Evidence map›Paper›PMID 30657875›Full record

GuidelineCardiovascular research2019

ESC Working Group on Cellular Biology of the Heart: position paper for Cardiovascular Research: tissue engineering strategies combined with cell therapies for cardiac repair in ischaemic heart disease and heart failure.

Rosalinda Madonna, Linda W Van Laake, Hans Erik Botker, Sean M Davidson, Raffaele De Caterina, Felix B Engel, Thomas Eschenhagen, Francesco Fernandez-Aviles, Derek J Hausenloy, Jean-Sebastien Hulot and 11 more

Registry-linked trialOpen access · bronzeAbstract readPractice GuidelineReview
In one paragraph

Guideline in Cardiovascular research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05632432 (Autologous Atrial Appendage Micrografts Transplanted During Coronary Artery Bypass Surgery), which is not on this map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
15.5field-weighted citation impact, top 1% 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.

NCT05632432 narecruitingnot on this mapstarted 2024, after this paper: background citation

Autologous Atrial Appendage Micrografts Transplanted During Coronary Artery Bypass Surgery: the AAMS2 Randomized, Double-blinded, and Placebo-controlled Trial

TypeinterventionalSponsorHospital District of Helsinki and UusimaaRan2024 to 2026Enrolled50ConditionsIschemic Heart Disease, Ischemic Cardiomyopathy, Heart Failure, Systolic, Heart Failure NYHA Class IIIArmsEpicardial AAMs-patch transplantation, RNA-stabilized whole blood sampling, Plasma sampling, Transthoracic echocardiography, Late-gadolinium enhancement cardiac magnetic resonance imaging (LGE-CMRI)
3 · Its place in the literature

Who cites it

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 121 citations in OpenAlex.

  1. Pooled it
  2. Adaptation of mesenchymal stromal cells to culture on collagen-based bioscaffold.Journal of materials science. Materials in medicine · 2026
    Article
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  18. Cell Therapy in the Treatment of Coronary Heart Disease.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Harnessing developmental cues for cardiomyocyte production.Development (Cambridge, England) · 2023
    Review
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

21 authors at 20 institutions in 13 countries.

Rosalinda MadonnaInstitute of Cardiology and Center of Excellence on Aging, "G. d'Annunzio" University-Chieti, Italy.
Linda W Van LaakeCardiology and UMC Utrecht Regenerative Medicine Center, University Medical Center Utrecht, The Netherlands.
Hans Erik BotkerDepartment of Cardiology, Aarhus University Hospital, Aarhus N, Denmark.
Sean M DavidsonThe Hatter Cardiovascular Institute, University College London, London, UK.
Raffaele De CaterinaInstitute of Cardiology and Center of Excellence on Aging, "G. d'Annunzio" University-Chieti, Italy.
Felix B EngelExperimental Renal and Cardiovascular Research, Department of Nephropathology, Institute of Pathology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany; Muscle Research Center Erlangen, MURCE.
Thomas EschenhagenInstitute of Experimental Pharmacology and Toxicology, University Medical Center Hamburg Eppendorf, Germany.
Francesco Fernandez-AvilesDepartment of Cardiology, Hospital General Universitario Gregorio Marañón, Instituto de Investigación Sanitaria Gregorio Marañón, Universidad Complutense, Madrid, Spain.
Derek J HausenloyThe Hatter Cardiovascular Institute, University College London, London, UK.
Jean-Sebastien HulotUniversité Paris-Descartes, Sorbonne Paris Cité, Paris, France.
Sandrine LecourHatter Cardiovascular Research Institute, University of Cape Town, South Africa.
Jonathan LeorTamman and Neufeld Cardiovascular Research Institutes, Sackler Faculty of Medicine, Tel-Aviv University and Sheba Medical Center, Tel-Hashomer, Israel.
Philippe MenaschéDepartment of Cardiovascular Surgery, Hôpital Européen Georges Pompidou, Paris, France.
Maurizio PesceUnità di Ingegneria Tissutale Cardiovascolare, Centro Cardiologico Monzino, IRCCS, Milan, Italy.
Cinzia PerrinoDepartment of Advanced Biomedical Sciences, Federico II University, Naples, Italy.
Fabrice PrunierInstitut Mitovasc, INSERM, CNRS, Université d'Angers, Service de Cardiologie, CHU Angers, Angers, France.
Sophie Van LinthoutBerlin-Brandenburg Center for Regenerative Therapies, Charité, University Medicine Berlin, Campus Virchow Klinikum, Berlin, Germany.
Kirsti YtrehusDepartment of Medical Biology, UiT, The Arctic University of Norway, Norway.
Wolfram-Hubertus ZimmermannInstitute of Pharmacology and Toxicology, University Medical Center Göttingen, Göttingen, Germany.
Peter FerdinandyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Nagyvárad tér 4, III-V Floor, H-1089 Budapest, Hungary.
Joost P G SluijterDepartment of Cardiology, Experimental Cardiology Laboratory, Regenerative Medicine Center, University Medical Center Utrecht, Utrecht University, Heidelberglaan 100, CX Utrecht, the Netherlands.
University Medical Center Utrecht · NLAarhus University Hospital · DKCentro Cardiologico Monzino · ITCentro de Investigación en Red en Enfermedades Cardiovasculares · ESCharité - Universitätsmedizin Berlin · DEFederico II University Hospital · ITFriedrich-Alexander-Universität Erlangen-Nürnberg · DEGerman Centre for Cardiovascular Research · DENational Heart Centre Singapore · SGParis Cardiovascular Research Center · FRSemmelweis University · HUSorbonne Paris Cité · FRTel Aviv University · ILUiT The Arctic University of Norway · NOUniversitätsmedizin Göttingen · DEUniversité d'Angers · FRUniversity College London · GBUniversity of Cape Town · ZAUniversity of Chieti-Pescara · ITUniversity of Pisa · IT

