The influence of omeprazole on platelet inhibition of clopidogrel in various CYP2C19 mutant alleles.
The influence of omeprazole on platelet inhibition of clopidogrel in various CYP2C19 mutant alleles.
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DOI:
10.1089/gtmb.2012.0119
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发表时间:
2012-10
影响因子:
1.4
通讯作者:
Qian Liu;Da-sheng Dang;Yu-feng Chen;Ming Yan;Guo-bing Shi;Qingchun Zhao
中科院分区:
文献类型:
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作者:
Qian Liu;Da-sheng Dang;Yu-feng Chen;Ming Yan;Guo-bing Shi;Qingchun Zhao
Currently, concerns of clopidogrel and proton pump inhibitors (especially omeprazole) interaction are raised, because they are both metabolized by CYP2C19. What is more, omeprazole can also inhibit the activity of CYP2C19. The study was to compare the influence of omeprazole on platelet inhibition of clopidogrel in various CYP2C19 mutant alleles. One hundred forty-two consecutive patients undergoing elective coronary stenting received aspirin and clopidogrel, and were randomized to omeprazole or the placebo. Enrolled patients were analyzed for adenosine diphosphate-induced platelet aggregation (ADP-Ag), and CYP2C19*2 and CYP2C19*3 were identified by polymerase chain reaction-restriction fragment length polymorphism. Of the patients included, 47 (33.1%) belonged to homozygous extensive metabolizers (homEMs) (CYP2C19*1/*1), 70 (49.3%) belonged to heterozygous extensive metabolizers (hetEMs) (*1/*2 or *1/*3), and 25 (17.6%) belonged to poor metabolizers (PMs) (*2/*3 or *2/*2). ADP-Ag had a significant difference among the three genotypic groups (p0.05). In conclusion, concomitant therapy with omeprazole appears to reduce the antiplatelet effect of clopidogrel most significantly in homEMs of CYP2C19.