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Updated: May 25, 2026

A Method to Study the C924T Polymorphism of the Thromboxane A2 Receptor Gene
Published on: April 1, 2019
Pharmacogenetics of clopidogrel: comparison between a standard and a rapid genetic testing
Claudia Saracini1, Anna Vestrini, Silvia Galora
1Department of Medical and Surgical Critical Care, University of Florence-Atherothrombotic Diseases Center, AOU Careggi, Florence, Italy. claudiasaracini@hotmail.it
Insights
The Verigene system accurately identifies clopidogrel poor metabolizer status, offering faster results and lower overall costs compared to TaqMan. This genetic testing aids in selecting optimal antiplatelet therapy for cardiovascular patients.
Area of Science:
- Pharmacogenomics
- Cardiovascular Medicine
- Clinical Chemistry
Background:
- CYP2C19 variant alleles influence clopidogrel response and cardiovascular event risk.
- Platelet function and CYP2C19 genetic testing can identify high-risk patients needing alternative antiplatelet strategies.
- Test accuracy, cost, and result availability are critical for clinical implementation of genetic testing.
Purpose of the Study:
- To compare the Verigene and TaqMan platforms for CYP2C19 genotyping in acute coronary syndrome patients.
- To evaluate the turnaround time and cost-effectiveness of the Verigene system versus TaqMan.
- To assess the clinical utility of rapid CYP2C19 genotyping for antiplatelet therapy decisions.
Main Methods:
- Genotyping of CYP2C19*2,*3,*4,*5, and *17 polymorphisms in 100 acute coronary syndrome patients.
- Comparison of results obtained from the Verigene system and the TaqMan system.
- Analysis of turnaround time and cost, including reagent and staff involvement.
Main Results:
- 100% concordance in genotyping results between Verigene and TaqMan for all five polymorphisms.
- Verigene system demonstrated a significantly shorter turnaround time compared to TaqMan.
- Despite lower reagent costs for TaqMan, Verigene offered a lower overall cost due to reduced manual staff involvement.
Conclusions:
- The Verigene system shows excellent performance for evaluating clopidogrel poor metabolizer status.
- Verigene provides genetic information within a clinically relevant timeframe (206 minutes) for therapeutic decisions.
- The Verigene system is a cost-effective and rapid method for CYP2C19 genotyping in clinical practice.
Aims:
CYP2C19 variant alleles are independent predictors of clopidogrel response variability and occurrence of major adverse cardiovascular events in high-risk vascular patients on clopidogrel therapy. Increasing evidence suggests a combination of platelet function testing with CYP2C19 genetic testing may be more effective in identifying high-risk individuals for alternative antiplatelet therapeutic strategies. A crucial point in evaluating the use of these polymorphisms in clinical practice, besides test accuracy, is the cost of the genetic test and rapid availability of the results. One hundred acute coronary syndrome patients were genotyped for CYP2C19*2,*3,*4,*5, and *17 polymorphisms with two platforms: Verigene(®) and the TaqMan(®) system.
Results:
Genotyping results obtained by the classical TaqMan approach and the rapid Verigene approach showed a 100% concordance for all the five polymorphisms investigated. The Verigene system had shorter turnaround time with respect to TaqMan. The cost of reagents for TaqMan genotyping was lower than that for the Verigene system, but the effective manual staff involvement and the relative cost resulted in higher cost for TaqMan than for Verigene.
Conclusions:
The Verigene system demonstrated good performance in terms of turnaround time and cost for the evaluation of the clopidogrel poor metabolizer status, giving genetic information in suitable time (206 min) for a therapeutic strategy decision.
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