Funding

British Heart Foundation FS/10/039/28270British Heart Foundation PG/16/85/32471British Heart Foundation PG/18/44/33790Department of Health
6 · The paper itself

Abstract

Morbidity and mortality from ischaemic heart disease (IHD) and heart failure (HF) remain significant in Europe and are increasing worldwide. Patients with IHD or HF might benefit from novel therapeutic strategies, such as cell-based therapies. We recently discussed the therapeutic potential of cell-based therapies and provided recommendations on how to improve the therapeutic translation of these novel strategies for effective cardiac regeneration and repair. Despite major advances in optimizing these strategies with respect to cell source and delivery method, the clinical outcome of cell-based therapy remains unsatisfactory. Major obstacles are the low engraftment and survival rate of transplanted cells in the harmful microenvironment of the host tissue, and the paucity or even lack of endogenous cells with repair capacity. Therefore, new ways of delivering cells and their derivatives are required in order to empower cell-based cardiac repair and regeneration in patients with IHD or HF. Strategies using tissue engineering (TE) combine cells with matrix materials to enhance cell retention or cell delivery in the transplanted area, and have recently received much attention for this purpose. Here, we summarize knowledge on novel approaches emerging from the TE scenario. In particular, we will discuss how combinations of cell/bio-materials (e.g. hydrogels, cell sheets, prefabricated matrices, microspheres, and injectable matrices) combinations might enhance cell retention or cell delivery in the transplantation areas, thereby increase the success rate of cell therapies for IHD and HF. We will not focus on the use of classical engineering approaches, employing fully synthetic materials, because of their unsatisfactory material properties which render them not clinically applicable. The overall aim of this Position Paper from the ESC Working Group Cellular Biology of the Heart is to provide recommendations on how to proceed in research with these novel TE strategies combined with cell-based therapies to boost cardiac repair in the clinical settings of IHD and HF.

Indexed as

RegenerationBiomedical ResearchCardiologyConsensusHeart FailureHumansMyocardial IschemiaMyocardiumRecovery of FunctionStem Cell TransplantationTissue EngineeringTreatment OutcomeBiomaterialsCardiac tissue engineeringCellsHeart failureIschaemic heart disease

Identifiers

PMID30657875
PMCPMC6383054
OpenAlexW2910905200

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.