Key result
CYP2C19 loss-of-function alleles (*2 or *3) were associated with higher platelet reactivity, whereas the *17 gain-of-function allele was associated with lower platelet reactivity.
Why the study?
Do CYP2C19 and PON1 polymorphisms affect clopidogrel bioactivation in Chinese, Malay, and Indian subjects?
Observational (n=389)
Do CYP2C19 and PON1 polymorphisms affect clopidogrel bioactivation in Chinese, Malay, and Indian subjects?
CYP2C19*2 and *3 polymorphisms significantly affect clopidogrel platelet reactivity in Asian populations, with varying allele frequencies among Chinese, Malay, and Indian subjects, suggesting ethnicity-specific genotyping strategies.
Answers are grounded in this paper and cite their sources.
Supports ethnicity-specific CYP2C19 considerations for clopidogrel in Asians; leaves open outcome impact of genotyping.
UNLABELLED: 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.
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Chan et al. (2012) conducted an observational in Patients on clopidogrel treatment (n=389). CYP2C19 and PON1 polymorphisms was evaluated on Platelet reactivity. CYP2C19 loss-of-function alleles (*2 or *3) were associated with higher platelet reactivity, whereas the *17 gain-of-function allele was associated with lower platelet reactivity.
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