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Clinical application and importance of one-step human CYP2C19 genotype detection
BACKGROUND: To directly achieve cytochrome P450 2C19 gene (CYP2C19) classification using one-step real-time fluorescent PCR detection and to verify the capabilities of this method with nucleic acid extracted from whole blood samples. METHODS: A human CYP2C19 genotyping kit based on one-step real-tim...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300956/ https://www.ncbi.nlm.nih.gov/pubmed/30360673 http://dx.doi.org/10.1177/0300060518787718 |
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author | Zheng, Ling-Jie Liu, Ning Yang, Kun Wang, Ai-Feng Tan, Zhi-Rong Li, Xiang |
author_facet | Zheng, Ling-Jie Liu, Ning Yang, Kun Wang, Ai-Feng Tan, Zhi-Rong Li, Xiang |
author_sort | Zheng, Ling-Jie |
collection | PubMed |
description | BACKGROUND: To directly achieve cytochrome P450 2C19 gene (CYP2C19) classification using one-step real-time fluorescent PCR detection and to verify the capabilities of this method with nucleic acid extracted from whole blood samples. METHODS: A human CYP2C19 genotyping kit based on one-step real-time fluorescent PCR detection was used to analyze whole blood or genomic DNA samples. This method was compared with pyrosequencing and another quantitative (q)PCR kit for its accuracy, repeatability, detection range analysis, sensitivity, specificity, and anti-interference analysis. RESULTS: The one-step real-time PCR method achieved a 100% accuracy rate compared with pyrosequencing and the other qPCR kit. When detecting different concentrations of known genes, concentrations of each sample ranging from 0.2 to 125 ng/µL could be correctly detected. The genotypes of samples treated with anticoagulants, including EDTA and sodium citrate, and chyle blood samples could be correctly detected. CONCLUSION: The one-step detection method demonstrated high accuracy and a wide detection range. It also had high levels of repeatability, sensitivity, and specificity for the assessment of genomic DNA test samples. |
format | Online Article Text |
id | pubmed-6300956 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-63009562019-01-11 Clinical application and importance of one-step human CYP2C19 genotype detection Zheng, Ling-Jie Liu, Ning Yang, Kun Wang, Ai-Feng Tan, Zhi-Rong Li, Xiang J Int Med Res Clinical Research Reports BACKGROUND: To directly achieve cytochrome P450 2C19 gene (CYP2C19) classification using one-step real-time fluorescent PCR detection and to verify the capabilities of this method with nucleic acid extracted from whole blood samples. METHODS: A human CYP2C19 genotyping kit based on one-step real-time fluorescent PCR detection was used to analyze whole blood or genomic DNA samples. This method was compared with pyrosequencing and another quantitative (q)PCR kit for its accuracy, repeatability, detection range analysis, sensitivity, specificity, and anti-interference analysis. RESULTS: The one-step real-time PCR method achieved a 100% accuracy rate compared with pyrosequencing and the other qPCR kit. When detecting different concentrations of known genes, concentrations of each sample ranging from 0.2 to 125 ng/µL could be correctly detected. The genotypes of samples treated with anticoagulants, including EDTA and sodium citrate, and chyle blood samples could be correctly detected. CONCLUSION: The one-step detection method demonstrated high accuracy and a wide detection range. It also had high levels of repeatability, sensitivity, and specificity for the assessment of genomic DNA test samples. SAGE Publications 2018-10-25 2018-12 /pmc/articles/PMC6300956/ /pubmed/30360673 http://dx.doi.org/10.1177/0300060518787718 Text en © The Author(s) 2018 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Clinical Research Reports Zheng, Ling-Jie Liu, Ning Yang, Kun Wang, Ai-Feng Tan, Zhi-Rong Li, Xiang Clinical application and importance of one-step human CYP2C19 genotype detection |
title | Clinical application and importance of one-step human CYP2C19 genotype detection |
title_full | Clinical application and importance of one-step human CYP2C19 genotype detection |
title_fullStr | Clinical application and importance of one-step human CYP2C19 genotype detection |
title_full_unstemmed | Clinical application and importance of one-step human CYP2C19 genotype detection |
title_short | Clinical application and importance of one-step human CYP2C19 genotype detection |
title_sort | clinical application and importance of one-step human cyp2c19 genotype detection |
topic | Clinical Research Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6300956/ https://www.ncbi.nlm.nih.gov/pubmed/30360673 http://dx.doi.org/10.1177/0300060518787718 |
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