Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population

Background. The role of genetic factors in the predisposition to develop ischemic stroke has been assessed by previous studies. The main goal of the current study was to determine any possible role of TNF-857C>T,TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms in risk for stroke. Materials a...

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Main Authors: Sofia Markoula, Anthoula Chatzikyriakidou, Sotirios Giannopoulos, Kargiotis Odysseas, Sofia Markou, Konstantinos Vemmos, Ioannis Georgiou, Athanassios P. Kyritsis
Format: Article
Language:English
Published: Wiley 2011-01-01
Series:Stroke Research and Treatment
Online Access:http://dx.doi.org/10.4061/2011/920584
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author Sofia Markoula
Anthoula Chatzikyriakidou
Sotirios Giannopoulos
Kargiotis Odysseas
Sofia Markou
Konstantinos Vemmos
Ioannis Georgiou
Athanassios P. Kyritsis
author_facet Sofia Markoula
Anthoula Chatzikyriakidou
Sotirios Giannopoulos
Kargiotis Odysseas
Sofia Markou
Konstantinos Vemmos
Ioannis Georgiou
Athanassios P. Kyritsis
author_sort Sofia Markoula
collection DOAJ
description Background. The role of genetic factors in the predisposition to develop ischemic stroke has been assessed by previous studies. The main goal of the current study was to determine any possible role of TNF-857C>T,TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms in risk for stroke. Materials and Methods. One hundred seventy-three patients with first ever ischemic stroke of solely atherosclerotic etiology in Northwest Greece and a control group of 179 healthy unrelated subjects were evaluated. Results. TNFα-857TT, TNFR136AA, and TNFR2676TT genotypes were significantly increased in the patient group compared to controls (𝑃=.008, OR = 2.47 (1.26–4.84), 𝑃=.005, OR = 1.97 (1.22–3.17), and 𝑃=.003, OR = 2.2 (1.43–3.37), resp.). In addition, the TNFR136A and the TNFR2676T alleles were found significantly increased in patients compared to controls (𝑃=.009, OR = 1.48 (1.1–2) and 𝑃=.001, OR = 1.75 (1.25–2.46), resp.). Conclusion. The high incidence of these genotypes and alleles in patient group suggests that they are potentially predisposing factors for stroke in the Greek population studied. Large-scale multicenter controlled studies are needed to verify these polymorphisms effects on stroke susceptibility.
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spelling doaj-art-b8a940eba84c4243bd730c1bdd34d27c2025-02-03T05:45:50ZengWileyStroke Research and Treatment2042-00562011-01-01201110.4061/2011/920584920584Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek PopulationSofia Markoula0Anthoula Chatzikyriakidou1Sotirios Giannopoulos2Kargiotis Odysseas3Sofia Markou4Konstantinos Vemmos5Ioannis Georgiou6Athanassios P. Kyritsis7Department of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceLaboratory of Medical Genetics, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceDepartment of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceNeurosurgical Research Institute, School of Medicine, University of Ioannina, 45110 Ioannina, GreeceDepartment of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceDepartment of Clinical Therapeutics, National and Kapodistrian, University of Athens, 11528 Athens, GreeceLaboratory of Medical Genetics, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceDepartment of Neurology, School of Medicine, University of Ioannina, University Campus, 45110 Ioannina, GreeceBackground. The role of genetic factors in the predisposition to develop ischemic stroke has been assessed by previous studies. The main goal of the current study was to determine any possible role of TNF-857C>T,TNFRSF1A36A>G, and TNFRSF1B676T>G polymorphisms in risk for stroke. Materials and Methods. One hundred seventy-three patients with first ever ischemic stroke of solely atherosclerotic etiology in Northwest Greece and a control group of 179 healthy unrelated subjects were evaluated. Results. TNFα-857TT, TNFR136AA, and TNFR2676TT genotypes were significantly increased in the patient group compared to controls (𝑃=.008, OR = 2.47 (1.26–4.84), 𝑃=.005, OR = 1.97 (1.22–3.17), and 𝑃=.003, OR = 2.2 (1.43–3.37), resp.). In addition, the TNFR136A and the TNFR2676T alleles were found significantly increased in patients compared to controls (𝑃=.009, OR = 1.48 (1.1–2) and 𝑃=.001, OR = 1.75 (1.25–2.46), resp.). Conclusion. The high incidence of these genotypes and alleles in patient group suggests that they are potentially predisposing factors for stroke in the Greek population studied. Large-scale multicenter controlled studies are needed to verify these polymorphisms effects on stroke susceptibility.http://dx.doi.org/10.4061/2011/920584
spellingShingle Sofia Markoula
Anthoula Chatzikyriakidou
Sotirios Giannopoulos
Kargiotis Odysseas
Sofia Markou
Konstantinos Vemmos
Ioannis Georgiou
Athanassios P. Kyritsis
Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
Stroke Research and Treatment
title Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
title_full Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
title_fullStr Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
title_full_unstemmed Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
title_short Association of TNF-857C>T, TNFRSF1A36A>G, and TNFRSF1B676T>G Polymorphisms with Ischemic Stroke in a Greek Population
title_sort association of tnf 857c t tnfrsf1a36a g and tnfrsf1b676t g polymorphisms with ischemic stroke in a greek population
url http://dx.doi.org/10.4061/2011/920584
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