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Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints
Early diagnosis of osteoarthritis (OA), before the onset of irreversible changes is crucial for understanding the disease process and identifying potential disease-modifying treatments from the earliest stage. OA is a whole joint disease and affects both cartilage and the underlying subchondral bone...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035167/ https://www.ncbi.nlm.nih.gov/pubmed/35461315 http://dx.doi.org/10.1038/s41598-022-10600-6 |
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author | Ajami, Sara Javaheri, Behzad Chang, Y.-M. Maruthainar, Nimalan Khan, Tahir Donaldson, James Pitsillides, Andrew A. Liu, Chaozong |
author_facet | Ajami, Sara Javaheri, Behzad Chang, Y.-M. Maruthainar, Nimalan Khan, Tahir Donaldson, James Pitsillides, Andrew A. Liu, Chaozong |
author_sort | Ajami, Sara |
collection | PubMed |
description | Early diagnosis of osteoarthritis (OA), before the onset of irreversible changes is crucial for understanding the disease process and identifying potential disease-modifying treatments from the earliest stage. OA is a whole joint disease and affects both cartilage and the underlying subchondral bone. However, spatial relationships between cartilage lesion severity (CLS) and microstructural changes in subchondral plate and trabecular bone remain elusive. Herein, we collected femoral heads from hip arthroplasty for primary osteoarthritis (n = 7) and femoral neck fracture (n = 6; non-OA controls) cases. Samples were regionally assessed for cartilage lesions by visual inspection using Outerbridge classification and entire femoral heads were micro-CT scanned. Scans of each femoral head were divided into 4 quadrants followed by morphometric analysis of subchondral plate and trabecular bone in each quadrant. Principal component analysis (PCA), a data reduction method, was employed to assess differences between OA and non-OA samples, and spatial relationship between CLS and subchondral bone changes. Mapping of the trabecular bone microstructure in OA patients with low CLS revealed trabecular organisation resembling non-OA patients, whereas clear differences were identifiable in subchondral plate architecture. The OA-related changes in subchondral plate architecture were summarised in the first principle component (PC1) which correlated with CLS in all quadrants, whilst by comparison such associations in trabecular bone were most prominent in the higher weight-bearing regions of the femoral head. Greater articular cartilage deterioration in OA was regionally-linked with lower BV/TV, TMD and thickness, and greater BS/BV and porosity in the subchondral plate; and with thinner, less separated trabeculae with greater TMD and BS/BV in the trabecular bone. Our findings suggest that impairment of subchondral bone microstructure in early stage of OA is more readily discernible in the cortical plate and that morphological characterisation of the femoral head bone microstructure may allow for earlier OA diagnosis and monitoring of progression. |
format | Online Article Text |
id | pubmed-9035167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90351672022-04-27 Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints Ajami, Sara Javaheri, Behzad Chang, Y.-M. Maruthainar, Nimalan Khan, Tahir Donaldson, James Pitsillides, Andrew A. Liu, Chaozong Sci Rep Article Early diagnosis of osteoarthritis (OA), before the onset of irreversible changes is crucial for understanding the disease process and identifying potential disease-modifying treatments from the earliest stage. OA is a whole joint disease and affects both cartilage and the underlying subchondral bone. However, spatial relationships between cartilage lesion severity (CLS) and microstructural changes in subchondral plate and trabecular bone remain elusive. Herein, we collected femoral heads from hip arthroplasty for primary osteoarthritis (n = 7) and femoral neck fracture (n = 6; non-OA controls) cases. Samples were regionally assessed for cartilage lesions by visual inspection using Outerbridge classification and entire femoral heads were micro-CT scanned. Scans of each femoral head were divided into 4 quadrants followed by morphometric analysis of subchondral plate and trabecular bone in each quadrant. Principal component analysis (PCA), a data reduction method, was employed to assess differences between OA and non-OA samples, and spatial relationship between CLS and subchondral bone changes. Mapping of the trabecular bone microstructure in OA patients with low CLS revealed trabecular organisation resembling non-OA patients, whereas clear differences were identifiable in subchondral plate architecture. The OA-related changes in subchondral plate architecture were summarised in the first principle component (PC1) which correlated with CLS in all quadrants, whilst by comparison such associations in trabecular bone were most prominent in the higher weight-bearing regions of the femoral head. Greater articular cartilage deterioration in OA was regionally-linked with lower BV/TV, TMD and thickness, and greater BS/BV and porosity in the subchondral plate; and with thinner, less separated trabeculae with greater TMD and BS/BV in the trabecular bone. Our findings suggest that impairment of subchondral bone microstructure in early stage of OA is more readily discernible in the cortical plate and that morphological characterisation of the femoral head bone microstructure may allow for earlier OA diagnosis and monitoring of progression. Nature Publishing Group UK 2022-04-23 /pmc/articles/PMC9035167/ /pubmed/35461315 http://dx.doi.org/10.1038/s41598-022-10600-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Ajami, Sara Javaheri, Behzad Chang, Y.-M. Maruthainar, Nimalan Khan, Tahir Donaldson, James Pitsillides, Andrew A. Liu, Chaozong Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title | Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title_full | Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title_fullStr | Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title_full_unstemmed | Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title_short | Spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
title_sort | spatial links between subchondral bone architectural features and cartilage degeneration in osteoarthritic joints |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9035167/ https://www.ncbi.nlm.nih.gov/pubmed/35461315 http://dx.doi.org/10.1038/s41598-022-10600-6 |
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