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Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]

BACKGROUND/AIM: We aimed to investigate the associations between endothelial nitric oxide synthase (eNOS) gene polymorphisms [G894T (rs1799983)], intron 4 (27-bpTR) variable number tandem repeat (VNTR) and T786C (rs2070744), and ischemic stroke in the Anatolian population. MATERIALS AND METHODS: Thi...

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Autores principales: ANLIAÇIK, Süleyman Ömer, TOKGÖZ, Serhat, ZAMANİ, Ayşe Gül, YILDIRIM, Mahmut Selman, İYİSOY, Mehmet Sinan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018372/
https://www.ncbi.nlm.nih.gov/pubmed/30997974
http://dx.doi.org/10.3906/sag-1808-57
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author ANLIAÇIK, Süleyman Ömer
TOKGÖZ, Serhat
ZAMANİ, Ayşe Gül
YILDIRIM, Mahmut Selman
İYİSOY, Mehmet Sinan
author_facet ANLIAÇIK, Süleyman Ömer
TOKGÖZ, Serhat
ZAMANİ, Ayşe Gül
YILDIRIM, Mahmut Selman
İYİSOY, Mehmet Sinan
author_sort ANLIAÇIK, Süleyman Ömer
collection PubMed
description BACKGROUND/AIM: We aimed to investigate the associations between endothelial nitric oxide synthase (eNOS) gene polymorphisms [G894T (rs1799983)], intron 4 (27-bpTR) variable number tandem repeat (VNTR) and T786C (rs2070744), and ischemic stroke in the Anatolian population. MATERIALS AND METHODS: This case-control study included 112 patients with “stroke of undetermined etiology” and 160 controls. Real-time polymerase chain reaction (RT-PCR) analysis was used to analyze these polymorphisms. Between-group frequencies of alleles and genotypes were compared using binary logistic regression analysis. RESULTS: No significant difference was observed between the two groups in terms of the genotype and allele distributions of the eNOS G894T (rs1799983) polymorphism (P > 0.05). The a alleles and the 4b/a and 4a/a genotypes of the intron 4 (27-bpTR) VNTR polymorphism had significantly higher frequencies in the patient group than in the control group (OR: 2.715, P < 0.001; OR: 3.396, P < 0.001; OR: 10.631, P = 0.016, respectively). On the contrary, the TC genotype and C alleles of the T786C (rs2070744) polymorphism had a significantly lower frequency in the patient group than in the control group (OR: 0.244, P < 0.001, OR: 0.605, P = 0.006, respectively). CONCLUSION: Our findings indicate that the eNOS G894T and T786C [rs2070744] polymorphisms are not associated with the risk of ischemic stroke, whereas the intron 4 [27-bpTR] VNTR may be a risk factor in the Anatolian population.
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spelling pubmed-70183722020-03-23 Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C] ANLIAÇIK, Süleyman Ömer TOKGÖZ, Serhat ZAMANİ, Ayşe Gül YILDIRIM, Mahmut Selman İYİSOY, Mehmet Sinan Turk J Med Sci Article BACKGROUND/AIM: We aimed to investigate the associations between endothelial nitric oxide synthase (eNOS) gene polymorphisms [G894T (rs1799983)], intron 4 (27-bpTR) variable number tandem repeat (VNTR) and T786C (rs2070744), and ischemic stroke in the Anatolian population. MATERIALS AND METHODS: This case-control study included 112 patients with “stroke of undetermined etiology” and 160 controls. Real-time polymerase chain reaction (RT-PCR) analysis was used to analyze these polymorphisms. Between-group frequencies of alleles and genotypes were compared using binary logistic regression analysis. RESULTS: No significant difference was observed between the two groups in terms of the genotype and allele distributions of the eNOS G894T (rs1799983) polymorphism (P > 0.05). The a alleles and the 4b/a and 4a/a genotypes of the intron 4 (27-bpTR) VNTR polymorphism had significantly higher frequencies in the patient group than in the control group (OR: 2.715, P < 0.001; OR: 3.396, P < 0.001; OR: 10.631, P = 0.016, respectively). On the contrary, the TC genotype and C alleles of the T786C (rs2070744) polymorphism had a significantly lower frequency in the patient group than in the control group (OR: 0.244, P < 0.001, OR: 0.605, P = 0.006, respectively). CONCLUSION: Our findings indicate that the eNOS G894T and T786C [rs2070744] polymorphisms are not associated with the risk of ischemic stroke, whereas the intron 4 [27-bpTR] VNTR may be a risk factor in the Anatolian population. The Scientific and Technological Research Council of Turkey 2019-04-18 /pmc/articles/PMC7018372/ /pubmed/30997974 http://dx.doi.org/10.3906/sag-1808-57 Text en Copyright © 2019 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
ANLIAÇIK, Süleyman Ömer
TOKGÖZ, Serhat
ZAMANİ, Ayşe Gül
YILDIRIM, Mahmut Selman
İYİSOY, Mehmet Sinan
Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title_full Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title_fullStr Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title_full_unstemmed Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title_short Investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [G894T, intron 4 VNTR and T786C]
title_sort investigation of the relationship between ischemic stroke and endothelial nitric oxide synthase gene polymorphisms [g894t, intron 4 vntr and t786c]
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7018372/
https://www.ncbi.nlm.nih.gov/pubmed/30997974
http://dx.doi.org/10.3906/sag-1808-57
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