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Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy
We demonstrate in this study the potential of near infrared (NIR) spectroscopy as a tool for monitoring progression of cartilage degeneration in an animal model. Osteoarthritic degeneration was artificially induced in one joint in laboratory rats, and the animals were sacrificed at four time points:...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597588/ https://www.ncbi.nlm.nih.gov/pubmed/28904358 http://dx.doi.org/10.1038/s41598-017-11844-3 |
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author | Afara, Isaac O. Prasadam, Indira Arabshahi, Zohreh Xiao, Yin Oloyede, Adekunle |
author_facet | Afara, Isaac O. Prasadam, Indira Arabshahi, Zohreh Xiao, Yin Oloyede, Adekunle |
author_sort | Afara, Isaac O. |
collection | PubMed |
description | We demonstrate in this study the potential of near infrared (NIR) spectroscopy as a tool for monitoring progression of cartilage degeneration in an animal model. Osteoarthritic degeneration was artificially induced in one joint in laboratory rats, and the animals were sacrificed at four time points: 1, 2, 4, and 6 weeks (3 animals/week). NIR spectra were acquired from both (injured and intact) knees. Subsequently, the joint samples were subjected to histological evaluation and glycosaminoglycan (GAG) content analysis, to assess disease severity based on the Mankin scoring system and to determine proteoglycan loss, respectively. Multivariate spectral techniques were then employed for classification (principal component analysis and support vector machines) and prediction (partial least squares regression) of the samples’ Mankin scores and GAG content from their NIR spectra. Our results demonstrate that NIR spectroscopy is sensitive to degenerative changes in articular cartilage, and is capable of distinguishing between mild (weeks 1&2; Mankin <=2) and advanced (weeks 4&6; Mankin =>3) cartilage degeneration. In addition, the spectral data contains information that enables estimation of the tissue’s Mankin score (error = 12.6%, R(2) = 86.2%) and GAG content (error = 7.6%, R(2) = 95%). We conclude that NIR spectroscopy is a viable tool for assessing cartilage degeneration post-injury, such as, post-traumatic osteoarthritis. |
format | Online Article Text |
id | pubmed-5597588 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55975882017-09-15 Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy Afara, Isaac O. Prasadam, Indira Arabshahi, Zohreh Xiao, Yin Oloyede, Adekunle Sci Rep Article We demonstrate in this study the potential of near infrared (NIR) spectroscopy as a tool for monitoring progression of cartilage degeneration in an animal model. Osteoarthritic degeneration was artificially induced in one joint in laboratory rats, and the animals were sacrificed at four time points: 1, 2, 4, and 6 weeks (3 animals/week). NIR spectra were acquired from both (injured and intact) knees. Subsequently, the joint samples were subjected to histological evaluation and glycosaminoglycan (GAG) content analysis, to assess disease severity based on the Mankin scoring system and to determine proteoglycan loss, respectively. Multivariate spectral techniques were then employed for classification (principal component analysis and support vector machines) and prediction (partial least squares regression) of the samples’ Mankin scores and GAG content from their NIR spectra. Our results demonstrate that NIR spectroscopy is sensitive to degenerative changes in articular cartilage, and is capable of distinguishing between mild (weeks 1&2; Mankin <=2) and advanced (weeks 4&6; Mankin =>3) cartilage degeneration. In addition, the spectral data contains information that enables estimation of the tissue’s Mankin score (error = 12.6%, R(2) = 86.2%) and GAG content (error = 7.6%, R(2) = 95%). We conclude that NIR spectroscopy is a viable tool for assessing cartilage degeneration post-injury, such as, post-traumatic osteoarthritis. Nature Publishing Group UK 2017-09-13 /pmc/articles/PMC5597588/ /pubmed/28904358 http://dx.doi.org/10.1038/s41598-017-11844-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Afara, Isaac O. Prasadam, Indira Arabshahi, Zohreh Xiao, Yin Oloyede, Adekunle Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title | Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title_full | Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title_fullStr | Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title_full_unstemmed | Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title_short | Monitoring osteoarthritis progression using near infrared (NIR) spectroscopy |
title_sort | monitoring osteoarthritis progression using near infrared (nir) spectroscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597588/ https://www.ncbi.nlm.nih.gov/pubmed/28904358 http://dx.doi.org/10.1038/s41598-017-11844-3 |
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