Evidence map›Paper›PMID 32985793›Full record

ArticleStem cells translational medicine2021

Systemic multipotent adult progenitor cells protect the cerebellum after asphyxia in fetal sheep.

Ruth Gussenhoven, Daan R M G Ophelders, Jeroen Dudink, Kay Pieterman, Martin Lammens, Robert W Mays, Luc J Zimmermann, Boris W Kramer, Tim G A M Wolfs, Reint K Jellema

Open access · goldAbstract read
In one paragraph

Article in Stem cells translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 6 citations in OpenAlex.

  1. 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

10 authors at 6 institutions in 3 countries.

Ruth GussenhovenDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.
Daan R M G OpheldersDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.
Jeroen DudinkDepartment of Neonatology, Wilhelmina Children's Hospital and Brain Centre Rudolf Magnus, University Medical Centre Utrecht, Utrecht, The Netherlands.
Kay PietermanBiomedical Imaging Group Rotterdam, Department of Radiology and Medical Informatics, Erasmus Medical Centre, Rotterdam, The Netherlands.
Martin LammensDepartment of Pathology, Antwerp University Hospital and University of Antwerp, Edegem, Belgium.
Robert W MaysRegenerative Medicine, Athersys, Inc., Cleveland, Ohio, USA.
Luc J ZimmermannDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.
Boris W KramerDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.
Tim G A M WolfsDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID 0000-0003-4417-4144
Reint K JellemaDepartment of Pediatrics, Maastricht University Medical Centre, Maastricht, The Netherlands.ORCID 0000-0002-6918-0930
Maastricht University Medical Centre · NLMaastricht University · NLAthersys (United States) · USErasmus University Rotterdam · NLUniversity of Antwerp · BEWilhelmina Children's Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Involvement of the cerebellum in the pathophysiology of hypoxic-ischemic encephalopathy (HIE) in preterm infants is increasingly recognized. We aimed to assess the neuroprotective potential of intravenously administered multipotent adult progenitor cells (MAPCs) in the preterm cerebellum. Instrumented preterm ovine fetuses were subjected to transient global hypoxia-ischemia (HI) by 25 minutes of umbilical cord occlusion at 0.7 of gestation. After reperfusion, two doses of MAPCs were administered intravenously. MAPCs are a plastic adherent bone-marrow-derived population of adult progenitor cells with neuroprotective potency in experimental and clinical studies. Global HI caused marked cortical injury in the cerebellum, histologically indicated by disruption of cortical strata, impeded Purkinje cell development, and decreased dendritic arborization. Furthermore, global HI induced histopathological microgliosis, hypomyelination, and disruption of white matter organization. MAPC treatment significantly prevented cortical injury and region-specifically attenuated white matter injury in the cerebellum following global HI. Diffusion tensor imaging (DTI) detected HI-induced injury and MAPC neuroprotection in the preterm cerebellum. This study has demonstrated in a preclinical large animal model that early systemic MAPC therapy improved structural injury of the preterm cerebellum following global HI. Microstructural improvement was detectable with DTI. These findings support the potential of MAPC therapy for the treatment of HIE and the added clinical value of DTI for the detection of cerebellar injury and the evaluation of cell-based therapy.

Indexed as

AsphyxiaCerebellumHypoxia-Ischemia, BrainMultipotent Stem CellsAdult Stem CellsAnimalsDiffusion Tensor ImagingDisease Models, AnimalFetusHumansInfant, NewbornInfant, PrematureSheepasphyxiacerebellumhypoxic-ischemic encephalopathyMAPCstem cells

Identifiers

PMID32985793
PMCPMC7780812
OpenAlexW3089231140

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.