Evidence map›Paper›PMID 29302333›Full record

ArticleNPJ Regenerative medicine2016

Intravenous delivery of adeno-associated virus 9-encoded IGF-1Ea propeptide improves post-infarct cardiac remodelling.

Enrique Gallego-Colon, Maria Villalba, Joanne Tonkin, Francisco Cruz, Juan Antonio Bernal, Luis J Jimenez-Borregureo, Michael D Schneider, Enrique Lara-Pezzi, Nadia Rosenthal

Erratum issuedAbstract read
In one paragraph

Article in NPJ Regenerative medicine, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
  2. Review
  3. Modified mRNA as a Treatment for Myocardial Infarction.International journal of molecular sciences · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Enrique Gallego-ColonImperial Centre for Translational Research, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Maria VillalbaCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Joanne TonkinImperial Centre for Translational Research, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Francisco CruzCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Juan Antonio BernalCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Luis J Jimenez-BorregureoCardiovascular Development and Repair Department, Centro Nacional de Investigaciones Cardiovasculares (CNIC), Madrid, Spain.
Michael D SchneiderImperial Centre for Translational Research, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Enrique Lara-PezziImperial Centre for Translational Research, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.
Nadia RosenthalImperial Centre for Translational Research, National Heart and Lung Institute, Faculty of Medicine, Imperial College London, London, UK.

Funding

Medical Research Council G0901467
6 · The paper itself

Abstract

The insulin-like growth factor Ea propeptide (IGF-1Ea) is a powerful enhancer of cardiac muscle growth and regeneration, also blocking age-related atrophy and beneficial in multiple skeletal muscle diseases. The therapeutic potential of IGF-1Ea compared with mature IGF-1 derives from its local action in the area of synthesis. We have developed an adeno-associated virus (AAV) vector for IGF-1Ea delivery to the heart to treat mice after myocardial infarction and examine the reparative effects of local IGF-1Ea production on left ventricular remodelling. A cardiotropic AAV9 vector carrying a cardiomyocyte-specific IGF-1Ea-luciferase bi-cistronic gene expression cassette (AAV9.IGF-1Ea) was administered intravenously to infarcted mice, 5 h after ischemia followed by reperfusion (I/R), as a model of myocardial infarction. Virally encoded IGF-1Ea in the heart improved global left ventricular function and remodelling, as measured by wall motion and thickness, 28 days after delivery, with higher viral titers yielding better improvement. The present study demonstrates that single intravenous AAV9-mediated IGF-1Ea Gene Therapy represents a tissue-targeted therapeutic approach to prevent the adverse remodelling after myocardial infarct.

Identifiers

PMID29302333
PMCPMC5744701

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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.