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Updated: May 7, 2026

Microfluidics in Assessing Platelet Function
Published on: November 8, 2024
Impact of CYP2C19 polymorphism on platelet function tests and coagulation and inflammatory biomarkers in patients
Koichi Kaikita1, Takamichi Ono, Satomi Iwashita
1Department of Cardiovascular Medicine, Graduate School of Medical Sciences, Kumamoto University.
Insights
Platelet function tests can identify patients with CYP2C19 reduced-function gene variants who have a higher risk of cardiovascular events. These tests help monitor the effectiveness of dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI).
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Clinical Biochemistry
Background:
- Patients with reduced-function CYP2C19 alleles on dual antiplatelet therapy (DAPT) show impaired platelet inhibition and increased event risk.
- Understanding the impact of CYP2C19 variants is crucial for optimizing antiplatelet therapy in patients undergoing percutaneous coronary intervention (PCI).
Purpose of the Study:
- To investigate the influence of CYP2C19 gene variants on platelet function, coagulation, and inflammatory biomarkers in patients undergoing elective PCI.
- To assess the utility of platelet function tests in identifying carriers of CYP2C19 reduced-function alleles.
Main Methods:
- Prospective, observational, multicenter study of 104 Japanese patients undergoing elective PCI.
- Analysis of CYP2C19 genotype, platelet function (light transmittance aggregometry, VerifyNow P2Y12), coagulation and inflammatory biomarkers, and hs-TnT levels at multiple time points post-PCI.
Main Results:
- 65% of patients were carriers of the CYP2C19 reduced-function allele.
- Carriers exhibited significantly higher on-clopidogrel platelet aggregation (PA) and platelet reactivity index (PRI) compared to non-carriers.
- No significant differences were observed in coagulation, inflammatory biomarkers, or hs-TnT levels between carriers and non-carriers.
Conclusions:
- Platelet function tests, specifically on-clopidogrel PA and PRI, are effective in identifying carriers of CYP2C19 reduced-function gene variants.
- These tests are valuable for monitoring DAPT efficacy in patients undergoing elective PCI, unlike coagulation or inflammatory biomarkers.
Aim:
Carriers of the reduced-function CYP2C19 allele receiving dual antiplatelet therapy (DAPT) with aspirin and clopidogrel exhibit diminished platelet inhibition and an increased risk of events. The purpose of this study was to investigate the effects of CYP2C19 gene variants on platelet function tests and coagulation and inflammatory biomarkers in patients undergoing elective percutaneous coronary intervention (PCI).
Methods:
This prospective, observational, multicenter study enrolled 104 consecutive Japanese patients undergoing elective PCI. We examined the CYP2C19 genotype, platelet function tests, the levels of coagulation and inflammatory biomarkers and the serum levels of high-sensitivity troponin T (hs-TnT) before, immediately after and one, two and 28 days after PCI.
Results:
A total of 68 (65%) of the 104 enrolled patients were carriers of the CYP2C19 reducedfunction allele. On-clopidogrel platelet aggregation (PA), measured using light transmittance aggregometry and the VerifyNow(®) P2Y12 system, and the platelet reactivity index (PRI) were significantly higher at all time points in the carriers than in the noncarriers (p<0.05), whereas there were no differences in the levels of the coagulation and inflammatory biomarkers or serum hs-TnT. Simple and multiple logistic regression analyses identified on-clopidogrel PA and PRI as being significant predictors of carriers of the CYP2C19 reduced-function allele.
Conclusions:
The present study suggests that platelet function tests, but not coagulation, inflammatory or cardiac biomarkers, are useful for identifying carriers of CYP2C19 reduced-function gene variants and monitoring the efficacy of DAPT in patients undergoing elective PCI.
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