Evidence map›Paper›PMID 25519993›Full record

ArticleJournal of the Royal Society, Interface2015

Neocartilage integration in temporomandibular joint discs: physical and enzymatic methods.

Meghan K Murphy, Boaz Arzi, Shannon M Prouty, Jerry C Hu, Kyriacos A Athanasiou

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.1field-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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Meghan K MurphyDepartment of Biomedical Engineering, University of California Davis, Davis, CA, USA.
Boaz ArziDepartment of Surgical and Radiological Sciences, William R. Pritchard Veterinary Medical Teaching Hospital, University of California Davis, Davis, CA, USA.
Shannon M ProutyDepartment of Biomedical Engineering, University of California Davis, Davis, CA, USA.
Jerry C HuDepartment of Biomedical Engineering, University of California Davis, Davis, CA, USA.
Kyriacos A AthanasiouDepartment of Biomedical Engineering, University of California Davis, Davis, CA, USA Department of Orthopaedic Surgery, University of California Davis, Davis, CA, USA athanasiou@ucdavis.edu.
University of California, Davis · USVeterinary Medical Teaching Hospital · US

Funding

Regenerating the fibrocartilage spectrum of the TMJ: from disc to condyleR01DE019666 · NIDCR · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ATHANASIOU, KYRIACOS A · 2010 to 2013
$1.4M
Engineering Lubrication in Tissue Engineered CartilageR01AR061496 · NIAMS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ATHANASIOU, KYRIACOS A, REDDI, AKEPATI HARI · 2011 to 2014
$1.3M
NIAMS NIH HHS R01AR061496NIDCR NIH HHS R01DE019666
6 · The paper itself

Abstract

Integration of engineered musculoskeletal tissues with adjacent native tissues presents a significant challenge to the field. Specifically, the avascularity and low cellularity of cartilage elicit the need for additional efforts in improving integration of neocartilage within native cartilage. Self-assembled neocartilage holds significant potential in replacing degenerated cartilage, though its stabilization and integration in native cartilage require further efforts. Physical and enzymatic stabilization methods were investigated in an in vitro model for temporomandibular joint (TMJ) disc degeneration. First, in phase 1, suture, glue and press-fit constructs were compared in TMJ disc intermediate zone defects. In phase 1, suturing enhanced interfacial shear stiffness and strength immediately; after four weeks, a 15-fold increase in stiffness and a ninefold increase in strength persisted over press-fit. Neither suture nor glue significantly altered neocartilage properties. In phase 2, the effects of the enzymatic stabilization regimen composed of lysyl oxidase, CuSO4 and hydroxylysine were investigated. A full factorial design was employed, carrying forward the best physical method from phase 1, suturing. Enzymatic stabilization significantly increased interfacial shear stiffness after eight weeks. Combined enzymatic stabilization and suturing led to a fourfold increase in shear stiffness and threefold increase in strength over press-fit. Histological analysis confirmed the presence of a collagen-rich interface. Enzymatic treatment additionally enhanced neocartilage mechanical properties, yielding a tensile modulus over 6 MPa and compressive instantaneous modulus over 1200 kPa at eight weeks. Suturing enhances stabilization of neocartilage, and enzymatic treatment enhances functional properties and integration of neocartilage in the TMJ disc. Methods developed here are applicable to other orthopaedic soft tissues, including knee meniscus and hyaline articular cartilage.

Indexed as

FibrocartilageTemporomandibular Joint DiscTemporomandibular Joint DisordersAnimalsHyaline CartilageProtein-Lysine 6-OxidaseSus scrofaTensile StrengthProtein-Lysine 6-Oxidasecyanoacrylatelysyl oxidasemosaicplastyporcinesuturetemporomandibular joint disc perforation

Identifiers

PMID25519993
PMCPMC4305410
OpenAlexW2103595580

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.