Evidence map›Paper›PMID 26353846›Full record

ArticleInternational urogynecology journal2016

Mesenchymal stem cell therapy in a rat model of birth-trauma injury: functional improvements and biodistribution.

Zhina Sadeghi, Justin Isariyawongse, Michael Kavran, Kenan Izgi, Gabriela Marini, Joseph Molter, Firouz Daneshgari, Chris A Flask, Arnold Caplan, Adonis Hijaz

Open access · greenAbstract read
In one paragraph

Article in International urogynecology journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

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  5. Mesenchymal stem cell-based therapy for female stress urinary incontinence.Frontiers in cell and developmental biology · 2023
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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 2 institutions in 2 countries.

Zhina SadeghiUrology Institute, University Hospitals of Case Medical Center, Department of Urology, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH, 44106, USA.
Justin IsariyawongseUrology Institute, University Hospitals of Case Medical Center, Department of Urology, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH, 44106, USA.
Michael KavranDepartment of Urology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Kenan IzgiDepartment of Urology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Gabriela MariniDepartment of Urology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Joseph MolterDepartment of Radiology, Case Western Reserve University, Cleveland, OH, USA.
Firouz DaneshgariDepartment of Urology, Case Western Reserve University School of Medicine, Cleveland, OH, USA.
Chris A FlaskDepartment of Radiology, Case Western Reserve University, Cleveland, OH, USA.
Arnold CaplanSkeletal Research Center, Biology Department, Case Western Reserve University, Cleveland, OH, USA.
Adonis HijazUrology Institute, University Hospitals of Case Medical Center, Department of Urology, Case Western Reserve University, 11100 Euclid Avenue, Cleveland, OH, 44106, USA. Adonis.Hijaz@UHhospitals.org.
Case Western Reserve University · USUniversity School · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Tissue recovery in the pathophysiology of stress urinary incontinenceK08DK090134 · NIDDK · CASE WESTERN RESERVE UNIVERSITY · PI HIJAZ, ADONIS K · 2011 to 2014
$594k
NCATS NIH HHS UL1 TR000439NIDDK NIH HHS 5K08DK090134NIDDK NIH HHS K08 DK090134
6 · The paper itself

Abstract

introduction and hypothesisWe evaluated the potential role of human mesenchymal stem cells (hMSCs) in improvement of urinary continence following birth-trauma injury.

methodsHuman MSCs were injected periurethrally or systemically into rats immediately after vaginal distention (VD) (n = 90). Control groups were non-VD (uninjured/untreated, n = 15), local or systemic saline (injection/control, n = 90), and dermofibroblast (cell therapy/control, n = 90). Leak-point pressure (LPP) was measured 4, 10, and 14 days later. Urethras were morphometrically evaluated. In another sets of VD and non-VD rats, the fate of periurethrally injected hMSC, biodistribution, and in vivo viability was studied using human Alu genomic repeat staining, PKH26 labeling, and luciferase-expression labeling, respectively.

resultsSaline- and dermofibroblast-treated control rats demonstrated lower LPP than non-VD controls at days 4 and 14 (P < 0.01). LPP after systemic hMSC and periurethral hMSC treatment were comparable with non-VD controls at 4, 10, and 14 days (P > 0.05). Local saline controls demonstrated extensive urethral tissue bleeding. The connective tissue area/urethral section area proportion and vascular density were higher in the local hMSC- versus the saline-treated group at 4 and 14 days, respectively. No positive Alu-stained nuclei were observed in urethras at 4, 10, and 14 days. PKH26-labelled cells were found in all urethras at 2 and 24 h. Bioluminescence study showed increased luciferase expression from day 0 to 1 following hMSC injection.

conclusionsHuman MSCs restored the continence mechanism with an immediate and sustained effect in the VD model, while saline and dermofibroblast therapy did not. Human MSCs remained at the site of periurethral injection for <7 days. We hypothesize that periurethral hMSC treatment improves vascular, connective tissue, and hemorrhage status of urethral tissues after acute VD injury.

Indexed as

Mesenchymal Stem Cell TransplantationParturitionAnimalsCell TrackingDisease Models, AnimalFemaleHumansMesenchymal Stem CellsPressureRatsRats, Sprague-DawleyUrethraUrinary IncontinenceBirth-trauma injuryMesenchymal stem cellMSC biodistributionStem cell fateStress urinary incontinence

Identifiers

PMID26353846
PMCPMC4890611
OpenAlexW1441236255

What OpenQuestion holds

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LicenceTDM
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.