Evidence map›Paper›PMID 36376770›Full record

ArticleStem cell reviews and reports2023

Autologous CD133 + Cells and Laser Revascularization in patients with severe Ischemic Cardiomyopathy.

Ahmed Abdel-Latif, Taha Ahmed, Steve W Leung, Talal Alnabelsi, Wadea Tarhuni, Michael E Sekela

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Article in Stem cell reviews and reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 56% of its field
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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Review
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

6 authors at 2 institutions in 2 countries.

Ahmed Abdel-LatifDepartment of Cardiovascular Medicine, Division of Cardiology, University of Kentucky, Lexington, KY, USA.ORCID 0000-0002-8178-7102
Taha AhmedDepartment of Cardiovascular Medicine, Division of Cardiology, University of Kentucky, Lexington, KY, USA.
Steve W LeungDepartment of Cardiovascular Medicine, Division of Cardiology, University of Kentucky, Lexington, KY, USA.
Talal AlnabelsiDepartment of Cardiovascular Medicine, Division of Cardiology, University of Kentucky, Lexington, KY, USA.
Wadea TarhuniDepartment of Internal Medicine, Division of Cardiology, Canadian Cardiac Research Center, University of Saskatchewan, SK, Saskatoon, Canada.
Michael E SekelaDepartment of Cardiothoracic Surgery, University of Kentucky, Lexington, KY, USA. mese223@uky.edu.
University of Kentucky · USUniversity of Saskatchewan · CA

Funding

Biological Substrates of Maladaptive Stress Response in Early ChildhoodR01MH124266 · NIMH · WASHINGTON UNIVERSITY · PI MELHEM, NADINE M., PERLMAN, SUSAN B · 2020 to 2024
$3.8M
Lysophosphatidic Acid Mediates Cardiac Inflammation After Acute InfarctionR01HL138488 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ABDEL-LATIF, AHMED · 2017 to 2021
$1.9M
NHLBI NIH HHS R01 HL138488NIMH NIH HHS R01 MH124266
6 · The paper itself

Abstract

objectiveWe tested the hypothesis that targeted TMLR combined with intramyocardial injection of autologous CD 133

methodsEight male patients (age 62 ± 2.4 years) with multivessel severe ischemic heart disease and no revascularization options were enrolled. Autologous CD 133 + endothelial progenitor cells were derived and purified from the bone marrow on the day of surgery using the clinical-grade closed CliniMACS system. Using a lateral thoracotomy approach, TMLR was performed, followed by transmyocardial transplantation of purified CD133 + cells (mean number of transplanted cells: 12.5 × 10

resultsNo major complications or death occurred during the procedure or during the peri-operative hospital stay. One patient died of cardiac cause 6 months post-procedure. There was a reported short-term improvement in anginal and heart failure symptoms and a modest reduction in the ischemic score as assessed by perfusion imaging.

conclusionsOur phase 1 clinical study examining the combination therapy of targeted transmyocardial laser revascularization therapy and autologous CD133 + endothelial progenitor cells in patients with chronic ICM and no revascularization options demonstrates the feasibility and short-term safety of this combined approach and warrants future larger phase 2 randomized clinical studies.

Indexed as

CardiomyopathiesHeart DiseasesMyocardial IschemiaAC133 AntigenHumansLasersMaleMiddle AgedMyocardial RevascularizationTreatment OutcomeAC133 AntigenPROM1 protein, humanAngiogenesisAutologous bone marrow-derived stem cellsIschemic heart disease

Identifiers

PMID36376770
OpenAlexW4308962182

What OpenQuestion holds

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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.