Literature DB >> 12473258

The endothelial nitric oxide synthase (Glu298Asp and -786T>C) gene polymorphisms are associated with coronary in-stent restenosis.

A H Gomma1, M A Elrayess, C J Knight, E Hawe, K M Fox, S E Humphries.   

Abstract

AIMS: Coronary stent deployment is a major advance in percutaneous treatment of ischaemic heart disease, but 10-40% of patients still develop angiographic restenosis by 6 months due to neointimal hyperplasia. Patient-specific factors, including genetic factors, can contribute to this process. We have conducted a prospective study to examine the involvement of genetic risk factors (eNOS, ACE, MMP-3, IL-6, and PECAM-1) in restenosis following coronary stent deployment. METHODS AND
RESULTS: A total of 226 patients who underwent elective and successful coronary artery stenting to de novo lesions in native coronary arteries were studied. Two hundred and five (90.7%) patients were restudied by coronary angiogram at 6 months and the stented lesions were assessed using an automated quantitative angiography system. Genotype was determined by polymerase chain reaction (PCR) and restriction enzyme digestion. Restenosis rate, defined as >or=50% diameter stenosis, was 29.3%. The overall genotype frequency distributions were in Hardy-Weinberg equilibrium for all variants. Carriers of the 298Asp allele of the eNOS Glu298Asp polymorphism showed a higher frequency of restenosis with an odds ratio of 1.88 (95%CI: 1.01-3.51, P=0.043) compared to 298Glu homozygotes. Carriers of the -786C allele of the eNOS -786T>C polymorphism also showed a higher frequency of restenosis with odds ratio of 2.06 (95%CI: 1.08-3.94, P=0.028). These effects were essentially additive and were independent of other classical risk factors. Other studied genes did not show significant association with coronary in-stent restenosis.
CONCLUSION: In patients with coronary artery disease, the possession of the 298Asp and -786C variants of the eNOS gene are a risk factor for coronary in-stent restenosis, demonstrating the importance of the nitric oxide system in restenosis. Copyright 2002 The European Society of Cardiology. Published by Elsevier Science Ltd.

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Year:  2002        PMID: 12473258     DOI: 10.1053/euhj.2002.3400

Source DB:  PubMed          Journal:  Eur Heart J        ISSN: 0195-668X            Impact factor:   29.983


  20 in total

1.  Endothelial nitric oxide synthase gene polymorphisms in non-arteritic anterior ischemic optic neuropathy.

Authors:  Tsutomu Sakai; Keigo Shikishima; Masato Matsushima; Kenji Kitahara
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2007-02       Impact factor: 3.117

2.  Reduction in plasma concentrations of N terminal pro B type natriuretic peptide following percutaneous coronary intervention.

Authors:  P R Kalra; A Gomma; C Daly; J R Clague; I B Squire; L L Ng; K F Fox
Journal:  Heart       Date:  2004-11       Impact factor: 5.994

3.  A promoter polymorphism of the endothelial nitric oxide synthase gene is associated with reduced mRNA and protein expression in failing human myocardium.

Authors:  Amit A Doshi; Mark T Ziolo; Honglan Wang; Emily Burke; Amanda Lesinski; Philip Binkley
Journal:  J Card Fail       Date:  2010-02-07       Impact factor: 5.712

4.  ALOX5AP variants are associated with in-stent restenosis after percutaneous coronary intervention.

Authors:  Svati H Shah; Elizabeth R Hauser; David Crosslin; Liyong Wang; Carol Haynes; Jessica Connelly; Sarah Nelson; Jessica Johnson; Shera Gadson; Charlotte L Nelson; David Seo; Simon Gregory; William E Kraus; Christopher B Granger; Pascal Goldschmidt-Clermont; L Kristin Newby
Journal:  Atherosclerosis       Date:  2008-02-12       Impact factor: 5.162

5.  Genetic risk factors for restenosis after percutaneous coronary intervention in Kazakh population.

Authors:  Elena V Zholdybayeva; Yerkebulan A Talzhanov; Akbota M Aitkulova; Pavel V Tarlykov; Gulmira N Kulmambetova; Aisha N Iskakova; Aliya U Dzholdasbekova; Olga A Visternichan; Dana Zh Taizhanova; Yerlan M Ramanculov
Journal:  Hum Genomics       Date:  2016-06-08       Impact factor: 4.639

Review 6.  Genetic causation of neointimal hyperplasia in hemodialysis vascular access dysfunction.

Authors:  Timmy Lee; Davinder Wadehra
Journal:  Semin Dial       Date:  2011-09-15       Impact factor: 3.455

7.  The Endothelial Nitric Oxide Synthase (NOS3-786T>C) Genetic Polymorphism in Chronic Heart Failure: Effects of Mutant -786C allele on Long-term Mortality.

Authors:  Sait Terzi; Ayşe Emre; Kemal Yesilcimen; Selçuk Yazıcı; Aysun Erdem; Ufuk Sadik Ceylan; Figen Ciloglu
Journal:  Acta Cardiol Sin       Date:  2017-07       Impact factor: 2.672

8.  Association between polymorphisms of eNOS and GPx-1 genes, activity of free-radical processes and in-stent restenosis.

Authors:  Yu A Shuvalova; A I Kaminnyi; A N Meshkov; R O Shirokov; A N Samko
Journal:  Mol Cell Biochem       Date:  2012-08-14       Impact factor: 3.396

Review 9.  Nitric oxide insufficiency and atherothrombosis.

Authors:  Barbara Voetsch; Richard C Jin; Joseph Loscalzo
Journal:  Histochem Cell Biol       Date:  2004-08-26       Impact factor: 4.304

10.  ACE (I/D) polymorphism and response to treatment in coronary artery disease: a comprehensive database and meta-analysis involving study quality evaluation.

Authors:  Georgios Kitsios; Elias Zintzaras
Journal:  BMC Med Genet       Date:  2009-06-04       Impact factor: 2.103

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