Long term outcomes of biomaterial-mediated repair of focal cartilage defects in a large animal model.


Journal

European cells & materials
ISSN: 1473-2262
Titre abrégé: Eur Cell Mater
Pays: Switzerland
ID NLM: 100973416

Informations de publication

Date de publication:
07 01 2021
Historique:
entrez: 7 1 2021
pubmed: 8 1 2021
medline: 14 1 2022
Statut: epublish

Résumé

The repair of focal cartilage defects remains one of the foremost issues in the field of orthopaedics. Chondral defects may arise from a variety of joint pathologies and left untreated, will likely progress to osteoarthritis. Current repair techniques, such as microfracture, result in short-term clinical improvements but have poor long-term outcomes. Emerging scaffold-based repair strategies have reported superior outcomes compared to microfracture and motivate the development of new biomaterials for this purpose. In this study, unique composite implants consisting of a base porous reinforcing component (woven poly(ε-caprolactone)) infiltrated with 1 of 2 hydrogels (self-assembling peptide or thermo-gelling hyaluronan) or bone marrow aspirate were evaluated. The objective was to evaluate cartilage repair with composite scaffold treatment compared to the current standard of care (microfracture) in a translationally relevant large animal model, the Yucatan minipig. While many cartilage-repair studies have shown some success in vivo, most are short term and not clinically relevant. Informed by promising 6-week findings, a 12-month study was carried out and those results are presented here. To aid in comparisons across platforms, several structural and functionally relevant outcome measures were performed. Despite positive early findings, the long-term results indicated less than optimal structural and mechanical results with respect to cartilage repair, with all treatment groups performing worse than the standard of care. This study is important in that it brings much needed attention to the importance of performing translationally relevant long-term studies in an appropriate animal model when developing new clinical cartilage repair approaches.

Identifiants

pubmed: 33411938
doi: 10.22203/eCM.v041a04
pii: vol041a04
pmc: PMC8626827
mid: NIHMS1749131
doi:

Substances chimiques

Biocompatible Materials 0
Hyaluronic Acid 9004-61-9

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

40-51

Subventions

Organisme : RRD VA
ID : I01 RX001213
Pays : United States
Organisme : Medical Research Council
ID : MR/R015651/1
Pays : United Kingdom
Organisme : NIAMS NIH HHS
ID : P30 AR069619
Pays : United States
Organisme : NIAMS NIH HHS
ID : P30 AR074992
Pays : United States

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