Journal
INTERNATIONAL HEART JOURNAL
Volume 57, Issue 5, Pages 586-592Publisher
INT HEART JOURNAL ASSOC
DOI: 10.1536/ihj.16-006
Keywords
Genetic polymorphism; CYP2C19*2 A allele frequency; P2Y(12) receptor; GPIIIa receptor gene; Clopidogrel efficacy; HTPR; MACEs recurrence
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Funding
- Key Research Project from Bureau of Education of Guangzhou [1201410730]
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To investigate the genotype frequencies of cytochrome P450, family2, subfamily C, polypeptide19 (CYP2C19); P2Y(12) receptor; and glycoprotein IIIa polymorphisms in patients with coronary heart disease and their impact on clopidogrel responsiveness and major adverse cardiac events (MACEs). A total of 146 coronary heart disease patients of Han ethnicity, on a clopidogrel regimen, were enrolled. Polymerase chain reaction and DNA sequencing were used to detect the genotype and allelic frequencies of CYP2C19 (*2,*3,*17), P2Y12 (C34T, G52T, T744C) and GPIIIa (T1565C) polymorphisms. Clinical and laboratory data were compared between the high on-treatment platelet reactivity (HTPR) versus normal groups. HTPR was identified in 35 (24%) patients. CYP2C19*2 (G681A) polymorphism was found to be significantly associated with HTPR (P < 0.05). A allele frequencies were significantly higher in the HTPR group versus the normal group (P < 0.05). On logistic regression analysis, CYP2C19*2 (G681A) polymorphism was found to be an independent risk factor associated with HTPR. No link could be established between genetic polymorphisms and recurrence of MACEs, or between HTPR and recurrence of MACEs. The genetic polymorphisms in CYP2C19*2 were closely associated with HTPR. The frequency of the A allele of CYP2C19*2 was significantly associated with HTPR, with A allele carriers being more likely to develop HTPR.
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