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Prognostic Value of sST2 in Heart Failure

In recent years, there has been growing interest in the risk stratification for heart failure, and the use of multiple biomarkers to identify different pathophysiological processes associated with this condition. One such biomarker is soluble suppression of tumorigenicity-2 (sST2), which has shown s...

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Autores principales: Sciatti, Edoardo, Merlo, Anna, Scangiuzzi, Claudio, Limonta, Raul, Gori, Mauro, D’Elia, Emilia, Aimo, Alberto, Vergaro, Giuseppe, Emdin, Michele, Senni, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299183/
https://www.ncbi.nlm.nih.gov/pubmed/37373664
http://dx.doi.org/10.3390/jcm12123970
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author Sciatti, Edoardo
Merlo, Anna
Scangiuzzi, Claudio
Limonta, Raul
Gori, Mauro
D’Elia, Emilia
Aimo, Alberto
Vergaro, Giuseppe
Emdin, Michele
Senni, Michele
author_facet Sciatti, Edoardo
Merlo, Anna
Scangiuzzi, Claudio
Limonta, Raul
Gori, Mauro
D’Elia, Emilia
Aimo, Alberto
Vergaro, Giuseppe
Emdin, Michele
Senni, Michele
author_sort Sciatti, Edoardo
collection PubMed
description In recent years, there has been growing interest in the risk stratification for heart failure, and the use of multiple biomarkers to identify different pathophysiological processes associated with this condition. One such biomarker is soluble suppression of tumorigenicity-2 (sST2), which has shown some potential for integration into clinical practice. sST2 is produced by both cardiac fibroblasts and cardiomyocytes in response to myocardial stress. Other sources of sST2 are endothelial cells of the aorta and coronary arteries and immune cells such as T cells. Indeed, ST2 is also associated with inflammatory and immune processes. We aimed at reviewing the prognostic value of sST2 in both chronic and acute heart failure. In this setting, we also provide a flowchart about its potential use in clinical practice.
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spelling pubmed-102991832023-06-28 Prognostic Value of sST2 in Heart Failure Sciatti, Edoardo Merlo, Anna Scangiuzzi, Claudio Limonta, Raul Gori, Mauro D’Elia, Emilia Aimo, Alberto Vergaro, Giuseppe Emdin, Michele Senni, Michele J Clin Med Review In recent years, there has been growing interest in the risk stratification for heart failure, and the use of multiple biomarkers to identify different pathophysiological processes associated with this condition. One such biomarker is soluble suppression of tumorigenicity-2 (sST2), which has shown some potential for integration into clinical practice. sST2 is produced by both cardiac fibroblasts and cardiomyocytes in response to myocardial stress. Other sources of sST2 are endothelial cells of the aorta and coronary arteries and immune cells such as T cells. Indeed, ST2 is also associated with inflammatory and immune processes. We aimed at reviewing the prognostic value of sST2 in both chronic and acute heart failure. In this setting, we also provide a flowchart about its potential use in clinical practice. MDPI 2023-06-11 /pmc/articles/PMC10299183/ /pubmed/37373664 http://dx.doi.org/10.3390/jcm12123970 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sciatti, Edoardo
Merlo, Anna
Scangiuzzi, Claudio
Limonta, Raul
Gori, Mauro
D’Elia, Emilia
Aimo, Alberto
Vergaro, Giuseppe
Emdin, Michele
Senni, Michele
Prognostic Value of sST2 in Heart Failure
title Prognostic Value of sST2 in Heart Failure
title_full Prognostic Value of sST2 in Heart Failure
title_fullStr Prognostic Value of sST2 in Heart Failure
title_full_unstemmed Prognostic Value of sST2 in Heart Failure
title_short Prognostic Value of sST2 in Heart Failure
title_sort prognostic value of sst2 in heart failure
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10299183/
https://www.ncbi.nlm.nih.gov/pubmed/37373664
http://dx.doi.org/10.3390/jcm12123970
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