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Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study
BACKGROUND: Plasmodium vivax malaria is characterized by relapses arising from the hypnozoite stages in the liver. The only currently registered drug for radical treatment to prevent relapse is primaquine. Primaquine, a prodrug, requires metabolism through the liver cytochrome CYP2D6 isoenzyme to it...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238304/ https://www.ncbi.nlm.nih.gov/pubmed/30442143 http://dx.doi.org/10.1186/s12936-018-2579-8 |
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author | Puaprasert, Kanokpich Chu, Cindy Saralamba, Naowarat Day, Nicholas P. J. Nosten, Francois White, Nicholas J. Dondorp, Arjen M. Imwong, Mallika |
author_facet | Puaprasert, Kanokpich Chu, Cindy Saralamba, Naowarat Day, Nicholas P. J. Nosten, Francois White, Nicholas J. Dondorp, Arjen M. Imwong, Mallika |
author_sort | Puaprasert, Kanokpich |
collection | PubMed |
description | BACKGROUND: Plasmodium vivax malaria is characterized by relapses arising from the hypnozoite stages in the liver. The only currently registered drug for radical treatment to prevent relapse is primaquine. Primaquine, a prodrug, requires metabolism through the liver cytochrome CYP2D6 isoenzyme to its active metabolite. Mutations in the CYP2D6 gene may thus affect primaquine efficacy. A SNPs genotyping technique was developed to characterize the CYP2D6 genetic variants and tested this in the patients with Plasmodium vivax infection collected in a Karen population on the Thailand–Myanmar border, where P. vivax malaria is endemic. METHODS: Direct sequencing of PCR-reamplified products (DSP) was used to uncover exonic CYP2D6 sequence variations. Subsequently, an allele-specific oligonucleotide probe real-time SNPs genotyping (ASO) assay was developed for rapid detection of the four clinically relevant CYP2D6 variants occurring in this population. These two in-house developed assays were used to genotype CYP2D6 mutations in blood samples obtained from 70 Karen adults. RESULTS: Results showed a high degree of concordance between the DSP and ASO methods. Six CYP2D6 point mutations were identified within the Karen population: C100T, C1039T, G1661C, G1846A, C2850T and G4180C, at frequencies of 0.43, 0.43, 0.76, 0.02, 0.32 and 0.76, respectively. The CYP2D6*2, *4, *5, *10 and *36 allelic frequencies were 0.33, 0.02, 0.03, 0.40 and 0.01, respectively. Alleles conferring an intermediate CYP2D6 metabolizer phenotype comprised 46% of the total number of alleles. CONCLUSION: The newly developed ASO assay is a reliable and rapid tool for large-scale CYP2D6 genotyping. The high frequency of the CYP2D6*10 allele in the Karen population warrants further assessment of its association with the radical curative efficacy of primaquine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2579-8) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6238304 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62383042018-11-23 Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study Puaprasert, Kanokpich Chu, Cindy Saralamba, Naowarat Day, Nicholas P. J. Nosten, Francois White, Nicholas J. Dondorp, Arjen M. Imwong, Mallika Malar J Methodology BACKGROUND: Plasmodium vivax malaria is characterized by relapses arising from the hypnozoite stages in the liver. The only currently registered drug for radical treatment to prevent relapse is primaquine. Primaquine, a prodrug, requires metabolism through the liver cytochrome CYP2D6 isoenzyme to its active metabolite. Mutations in the CYP2D6 gene may thus affect primaquine efficacy. A SNPs genotyping technique was developed to characterize the CYP2D6 genetic variants and tested this in the patients with Plasmodium vivax infection collected in a Karen population on the Thailand–Myanmar border, where P. vivax malaria is endemic. METHODS: Direct sequencing of PCR-reamplified products (DSP) was used to uncover exonic CYP2D6 sequence variations. Subsequently, an allele-specific oligonucleotide probe real-time SNPs genotyping (ASO) assay was developed for rapid detection of the four clinically relevant CYP2D6 variants occurring in this population. These two in-house developed assays were used to genotype CYP2D6 mutations in blood samples obtained from 70 Karen adults. RESULTS: Results showed a high degree of concordance between the DSP and ASO methods. Six CYP2D6 point mutations were identified within the Karen population: C100T, C1039T, G1661C, G1846A, C2850T and G4180C, at frequencies of 0.43, 0.43, 0.76, 0.02, 0.32 and 0.76, respectively. The CYP2D6*2, *4, *5, *10 and *36 allelic frequencies were 0.33, 0.02, 0.03, 0.40 and 0.01, respectively. Alleles conferring an intermediate CYP2D6 metabolizer phenotype comprised 46% of the total number of alleles. CONCLUSION: The newly developed ASO assay is a reliable and rapid tool for large-scale CYP2D6 genotyping. The high frequency of the CYP2D6*10 allele in the Karen population warrants further assessment of its association with the radical curative efficacy of primaquine. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2579-8) contains supplementary material, which is available to authorized users. BioMed Central 2018-11-15 /pmc/articles/PMC6238304/ /pubmed/30442143 http://dx.doi.org/10.1186/s12936-018-2579-8 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Puaprasert, Kanokpich Chu, Cindy Saralamba, Naowarat Day, Nicholas P. J. Nosten, Francois White, Nicholas J. Dondorp, Arjen M. Imwong, Mallika Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title | Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title_full | Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title_fullStr | Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title_full_unstemmed | Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title_short | Real time PCR detection of common CYP2D6 genetic variants and its application in a Karen population study |
title_sort | real time pcr detection of common cyp2d6 genetic variants and its application in a karen population study |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6238304/ https://www.ncbi.nlm.nih.gov/pubmed/30442143 http://dx.doi.org/10.1186/s12936-018-2579-8 |
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