Effects of osteochondral fragmentation and intra-articular triamcinolone acetonide treatment on subchondral bone in the equine carpus.
Abstract: To determine the effects of osteochondral fragmentation and intra-articular corticosteroid treatment on dynamics of bone remodelling and fragility, 12 horses each had a unilateral, 8 mm osteochondral fragment created in the distal aspect of one radiocarpal bone. Six of the horses were treated in the fragmented joint, and the other 6 were treated in the nonfragmented joint with 12 mg of triamcinolone acetonide (TA) 14 and 28 days after surgery. All horses were exercised on a high-speed treadmill starting 15 days, and ending 72 days after surgery. Horses treated with TA in the fragmented joints were significantly less lame than those treated in the nonfragmented joints. Third carpal bones from joints with fragments showed significantly more vascularity, single labelled surface, total labelled surface and mineralising surface in subchondral and subjacent trabecular bone. Trends were also seen towards higher vascular canal volume and osteochondral junction remodelling sites in third carpal bones from fragmented joints. No significant differences were seen in microdamage density or size between fragmented and nonfragmented joints. No significant influence of TA treatment was seen on any parameter measured. The results from this study show that osteochondral fragmentation induces significant changes in remodelling of opposing bones, and that the administration of corticosteroids into joints with fragmentation does not significantly alter bone remodelling or fragility.
Publication Date: 1998-02-12 PubMed ID: 9458401DOI: 10.1111/j.2042-3306.1998.tb04090.xGoogle Scholar: Lookup
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- Clinical Trial
- Controlled Clinical Trial
- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This study analyzes how osteochondral fragmentation and an intra-articular corticosteroid treatment impact bone remodelling and fragility in horses. The researchers found that the corticosteroid treatment did not significantly change bone remodelling or fragility, but the fragmentation did have a significant impact.
Experiment Design
- The study involved 12 horses, in each of them, a unilateral, 8 mm osteochondral fragment was created in the distal aspect of one radiocarpal bone.
- Half of the horses were treated in the fragmented joint, and the other half were treated in the nonfragmented joint with 12 mg of triamcinolone acetonide (TA), a corticosteroid. The treatment was administered 14 and 28 days after surgery.
- All horses were exercised on a high-speed treadmill starting 15 days and ending 72 days after surgery.
Finding 1: Lameness Reduction after TA Treatment
- Horses that underwent the TA treatment on the joints with fragments showed significantly less lameness compared to those treated in the nonfragmented joints, suggesting a potential pain-relieving effect of TA on injured joints.
Finding 2: Increased Vascularity and Remodelling in Fragmented Joints
- Significantly higher vascularity, single labelled surface, total labelled surface, and mineralising surface were observed in the subchondral and subjacent trabecular bone of joints with fragments.
- There also appeared to be a trend towards higher vascular canal volume and osteochondral junction remodelling sites in the bones from fragmented joints.
Finding 3: No Significant Impact of TA on Bone Remodelling
- No significant variations were found in microdamage density or size, between fragmented and nonfragmented joints.
- Most importantly, the TA treatment did not have a significant impact on bone remodelling or fragility, suggesting that the corticosteroid, while helpful in reducing lameness, does not significantly influence these parameters.
Implication of the Findings
- The results indicate that while osteochondral fragmentation significantly alters bone remodelling, the administration of TA into joints with fragments does not significantly alter this remodelling process or the fragility of the bone.
- The findings could have clinical significance for understanding how to manage joint injury and osteoarthritis in horses, and potentially in other animals or humans as well.
Cite This Article
APA
Kawcak CE, Norrdin RW, Frisbie DD, Trotter GW, Mcilwraith CW.
(1998).
Effects of osteochondral fragmentation and intra-articular triamcinolone acetonide treatment on subchondral bone in the equine carpus.
Equine Vet J, 30(1), 66-71.
https://doi.org/10.1111/j.2042-3306.1998.tb04090.x Publication
Researcher Affiliations
- Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins 80523, USA.
MeSH Terms
- Animals
- Anti-Inflammatory Agents / administration & dosage
- Anti-Inflammatory Agents / pharmacology
- Anti-Inflammatory Agents / therapeutic use
- Bone Development / drug effects
- Bone Development / physiology
- Bone Remodeling / drug effects
- Bone Remodeling / physiology
- Carpal Bones / injuries
- Carpus, Animal / blood supply
- Carpus, Animal / drug effects
- Carpus, Animal / pathology
- Exercise Test / methods
- Exercise Test / veterinary
- Fractures, Bone / drug therapy
- Fractures, Bone / physiopathology
- Fractures, Bone / veterinary
- Horses / injuries
- Horses / physiology
- Injections, Intra-Articular / veterinary
- Lameness, Animal / etiology
- Lameness, Animal / physiopathology
- Lameness, Animal / prevention & control
- Triamcinolone Acetonide / administration & dosage
- Triamcinolone Acetonide / pharmacology
- Triamcinolone Acetonide / therapeutic use
Citations
This article has been cited 4 times.- Sullivan SN, Altmann NN, Brokken MT, Durgam SS. In vitro Effects of Methylprednisolone Acetate on Equine Deep Digital Flexor Tendon-Derived Cells.. Front Vet Sci 2020;7:486.
- Donnell JR, Frisbie DD. Use of firocoxib for the treatment of equine osteoarthritis.. Vet Med (Auckl) 2014;5:159-168.
- McIlwraith CW, Frisbie DD, Kawcak CE. The horse as a model of naturally occurring osteoarthritis.. Bone Joint Res 2012 Nov;1(11):297-309.
- Gregory MH, Capito N, Kuroki K, Stoker AM, Cook JL, Sherman SL. A review of translational animal models for knee osteoarthritis.. Arthritis 2012;2012:764621.
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