The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome

Background. Extensive evidence, arising from models of endothelial nitric oxide synthase gene (NOS3)-knockout mice supports the role of endothelial malfunction in the pathogenesis of the metabolic syndrome (MS). Aims. The aim of this study was to evaluate the role of −786T/C polymorphism in the etio...

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Main Authors: Blazej Misiak, Marta Krolik, Anna Kukowka, Anna Lewera, Przemyslaw Leszczynski, Joanna Stankiewicz-Olczyk, Ryszard Slezak
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2011/458750
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author Blazej Misiak
Marta Krolik
Anna Kukowka
Anna Lewera
Przemyslaw Leszczynski
Joanna Stankiewicz-Olczyk
Ryszard Slezak
author_facet Blazej Misiak
Marta Krolik
Anna Kukowka
Anna Lewera
Przemyslaw Leszczynski
Joanna Stankiewicz-Olczyk
Ryszard Slezak
author_sort Blazej Misiak
collection DOAJ
description Background. Extensive evidence, arising from models of endothelial nitric oxide synthase gene (NOS3)-knockout mice supports the role of endothelial malfunction in the pathogenesis of the metabolic syndrome (MS). Aims. The aim of this study was to evaluate the role of −786T/C polymorphism in the etiology of MS and assess previously reported interaction with cigarette smoking. Methods. Based on International Diabetes Federation 2005 criteria, we recruited randomly 152 subjects with MS and 75 subjects without MS. Results. Allelic and genotype frequencies did not differ significantly between both groups. Total cholesterol level (CHOLT) and intima-media thickness of carotid arteries were significantly higher in −786CC homozygotes, in comparison with −786TC and −786TT patients. Regarding current smoking status, −786C allele was associated with higher CHOLT than −786T allele. Conclusion. Our study indicates the putative role of −786T/C polymorphism in the development of hypercholesterolemia, in patients with MS, which might be enhanced by cigarette smoking.
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publishDate 2011-01-01
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series International Journal of Endocrinology
spelling doaj-art-387dc517a34743dbb1645b438dba566d2025-02-03T05:58:39ZengWileyInternational Journal of Endocrinology1687-83371687-83452011-01-01201110.1155/2011/458750458750The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic SyndromeBlazej Misiak0Marta Krolik1Anna Kukowka2Anna Lewera3Przemyslaw Leszczynski4Joanna Stankiewicz-Olczyk5Ryszard Slezak6Department of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandDepartment of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandDepartment of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandDepartment of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandDepartment of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandCopper Health Centre, The Outpatient Clinic of Endocrinology, 59-300 Lubin, PolandDepartment of Genetics, Wroclaw Medical University, 50-368 Wroclaw, PolandBackground. Extensive evidence, arising from models of endothelial nitric oxide synthase gene (NOS3)-knockout mice supports the role of endothelial malfunction in the pathogenesis of the metabolic syndrome (MS). Aims. The aim of this study was to evaluate the role of −786T/C polymorphism in the etiology of MS and assess previously reported interaction with cigarette smoking. Methods. Based on International Diabetes Federation 2005 criteria, we recruited randomly 152 subjects with MS and 75 subjects without MS. Results. Allelic and genotype frequencies did not differ significantly between both groups. Total cholesterol level (CHOLT) and intima-media thickness of carotid arteries were significantly higher in −786CC homozygotes, in comparison with −786TC and −786TT patients. Regarding current smoking status, −786C allele was associated with higher CHOLT than −786T allele. Conclusion. Our study indicates the putative role of −786T/C polymorphism in the development of hypercholesterolemia, in patients with MS, which might be enhanced by cigarette smoking.http://dx.doi.org/10.1155/2011/458750
spellingShingle Blazej Misiak
Marta Krolik
Anna Kukowka
Anna Lewera
Przemyslaw Leszczynski
Joanna Stankiewicz-Olczyk
Ryszard Slezak
The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
International Journal of Endocrinology
title The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
title_full The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
title_fullStr The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
title_full_unstemmed The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
title_short The Role of −786T/C Polymorphism in the Endothelial Nitric Oxide Synthase Gene in Males with Clinical and Biochemical Features of the Metabolic Syndrome
title_sort role of 786t c polymorphism in the endothelial nitric oxide synthase gene in males with clinical and biochemical features of the metabolic syndrome
url http://dx.doi.org/10.1155/2011/458750
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