Evidence map›Paper›PMID 28988439›Full record

ReviewESC heart failure2018

Rationale of the FIBROTARGETS study designed to identify novel biomarkers of myocardial fibrosis.

João Pedro Ferreira, Jean-Loup Machu, Nicolas Girerd, Frederic Jaisser, Thomas Thum, Javed Butler, Arantxa González, Javier Diez, Stephane Heymans, Kenneth McDonald and 5 more

Abstract readReview
In one paragraph

Review in ESC heart failure, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Highlights in heart failure.ESC heart failure · 2019
    Pooled it
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

João Pedro FerreiraCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.
Jean-Loup MachuCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.
Nicolas GirerdCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.
Frederic JaisserCentre de Recherche des Cordeliers, Inserm U1138, Université Pierre et Marie Curie, Paris, France.
Thomas ThumInstitute of Molecular and Translational Therapeutic Strategies (IMTTS), Hannover Medical School, Hanover, Germany.
Javed ButlerCardiology Division, Stony Brook University, Stony Brook, NY, USA.
Arantxa GonzálezProgram of Cardiovascular Diseases, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Javier DiezProgram of Cardiovascular Diseases, Center for Applied Medical Research, University of Navarra, Pamplona, Spain.
Stephane HeymansCenter for Heart Failure Research, Cardiovascular Research Institute Maastricht (CARIM), University Hospital Maastricht, Maastricht, The Netherlands.
Kenneth McDonaldUniversity College Dublin, Dublin, Ireland.
Mariann GyöngyösiDepartment of Cardiology, Medical University of Vienna, Vienna, Austria.
Hueseyin FiratFiralis S.A.S., Huningue, France.
Patrick RossignolCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.
Anne PizardCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.
Faiez ZannadCentre d'Investigation Clinique 1433 Module Plurithématique, INSERM U1116, Université de Lorraine, CHRU de Nancy, F-CRIN INI-CRCT, Hopitaux de Brabois, Institut Lorrain du Coeur et des Vaisseaux Louis Mathieu, 4 rue du Morvan, 54500, Vandœuvre-lès-Nancy, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsMyocardial 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

resultsThe 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.

conclusionsThe 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.

Indexed as

AnimalsBiomarkersCardiomyopathiesFibrosisHumansMyocardiumResearch DesignBiomarkersFibrotic bioprofilesHeart failureMyocardial fibrosis

Identifiers

PMID28988439
PMCPMC5793978

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.