Evidence map›Paper›PMID 28468789›Full record

ArticleJournal of the American Heart Association2017

Intracoronary Administration of Allogeneic Adipose Tissue-Derived Mesenchymal Stem Cells Improves Myocardial Perfusion But Not Left Ventricle Function, in a Translational Model of Acute Myocardial Infarction.

Joaquim Bobi, Núria Solanes, Rodrigo Fernández-Jiménez, Carlos Galán-Arriola, Ana Paula Dantas, Leticia Fernández-Friera, Carolina Gálvez-Montón, Elisabet Rigol-Monzó, Jaume Agüero, José Ramírez and 8 more

Abstract read
In one paragraph

Article in Journal of the American Heart Association, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
–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

32 citing papers in PubMed.

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  15. Extracellular Vesicle-Based Therapeutics for Heart Repair.Nanomaterials (Basel, Switzerland) · 2021
    Review
  16. Review
  17. CD73Frontiers in cell and developmental biology · 2021
    Article
  18. Review
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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

18 authors.

Joaquim BobiAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Núria SolanesAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Rodrigo Fernández-JiménezCentro Nacional de Investigaciones Cardiovasculares Carlos III, CNIC, Madrid, Spain.
Carlos Galán-ArriolaCentro Nacional de Investigaciones Cardiovasculares Carlos III, CNIC, Madrid, Spain.
Ana Paula DantasAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Leticia Fernández-FrieraCentro Nacional de Investigaciones Cardiovasculares Carlos III, CNIC, Madrid, Spain.
Carolina Gálvez-MontónICREC Research Program, Health Science Research Institute Germans Trias i Pujol, Badalona, Spain.
Elisabet Rigol-MonzóServei d'Immunologia, Hospital Clínic de Barcelona, Barcelona, Spain.
Jaume AgüeroCentro Nacional de Investigaciones Cardiovasculares Carlos III, CNIC, Madrid, Spain.
José RamírezServei d'Anatomia Patològica, Hospital Clínic de Barcelona, Barcelona, Spain.
Mercè RoquéAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Antoni Bayés-GenísICREC Research Program, Health Science Research Institute Germans Trias i Pujol, Badalona, Spain.
Javier Sánchez-GonzálezPhilips Healthcare, Madrid, Spain.
Ana García-ÁlvarezAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Manel SabatéAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain.
Santiago RouraICREC Research Program, Health Science Research Institute Germans Trias i Pujol, Badalona, Spain.
Borja IbáñezCentro Nacional de Investigaciones Cardiovasculares Carlos III, CNIC, Madrid, Spain.
Montserrat RigolAugust Pi i Sunyer Biomedical Research Institute (IDIBAPS), Institut de Malalties Cardiovasculars, Hospital Clínic de Barcelona, Universitat de Barcelona, Spain mrigol@clinic.cat.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutologous adipose tissue-derived mesenchymal stem cells (ATMSCs) therapy is a promising strategy to improve post-myocardial infarction outcomes. In a porcine model of acute myocardial infarction, we studied the long-term effects and the mechanisms involved in allogeneic ATMSCs administration on myocardial performance. METHODS AND

resultsThirty-eight pigs underwent 50 minutes of coronary occlusion; the study was completed in 33 pigs. After reperfusion, allogeneic ATMSCs or culture medium (vehicle) were intracoronarily administered. Follow-ups were performed at short (2 days after acute myocardial infarction vehicle-treated, n=10; ATMSCs-treated, n=9) or long term (60 days after acute myocardial infarction vehicle-treated, n=7; ATMSCs-treated, n=7). At short term, infarcted myocardium analysis showed reduced apoptosis in the ATMSCs-treated animals (48.6±6% versus 55.9±5.7% in vehicle;

conclusionsIn this porcine acute myocardial infarction model, allogeneic ATMSCs-based therapy was associated with increased cardioprotective and reparative mechanisms and with better cardiac magnetic resonance-measured perfusion. No effect on left ventricular volumes or ejection fraction was observed.

Indexed as

Coronary CirculationMesenchymal Stem CellsVentricular Function, LeftAdipose TissueAngiogenic ProteinsAnimalsCells, CulturedComputed Tomography AngiographyCoronary AngiographyCytokinesDisease Models, AnimalGreen Fluorescent ProteinsMagnetic Resonance ImagingMaleMesenchymal Stem Cell TransplantationMultidetector Computed TomographyAngiogenic ProteinsCytokinesGreen Fluorescent Proteinsadipose tissue‐derived mesenchymal stem cellsallogeneic originmyocardial infarctionmyocardial perfusionvascular density

Identifiers

PMID28468789
PMCPMC5524109

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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.