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Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation

BACKGROUND: Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are essential for the cardiac extracellular matrix (ECM) remodeling. We investigated differences in serum levels of these markers between patients with atrial fibrillation (AF) and sinus rhythm (SR). METHODS: Serum leve...

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Autores principales: Kalogeropoulos, Andreas S, Tsiodras, Sotirios, Rigopoulos, Angelos G, Sakadakis, Eleftherios A, Triantafyllis, Andreas, Kremastinos, Dimitrios TH, Rizos, Ioannis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276440/
https://www.ncbi.nlm.nih.gov/pubmed/22204652
http://dx.doi.org/10.1186/1471-2261-11-77
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author Kalogeropoulos, Andreas S
Tsiodras, Sotirios
Rigopoulos, Angelos G
Sakadakis, Eleftherios A
Triantafyllis, Andreas
Kremastinos, Dimitrios TH
Rizos, Ioannis
author_facet Kalogeropoulos, Andreas S
Tsiodras, Sotirios
Rigopoulos, Angelos G
Sakadakis, Eleftherios A
Triantafyllis, Andreas
Kremastinos, Dimitrios TH
Rizos, Ioannis
author_sort Kalogeropoulos, Andreas S
collection PubMed
description BACKGROUND: Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are essential for the cardiac extracellular matrix (ECM) remodeling. We investigated differences in serum levels of these markers between patients with atrial fibrillation (AF) and sinus rhythm (SR). METHODS: Serum levels of MMP-2, MMP-3, MMP-9 and TIMP-1 were measured in 86 patients: 27 on SR without any AF history, 33 with paroxysmal and 26 with permanent AF. All subjects had essential hypertension, normal systolic function and no coronary artery disease. RESULTS: Patients with AF had higher MMP-2, MMP-3 and MMP-9 and lower TIMP-1 compared to SR subjects (all p < 0.001). Paroxysmal AF was associated with higher MMP-2 levels compared to permanent AF (p < 0.001). Matrix metalloproteinase-9 but not MMP-3 was higher in permanent compared to paroxysmal AF group (p < 0.001). Patients with AF had lower levels of TIMP-1 compared to those with SR while permanent AF subjects had lower TIMP-1 levels than those with paroxysmal AF (p < 0.001 for both comparisons). Lower TIMP-1 was the only independent factor associated with AF (OR: 0.259, 95%CI: 0.104-0.645, p = 0.004). CONCLUSIONS: In hypertensives, paroxysmal AF and permanent AF differ with respect to serum MMPs. Increased MMP-2 is associated with paroxysmal, whereas increased MMP-9 with permanent AF. Additionally, lower levels of TIMP-1 had a strong association with AF incidence.
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spelling pubmed-32764402012-02-10 Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation Kalogeropoulos, Andreas S Tsiodras, Sotirios Rigopoulos, Angelos G Sakadakis, Eleftherios A Triantafyllis, Andreas Kremastinos, Dimitrios TH Rizos, Ioannis BMC Cardiovasc Disord Research Article BACKGROUND: Matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMPs) are essential for the cardiac extracellular matrix (ECM) remodeling. We investigated differences in serum levels of these markers between patients with atrial fibrillation (AF) and sinus rhythm (SR). METHODS: Serum levels of MMP-2, MMP-3, MMP-9 and TIMP-1 were measured in 86 patients: 27 on SR without any AF history, 33 with paroxysmal and 26 with permanent AF. All subjects had essential hypertension, normal systolic function and no coronary artery disease. RESULTS: Patients with AF had higher MMP-2, MMP-3 and MMP-9 and lower TIMP-1 compared to SR subjects (all p < 0.001). Paroxysmal AF was associated with higher MMP-2 levels compared to permanent AF (p < 0.001). Matrix metalloproteinase-9 but not MMP-3 was higher in permanent compared to paroxysmal AF group (p < 0.001). Patients with AF had lower levels of TIMP-1 compared to those with SR while permanent AF subjects had lower TIMP-1 levels than those with paroxysmal AF (p < 0.001 for both comparisons). Lower TIMP-1 was the only independent factor associated with AF (OR: 0.259, 95%CI: 0.104-0.645, p = 0.004). CONCLUSIONS: In hypertensives, paroxysmal AF and permanent AF differ with respect to serum MMPs. Increased MMP-2 is associated with paroxysmal, whereas increased MMP-9 with permanent AF. Additionally, lower levels of TIMP-1 had a strong association with AF incidence. BioMed Central 2011-12-28 /pmc/articles/PMC3276440/ /pubmed/22204652 http://dx.doi.org/10.1186/1471-2261-11-77 Text en Copyright ©2011 Kalogeropoulos et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kalogeropoulos, Andreas S
Tsiodras, Sotirios
Rigopoulos, Angelos G
Sakadakis, Eleftherios A
Triantafyllis, Andreas
Kremastinos, Dimitrios TH
Rizos, Ioannis
Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title_full Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title_fullStr Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title_full_unstemmed Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title_short Novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
title_sort novel association patterns of cardiac remodeling markers in patients with essential hypertension and atrial fibrillation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276440/
https://www.ncbi.nlm.nih.gov/pubmed/22204652
http://dx.doi.org/10.1186/1471-2261-11-77
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