Level D· Scientific groundwork from lab and animal studiesAnimal StudyPubMed

Evaluating the efficacy of tissue-engineered human amniotic membrane in the treatment of myocardial infarction.

Khorramirouz R., Kameli SM., Fendereski K., Daryabari SS., Kajbafzadeh AM.

Animal Study on Cardiovascular Disease, published in Regen Med (2019) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
Read the A–D evidence level guide

This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Animal Study
Journal
Regen Med (2019)
Country
England
Reported sample size
—
Source database
PubMed
PMID
30741604
DOI
10.2217/rme-2018-0024
Citations
23

Abstract (original English)

Aim The aim of this study was to evaluate the efficacy of tissue-engineered amniotic membrane (AM) in the treatment of myocardial infarction lesions. Materials & methods 20 rats were subjected to coronary arterial ligation in order to induce myocardial infarction injury. Decellularized human AMs were seeded with 2 × 10 5 adipose-derived mesenchymal stem cells and were implanted in the infarcted hearts. Results & conclusion Histological and immunohistochemical evaluations indicated the regeneration of cardiomyocytes and reduction of inflammation and fibrosis in the patch-implanted group compared with a control group, 14 days after the surgery. Terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate biotin nick-end labeling assay was suggestive for apoptosis reduction in the patch-implanted specimens. This study suggested that human AM can be developed into a novel treatment for treating postmyocardial infarction.

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

How we grade evidence
AmnionAnimalsApoptosisHumansMyocardial InfarctionMyocytes, CardiacRatsRegenerative MedicineTissue Engineering

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