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Contrast enhanced μCT imaging of early articular changes in a pre-clinical model of osteoarthritis.

Authors :
Reece DS
Thote T
Lin ASP
Willett NJ
Guldberg RE
Source :
Osteoarthritis and cartilage [Osteoarthritis Cartilage] 2018 Jan; Vol. 26 (1), pp. 118-127. Date of Electronic Publication: 2017 Oct 28.
Publication Year :
2018

Abstract

Objective: The objective of this study was to characterize early osteoarthritis (OA) development in cartilage and bone tissues in the rat medial meniscus transection (MMT) model using non-destructive equilibrium partitioning of an ionic contrast agent micro-computed tomography (EPIC-μCT) imaging. Cartilage fibrillation, one of the first physiological developments in OA, was quantified in the rat tibial plateau as three-dimensional (3D) cartilage surface roughness using a custom surface-rendering algorithm.<br />Methods: Male Lewis rats underwent MMT or sham-operation in the left leg. At 1- and 3-weeks post-surgery, the animals (n = 7-8 per group) were euthanized and the left legs were scanned using EPIC-μCT imaging to quantify cartilage and bone parameters. In addition, a custom algorithm was developed to measure the roughness of 3D surfaces. This algorithm was validated and used to quantify cartilage surface roughness changes as a function of time post-surgery.<br />Results: MMT surgery resulted in significantly greater cartilage damage and subchondral bone sclerosis with the damage increasing in both severity and area from 1- to 3-weeks post-surgery. Analysis of rendered 3D surfaces could accurately distinguish early changes in joints developing OA, detecting significant increases of 45% and 124% in surface roughness at 1- and 3-weeks post-surgery respectively.<br />Conclusion: Disease progression in the MMT model progresses sequentially through changes in the cartilage articular surface, extracellular matrix composition, and then osteophyte mineralization and subchondral bone sclerosis. Cartilage surface roughness is a quantitative, early indicator of degenerative joint disease in small animal OA models and can potentially be used to evaluate therapeutic strategies.<br /> (Copyright © 2017 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights reserved.)

Details

Language :
English
ISSN :
1522-9653
Volume :
26
Issue :
1
Database :
MEDLINE
Journal :
Osteoarthritis and cartilage
Publication Type :
Academic Journal
Accession number :
29107695
Full Text :
https://doi.org/10.1016/j.joca.2017.10.017