Evidence map›Paper›PMID 31386550›Full record

ArticleThe American journal of sports medicine2019

Long-term Evaluation of Meniscal Tissue Formation in 3-dimensional-Printed Scaffolds With Sequential Release of Connective Tissue Growth Factor and TGF-β3 in an Ovine Model.

Yusuke Nakagawa, Lisa A Fortier, Jeremy J Mao, Chang Hun Lee, Margaret B Goodale, Matthew F Koff, Tyler J Uppstrom, Brett Croen, Susumu Wada, Camila B Carballo and 2 more

Open access · greenAbstract read
In one paragraph

Article in The American journal of sports medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 44 citations in OpenAlex.

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  9. Oxo-M and 4-PPBP DeliveryFrontiers in bioengineering and biotechnology · 2022
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  15. Meniscal substitution, a developing and long-awaited demand.Journal of experimental orthopaedics · 2020
    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

12 authors at 4 institutions in 2 countries.

Yusuke NakagawaLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Lisa A FortierDepartment of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Jeremy J MaoTissue Engineering and Regenerative Medicine Laboratory, Columbia University Medical Center, Columbia University, New York, New York, USA.
Chang Hun LeeTissue Engineering and Regenerative Medicine Laboratory, Columbia University Medical Center, Columbia University, New York, New York, USA.
Margaret B GoodaleDepartment of Clinical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, New York, USA.
Matthew F KoffDepartment of Radiology and Imaging, Hospital for Special Surgery, New York, New York, USA.
Tyler J UppstromLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Brett CroenLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Susumu WadaLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Camila B CarballoLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Hollis G PotterDepartment of Radiology and Imaging, Hospital for Special Surgery, New York, New York, USA.
Scott A RodeoLaboratory for Joint Tissue Repair and Regeneration, Orthopedic Soft Tissue Research Program, Hospital for Special Surgery, New York, New York, USA.
Hospital for Special Surgery · USColumbia University Irving Medical Center · USCornell University · USTokyo Medical and Dental University · JP

Funding

Meniscus Regeneration by Endogenous Stem/Progenitor CellsR01AR065023 · NIAMS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI FORTIER, LISA A, LEE, CHANG HUN · 2014 to 2018
$4.6M
NIAMS NIH HHS R01 AR065023
6 · The paper itself

Abstract

backgroundArtificial meniscal scaffolds are being developed to prevent development of osteoarthritis after meniscectomy. Previously, it was reported that 3-dimensional (3D) anatomic scaffolds loaded with connective tissue growth factor (CTGF) and transforming growth factor β3 (TGF-β3) achieved meniscal regeneration in an ovine model. This was a relatively short-term study (3 months postoperative), and outcome analyses did not include magnetic resonance imaging (MRI). PURPOSE: To evaluate long-term outcome of meniscal replacement with growth factor-laden poly-ε-caprolactone (PCL) scaffolds. STUDY

designControlled laboratory study.

methodsAnatomically shaped ovine meniscal scaffolds were fabricated from PCL with a 3D printer based on MRI data. Skeletally mature sheep (N = 34) were randomly allocated to 3 groups: scaffold without growth factor (0-µg group), scaffold with CTGF microspheres (µS) (5 µg) + TGF-β3 µS (5 µg) (5-µg group), and scaffold with CTGF µS (10 µg) + TGF-β3 µS (10 µg) (10-µg group). Unilateral medial meniscal replacement was performed. Animals were euthanized at 6 or 12 months. Regenerated meniscus, articular cartilage status, and synovial reaction were evaluated quantitatively with gross inspection, histology, and MRI. Kruskal-Wallis and Dunn tests were used to compare the 3 groups.

resultsRemnants of the PCL scaffold were evident in the 6-month specimens and were decreased but still present at 12 months in most animals. There were no significant differences among groups in gross inspection, histology, or MRI for either meniscal regeneration or articular cartilage protection. All experimental groups exhibited articular cartilage degeneration as compared with control (nonoperated). In terms of synovitis, there were no clear differences among groups, suggesting that growth factors did not increase inflammation and fibrosis. MRI revealed that meniscal extrusion was observed in most animals (82.7%).

conclusionPreviously, the combination of CTGF and TGF-β3 was shown to stimulate mesenchymal stem cells into a fibrochondrocyte lineage. CTGF and TGF-β3 did not aggravate synovitis, suggesting no adverse response to the combination of 3D-printed PCL scaffold combined with CTGF and TGF-β3. Further work will be required to improve scaffold fixation to avoid meniscal extrusion. CLINICAL RELEVANCE: A significant advantage of this technique is the ability to print custom-fit scaffolds from MRI-generated templates. In addition, average-size menisci could be printed and available for off-the-shelf applications. Based on the 1-year duration of the study, the approach appears to be promising for meniscal regeneration in humans.

Indexed as

AnimalsConnective Tissue Growth FactorMeniscusModels, AnimalPrinting, Three-DimensionalSheepTissue ScaffoldsTransforming Growth Factor beta3Connective Tissue Growth FactorTransforming Growth Factor beta33D printed scaffoldsgrowth factorsmeniscusovine knee

Identifiers

PMID31386550
PMCPMC7422478
OpenAlexW2965351748

What OpenQuestion holds

Textmetadata
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.