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dc.creatorFerreira, J.P. (João Pedro)-
dc.creatorMachu, J.L. (Jean-Loup)-
dc.creatorGirerd, N. (Nicolas)-
dc.creatorJaisser, F. (Frederic)-
dc.creatorThum, T. (Thomas)-
dc.creatorButler, J. (Javed)-
dc.creatorGonzalez, A. (Arantxa)-
dc.creatorDiez, J. (Javier)-
dc.creatorHeymans, S. (Stephane)-
dc.creatorMcDonald, K. (Kenneth)-
dc.creatorGyöngyösi, M. (Mariann)-
dc.creatorFirat, H. (Hueseyin)-
dc.creatorRossignol, P.(Patrick)-
dc.creatorPizard, A. (Anne)-
dc.creatorZannad, F. (Faiez)-
dc.date.accessioned2023-03-13T12:30:27Z-
dc.date.available2023-03-13T12:30:27Z-
dc.date.issued2018-
dc.identifier.citationFerreira, J.P. (João Pedro); Machu, J.L. (Jean-Loup); Girerd, N. (Nicolas); et al. "Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis". Esc hear failure. 5 (1), 2018, 139 - 148es_ES
dc.identifier.issn2055-5822-
dc.identifier.urihttps://hdl.handle.net/10171/65677-
dc.description.abstractAims 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.es_ES
dc.description.sponsorshipThis work was funded through the European Commission Seventh Framework Programme (FIBROTARGETS project grant HEALTH-2013-602904) and the REBIRTH Excellence Cluster, Hannover Medical School (to T.T.).es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/602904/EUes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.subjectMyocardial fibrosises_ES
dc.subjectFibrotic bioprofileses_ES
dc.subjectHeart failurees_ES
dc.titleRationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosises_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.description.noteThis is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.es_ES
dc.identifier.doi10.1002/ehf2.12218-
dadun.citation.endingPage148es_ES
dadun.citation.number1es_ES
dadun.citation.publicationNameEsc hear failurees_ES
dadun.citation.startingPage139es_ES
dadun.citation.volume5es_ES

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