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The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis

MATERIALS AND METHODS: The experiment was carried out on 100 symptomatic patients with internal carotid artery stenosis that underwent carotid endarterectomy. Every patient had the wall of the carotid artery resected during organ harvesting surgery in order to evaluate some cytokines (TGF-β, VEGF, F...

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Autores principales: Janczak, Dariusz, Ziolkowski, Piotr, Garcarek, Jerzy, Janczak, Dawid, Dorobisz, Karolina, Chabowski, Mariusz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283111/
https://www.ncbi.nlm.nih.gov/pubmed/25128019
http://dx.doi.org/10.1186/1749-8090-9-139
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author Janczak, Dariusz
Ziolkowski, Piotr
Garcarek, Jerzy
Janczak, Dawid
Dorobisz, Karolina
Chabowski, Mariusz
author_facet Janczak, Dariusz
Ziolkowski, Piotr
Garcarek, Jerzy
Janczak, Dawid
Dorobisz, Karolina
Chabowski, Mariusz
author_sort Janczak, Dariusz
collection PubMed
description MATERIALS AND METHODS: The experiment was carried out on 100 symptomatic patients with internal carotid artery stenosis that underwent carotid endarterectomy. Every patient had the wall of the carotid artery resected during organ harvesting surgery in order to evaluate some cytokines (TGF-β, VEGF, FGF, TNF-α) and to perform the immunohistochemistry (IHC). An immunoreactive score (IRS) was calculated based on the staining intensity and the number of cells stained. Over a 3-year period, 7 patients died, and 2 patients were lost to follow-up. The study group consisted of 91 patients. The control group comprised 20 young organ donors with confirmed death brain, who had their normal carotid artery sampled. RESULTS: In all healthy donors (control group) with normal carotid arteries the three cytokines (TGF-β, VEGF, TNF-α) were not discovered. The presence of FGF was confirmed in 25% of healthy donors, probably due to an intima fibroblasts activity, responsible for the synthesis of elastin and collagen to the extracellular matrix (ECM). Only three cytokines (TGF-β, FGF, TNF-α) were found within atheromatous plaques (study group). CONCLUSIONS: Our research confirmed that these factors may accelerate the development of atheromatic plaque and its destabilisation. The aim of the study was the evaluation of the inflammatory cytokines within atheromatic carotid plaque. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1749-8090-9-139) contains supplementary material, which is available to authorized users.
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spelling pubmed-42831112015-01-06 The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis Janczak, Dariusz Ziolkowski, Piotr Garcarek, Jerzy Janczak, Dawid Dorobisz, Karolina Chabowski, Mariusz J Cardiothorac Surg Research Article MATERIALS AND METHODS: The experiment was carried out on 100 symptomatic patients with internal carotid artery stenosis that underwent carotid endarterectomy. Every patient had the wall of the carotid artery resected during organ harvesting surgery in order to evaluate some cytokines (TGF-β, VEGF, FGF, TNF-α) and to perform the immunohistochemistry (IHC). An immunoreactive score (IRS) was calculated based on the staining intensity and the number of cells stained. Over a 3-year period, 7 patients died, and 2 patients were lost to follow-up. The study group consisted of 91 patients. The control group comprised 20 young organ donors with confirmed death brain, who had their normal carotid artery sampled. RESULTS: In all healthy donors (control group) with normal carotid arteries the three cytokines (TGF-β, VEGF, TNF-α) were not discovered. The presence of FGF was confirmed in 25% of healthy donors, probably due to an intima fibroblasts activity, responsible for the synthesis of elastin and collagen to the extracellular matrix (ECM). Only three cytokines (TGF-β, FGF, TNF-α) were found within atheromatous plaques (study group). CONCLUSIONS: Our research confirmed that these factors may accelerate the development of atheromatic plaque and its destabilisation. The aim of the study was the evaluation of the inflammatory cytokines within atheromatic carotid plaque. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/1749-8090-9-139) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-15 /pmc/articles/PMC4283111/ /pubmed/25128019 http://dx.doi.org/10.1186/1749-8090-9-139 Text en © Janczak et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Janczak, Dariusz
Ziolkowski, Piotr
Garcarek, Jerzy
Janczak, Dawid
Dorobisz, Karolina
Chabowski, Mariusz
The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title_full The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title_fullStr The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title_full_unstemmed The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title_short The cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
title_sort cytokines within the carotid plaque in symptomatic patients with internal carotid artery stenosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4283111/
https://www.ncbi.nlm.nih.gov/pubmed/25128019
http://dx.doi.org/10.1186/1749-8090-9-139
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