Cargando…

Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants

In precision medicine, multiple factors are involved in clinical decision-making because of ethnic and racial genetic diversity, family history and other health factors. Although advanced techniques have evolved, there is still an economic obstacle to pharmacogenetic (PGx) implementation in developi...

Descripción completa

Detalles Bibliográficos
Autores principales: Nandar, Yu Myat, Duangmano, Suwit, Lucksiri, Aroonrut, Sirikul, Chonticha, Palacajornsuk, Poonsub, Anukul, Nampeung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808490/
https://www.ncbi.nlm.nih.gov/pubmed/36606140
http://dx.doi.org/10.3892/br.2022.1582
_version_ 1784862953957228544
author Nandar, Yu Myat
Duangmano, Suwit
Lucksiri, Aroonrut
Sirikul, Chonticha
Palacajornsuk, Poonsub
Anukul, Nampeung
author_facet Nandar, Yu Myat
Duangmano, Suwit
Lucksiri, Aroonrut
Sirikul, Chonticha
Palacajornsuk, Poonsub
Anukul, Nampeung
author_sort Nandar, Yu Myat
collection PubMed
description In precision medicine, multiple factors are involved in clinical decision-making because of ethnic and racial genetic diversity, family history and other health factors. Although advanced techniques have evolved, there is still an economic obstacle to pharmacogenetic (PGx) implementation in developing countries. The aim of the present study was to provide an alternative pipeline that roughly estimate patient carrier type and prescreen out wild-type samples before sequencing or genotyping to determine genetic status. Fast co-amplification at lower denaturation temperature (COLD)-PCR was used to differentiate genetic variant non-carriers from carriers. The majority of drugs are hepatically cleared by cytochrome P450 (CYP) enzymes and genes encoding CYP enzymes are highly variable. Of all the CYPs, CYP2 family of CYP2C9, CYP2C19, and CYP2D6 isoforms have clinically significant impact on drugs of PGx testing. Therefore, five variants associated with these CYPs were selected for preliminary testing with this novel pipeline. For fast COLD-PCR, the optimal annealing temperature and critical denaturation temperature were determined and evaluated via Sanger sequencing of 27 randomly collected samples. According to precise Tc, to perform in a single-reaction is difficult. However, in this study, this issue was resolved by combination of precise Tc using 10+10+20 cycles. The results showed 100% sensitivity and specificity, with perfect agreement (κ=1.0) compared with Sanger sequencing. The present study provides a prescreening platform by introducing multiplex fast COLD-PCR as a pharmacoeconomic implementation. Our study just present in five variants which are not enough to describe patient metabolic status. Therefore, other actional genetic variants are still needed to cover the actual patient's genotypes. Nevertheless, the proposed method can well-present its efficiency and reliability for serving as a PGx budget platform in the future.
format Online
Article
Text
id pubmed-9808490
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-98084902023-01-04 Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants Nandar, Yu Myat Duangmano, Suwit Lucksiri, Aroonrut Sirikul, Chonticha Palacajornsuk, Poonsub Anukul, Nampeung Biomed Rep Articles In precision medicine, multiple factors are involved in clinical decision-making because of ethnic and racial genetic diversity, family history and other health factors. Although advanced techniques have evolved, there is still an economic obstacle to pharmacogenetic (PGx) implementation in developing countries. The aim of the present study was to provide an alternative pipeline that roughly estimate patient carrier type and prescreen out wild-type samples before sequencing or genotyping to determine genetic status. Fast co-amplification at lower denaturation temperature (COLD)-PCR was used to differentiate genetic variant non-carriers from carriers. The majority of drugs are hepatically cleared by cytochrome P450 (CYP) enzymes and genes encoding CYP enzymes are highly variable. Of all the CYPs, CYP2 family of CYP2C9, CYP2C19, and CYP2D6 isoforms have clinically significant impact on drugs of PGx testing. Therefore, five variants associated with these CYPs were selected for preliminary testing with this novel pipeline. For fast COLD-PCR, the optimal annealing temperature and critical denaturation temperature were determined and evaluated via Sanger sequencing of 27 randomly collected samples. According to precise Tc, to perform in a single-reaction is difficult. However, in this study, this issue was resolved by combination of precise Tc using 10+10+20 cycles. The results showed 100% sensitivity and specificity, with perfect agreement (κ=1.0) compared with Sanger sequencing. The present study provides a prescreening platform by introducing multiplex fast COLD-PCR as a pharmacoeconomic implementation. Our study just present in five variants which are not enough to describe patient metabolic status. Therefore, other actional genetic variants are still needed to cover the actual patient's genotypes. Nevertheless, the proposed method can well-present its efficiency and reliability for serving as a PGx budget platform in the future. D.A. Spandidos 2022-10-31 /pmc/articles/PMC9808490/ /pubmed/36606140 http://dx.doi.org/10.3892/br.2022.1582 Text en Copyright: © Nandar et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Nandar, Yu Myat
Duangmano, Suwit
Lucksiri, Aroonrut
Sirikul, Chonticha
Palacajornsuk, Poonsub
Anukul, Nampeung
Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title_full Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title_fullStr Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title_full_unstemmed Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title_short Introduction of new alternative pipeline using multiplexed fast COLD‑PCR together with sequencing approach highlighting pharmacoeconomics by detection of CYP variants
title_sort introduction of new alternative pipeline using multiplexed fast cold‑pcr together with sequencing approach highlighting pharmacoeconomics by detection of cyp variants
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9808490/
https://www.ncbi.nlm.nih.gov/pubmed/36606140
http://dx.doi.org/10.3892/br.2022.1582
work_keys_str_mv AT nandaryumyat introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants
AT duangmanosuwit introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants
AT lucksiriaroonrut introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants
AT sirikulchonticha introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants
AT palacajornsukpoonsub introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants
AT anukulnampeung introductionofnewalternativepipelineusingmultiplexedfastcoldpcrtogetherwithsequencingapproachhighlightingpharmacoeconomicsbydetectionofcypvariants