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Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis
AIMS: Myocardial fibrosis alters the cardiac architecture favouring the development of cardiac dysfunction, including arrhythmias and heart failure. Reducing myocardial fibrosis may improve outcomes through the targeted diagnosis and treatment of emerging fibrotic pathways. The European‐Commission‐f...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793978/ https://www.ncbi.nlm.nih.gov/pubmed/28988439 http://dx.doi.org/10.1002/ehf2.12218 |
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author | Ferreira, João Pedro Machu, Jean‐Loup Girerd, Nicolas Jaisser, Frederic Thum, Thomas Butler, Javed González, Arantxa Diez, Javier Heymans, Stephane McDonald, Kenneth Gyöngyösi, Mariann Firat, Hueseyin Rossignol, Patrick Pizard, Anne Zannad, Faiez |
author_facet | Ferreira, João Pedro Machu, Jean‐Loup Girerd, Nicolas Jaisser, Frederic Thum, Thomas Butler, Javed González, Arantxa Diez, Javier Heymans, Stephane McDonald, Kenneth Gyöngyösi, Mariann Firat, Hueseyin Rossignol, Patrick Pizard, Anne Zannad, Faiez |
author_sort | Ferreira, João Pedro |
collection | PubMed |
description | AIMS: Myocardial fibrosis alters the cardiac architecture favouring the development of cardiac dysfunction, including arrhythmias and heart failure. Reducing myocardial fibrosis may improve outcomes through the targeted diagnosis and treatment of emerging fibrotic pathways. The European‐Commission‐funded ‘FIBROTARGETS’ is a multinational academic and industrial consortium with the main aims of (i) characterizing novel key mechanistic pathways involved in the metabolism of fibrillary collagen that may serve as biotargets, (ii) evaluating the potential anti‐fibrotic properties of novel or repurposed molecules interfering with the newly identified biotargets, and (iii) characterizing bioprofiles based on distinct mechanistic phenotypes involving the aforementioned biotargets. These pathways will be explored by performing a systematic and collaborative search for mechanisms and targets of myocardial fibrosis. These mechanisms will then be translated into individualized diagnostic tools and specific therapeutic pharmacological options for heart failure. METHODS AND RESULTS: The FIBROTARGETS consortium has merged data from 12 patient cohorts in a common database available to individual consortium partners. The database consists of >12 000 patients with a large spectrum of cardiovascular clinical phenotypes. It integrates community‐based population cohorts, cardiovascular risk cohorts, and heart failure cohorts. CONCLUSIONS: The FIBROTARGETS biomarker programme is aimed at exploring fibrotic pathways allowing the bioprofiling of patients into specific ‘fibrotic’ phenotypes and identifying new therapeutic targets that will potentially enable the development of novel and tailored anti‐fibrotic therapies for heart failure. |
format | Online Article Text |
id | pubmed-5793978 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57939782018-02-14 Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis Ferreira, João Pedro Machu, Jean‐Loup Girerd, Nicolas Jaisser, Frederic Thum, Thomas Butler, Javed González, Arantxa Diez, Javier Heymans, Stephane McDonald, Kenneth Gyöngyösi, Mariann Firat, Hueseyin Rossignol, Patrick Pizard, Anne Zannad, Faiez ESC Heart Fail Original Research Articles AIMS: Myocardial fibrosis alters the cardiac architecture favouring the development of cardiac dysfunction, including arrhythmias and heart failure. Reducing myocardial fibrosis may improve outcomes through the targeted diagnosis and treatment of emerging fibrotic pathways. The European‐Commission‐funded ‘FIBROTARGETS’ is a multinational academic and industrial consortium with the main aims of (i) characterizing novel key mechanistic pathways involved in the metabolism of fibrillary collagen that may serve as biotargets, (ii) evaluating the potential anti‐fibrotic properties of novel or repurposed molecules interfering with the newly identified biotargets, and (iii) characterizing bioprofiles based on distinct mechanistic phenotypes involving the aforementioned biotargets. These pathways will be explored by performing a systematic and collaborative search for mechanisms and targets of myocardial fibrosis. These mechanisms will then be translated into individualized diagnostic tools and specific therapeutic pharmacological options for heart failure. METHODS AND RESULTS: The FIBROTARGETS consortium has merged data from 12 patient cohorts in a common database available to individual consortium partners. The database consists of >12 000 patients with a large spectrum of cardiovascular clinical phenotypes. It integrates community‐based population cohorts, cardiovascular risk cohorts, and heart failure cohorts. CONCLUSIONS: The FIBROTARGETS biomarker programme is aimed at exploring fibrotic pathways allowing the bioprofiling of patients into specific ‘fibrotic’ phenotypes and identifying new therapeutic targets that will potentially enable the development of novel and tailored anti‐fibrotic therapies for heart failure. John Wiley and Sons Inc. 2017-10-07 /pmc/articles/PMC5793978/ /pubmed/28988439 http://dx.doi.org/10.1002/ehf2.12218 Text en © 2017 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of the European Society of Cardiology. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Research Articles Ferreira, João Pedro Machu, Jean‐Loup Girerd, Nicolas Jaisser, Frederic Thum, Thomas Butler, Javed González, Arantxa Diez, Javier Heymans, Stephane McDonald, Kenneth Gyöngyösi, Mariann Firat, Hueseyin Rossignol, Patrick Pizard, Anne Zannad, Faiez Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title | Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title_full | Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title_fullStr | Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title_full_unstemmed | Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title_short | Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis |
title_sort | rationale of the fibrotargets study designed to identify novel biomarkers of myocardial fibrosis |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5793978/ https://www.ncbi.nlm.nih.gov/pubmed/28988439 http://dx.doi.org/10.1002/ehf2.12218 |
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