Key result
Carriage of the CYP2C19 681A allele and the P2RY12 H2 haplotype were significantly associated with high residual platelet reactivity in patients with stable angina receiving clopidogrel.
Why the study?
The study aimed to assess the distribution of CYP2C19 G681A, P2RY12 H1/H2, and ITGB3 T1565C polymorphic variants and their effect on platelet activity and clopidogrel efficacy in patients with stable stenocardia in the Grodno region.
Do CYP2C19, P2RY12, and ITGB3 genetic polymorphisms affect platelet activity and clopidogrel efficacy in patients with stable stenocardia?
Observational (n=185)
No
Do CYP2C19, P2RY12, and ITGB3 genetic polymorphisms affect platelet activity and clopidogrel efficacy in patients with stable stenocardia?
Polymorphisms in the CYP2C19 and P2RY12 genes are associated with high residual platelet reactivity in patients with stable stenocardia receiving clopidogrel.
Does not support routine genotyping; leaves open whether CYP2C19/P2RY12 variants predict outcomes in stable stenocardia.
The aim of the study was to assess the distribution of polymorphic variants G681A of the CYP2C19 gene, H1/H2 of the P2RY12 gene, and T1565C of the ITGB3 gene and to study their effect on the platelet activity and clopidogrel efficacy in patients with stable stenocardia living in the Grodno region. The study included 92 patients with stable stenocardia, 89 of them underwent elective percutaneous coronary intervention (PCI), and 93 practically healthy people. The survey data (general clinical, aggregometry, general blood count and platelet indices, and polymerase chain reaction genotyping) were analyzed using the STATISTICA 10.0 software.A high prevalence of carriage of genotypes associated with possible variability in response to clopidogrel therapy was revealed both among patients with stable stenocardia and among practically healthy individuals in the Grodno region. The frequency of occurrence of studying genotypes among patients with stable stanocardia was 23.9 % for the CYP2C19 gene (polymorphic locus G681A), 40.2 % for the P2RY12 gene (polymorphic locus H1/H2), and 31.5 % for the gene ITGB3 (polymorphic locus T1565C). For the group of practically healthy individuals, the distribution of these genotypes was 18.3; 46.2; 37.6 %, respectively. Associations were revealed between the carriage of the 681A allele of the CYP2C19 gene and the H2 haplotype of the P2RY12 gene with high residual platelet reactivity during clopidogrel therapy in patients with stable stenocardia. An association was found between the carriage of the H2 haplotype of the H1/H2 polymorphism of the P2RY12 gene with high platelet MPV values and a higher frequency of large platelets (P-LCR) in patients with stable stenocardia.
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Pronko et al. (2021) conducted an observational in Stable stenocardia (n=185). CYP2C19 681A allele vs. CYP2C19 GG genotype was evaluated on High residual platelet reactivity (ADP-test > 50 U) (p=<0.05). Carriage of the CYP2C19 681A allele and the P2RY12 H2 haplotype were significantly associated with high residual platelet reactivity in patients with stable angina receiving clopidogrel.
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