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Endostatin a Potential Biomarker for Heart Failure with Preserved Ejection Fraction
BACKGROUND: Endostatin is a circulating endogenous angiogenesis inhibitor preventing neovascularization. Previous studies demonstrated the prognostic value of Endostatin among patients with heart failure with reduced ejection fraction (HFrEF). However, the role of Endostatin among patients with hear...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Cardiologia - SBC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729781/ https://www.ncbi.nlm.nih.gov/pubmed/28977054 http://dx.doi.org/10.5935/abc.20170144 |
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author | Barroso, Michael Coll Boehme, Philip Kramer, Frank Mondritzki, Thomas Koehler, Till Gülker, Jan-Erik Karoff, Martin Dinh, Wilfried |
author_facet | Barroso, Michael Coll Boehme, Philip Kramer, Frank Mondritzki, Thomas Koehler, Till Gülker, Jan-Erik Karoff, Martin Dinh, Wilfried |
author_sort | Barroso, Michael Coll |
collection | PubMed |
description | BACKGROUND: Endostatin is a circulating endogenous angiogenesis inhibitor preventing neovascularization. Previous studies demonstrated the prognostic value of Endostatin among patients with heart failure with reduced ejection fraction (HFrEF). However, the role of Endostatin among patients with heart failure with preserved ejection fraction (HFpEF) remains unclear. OBJECTIVE: This study aimed to investigate the association between serum Endostatin levels, natriuretic peptide levels and the severity of left ventricular diastolic dysfunction and the diagnosis of HFpEF. METHODS: Endostatin serum concentrations were measured in 301 patients comprising 77 HFpEF patients, 169 patients with asymptomatic left ventricular diastolic dysfunction (ALVDD), and 55 controls with normal cardiac function. RESULTS: Endostatin serum levels were significantly elevated in patients with HFpEF (median/interquartile range 179.0 [159-220]) and ALVDD (163.8 [145.4-191.3]) compared to controls (149.1 [130.6-176.9]), p < 0.001 and p = 0.004, respectively) and significant correlated with N-terminal pro B-type natriuretic peptide (NT-proBNP). CONCLUSIONS: This hypothesis-generating pilot study gives first evidence that Endostatin correlates with the severity of diastolic dysfunction and may become a novel biomarker for HFpEF. We hypothesize a rise in Endostatin levels may reflect inhibition of adaptive angiogenesis and adverse cardiac remodeling. |
format | Online Article Text |
id | pubmed-5729781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Sociedade Brasileira de Cardiologia - SBC |
record_format | MEDLINE/PubMed |
spelling | pubmed-57297812017-12-18 Endostatin a Potential Biomarker for Heart Failure with Preserved Ejection Fraction Barroso, Michael Coll Boehme, Philip Kramer, Frank Mondritzki, Thomas Koehler, Till Gülker, Jan-Erik Karoff, Martin Dinh, Wilfried Arq Bras Cardiol Original Articles BACKGROUND: Endostatin is a circulating endogenous angiogenesis inhibitor preventing neovascularization. Previous studies demonstrated the prognostic value of Endostatin among patients with heart failure with reduced ejection fraction (HFrEF). However, the role of Endostatin among patients with heart failure with preserved ejection fraction (HFpEF) remains unclear. OBJECTIVE: This study aimed to investigate the association between serum Endostatin levels, natriuretic peptide levels and the severity of left ventricular diastolic dysfunction and the diagnosis of HFpEF. METHODS: Endostatin serum concentrations were measured in 301 patients comprising 77 HFpEF patients, 169 patients with asymptomatic left ventricular diastolic dysfunction (ALVDD), and 55 controls with normal cardiac function. RESULTS: Endostatin serum levels were significantly elevated in patients with HFpEF (median/interquartile range 179.0 [159-220]) and ALVDD (163.8 [145.4-191.3]) compared to controls (149.1 [130.6-176.9]), p < 0.001 and p = 0.004, respectively) and significant correlated with N-terminal pro B-type natriuretic peptide (NT-proBNP). CONCLUSIONS: This hypothesis-generating pilot study gives first evidence that Endostatin correlates with the severity of diastolic dysfunction and may become a novel biomarker for HFpEF. We hypothesize a rise in Endostatin levels may reflect inhibition of adaptive angiogenesis and adverse cardiac remodeling. Sociedade Brasileira de Cardiologia - SBC 2017-11 /pmc/articles/PMC5729781/ /pubmed/28977054 http://dx.doi.org/10.5935/abc.20170144 Text en http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Barroso, Michael Coll Boehme, Philip Kramer, Frank Mondritzki, Thomas Koehler, Till Gülker, Jan-Erik Karoff, Martin Dinh, Wilfried Endostatin a Potential Biomarker for Heart Failure with Preserved Ejection Fraction |
title | Endostatin a Potential Biomarker for Heart Failure with Preserved
Ejection Fraction |
title_full | Endostatin a Potential Biomarker for Heart Failure with Preserved
Ejection Fraction |
title_fullStr | Endostatin a Potential Biomarker for Heart Failure with Preserved
Ejection Fraction |
title_full_unstemmed | Endostatin a Potential Biomarker for Heart Failure with Preserved
Ejection Fraction |
title_short | Endostatin a Potential Biomarker for Heart Failure with Preserved
Ejection Fraction |
title_sort | endostatin a potential biomarker for heart failure with preserved
ejection fraction |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5729781/ https://www.ncbi.nlm.nih.gov/pubmed/28977054 http://dx.doi.org/10.5935/abc.20170144 |
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