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Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Relationship between clopidogrel-related polymorphisms and variable platelet reactivity at 1 year: A cohort study
Xiaodong Wang1, Yan Lai2, Yu Luo1
1Department of Cardiology, Shanghai East Hospital, Tongji University School of Medicine, Shanghai 200120, China.
Clopidogrel gene variations affect platelet reactivity and major adverse cardiovascular events in Chinese patients. Specific polymorphisms like CYP2C19*2 and P2Y12 increase risks, while CYP2C19*17 offers protection, without impacting cardiac death rates.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Genetics
Background:
- Clopidogrel is a widely used antiplatelet medication.
- Genetic variations can influence clopidogrel's efficacy and patient outcomes.
- Understanding these genetic effects is crucial for personalized treatment.
Purpose of the Study:
- To investigate the impact of clopidogrel-related gene polymorphisms on platelet reactivity.
- To assess the relationship between these polymorphisms and clinical outcomes in Chinese Han patients undergoing percutaneous coronary intervention.
- To identify specific genetic markers associated with treatment response and adverse events.
Main Methods:
- A cohort of 336 patients receiving percutaneous coronary intervention was studied over 1 year.
- DNA genotyping was performed to assess various alleles, including CYP2C19*2, CYP2C19*3, CYP2C19*17, ABCB1, ITGB3, CYP2C9*3, CYP2B6*9, and P2Y12.
- Platelet reactivity was measured using the VerifyNow assay.
Main Results:
- Clinical endpoints were associated with prior heart disease, stroke, and diabetes.
- High on-treatment platelet reactivity (HTPR) was linked to older age, male gender, hypertension, and chronic renal failure.
- CYP2C19*2 and P2Y12 polymorphisms correlated with increased endpoints and HTPR, while CYP2C19*17 showed reduced platelet reactivity and fewer endpoints.
Conclusions:
- Clopidogrel-related gene polymorphisms significantly influence platelet reactivity and major adverse cardiovascular events in Han Chinese patients.
- The CYP2C19*2 and P2Y12 variants are associated with increased risk, whereas CYP2C19*17 is associated with improved outcomes.
- These genetic factors affect cardiovascular events but do not appear to influence cardiac death.
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