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Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis

In patients with aortic stenosis (AS), a novel staging classification of extra-valvular left and right heart damage with prognostic relevance was introduced in 2017. The aim of the study was to evaluate the biomarkers of cardiovascular tissue remodelling in relation to this novel staging classificat...

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Autores principales: Bäz, Laura, Dannberg, Gudrun, Grün, Katja, Westphal, Julian, Möbius-Winkler, Sven, Jung, Christian, Pfeil, Alexander, Schulze, P. Christian, Franz, Marcus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312014/
https://www.ncbi.nlm.nih.gov/pubmed/32545310
http://dx.doi.org/10.3390/ijms21114174
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author Bäz, Laura
Dannberg, Gudrun
Grün, Katja
Westphal, Julian
Möbius-Winkler, Sven
Jung, Christian
Pfeil, Alexander
Schulze, P. Christian
Franz, Marcus
author_facet Bäz, Laura
Dannberg, Gudrun
Grün, Katja
Westphal, Julian
Möbius-Winkler, Sven
Jung, Christian
Pfeil, Alexander
Schulze, P. Christian
Franz, Marcus
author_sort Bäz, Laura
collection PubMed
description In patients with aortic stenosis (AS), a novel staging classification of extra-valvular left and right heart damage with prognostic relevance was introduced in 2017. The aim of the study was to evaluate the biomarkers of cardiovascular tissue remodelling in relation to this novel staging classification. Patients were categorized according to the novel staging classification into stages 0 to 4. The levels of matrix metalloproteinase 9 (MMP-9), tissue inhibitor of metalloproteinases 1 (TIMP-1), B and C domain containing tenascin-C (B(+) Tn-C, C(+) Tn-C), the ED-A and ED-B domain containing fibronectin (ED-A(+) Fn, ED-B(+) Fn), endothelin 1 (ET-1) and neutrophil gelatinase-associated lipocalin (NGAL) were determined in serum by ELISA. There were significantly decreased serum levels of MMP-9 and increased levels of B(+) Tn-C and C(+) Tn-C when comparing stages 0 and 1 with stage 2, with no further dynamics in stages 3 and 4. In contrast, for TIMP-1, C(+) Tn-C, ED-A(+) Fn, ET-1 and NGAL, significantly increased serum levels could be detected in stages 3 and 4 compared to both stages 0 and 1 and stage 2. ED-A(+) Fn and ET-1 could be identified as independent predictors of the presence of stage 3 and/or 4. To the best of our knowledge, this is the first study identifying novel serum biomarkers differentially reflecting the patterns of left and right heart extra-valvular damage in patients suffering from AS. Our findings might indicate a more precise initial diagnosis and risk stratification.
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spelling pubmed-73120142020-06-25 Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis Bäz, Laura Dannberg, Gudrun Grün, Katja Westphal, Julian Möbius-Winkler, Sven Jung, Christian Pfeil, Alexander Schulze, P. Christian Franz, Marcus Int J Mol Sci Article In patients with aortic stenosis (AS), a novel staging classification of extra-valvular left and right heart damage with prognostic relevance was introduced in 2017. The aim of the study was to evaluate the biomarkers of cardiovascular tissue remodelling in relation to this novel staging classification. Patients were categorized according to the novel staging classification into stages 0 to 4. The levels of matrix metalloproteinase 9 (MMP-9), tissue inhibitor of metalloproteinases 1 (TIMP-1), B and C domain containing tenascin-C (B(+) Tn-C, C(+) Tn-C), the ED-A and ED-B domain containing fibronectin (ED-A(+) Fn, ED-B(+) Fn), endothelin 1 (ET-1) and neutrophil gelatinase-associated lipocalin (NGAL) were determined in serum by ELISA. There were significantly decreased serum levels of MMP-9 and increased levels of B(+) Tn-C and C(+) Tn-C when comparing stages 0 and 1 with stage 2, with no further dynamics in stages 3 and 4. In contrast, for TIMP-1, C(+) Tn-C, ED-A(+) Fn, ET-1 and NGAL, significantly increased serum levels could be detected in stages 3 and 4 compared to both stages 0 and 1 and stage 2. ED-A(+) Fn and ET-1 could be identified as independent predictors of the presence of stage 3 and/or 4. To the best of our knowledge, this is the first study identifying novel serum biomarkers differentially reflecting the patterns of left and right heart extra-valvular damage in patients suffering from AS. Our findings might indicate a more precise initial diagnosis and risk stratification. MDPI 2020-06-11 /pmc/articles/PMC7312014/ /pubmed/32545310 http://dx.doi.org/10.3390/ijms21114174 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Bäz, Laura
Dannberg, Gudrun
Grün, Katja
Westphal, Julian
Möbius-Winkler, Sven
Jung, Christian
Pfeil, Alexander
Schulze, P. Christian
Franz, Marcus
Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title_full Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title_fullStr Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title_full_unstemmed Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title_short Serum Biomarkers of Cardiovascular Remodelling Reflect Extra-Valvular Cardiac Damage in Patients with Severe Aortic Stenosis
title_sort serum biomarkers of cardiovascular remodelling reflect extra-valvular cardiac damage in patients with severe aortic stenosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7312014/
https://www.ncbi.nlm.nih.gov/pubmed/32545310
http://dx.doi.org/10.3390/ijms21114174
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