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A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application

BACKGROUND: Angiotensin-converting enzyme (ACE) plays a major role in blood pressure regulation and cardiovascular homeostasis. The wide distribution and multifunctional properties of ACE suggest it’s involvement in various pathophysiological conditions. RESULTS: In this study, a novel visual detect...

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Autores principales: Yang, Xue-min, Liang, Jian-ping, Huang, Xiao-juan, Wang, Xiang-rong, Sun, Yang, Dong, Chen, Cui, Ya-li, Hui, Wen-li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791644/
https://www.ncbi.nlm.nih.gov/pubmed/33413084
http://dx.doi.org/10.1186/s12575-020-00140-6
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author Yang, Xue-min
Liang, Jian-ping
Huang, Xiao-juan
Wang, Xiang-rong
Sun, Yang
Dong, Chen
Cui, Ya-li
Hui, Wen-li
author_facet Yang, Xue-min
Liang, Jian-ping
Huang, Xiao-juan
Wang, Xiang-rong
Sun, Yang
Dong, Chen
Cui, Ya-li
Hui, Wen-li
author_sort Yang, Xue-min
collection PubMed
description BACKGROUND: Angiotensin-converting enzyme (ACE) plays a major role in blood pressure regulation and cardiovascular homeostasis. The wide distribution and multifunctional properties of ACE suggest it’s involvement in various pathophysiological conditions. RESULTS: In this study, a novel visual detection method for ACE I/D polymorphisms was designed by integrating direct PCR without the need for DNA extraction using gold magnetic nanoparticles (GMNPs)-based lateral flow assay (LFA) biosensor. The entire detection procedure could enable the genotyping of clinical samples in about 80 min. The detection limit was 0.75 ng and results could be obtained in 5 min using the LFA device. Three hundred peripheral blood samples were analyzed using the direct PCR-LFA system and then verified by sequencing to determine accuracy and repeatability. A clinical preliminary study was then performed to analyze a total of 633 clinical samples. CONCLUSIONS: After grouping based on age, we found a significant difference between the genotypes and the age of patients in the CHD group. The introduction of this method into clinical practice may be helpful for the diagnosis of diseases caused by large fragment gene insertions/deletions.
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spelling pubmed-77916442021-01-11 A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application Yang, Xue-min Liang, Jian-ping Huang, Xiao-juan Wang, Xiang-rong Sun, Yang Dong, Chen Cui, Ya-li Hui, Wen-li Biol Proced Online Research BACKGROUND: Angiotensin-converting enzyme (ACE) plays a major role in blood pressure regulation and cardiovascular homeostasis. The wide distribution and multifunctional properties of ACE suggest it’s involvement in various pathophysiological conditions. RESULTS: In this study, a novel visual detection method for ACE I/D polymorphisms was designed by integrating direct PCR without the need for DNA extraction using gold magnetic nanoparticles (GMNPs)-based lateral flow assay (LFA) biosensor. The entire detection procedure could enable the genotyping of clinical samples in about 80 min. The detection limit was 0.75 ng and results could be obtained in 5 min using the LFA device. Three hundred peripheral blood samples were analyzed using the direct PCR-LFA system and then verified by sequencing to determine accuracy and repeatability. A clinical preliminary study was then performed to analyze a total of 633 clinical samples. CONCLUSIONS: After grouping based on age, we found a significant difference between the genotypes and the age of patients in the CHD group. The introduction of this method into clinical practice may be helpful for the diagnosis of diseases caused by large fragment gene insertions/deletions. BioMed Central 2021-01-07 /pmc/articles/PMC7791644/ /pubmed/33413084 http://dx.doi.org/10.1186/s12575-020-00140-6 Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Yang, Xue-min
Liang, Jian-ping
Huang, Xiao-juan
Wang, Xiang-rong
Sun, Yang
Dong, Chen
Cui, Ya-li
Hui, Wen-li
A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title_full A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title_fullStr A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title_full_unstemmed A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title_short A Novel PCR Method for Detecting ACE Gene Insertion/Deletion Polymorphisms and its Clinical Application
title_sort novel pcr method for detecting ace gene insertion/deletion polymorphisms and its clinical application
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7791644/
https://www.ncbi.nlm.nih.gov/pubmed/33413084
http://dx.doi.org/10.1186/s12575-020-00140-6
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