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A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure

Heart failure (HF) is a complex clinical syndrome that causes systemic hypoperfusion and failure to meet the body’s metabolic demands. In an attempt to compensate, chronic upregulation of the sympathetic nervous system and renin-angiotensin-aldosterone leads to further myocardial injury, HF progress...

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Detalles Bibliográficos
Autor principal: Deng, Mario C
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479277/
https://www.ncbi.nlm.nih.gov/pubmed/29737882
http://dx.doi.org/10.2217/bmm-2018-0097
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author Deng, Mario C
author_facet Deng, Mario C
author_sort Deng, Mario C
collection PubMed
description Heart failure (HF) is a complex clinical syndrome that causes systemic hypoperfusion and failure to meet the body’s metabolic demands. In an attempt to compensate, chronic upregulation of the sympathetic nervous system and renin-angiotensin-aldosterone leads to further myocardial injury, HF progression and reduced O(2) delivery. This triggers progressive organ dysfunction, immune system activation and profound metabolic derangements, creating a milieu similar to other chronic systemic diseases and presenting as advanced HF with severely limited prognosis. We hypothesize that 1-year survival in advanced HF is linked to functional recovery potential (FRP), a novel clinical composite parameter that includes HF severity, secondary organ dysfunction, co-morbidities, frailty, disabilities as well as chronological age and that can be diagnosed by a molecular biomarker.
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spelling pubmed-64792772019-04-29 A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure Deng, Mario C Biomark Med Perspective Heart failure (HF) is a complex clinical syndrome that causes systemic hypoperfusion and failure to meet the body’s metabolic demands. In an attempt to compensate, chronic upregulation of the sympathetic nervous system and renin-angiotensin-aldosterone leads to further myocardial injury, HF progression and reduced O(2) delivery. This triggers progressive organ dysfunction, immune system activation and profound metabolic derangements, creating a milieu similar to other chronic systemic diseases and presenting as advanced HF with severely limited prognosis. We hypothesize that 1-year survival in advanced HF is linked to functional recovery potential (FRP), a novel clinical composite parameter that includes HF severity, secondary organ dysfunction, co-morbidities, frailty, disabilities as well as chronological age and that can be diagnosed by a molecular biomarker. Future Medicine Ltd 2018-06 2018-05-08 /pmc/articles/PMC6479277/ /pubmed/29737882 http://dx.doi.org/10.2217/bmm-2018-0097 Text en © 2018 Mario Deng This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Perspective
Deng, Mario C
A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title_full A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title_fullStr A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title_full_unstemmed A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title_short A peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
title_sort peripheral blood transcriptome biomarker test to diagnose functional recovery potential in advanced heart failure
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6479277/
https://www.ncbi.nlm.nih.gov/pubmed/29737882
http://dx.doi.org/10.2217/bmm-2018-0097
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