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Published on: May 14, 2020
The Bone Cartilage Interface and Osteoarthritis
1Dental Physical Sciences Imaging Unit, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, Mile End Campus, London, E1 4NS, UK. a.boyde@qmul.ac.uk.
Osteoarthritis (OA) involves damage to joint tissues like cartilage and bone. This review details microstructural changes in equine and human OA, revealing how bone resorption and repair processes contribute to joint destruction.
Area of Science:
- Orthopedics
- Biomaterials Science
- Veterinary Medicine
Background:
- Osteoarthritis (OA) is a degenerative joint disease affecting both humans and equines.
- Understanding the microstructural changes at the osteochondral junction is crucial for OA pathogenesis.
- Previous studies on equine and human OA tissue provide valuable insights into disease mechanisms.
Purpose of the Study:
- To review and synthesize findings on the microstructural changes in articular cartilage and subchondral bone in osteoarthritis.
- To elucidate the role of bone resorption and repair processes in the progression of OA.
- To analyze the contribution of specific microstructural features to joint destruction in OA.
Main Methods:
- Re-utilization of tissue samples from prior studies.
- Scanning electron microscopy for high-resolution imaging.
- Novel light microscopy techniques.
- X-ray micro-tomography for 3D structural analysis.
Main Results:
- Overload exercise and rest periods downregulate turnover at the osteochondral junction, predisposing to microfracture.
- Resorption canals, loss of articular calcified cartilage (ACC), and subchondral bone (SCB) cracking are key OA features.
- High-Density Mineral Infill (HDMI) seals cracks, extruding as High-Density Mineral Protrusions (HDMP) into hyaline articular cartilage (HAC), leading to fragmentation and destruction.
- SCB densification with woven bone, HAC fibrillation, eburnation, and repair with abnormal tissues characterize advanced OA.
Conclusions:
- The interplay between bone resorption and repair at the osteochondral junction is a critical driver of OA.
- Microstructural alterations, including HDMI and HDMP, significantly contribute to cartilage and bone destruction in OA.
- This review highlights the complex pathological cascade in OA, emphasizing the need for targeted therapeutic strategies.
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