Evidence map›Paper›PMID 26738900›Full record

ArticleThe Journal of bone and joint surgery. American volume2016

Addition of Mesenchymal Stem Cells to Autologous Platelet-Enhanced Fibrin Scaffolds in Chondral Defects: Does It Enhance Repair?

Laurie R Goodrich, Albert C Chen, Natasha M Werpy, Ashley A Williams, John D Kisiday, Alvin W Su, Esther Cory, Paul S Morley, C Wayne McIlwraith, Robert L Sah and 1 more

Abstract read
In one paragraph

Article in The Journal of bone and joint surgery. American volume, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 1 pooled it
10.5field-weighted citation impact, top 1% 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

25 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

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  16. The challenges of promoting osteogenesis in segmental bone defects and osteoporosis.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
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  17. Article
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  20. Current and novel injectable hydrogels to treat focal chondral lesions: Properties and applicability.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2018
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Laurie R GoodrichGail Holmes Equine Orthopedic Research Center, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523.
Albert C ChenDepartment of Bioengineering, Mail Code 0412, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412.
Natasha M WerpyLarge Animal Clinical Sciences, 2015 S.W. 16th Avenue, Gainesville, FL 32608.
Ashley A WilliamsDepartment of Orthopedic Surgery, Stanford University School of Medicine, 450 Broadway Street, Redwood City, CA 94063.
John D KisidayGail Holmes Equine Orthopedic Research Center, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523.
Alvin W SuDepartment of Bioengineering, Mail Code 0412, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412.
Esther CoryDepartment of Bioengineering, Mail Code 0412, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412.
Paul S MorleyGail Holmes Equine Orthopedic Research Center, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523.
C Wayne McIlwraithGail Holmes Equine Orthopedic Research Center, Colorado State University, 300 West Drake Road, Fort Collins, CO 80523.
Robert L SahDepartment of Bioengineering, Mail Code 0412, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0412.
Constance R ChuDepartment of Orthopedic Surgery, Stanford University School of Medicine, 450 Broadway Street, Redwood City, CA 94063. chucr@stanford.edu.
Colorado State University · USUniversity of California, San Diego · US

Funding

TISSUE ACQUISITION, MORPHOLOGY, AND CELL CULTUREP01AG007996 · NIA · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI TERKELTAUB, ROBERT A. · 1989 to 2016
$26.0M
Enhanced Clinical Diagnosis of Early OsteoarthritisR01AR052784 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, CONSTANCE R · 2006 to 2015
$4.1M
Developing Articular Cartilage: Function &RemodelingR01AR044058 · NIAMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SAH, ROBERT L · 2000 to 2010
$3.3M
Chondrogenesis In SituR01AR051963 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, CONSTANCE R · 2007 to 2011
$1.9M
Multicenter Cartilage Repair Preclinical Trial in HorsesRC2AR058929 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHU, CONSTANCE R · 2009 to 2010
$1.7M
Gene Therapeutic Approaches to Cartilage RepairK08AR054903 · NIAMS · COLORADO STATE UNIVERSITY · PI GOODRICH, LAURIE · 2008 to 2012
$720k
NIAMS NIH HHS 1K08AR054903-01A2NIAMS NIH HHS R01 AR044058NIAMS NIH HHS R01 AR051963NIAMS NIH HHS R01 AR052784NIAMS NIH HHS RC2 AR058929NIA NIH HHS P01 AG007996
6 · The paper itself

Abstract

backgroundThe chondrogenic potential of culture-expanded bone-marrow-derived mesenchymal stem cells (BMDMSCs) is well described. Numerous studies have also shown enhanced repair when BMDMSCs, scaffolds, and growth factors are placed into chondral defects. Platelets provide a rich milieu of growth factors and, along with fibrin, are readily available for clinical use. The objective of this study was to determine if the addition of BMDMSCs to an autologous platelet-enriched fibrin (APEF) scaffold enhances chondral repair compared with APEF alone.

methodsA 15-mm-diameter full-thickness chondral defect was created on the lateral trochlear ridge of both stifle joints of twelve adult horses. In each animal, one defect was randomly assigned to receive APEF+BMDMSCs and the contralateral defect received APEF alone. Repair tissues were evaluated one year later with arthroscopy, histological examination, magnetic resonance imaging (MRI), micro-computed tomography (micro-CT), and biomechanical testing.

resultsThe arthroscopic findings, MRI T2 map, histological scores, structural stiffness, and material stiffness were similar (p > 0.05) between the APEF and APEF+BMDMSC-treated repairs at one year. Ectopic bone was observed within the repair tissue in four of twelve APEF+BMDMSC-treated defects. Defects repaired with APEF alone had less trabecular bone edema (as seen on MRI) compared with defects repaired with APEF+BMDMSCs. Micro-CT analysis showed thinner repair tissue in defects repaired with APEF+BMDMSCs than in those treated with APEF alone (p < 0.05).

conclusionsAPEF alone resulted in thicker repair tissue than was seen with APEF+BMDMSCs. The addition of BMDMSCs to APEF did not enhance cartilage repair and stimulated bone formation in some cartilage defects. CLINICAL RELEVANCE: APEF supported repair of critical-size full-thickness chondral defects in horses, which was not improved by the addition of BMDMSCs. This work supports further investigation to determine whether APEF enhances cartilage repair in humans.

Indexed as

AnimalsArthroscopyBiopsy, NeedleBlood PlateletsCartilage, ArticularCartilage DiseasesDisease Models, AnimalFibrinFollow-Up StudiesHorsesHumansImmunohistochemistryMagnetic Resonance ImagingMesenchymal Stem Cell TransplantationRandom AllocationTissue EngineeringFibrin

Identifiers

PMID26738900
PMCPMC4697360
OpenAlexW2413431790

What OpenQuestion holds

Textmetadata
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.