Intrafascicular chondroid‐like bodies in the ageing equine superficial digital flexor tendon comprise glycosaminoglycans and type II collagen. Issue 12 (24th February 2021)

• Record Type: Journal Article
• Authors: Ali, Othman J.; Ehrle, Anna; Comerford, Eithne J.; Canty‐Laird, Elizabeth G.; Mead, Ashleigh; Clegg, Peter D.; Maddox, Thomas W.
• Is Part Of: Journal of orthopaedic research. Volume 39:Issue 12(2021)
• Page Start: 2755
• Page End: 2766
• Publication Date: 2021-02-24
• Subjects: ageing -- fascicle -- inclusion body -- interfascicular matrix -- superficial digital flexor tendon; Orthopedics -- Periodicals; Musculoskeletal system -- Periodicals; 616.7
• DOI: 10.1002/jor.25002
• Languages: English
• ISSNs: 0736-0266

Abstract

Abstract: The superficial digital flexor tendon (SDFT) is considered functionally equivalent to the human Achilles tendon. Circular chondroid depositions scattered amongst the fascicles of the equine SDFT are rarely reported. The purpose of this study was the detailed characterization of intrafascicular chondroid‐like bodies (ICBs) in the equine SDFT, and the assessment of the effect of ageing on the presence and distribution of these structures. Ultrahigh field magnetic resonance imaging (9.4T) series of SDFT samples of young (1–9 years) and aged (17–25 years) horses were obtained, and three‐dimensional reconstruction of ICBs was performed. Morphological evaluation of the ICBs included histology, immunohistochemistry and transmission electron microscopy. The number, size, and position of ICBs was determined and compared between age groups. There was a significant difference ( p = .008) in the ICB count between young and old horses with ICBs present in varying number (13–467; median = 47, mean = 132.6), size and distribution in the SDFT of aged horses only. There were significantly more ICBs in the tendon periphery when compared with the tendon core region ( p = .010). Histological characterization identified distinctive cells associated with increased glycosaminoglycan and type II collagen extracellular matrix content. Ageing and repetitive strain frequently cause tendon micro‐damage before the development of clinical tendinopathy. Documentation of the presence and distribution of ICBs is a first step towards improving our understanding of the impact of these structures on the viscoelastic properties, and ultimately their effect on the risk of age‐related tendinopathy in energy‐storing tendons.