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The osteoarthritis bone score (OABS): a new histological scoring system for the characterisation of bone marrow lesions in osteoarthritis.

Koushesh, S; Shahtaheri, SM; McWilliams, DF; Walsh, DA; Sheppard, MN; Westaby, J; Haybatollahi, SM; Howe, FA; Sofat, N (2022) The osteoarthritis bone score (OABS): a new histological scoring system for the characterisation of bone marrow lesions in osteoarthritis. Osteoarthritis Cartilage, 30 (5). pp. 746-755. ISSN 1522-9653 https://doi.org/10.1016/j.joca.2022.01.008
SGUL Authors: Sofat, Nidhi Koushesh, Soraya Sheppard, Mary Noelle Westaby, Joseph David Howe, Franklyn Arron

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Abstract

OBJECTIVES: Bone marrow lesions (BMLs) are associated with pain in osteoarthritis (OA), but histological scores for OA focus on cartilage pathology. We developed a new scoring system, the Osteoarthritis Bone Score (OABS), to characterise OA-related BMLs. METHODS: BML/non-BML tissues identified by Magnetic Resonance Imaging (MRI) in 10 knee OA subjects were harvested at total knee replacement (TKR). Osteochondral tissue from a further 140 TKR and 23 post-mortem (PM) cases was assessed. Histological features distinguishing MRI-defined BML/non-BML tissues on qualitative analysis were classified as present (0) or absent (1), summated for the OABS, validated by Rasch analysis and sensitivity to distinguish between sample groups. Immunohistochemistry for PGP9.5 assessed innervation. RESULTS: Subchondral characteristics associated with BML tissues were cysts, fibrosis, hypervascularity, cartilage islands, trabecular thickening, loss of tidemark integrity and inflammatory cell infiltration. PGP9.5 immunoreactive perivascular nerves were associated with BMLs. OABS performed well as a measurement tool, displayed good reliability (Cronbach alpha = 0.68), had a 2-factor structure (trabecular/non-trabecular), with moderate correlation between the two factors (r = 0.56, 95% CI 0.46, 0.65). OABS scores were higher in TKR than PM cases with chondropathy, median difference 1.5 (95% CI -2, 0). OABS and Mankin scores similarly distinguished TKR from non-OA controls, but only OABS was higher in BML than non-BML tissues, median difference -4 (95% CI -5 to -2). CONCLUSIONS: OABS identifies and validly quantifies histopathological changes associated with OA BMLs. Histopathology underlying BMLs may represent 2 inter-related pathological processes affecting trabecular/non-trabecular structures. Increased vascularity/perivascular innervation in BMLs might contribute to pain.

Item Type: Article
Additional Information: Crown Copyright © 2022 Published by Elsevier Ltd on behalf of Osteoarthritis Research Society International. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
Keywords: Bone marrow lesions, Grading, Histology, Magnetic resonance imaging, Osteoarthritis, Scoring system, Bone Diseases, Bone Marrow, Bone and Bones, Cartilage Diseases, Humans, Knee Joint, Magnetic Resonance Imaging, Osteoarthritis, Knee, Pain, Reproducibility of Results, Bone and Bones, Knee Joint, Bone Marrow, Humans, Bone Diseases, Cartilage Diseases, Osteoarthritis, Knee, Pain, Magnetic Resonance Imaging, Reproducibility of Results, 1103 Clinical Sciences, Arthritis & Rheumatology
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Academic Structure > Molecular and Clinical Sciences Research Institute (MCS)
Journal or Publication Title: Osteoarthritis Cartilage
ISSN: 1522-9653
Language: eng
Dates:
DateEvent
21 April 2022Published
3 February 2022Published Online
26 January 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MC_PC_19095Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
M11-F3Rosetrees Trusthttp://dx.doi.org/10.13039/501100000833
204809/16/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
20777National Institute for Health Researchhttp://dx.doi.org/10.13039/501100000272
PubMed ID: 35124198
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/114076
Publisher's version: https://doi.org/10.1016/j.joca.2022.01.008

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