High detail radiography and histology of the centrodistal tarsal joint of Icelandic horses age 6 months to 6 years

• Published in: Equine veterinary journal 2004-01, Vol.36 (1), p.5-11
• Main Authors: Björnsdóttir, S., Ekman, S., Eksell, P., Lord, P.
• Format: Article
• Language: English
• Subjects: Age Factors; Animals; Biomechanical Phenomena; bone spavin; distal tarsal joints; Gait - physiology; Genetic Predisposition to Disease; high detail radiograpy; Hindlimb; histology; horse; Horse Diseases - diagnostic imaging; Horse Diseases - epidemiology; Horse Diseases - pathology; Horses; Iceland - epidemiology; Icelandic; Joint Diseases - diagnostic imaging; Joint Diseases - epidemiology; Joint Diseases - pathology; Joint Diseases - veterinary; Lameness, Animal; Osteoarthritis - diagnostic imaging; Osteoarthritis - epidemiology; Osteoarthritis - pathology; Osteoarthritis - veterinary; Prevalence; Radiography; Tarsus, Animal - diagnostic imaging; Tarsus, Animal - pathology; Tarsus, Animal - physiology
• ISSN: 0425-1644; 2042-3306
• DOI: 10.2746/0425164044864679

Summary Reasons for performing study: Osteoarthrosis (OA) in the distal tarsal joints, bone spavin, is a well known condition which is common in Icelandic horses age 6–12 years. Objectives: To determine the nature, location and age of appearance of early radiographic and histological changes in the centrodistal tarsal joint (CD) of young Icelandic horses. Methods: Slab sections from the CD of young Icelandic horses were examined by high detail radiography (age 6 months to 6 years, n = 111) and histology (age 6 months to 4 years, n = 82) to detect and describe the early changes indicative of OA. Horses younger than 5 years were unridden. Results: Chondronecrotic lesions histologically similar to those described in the early pathogenesis of OA were seen in 33% of the joints, located both medially and laterally. Radiographic sclerosis of the subchondral bone was recorded in 60% of the specimens, most often medially. Medial location was not associated with chondronecrosis, but was strongly related to age. Sclerosis was an infrequent finding on the lateral side, and was probably secondary to chondronecrosis in the corresponding part of the joint. Small defects in the subchondral bone were considered to be the most specific radiographic sign of OA as they were strongly associated with chondronecrosis. Conclusions: The high prevalence of chondronecrosis in the young horses indicates an early onset and slow progression of the disease. The early appearance also shows that the initiation of the disease is unrelated to the use of horses for riding. As clinical manifestation of OA in the distal tarsal joints is most often described in mature or old horses, the first stages of the disease are not likely to result in clinical signs. Subchondral bone sclerosis did not appear to be a primary factor in the development of OA in the CD but was considered to reflect an uneven distribution of biomechanical forces within the joint. Potential relevance: The development of OA in the CD of young Icelandic horses seems to be due to poor conformation or joint architecture rather than trauma or overloading. These aetiological factors are likely to be of importance for OA in the distal tarsal joints in other breeds as well. The influence of hindlimb conformation and the architecture of the distal tarsal joints on the biomechanics of joints need to be investigated, preferably by locomotion analysis in young horses.