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Published on: April 1, 2019
Association of ABCB1 Gene Polymorphisms and Clopidogrel Responsiveness in Iranian Patients undergoing Percutaneous
Soha Namazi1, Ebrahim Sahebi2, Negar Azarpira3
1Department of Clinical Pharmacy, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Insights
This study found no link between ABCB1 gene variations and clopidogrel response in Iranian patients after percutaneous coronary intervention (PCI). Genetic factors did not significantly impact antiplatelet effectiveness in this population.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Molecular Biology
Background:
- Clopidogrel is a key antiplatelet drug for preventing stent thrombosis after percutaneous coronary intervention (PCI).
- Individual variability in clopidogrel response can lead to suboptimal antiplatelet effects, increasing risks.
- The ABCB1 gene (ATP-Binding Cassette, Subfamily B, member 1) is implicated in drug transport and may influence clopidogrel efficacy.
Purpose of the Study:
- To investigate the association between ABCB1 gene polymorphism and clopidogrel responsiveness in Iranian patients undergoing PCI.
- To determine if genetic variations in ABCB1 affect platelet aggregation levels in response to clopidogrel.
- To explore the influence of demographic factors on clopidogrel responsiveness.
Main Methods:
- Sixty-seven Iranian patients undergoing PCI were enrolled.
- Blood samples were collected at baseline, 2 hours, 24 hours, and 30 days post-clopidogrel loading dose.
- Platelet aggregation was measured using light transmittance aggregometry (LTA) with adenosine diphosphate (ADP) stimulation.
- ABCB1 genotyping was performed using restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR).
Main Results:
- The allelic frequencies for ABCB1 genotypes were: wild type (20.9%), heterozygote (74.6%), and homozygote (4.5%).
- No statistically significant association was found between ABCB1 gene polymorphism and clopidogrel non-responsiveness.
- Demographic characteristics did not show significant differences among patients.
- Neither genetic nor demographic factors significantly affected platelet activity in response to clopidogrel.
Conclusions:
- ABCB1 gene polymorphism does not appear to be a significant predictor of clopidogrel responsiveness in the studied Iranian population after PCI.
- Genetic and demographic factors investigated did not significantly influence clopidogrel's antiplatelet effect in this cohort.
- Further research may be needed to identify other factors contributing to clopidogrel variability in this population.
Abstract:
Clopidogrel is an antiplatelet agent currently used for preventing stent thrombosis. Despite certain clinical benefits of clopidogrel in patients undergoing percutaneous coronary intervention (PCI), adequate antiplatelet effect has not been obtained in some patients. The present study was designed to investigate the potential association of ABCB1 (ATP-Binding Cassette, Subfamily B, member1) gene polymorphism, and clopidogrel responsiveness in Iranian patients after PCI. Sixty-seven patients were included in the study. Blood samples were taken from patients at baseline, 2 h after administration of 600-mg loading dose of clopidogrel, 24 h and 30 days after PCI. Platelet aggregation was measured by light transmittance aggregometry (LTA) with two levels of adenosine diphosphate (ADP) concentrations (5 and 20 µM). ABCB1 genotyping was performed by restriction fragment length polymorphism-polymerase chain reaction (RFLP-PCR). The allelic frequencies of wild type, heterozygote, and homozygote genotypes of ABCB1 were 20.9%, 74.6%, and 4.5%, respectively. There was no significant association between polymorphism of ABCB1 and clopidogrel non-responsiveness (P > 0.05) in various situations. No significant difference was observed for demographic characteristics. Genetic and demographic factors had no significant effect on the platelet activity of clopidogrel in an Iranian population.
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