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The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review

BACKGROUND: Intra-articular (IA) corticosteroid therapy has been used for the treatment of inflammation and pain in the knee since the 1950s. PURPOSE: To review the current literature on the effects of IA corticosteroids on articular cartilage. STUDY DESIGN: Systematic review. METHODS: A MEDLINE and...

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Autores principales: Wernecke, Chloe, Braun, Hillary J., Dragoo, Jason L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2015
Materias:
42
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4622344/
https://www.ncbi.nlm.nih.gov/pubmed/26674652
http://dx.doi.org/10.1177/2325967115581163
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author Wernecke, Chloe
Braun, Hillary J.
Dragoo, Jason L.
author_facet Wernecke, Chloe
Braun, Hillary J.
Dragoo, Jason L.
author_sort Wernecke, Chloe
collection PubMed
description BACKGROUND: Intra-articular (IA) corticosteroid therapy has been used for the treatment of inflammation and pain in the knee since the 1950s. PURPOSE: To review the current literature on the effects of IA corticosteroids on articular cartilage. STUDY DESIGN: Systematic review. METHODS: A MEDLINE and SCOPUS database search was performed, and studies were selected for basic science and clinical trial research on corticosteroids with direct outcome measures of cartilage health. Preliminary searches yielded 1929 articles, and final analysis includes 40 studies. RESULTS: Methylprednisolone, dexamethasone, hydrocortisone, betamethasone, prednisolone, and triamcinolone were reported to display dose-dependent deleterious effects on cartilage morphology, histology, and viability in both in vitro and in vivo models. The beneficial animal in vivo effects of methylprednisolone, hydrocortisone, and triamcinolone occurred at low doses (usually <2-3 mg/dose or 8-12 mg/cumulative total dose in vivo), at which increased cell growth and recovery from damage was observed; the single human clinical trial indicated a beneficial effect of triamcinolone. However, at higher doses (>3 mg/dose or 18-24 mg/cumulative total dose in vivo), corticosteroids were associated with significant gross cartilage damage and chondrocyte toxicity. Dose and time dependency of corticosteroid chondrotoxicity was supported in the in vitro results, however, without clear dose thresholds. CONCLUSION: Corticosteroids have a time- and dose-dependent effect on articular cartilage, with beneficial effects occurring at low doses and durations and detrimental effects at high doses and durations. Clinically, beneficial effects are supported for IA administration, but the lowest efficacious dose should be used.
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spelling pubmed-46223442015-12-15 The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review Wernecke, Chloe Braun, Hillary J. Dragoo, Jason L. Orthop J Sports Med 42 BACKGROUND: Intra-articular (IA) corticosteroid therapy has been used for the treatment of inflammation and pain in the knee since the 1950s. PURPOSE: To review the current literature on the effects of IA corticosteroids on articular cartilage. STUDY DESIGN: Systematic review. METHODS: A MEDLINE and SCOPUS database search was performed, and studies were selected for basic science and clinical trial research on corticosteroids with direct outcome measures of cartilage health. Preliminary searches yielded 1929 articles, and final analysis includes 40 studies. RESULTS: Methylprednisolone, dexamethasone, hydrocortisone, betamethasone, prednisolone, and triamcinolone were reported to display dose-dependent deleterious effects on cartilage morphology, histology, and viability in both in vitro and in vivo models. The beneficial animal in vivo effects of methylprednisolone, hydrocortisone, and triamcinolone occurred at low doses (usually <2-3 mg/dose or 8-12 mg/cumulative total dose in vivo), at which increased cell growth and recovery from damage was observed; the single human clinical trial indicated a beneficial effect of triamcinolone. However, at higher doses (>3 mg/dose or 18-24 mg/cumulative total dose in vivo), corticosteroids were associated with significant gross cartilage damage and chondrocyte toxicity. Dose and time dependency of corticosteroid chondrotoxicity was supported in the in vitro results, however, without clear dose thresholds. CONCLUSION: Corticosteroids have a time- and dose-dependent effect on articular cartilage, with beneficial effects occurring at low doses and durations and detrimental effects at high doses and durations. Clinically, beneficial effects are supported for IA administration, but the lowest efficacious dose should be used. SAGE Publications 2015-04-27 /pmc/articles/PMC4622344/ /pubmed/26674652 http://dx.doi.org/10.1177/2325967115581163 Text en © The Author(s) 2015 http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License (http://www.creativecommons.org/licenses/by-nc-nd/3.0/) which permits non-commercial use, reproduction and distribution of the work as published without adaptation or alteration, without further permission provided the original work is attributed as specified on the SAGE and Open Access page (http://www.uk.sagepub.com/aboutus/openaccess.htm).
spellingShingle 42
Wernecke, Chloe
Braun, Hillary J.
Dragoo, Jason L.
The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title_full The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title_fullStr The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title_full_unstemmed The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title_short The Effect of Intra-articular Corticosteroids on Articular Cartilage: A Systematic Review
title_sort effect of intra-articular corticosteroids on articular cartilage: a systematic review
topic 42
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4622344/
https://www.ncbi.nlm.nih.gov/pubmed/26674652
http://dx.doi.org/10.1177/2325967115581163
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