@article{aa7e2bf43e354adfa45bcfb9da6cd0ee,
title = "Long term outcomes of biomaterial -mediated repair of focal cartilage defects in a large animal model",
abstract = "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.",
keywords = "Articular cartilage repair, Biomaterials, Cartilage biomechanics, Cartilage defects, Large animal models, Long-term outcomes, Orthopaedics, Scaffolds, Tissue engineering",
author = "Sennett, {M. L.} and Friedman, {J. M.} and Ashley, {B. S.} and Stoeckl, {B. D.} and Patel, {J. M.} and M. Alini and M. Cucchiarini and D. Eglin and H. Madry and A. Mata and C. Semino and Stoddart, {M. J.} and B. Johnstone and Moutos, {F. T.} and Estes, {B. T.} and F. Guilak and Mauck, {R. L.} and Dodge, {George R.}",
note = "Funding Information: This study was supported by the ?O Foundation ?cute Cartilage Injury Consortium. ?dditional support was provided by the Department of Veteran{\textquoteright}s ?ffairs (I01 RX001213) and the NIH through the Penn Center for Musculoskeletal Diseases Histology and Biomechanics Cores (P30 ?R069619) and the Washington University Musculoskeletal Research Center (P30 ?R074992). We gratefully acknowledge Dr. Sandra Steiner for her guidance and oversight of the ?O Foundation ?cute Cartilage Injury fig. 7. blinded histological scoring. Significant differences were found in the overall assessment, matrix stain, cell morphology, deep clustering, basal integration, subchondral involvement, surface assessment, and deep assessment parameters. ^ = indicates significant difference from anchor group, & = significant difference from both anchor and MFX groups. Bars indicate median and interquartile range. Funding Information: This study was supported by the AO Foundation Acute Cartilage Injury Consortium. Additional support was provided by the Department of Veteran{\textquoteright}s Affairs (I01 RX001213) and the NIH through the Penn Center for Musculoskeletal Diseases Histology and Biomechanics Cores (P30 AR069619) and the Washington University Musculoskeletal Research Center (P30 AR074992). We gratefully acknowledge Dr. Sandra Steiner for her guidance and oversight of the AO Foundation Acute Cartilage Injury Consortium. In addition, the authors are grateful for the expert guidance and encouragement throughout this project from the AO Exploratory Research Collaborative advisors, Dr. Mats Brittberg and the late Dr. Peter Roughley. Publisher Copyright: {\textcopyright} 2021, AO Research Institute Davos. All rights reserved.",
year = "2021",
doi = "10.22203/eCM.v041a04",
language = "English",
volume = "41",
pages = "40--51",
journal = "European Cells and Materials",
issn = "1473-2262",
publisher = "AO Research Institute",
}