antiplatelet Effect of Clopidogrel and Ticlopidine
    Asai, Toru
    Ishiguro, Hisaaki
    Umemoto, Norio
    Morishima, Mikio
    Harata, Syuji
    Shimizu, Kiyokazu
    Murohara, Toyoaki
    Maeda, Akimitsu
    Ando, Hitoshi
    Fujimura, Akio
    CIRCULATION, 2010, 122 (21)
  • [38] CYP2C19 Polymorphisms and Antiplatelet Effects of Clopidogrel in Acute Ischemic Stroke in China
    Jia, Dong-mei
    Chen, Zhi-bin
    Zhang, Mei-juan
    Yang, Wen-jie
    Jin, Jia-li
    Xia, Yong-quan
    Zhang, Chun-lei
    Shao, Yuan
    Chen, Cong
    Xu, Yun
    STROKE, 2013, 44 (06) : 1717 - 1719
  • [39] Effects of combined CYP2C19 and 2D6 polymorphisms on the pharmacokinetics of fluoxetine in Chinese subjects
    Yin, Ophelia Q. P.
    Lam, Vincent
    Tomlinson, Brian
    Chow, Moses S. S.
    JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 46 (09): : 1093 - 1093
  • [40] 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