Evidence map›Paper›PMID 30016405›Full record

ReviewCardiovascular research2018

Future directions for therapeutic strategies in post-ischaemic vascularization: a position paper from European Society of Cardiology Working Group on Atherosclerosis and Vascular Biology.

Andrea Caporali, Magnus Bäck, Mat J Daemen, Imo E Hoefer, Elizabeth A Jones, Esther Lutgens, Christian M Matter, Marie-Luce Bochaton-Piallat, Arndt F Siekmann, Judith C Sluimer and 6 more

Open access · bronzeAbstract readReviewConsensus Statement
In one paragraph

Review in Cardiovascular research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.1field-weighted citation impact, top 22% of its field
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

11 citing papers in PubMed, 22 citations in OpenAlex.

  1. Gene Therapy for Heart Failure.Journal of cardiovascular translational research · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Biomedicines · 2022
    Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
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

16 authors at 16 institutions in 9 countries.

Andrea CaporaliUniversity/British Heart Foundation Centre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Magnus BäckDivision of Valvular and Coronary Disease, Department of Medicine, Center for Molecular Medicine, Karolinska Institutet and University Hospital Stockholm, Stockholm, Sweden.
Mat J DaemenDepartment of Pathology, Academic Medical Hospital, University of Amsterdam, Amsterdam, The Netherlands.
Imo E HoeferLaboratory of Experimental Cardiology and Laboratory of Clinical Chemistry and Hematology, UMC Utrecht, Utrecht, Netherlands.
Elizabeth A JonesDepartment of Cardiovascular Science, KU Leuven, Leuven, Belgium.
Esther LutgensDepartment of Medical Biochemistry, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Christian M MatterDepartment of Cardiology, University Heart Center, University Hospital Zurich, Zurich, Switzerland.
Marie-Luce Bochaton-PiallatDepartment of Pathology and Immunology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Arndt F SiekmannMax Planck Institute for Molecular Biomedicine, Muenster, Germany.
Judith C SluimerUniversity/British Heart Foundation Centre for Cardiovascular Science, The Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Sabine SteffensLudwig-Maximilians-University, German Centre for Cardiovascular Research (DZHK), Partner Site Munich Heart Alliance, Munich, Germany.
José TuñónIIS-Fundación Jiménez Díaz, Madrid, Spain.
Cecile VindisINSERM U1048/Institute of Metabolic and Cardiovascular Diseases, Toulouse, France.
Jolanda J WentzelDepartment of Cardiology, Biomechanics Laboratory, Erasmus MC, Rotterdam, The Netherlands.
Seppo Ylä-HerttualaA.I. Virtanen Institute, University of Eastern Finland, Kuopio, Finland.
Paul C EvansDepartment of Infection, Immunity and Cardiovascular Disease, Faculty of Medicine, Dentistry and Health, the INSIGNEO Institute for In Silico Medicine and the Bateson Centre, University of Sheffield, Sheffield, UK.
Erasmus University Rotterdam · NLGerman Centre for Cardiovascular Research · DEHospital Universitario Fundación Jiménez Díaz · ESInstitut des Maladies Métaboliques et Cardiovasculaires · FRKU Leuven · BELudwig-Maximilians-Universität München · DEMax Planck Institute for Molecular Biomedicine · DEThe Queen's Medical Research Institute · GBUniversité de Lorraine · FRUniversity Hospital of Zurich · CHUniversity Medical Center Utrecht · NLUniversity of Amsterdam · NLUniversity of Eastern Finland · FIUniversity of Edinburgh · GBUniversity of Geneva · CHUniversity of Sheffield · GB

Funding

British Heart Foundation PG/16/58/32275
6 · The paper itself

Abstract

Modulation of vessel growth holds great promise for treatment of cardiovascular disease. Strategies to promote vascularization can potentially restore function in ischaemic tissues. On the other hand, plaque neovascularization has been shown to associate with vulnerable plaque phenotypes and adverse events. The current lack of clinical success in regulating vascularization illustrates the complexity of the vascularization process, which involves a delicate balance between pro- and anti-angiogenic regulators and effectors. This is compounded by limitations in the models used to study vascularization that do not reflect the eventual clinical target population. Nevertheless, there is a large body of evidence that validate the importance of angiogenesis as a therapeutic concept. The overall aim of this Position Paper of the ESC Working Group of Atherosclerosis and Vascular biology is to provide guidance for the next steps to be taken from pre-clinical studies on vascularization towards clinical application. To this end, the current state of knowledge in terms of therapeutic strategies for targeting vascularization in post-ischaemic disease is reviewed and discussed. A consensus statement is provided on how to optimize vascularization studies for the identification of suitable targets, the use of animal models of disease, and the analysis of novel delivery methods.

Indexed as

Neovascularization, PathologicNeovascularization, PhysiologicAngiogenic ProteinsAnimalsBlood VesselsCardiovascular DiseasesCell TransplantationDiffusion of InnovationDisease Models, AnimalForecastingGene Expression RegulationGenetic TherapyHumansMyocardiumRecovery of FunctionRNA, UntranslatedAngiogenic ProteinsRNA, Untranslated

Identifiers

PMID30016405
PMCPMC6106103
OpenAlexW2884736809

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.