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Updated: Oct 16, 2025

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
The correlation between platelet responsiveness to clopidogrel and CYP2C19 polymorphism in patients with peripheral
N M El-Khodary1, A M El-Behery, N A El-Askary
1Clinical Pharmacy and Pharmacy Practice Department, Faculty of Pharmacy, Damanhour University, Damanhour, Egypt. nohamahmoud_55@hotmail.com.
Insights
Clopidogrel resistance, affecting 22% of Egyptians studied, is linked to the CYP2C19*2 gene, obesity, and diabetes. These factors are crucial for predicting patient response to clopidogrel therapy.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Clinical Chemistry
Background:
- High platelet reactivity post-clopidogrel treatment is observed in patients undergoing vascular interventions.
- Understanding genetic and clinical predictors of clopidogrel response is vital for optimizing treatment.
Purpose of the Study:
- To determine the frequency of the CYP2C19*2 genetic polymorphism in an Egyptian population.
- To assess the contribution of CYP2C19*2 and other clinical factors to clopidogrel resistance.
Main Methods:
- Platelet aggregation analysis was performed on 50 patients receiving clopidogrel.
- Single-nucleotide polymorphism (SNP) genotyping for CYP2C19*2 was conducted using quantitative real-time polymerase chain reaction (QRT-PCR).
Main Results:
- Clopidogrel resistance was found in 22% of the Egyptian cohort.
- CYP2C19*2 genotype, high body mass index (BMI), diabetes, high fasting blood glucose (FBG), and high glycosylated hemoglobin (HbA1c) were associated with resistance.
- Multivariate analysis identified CYP2C19*2 genotype and high BMI as the strongest predictors of clopidogrel resistance.
Conclusions:
- Clopidogrel resistance in peripheral vascular disease patients is associated with the CYP2C19*2 allele, obesity, and diabetes.
- These factors warrant consideration before initiating clopidogrel therapy to personalize treatment strategies.
Objective:
Several patients undergoing endovascular intervention and bypass surgery present with high platelet reactivity following clopidogrel treatment. We aimed to determine the frequency of the genetic polymorphism of CYP2C19*2 and the contribution of this polymorphism along with other clinical parameters to clopidogrel response in an Egyptian population.
Patients And Methods:
A total of 50 patients receiving clopidogrel at a maintenance dose of 75 mg daily post vascular intervention from January 1, 2019, to May 30, 2020, were enrolled in this study. Clopidogrel resistance was determined through platelet aggregation analysis using Chrono-Log® platelet aggregometer. Single-nucleotide polymorphism (SNP) genotyping was performed using quantitative real-time polymerase chain reaction (QRT-PCR).
Results:
The incidence of clopidogrel resistance among this Egyptian population is about 22%. Univariate analysis demonstrated that CYP2C19*2 genotype (p = 0.001), high body mass index (BMI; p = 0.025), diabetes (p = 0.037), high fasting blood glucose (FBG) level (p = 0.037), and high glycosylated hemoglobin (HbA1c) level (p = 0.004) were significantly associated with clopidogrel resistance. Multivariate analysis showed that CYP2C19*2 genotype (odds ratio (OR), 927.71; 95% confidence interval (CI), 1.915-449496.2; p = 0.030) and high BMI (OR, 1.789; 95% CI, 1.044-3.064; p = 0.034) were the most powerful predictors of clopidogrel resistance.
Conclusions:
Clopidogrel resistance in patients with peripheral vascular disease is associated with the presence of CYP2C19*2 allele, obesity, and diabetes; these factors should be considered prior to clopidogrel administration.
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