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Biologic adjuvants for fracture healing

Bone tissue has an exceptional quality to regenerate to native tissue in response to injury. However, the fracture repair process requires mechanical stability or a viable biological microenvironment or both to ensure successful healing to native tissue. An improved understanding of the molecular an...

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Detalles Bibliográficos
Autores principales: Virk, Mandeep S, Lieberman, Jay R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674596/
https://www.ncbi.nlm.nih.gov/pubmed/23198865
http://dx.doi.org/10.1186/ar4053
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author Virk, Mandeep S
Lieberman, Jay R
author_facet Virk, Mandeep S
Lieberman, Jay R
author_sort Virk, Mandeep S
collection PubMed
description Bone tissue has an exceptional quality to regenerate to native tissue in response to injury. However, the fracture repair process requires mechanical stability or a viable biological microenvironment or both to ensure successful healing to native tissue. An improved understanding of the molecular and cellular events that occur during bone repair and remodeling has led to the development of biologic agents that can augment the biological microenvironment and enhance bone repair. Orthobiologics, including stem cells, osteoinductive growth factors, osteoconductive matrices, and anabolic agents, are available clinically for accelerating fracture repair and treatment of compromised bone repair situations like delayed unions and nonunions. Preclinical and clinical studies using biologic agents like recombinant bone morphogenetic proteins have demonstrated an efficacy similar or better than that of autologous bone graft in acute fracture healing. A lack of standardized outcome measures for comparison of biologic agents in clinical fracture repair trials, frequent off-label use, and a limited understanding of the biological activity of these agents at the bone repair site have limited their efficacy in clinical applications.
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spelling pubmed-36745962013-06-10 Biologic adjuvants for fracture healing Virk, Mandeep S Lieberman, Jay R Arthritis Res Ther Review Bone tissue has an exceptional quality to regenerate to native tissue in response to injury. However, the fracture repair process requires mechanical stability or a viable biological microenvironment or both to ensure successful healing to native tissue. An improved understanding of the molecular and cellular events that occur during bone repair and remodeling has led to the development of biologic agents that can augment the biological microenvironment and enhance bone repair. Orthobiologics, including stem cells, osteoinductive growth factors, osteoconductive matrices, and anabolic agents, are available clinically for accelerating fracture repair and treatment of compromised bone repair situations like delayed unions and nonunions. Preclinical and clinical studies using biologic agents like recombinant bone morphogenetic proteins have demonstrated an efficacy similar or better than that of autologous bone graft in acute fracture healing. A lack of standardized outcome measures for comparison of biologic agents in clinical fracture repair trials, frequent off-label use, and a limited understanding of the biological activity of these agents at the bone repair site have limited their efficacy in clinical applications. BioMed Central 2012 2012-11-30 /pmc/articles/PMC3674596/ /pubmed/23198865 http://dx.doi.org/10.1186/ar4053 Text en Copyright ©2012 BioMed Central Ltd
spellingShingle Review
Virk, Mandeep S
Lieberman, Jay R
Biologic adjuvants for fracture healing
title Biologic adjuvants for fracture healing
title_full Biologic adjuvants for fracture healing
title_fullStr Biologic adjuvants for fracture healing
title_full_unstemmed Biologic adjuvants for fracture healing
title_short Biologic adjuvants for fracture healing
title_sort biologic adjuvants for fracture healing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3674596/
https://www.ncbi.nlm.nih.gov/pubmed/23198865
http://dx.doi.org/10.1186/ar4053
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