Key result
An extraction-free real-time PCR method with melting curve analysis accurately identified CYP2C19 *2/3/17 genotypes in 93 clinical blood samples within 1 hour, confirmed by Sanger sequencing.
Why the study?
Detecting CYP2C19 gene polymorphisms classifies patients into metabolic types to guide clopidogrel therapy, but rapid, low-cost detection methods are needed.
Does an extraction-free real-time PCR method accurately detect CYP2C19 *2/3/17 polymorphisms compared to Sanger sequencing?
Does an extraction-free real-time PCR method accurately detect CYP2C19 *2/3/17 polymorphisms compared to Sanger sequencing?
An extraction-free real-time PCR method provides rapid and accurate detection of CYP2C19 polymorphisms, offering a practical tool for guiding clopidogrel therapy in resource-limited settings.
Supports rapid CYP2C19 genotyping in labs; leaves open prospective outcome trials before guiding clopidogrel therapy.
Drug‐metabolizing enzymes play an important role in the metabolism of drugs in vivo. Their activity is an important factor affecting the rate of drug metabolism, which directly determines the intensity and persistence of drug action. Patients taking medication can be divided into different metabolic types through detection of CYP2C19 drug‐metabolizing enzyme gene polymorphisms, which can then be used for medication guidance for clopidogrel. Here, we describe a detection method based on real‐time polymerase chain reaction (PCR). This method uses multicolor melting curve analysis to accurately identify different mutation sites and genotypes of CYP2C19 * 2, CYP2C19 * 3, and CYP2C19 * 17. The detection limit of plasmid samples was 1 copies μL−1; that of genomic samples was 0.1 ng μL−1. The system can detect nine types of CYP2C19 * 2/3/17 at three sites in one tube, quickly achieving detection within 1 h. Combined with the sample release agent, sample extraction was completed in 5 s, achieving rapid diagnosis without extraction for timely diagnosis and treatment. Furthermore, the system is not limited to blood samples and can also be applied to oropharyngeal and saliva samples, increasing sampling diversity and convenience. When using clinical blood samples (n = 93), the detection system we established was able to quickly and accurately identify different genotypes, and the accuracy and effectiveness of the detection were confirmed by Sanger sequencing. Due to its accuracy, rapidity, simple operation, and low cost, detection technology based on real‐time polymerase amplification combined with melting curve analysis is expected to become a powerful tool for detecting and guiding clopidogrel use in countries with limited resources.
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Guo et al. (2023) studied CYP2C19 polymorphisms (n=93). Real-time PCR with multicolor melting curve analysis vs. Sanger sequencing was evaluated on Identification of different genotypes of CYP2C19 *2, *3, and *17. An extraction-free real-time PCR method with melting curve analysis accurately identified CYP2C19 *2/3/17 genotypes in 93 clinical blood samples within 1 hour, confirmed by Sanger sequencing.
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