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Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair

Microfracture of cartilage defects may induce alterations of the subchondral bone in the mid- and long-term, yet very little is known about their onset. Possibly, these changes may be avoided by an enhanced microfracture technique with additional application of bone marrow aspirate. In this study, f...

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Autores principales: Gao, Liang, Orth, Patrick, Müller-Brandt, Kathrin, Goebel, Lars K. H., Cucchiarini, Magali, Madry, Henning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366926/
https://www.ncbi.nlm.nih.gov/pubmed/28345610
http://dx.doi.org/10.1038/srep45189
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author Gao, Liang
Orth, Patrick
Müller-Brandt, Kathrin
Goebel, Lars K. H.
Cucchiarini, Magali
Madry, Henning
author_facet Gao, Liang
Orth, Patrick
Müller-Brandt, Kathrin
Goebel, Lars K. H.
Cucchiarini, Magali
Madry, Henning
author_sort Gao, Liang
collection PubMed
description Microfracture of cartilage defects may induce alterations of the subchondral bone in the mid- and long-term, yet very little is known about their onset. Possibly, these changes may be avoided by an enhanced microfracture technique with additional application of bone marrow aspirate. In this study, full-thickness chondral defects in the knee joints of minipigs were either treated with (1) debridement down to the subchondral bone plate alone, (2) debridement with microfracture, or (3) microfracture with additional application of bone marrow aspirate. At 4 weeks after microfracture, the loss of subchondral bone below the defects largely exceeded the original microfracture holes. Of note, a significant increase of osteoclast density was identified in defects treated with microfracture alone compared with debridement only. Both changes were significantly counteracted by the adjunct treatment with bone marrow. Debridement and microfracture without or with bone marrow were equivalent regarding the early cartilage repair. These data suggest that microfracture induced a substantial early resorption of the subchondral bone and also highlight the potential value of bone marrow aspirate as an adjunct to counteract these alterations. Clinical studies are warranted to further elucidate early events of osteochondral repair and the effect of enhanced microfracture techniques.
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spelling pubmed-53669262017-03-28 Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair Gao, Liang Orth, Patrick Müller-Brandt, Kathrin Goebel, Lars K. H. Cucchiarini, Magali Madry, Henning Sci Rep Article Microfracture of cartilage defects may induce alterations of the subchondral bone in the mid- and long-term, yet very little is known about their onset. Possibly, these changes may be avoided by an enhanced microfracture technique with additional application of bone marrow aspirate. In this study, full-thickness chondral defects in the knee joints of minipigs were either treated with (1) debridement down to the subchondral bone plate alone, (2) debridement with microfracture, or (3) microfracture with additional application of bone marrow aspirate. At 4 weeks after microfracture, the loss of subchondral bone below the defects largely exceeded the original microfracture holes. Of note, a significant increase of osteoclast density was identified in defects treated with microfracture alone compared with debridement only. Both changes were significantly counteracted by the adjunct treatment with bone marrow. Debridement and microfracture without or with bone marrow were equivalent regarding the early cartilage repair. These data suggest that microfracture induced a substantial early resorption of the subchondral bone and also highlight the potential value of bone marrow aspirate as an adjunct to counteract these alterations. Clinical studies are warranted to further elucidate early events of osteochondral repair and the effect of enhanced microfracture techniques. Nature Publishing Group 2017-03-27 /pmc/articles/PMC5366926/ /pubmed/28345610 http://dx.doi.org/10.1038/srep45189 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Gao, Liang
Orth, Patrick
Müller-Brandt, Kathrin
Goebel, Lars K. H.
Cucchiarini, Magali
Madry, Henning
Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title_full Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title_fullStr Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title_full_unstemmed Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title_short Early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
title_sort early loss of subchondral bone following microfracture is counteracted by bone marrow aspirate in a translational model of osteochondral repair
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5366926/
https://www.ncbi.nlm.nih.gov/pubmed/28345610
http://dx.doi.org/10.1038/srep45189
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