Evidence map›Paper›PMID 34884856›Full record

ReviewInternational journal of molecular sciences2021

Therapeutic Acellular Scaffolds for Limiting Left Ventricular Remodelling-Current Status and Future Directions.

Sadia Perveen, Daniela Rossin, Emanuela Vitale, Rachele Rosso, Roberto Vanni, Caterina Cristallini, Raffaella Rastaldo, Claudia Giachino

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
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  4. 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

8 authors.

Sadia PerveenDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.ORCID 0000-0003-0959-2076
Daniela RossinDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.ORCID 0000-0001-5741-5774
Emanuela VitaleDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.
Rachele RossoDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.ORCID 0000-0003-0573-3388
Roberto VanniDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.
Caterina CristalliniInstitute for Chemical and Physical Processes, CNR, 56126 Pisa, Italy.
Raffaella RastaldoDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.ORCID 0000-0002-8673-9409
Claudia GiachinoDepartment of Clinical and Biological Sciences, University of Turin, 10043 Orbassano, Italy.

Funding

European Union Translational EU project INCIPIT M-ERA.NET 2University of Turin GIAC_RILO_20_03University of Turin RASR_RILO_20_01
6 · The paper itself

Abstract

Myocardial infarction (MI) is one of the leading causes of heart-related deaths worldwide. Following MI, the hypoxic microenvironment triggers apoptosis, disrupts the extracellular matrix and forms a non-functional scar that leads towards adverse left ventricular (LV) remodelling. If left untreated this eventually leads to heart failure. Besides extensive advancement in medical therapy, complete functional recovery is never accomplished, as the heart possesses limited regenerative ability. In recent decades, the focus has shifted towards tissue engineering and regenerative strategies that provide an attractive option to improve cardiac regeneration, limit adverse LV remodelling and restore function in an infarcted heart. Acellular scaffolds possess attractive features that have made them a promising therapeutic candidate. Their application in infarcted areas has been shown to improve LV remodelling and enhance functional recovery in post-MI hearts. This review will summarise the updates on acellular scaffolds developed and tested in pre-clinical and clinical scenarios in the past five years with a focus on their ability to overcome damage caused by MI. It will also describe how acellular scaffolds alone or in combination with biomolecules have been employed for MI treatment. A better understanding of acellular scaffolds potentialities may guide the development of customised and optimised therapeutic strategies for MI treatment.

Indexed as

Tissue ScaffoldsVentricular RemodelingAnimalsBiocompatible MaterialsCardiotonic AgentsEnzyme InhibitorsExtracellular MatrixExtracellular VesiclesGenetic TherapyHumansIntercellular Signaling Peptides and ProteinsMyocardial InfarctionPolymersProteinsBiocompatible MaterialsCardiotonic AgentsEnzyme InhibitorsIntercellular Signaling Peptides and ProteinsPolymersProteinsacellular scaffoldscardiac regenerationconductive polymersextracellular matrixmyocardial infarctionnanoparticlestissue engineeringventricular remodelling

Identifiers

PMID34884856
PMCPMC8658014

What OpenQuestion holds

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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.