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Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow
BACKGROUND AND AIMS: The aim of this study was to explore potential associations of the intron 4 variable number of tandem repeats (VNTR) and E298A polymorphisms of the endothelial nitric oxide synthase (eNOS) gene with slow coronary flow (SCF). The association between plasma nitrate and nitrite (NO...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Akadémiai Kiadó
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700696/ https://www.ncbi.nlm.nih.gov/pubmed/29201435 http://dx.doi.org/10.1556/1646.9.2017.17 |
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author | Sezgin, Nurzen Tekin, Abdullah Atac, Fatma Belgin Verdi, Hasibe Sezgin, Alpay Turan |
author_facet | Sezgin, Nurzen Tekin, Abdullah Atac, Fatma Belgin Verdi, Hasibe Sezgin, Alpay Turan |
author_sort | Sezgin, Nurzen |
collection | PubMed |
description | BACKGROUND AND AIMS: The aim of this study was to explore potential associations of the intron 4 variable number of tandem repeats (VNTR) and E298A polymorphisms of the endothelial nitric oxide synthase (eNOS) gene with slow coronary flow (SCF). The association between plasma nitrate and nitrite (NO(x)) concentrations and eNOS gene polymorphisms was also assessed. MATERIALS AND METHODS: The intron 4 VNTR and E298A polymorphisms of the eNOS gene were evaluated in the isolated DNA blood samples obtained from the SCF patient group (n = 30) and healthy group consisted of age- and sex-matched controls (n = 61). RESULTS: Plasma NO(x) level was significantly lower in patients with SCF than in controls. In addition, patients with SCF have significantly lower nitric oxide levels than control subjects within each genotype variants. The allele and genotyped frequencies of the eNOS intron 4 VNTR and E298A polymorphisms were similar between patients with SCF and the controls. Plasma NO(x) concentrations with respect to the relevant genotypes were found insignificant. DISCUSSION AND CONCLUSION: Plasma NO(x) is lower in patients with SCF than in healthy subjects. Our findings may suggest the lack of association between intron 4 VNTR and E298A polymorphisms of the eNOS gene and SCF. |
format | Online Article Text |
id | pubmed-5700696 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Akadémiai Kiadó |
record_format | MEDLINE/PubMed |
spelling | pubmed-57006962017-12-01 Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow Sezgin, Nurzen Tekin, Abdullah Atac, Fatma Belgin Verdi, Hasibe Sezgin, Alpay Turan Interv Med Appl Sci Original Paper BACKGROUND AND AIMS: The aim of this study was to explore potential associations of the intron 4 variable number of tandem repeats (VNTR) and E298A polymorphisms of the endothelial nitric oxide synthase (eNOS) gene with slow coronary flow (SCF). The association between plasma nitrate and nitrite (NO(x)) concentrations and eNOS gene polymorphisms was also assessed. MATERIALS AND METHODS: The intron 4 VNTR and E298A polymorphisms of the eNOS gene were evaluated in the isolated DNA blood samples obtained from the SCF patient group (n = 30) and healthy group consisted of age- and sex-matched controls (n = 61). RESULTS: Plasma NO(x) level was significantly lower in patients with SCF than in controls. In addition, patients with SCF have significantly lower nitric oxide levels than control subjects within each genotype variants. The allele and genotyped frequencies of the eNOS intron 4 VNTR and E298A polymorphisms were similar between patients with SCF and the controls. Plasma NO(x) concentrations with respect to the relevant genotypes were found insignificant. DISCUSSION AND CONCLUSION: Plasma NO(x) is lower in patients with SCF than in healthy subjects. Our findings may suggest the lack of association between intron 4 VNTR and E298A polymorphisms of the eNOS gene and SCF. Akadémiai Kiadó 2017-09-22 2017-09 /pmc/articles/PMC5700696/ /pubmed/29201435 http://dx.doi.org/10.1556/1646.9.2017.17 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium for non-commercial purposes, provided the original author and source are credited. |
spellingShingle | Original Paper Sezgin, Nurzen Tekin, Abdullah Atac, Fatma Belgin Verdi, Hasibe Sezgin, Alpay Turan Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title | Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title_full | Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title_fullStr | Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title_full_unstemmed | Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title_short | Endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
title_sort | endothelial nitric oxide synthase gene polymorphisms in patients with slow coronary flow |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700696/ https://www.ncbi.nlm.nih.gov/pubmed/29201435 http://dx.doi.org/10.1556/1646.9.2017.17 |
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