Evidence map›Paper›PMID 42441008›Full record

ArticleHealth science reports2026

Unlocking the Cardioprotective Action of Human Amniotic Mesenchymal Stem Cells: A Review of the Current Documents.

Reza Arefnezhd, Farzaneh Moammer, Amirhossein Ghaneimoghadam, Shaghayegh Khodabakhshian, Sina Safdari, Reza Nasiri, Hossein Fatemian, Mohammad Reza Alipour, Seyyed Kiarash Sadat Rafiei, Fatemeh Rezaei-Tazangi and 1 more

Abstract read
In one paragraph

Article in Health science reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Reza ArefnezhdStudent Research Committee Fasa University of Medical Sciences Fasa Iran.
Farzaneh MoammerStudent Research Committee, School of Medicine Guilan University of Medical Sciences Rasht Iran.
Amirhossein GhaneimoghadamChildren Growth Disorder Research Center Shahid Sadoughi University of Medical Sciences Yazd Iran.
Shaghayegh KhodabakhshianDepartment of Education Student Research Center Jask Iran.
Sina SafdariStudent Research Committee Dezful University of Medical Sciences Dezful Iran.
Reza NasiriSchool of Medicine Shiraz University of Medical Sciences Shiraz Iran.
Hossein FatemianSchool of Medicine Shiraz University of Medical Sciences Shiraz Iran.
Mohammad Reza AlipourDepartment of Nursing, School of Nursing Islamic Azad University of Mashhad Mashhad Iran.
Seyyed Kiarash Sadat RafieiStudent Research Committee, School of Medicine Shahid Beheshti University of Medical Sciences Tehran Iran.
Fatemeh Rezaei-TazangiDepartment of Anatomy, School of Medicine Fasa Univerity of Medical Sciences Fasa Iran.ORCID https://orcid.org/0000-0003-1402-6482
Marziye Ranjbar TavakoliPharmaceutical Sciences and Cosmetic Products Research Center Kerman University of Medical Sciences Kerman Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aims: Cardiovascular diseases (CVDs), such as heart failure (HF), myocardial ischemic-reperfusion injury (MIRI), and myocardial infarction (MI), are defined as one of the most known causes of mortality and morbidity worldwide, responsible for 30% of global death rate. The etiologic factors for CVDs have not been exactly comprehended; however, a number of modifiable and nonmodifiable risk factors have been recognized, like smoking, physical activity, and the history of some diseases (e.g., hyperlipidemia, hypertension, and obesity). Although the current therapeutic approaches for these diseases, which are on the basis of conventional pharmacotherapy and surgery, have been largely effective in dwindling mortality and alleviating symptoms, the presence of serious side effects and injury to the different body organs and restricted clinical application are the main barriers of these methods. Therefore, there is an unmet need to recommend alternative and effective strategies with the minimum side effects for CVDs. Results: Recently, mesenchymal stem cell (MSC)-based therapies have opened a new window to patients with diverse health problems. MSCs can be isolated from different sources, for example, adipose tissue, bone marrow, umbilical cord, amniotic membrane, and amniotic fluid, and have reflected remarkable pharmacological and biological abilities. An increasing body of evidence has paid special attention to MSCs derived from the amniotic membrane and amniotic fluid for treating health-threatening conditions, particularly CVDs, in light of their safety and facility in collecting without considerable ethical issues. Conclusion: This narrative review delves into the cardioprotective potential of human amniotic mesenchymal stem cells against the three main cardiovascular disorders with high lethality, including HF, MIRI, and MI, with a mechanistic insight.

Indexed as

heart failurehuman amniotic mesenchymal stem cellsmyocardial infarctionmyocardial ischemic reperfusion injury

Identifiers

PMID42441008
PMCPMC13334615

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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.