Abstract
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.
Highlights
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
Gene sequence variations of the platelet P2Y12 receptor are associated with coronary artery disease / U
Common variation in the platelet receptor P2RY12 gene is associated with residual on-clopidogrel platelet reactivity in patients undergoing elective percutaneous coronary interventions / G
Summary
Примечание. # – достоверные отличия (p < 0,05) между мужчинами и женщинами внутри группы. [39] не выявлено взаимосвязи между полиморфизмом T1565C гена ITGB3 со значениями MPV как у здоровых лиц, так и у пациентов с острым коронарным синдромом. Частота встречаемости указанных генотипов среди пациентов со стабильной стенокардией составила 23,9 % для гена CYP2C19 (полиморфный локус G681A), 40,2 % для гена P2RY12 (полиморфный локус H1/H2), 31,5 % для гена ITGB3 (полиморфный локус T1565C), среди практически здоровых лиц ‒ 18,3; 46,2 и 37,6 % соответственно. Выявлены ассоциации между носительством аллеля 681A гена CYP2C19 и гаплотипа Н2 гена P2RY12 с высокой остаточной реактивностью тромбоцитов на фоне терапии клопидогрелем у пациентов с ССН. Обнаружена ассоциация между носительством гаплотипа Н2 полиморфизма Н1/Н2 гена P2RY12 с высокими значениями MPV тромбоцитов и более высокой частотой встречаемости крупных тромбоцитов (P-LCR) у пациентов с ССН.
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