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In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee

The in vivo measurement of articular cartilage deformation is essential to understand how mechanical forces distribute throughout the healthy tissue and change over time in the pathologic joint. Displacements or strain may serve as a functional imaging biomarker for healthy, diseased, and repaired t...

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Autores principales: Chan, Deva D., Cai, Luyao, Butz, Kent D., Trippel, Stephen B., Nauman, Eric A., Neu, Corey P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707486/
https://www.ncbi.nlm.nih.gov/pubmed/26752228
http://dx.doi.org/10.1038/srep19220
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author Chan, Deva D.
Cai, Luyao
Butz, Kent D.
Trippel, Stephen B.
Nauman, Eric A.
Neu, Corey P.
author_facet Chan, Deva D.
Cai, Luyao
Butz, Kent D.
Trippel, Stephen B.
Nauman, Eric A.
Neu, Corey P.
author_sort Chan, Deva D.
collection PubMed
description The in vivo measurement of articular cartilage deformation is essential to understand how mechanical forces distribute throughout the healthy tissue and change over time in the pathologic joint. Displacements or strain may serve as a functional imaging biomarker for healthy, diseased, and repaired tissues, but unfortunately intratissue cartilage deformation in vivo is largely unknown. Here, we directly quantified for the first time deformation patterns through the thickness of tibiofemoral articular cartilage in healthy human volunteers. Magnetic resonance imaging acquisitions were synchronized with physiologically relevant compressive loading and used to visualize and measure regional displacement and strain of tibiofemoral articular cartilage in a sagittal plane. We found that compression (of 1/2 body weight) applied at the foot produced a sliding, rigid-body displacement at the tibiofemoral cartilage interface, that loading generated subject- and gender-specific and regionally complex patterns of intratissue strains, and that dominant cartilage strains (approaching 12%) were in shear. Maximum principle and shear strain measures in the tibia were correlated with body mass index. Our MRI-based approach may accelerate the development of regenerative therapies for diseased or damaged cartilage, which is currently limited by the lack of reliable in vivo methods for noninvasive assessment of functional changes following treatment.
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spelling pubmed-47074862016-01-20 In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee Chan, Deva D. Cai, Luyao Butz, Kent D. Trippel, Stephen B. Nauman, Eric A. Neu, Corey P. Sci Rep Article The in vivo measurement of articular cartilage deformation is essential to understand how mechanical forces distribute throughout the healthy tissue and change over time in the pathologic joint. Displacements or strain may serve as a functional imaging biomarker for healthy, diseased, and repaired tissues, but unfortunately intratissue cartilage deformation in vivo is largely unknown. Here, we directly quantified for the first time deformation patterns through the thickness of tibiofemoral articular cartilage in healthy human volunteers. Magnetic resonance imaging acquisitions were synchronized with physiologically relevant compressive loading and used to visualize and measure regional displacement and strain of tibiofemoral articular cartilage in a sagittal plane. We found that compression (of 1/2 body weight) applied at the foot produced a sliding, rigid-body displacement at the tibiofemoral cartilage interface, that loading generated subject- and gender-specific and regionally complex patterns of intratissue strains, and that dominant cartilage strains (approaching 12%) were in shear. Maximum principle and shear strain measures in the tibia were correlated with body mass index. Our MRI-based approach may accelerate the development of regenerative therapies for diseased or damaged cartilage, which is currently limited by the lack of reliable in vivo methods for noninvasive assessment of functional changes following treatment. Nature Publishing Group 2016-01-11 /pmc/articles/PMC4707486/ /pubmed/26752228 http://dx.doi.org/10.1038/srep19220 Text en Copyright © 2016, Macmillan Publishers Limited 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
Chan, Deva D.
Cai, Luyao
Butz, Kent D.
Trippel, Stephen B.
Nauman, Eric A.
Neu, Corey P.
In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title_full In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title_fullStr In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title_full_unstemmed In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title_short In vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
title_sort in vivo articular cartilage deformation: noninvasive quantification of intratissue strain during joint contact in the human knee
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707486/
https://www.ncbi.nlm.nih.gov/pubmed/26752228
http://dx.doi.org/10.1038/srep19220
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