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Veterinary journal (London, England : 1997)2013; 197(1); 103-111; doi: 10.1016/j.tvjl.2013.03.049

Computed tomography and magnetic resonance imaging in the study of joint development in the equine pelvic limb.

Abstract: Osteochondrosis dissecans (OCD) is a focal failure of endochondral ossification of the epiphysis characterized by the presence of cartilage flaps and osteochondral fragments. The objective of this study was to image epiphyseal development in the equine pelvic limb to determine whether there was a variation in site maturation that could be a predisposing factor for OCD. Pelvic limbs (fetuses and foals) were studied post-mortem. The epiphyses of the distal femur, tibia and talus were scanned with computed tomography (CT) and 1.5T magnetic resonance imaging (MRI) to investigate the degree and pattern of ossification, the regularity of the ossification front and cartilage percentage (articular epiphyseal cartilage thickness as a percentage of total epiphyseal diameter) at predetermined sites. The secondary ossification centers (SOCs) were first identified in the femoral epiphyses at 7months, and both tibia and talus at 8months of gestation (MOG). At ⩾8 MOG the cartilage percentage was higher at the majority of OCD-susceptible sites when compared to control sites. At 8-9 MOG the lateral trochlear ridge of the femur, medial malleolus of the tibia (MM), cranial part of the distal intermediate ridge of the tibia (DIRT(Cr)), all OCD susceptible sites, had the greatest cartilage percentage compared to all other sites assessed. Post-partum, the cartilage percentage of the MM and DIRT(Cr), common sites of OCD, remained high. CT and MRI images illustrate equine epiphyseal development and provide additional evidence that greater cartilage thickness at specific joint sites could play a role in the development of OCD.
Publication Date: 2013-05-18 PubMed ID: 23688440DOI: 10.1016/j.tvjl.2013.03.049Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study aims to examine the development of joints in equine pelvic limbs through computed tomography (CT) and magnetic resonance imaging (MRI), to understand whether certain variations might predispose horses to Osteochondrosis Dissecans (OCD), a condition characterized by the failure of bone beneath the cartilage to form properly.

Introduction and Objective

  • The research focuses on studying equine pelvic limb development using CT and MRI in a bid to ascertain variations that may predispose horses to Osteochondrosis Dissecans; a bone and cartilage condition in horses.

Methodology

  • Equine pelvic limbs were examined post-mortem.
  • The researchers specifically targeted the epiphyses of the distal femur, tibia, and talus.
  • With the help of CT and 1.5T MRI, they investigated ossification patterns, the regularity of the ossification front, and the percentage of cartilage at certain sites.

Findings

  • The secondary ossification centers (SOCs) were first observed in the femoral epiphyses at 7 months of gestation, while in the tibia and talus, they were identified at 8 months of gestation.
  • A higher percentage of cartilage was noted at the majority of OCD-susceptible sites when compared to control sites from 8 months of gestation onwards.
  • At 8-9 months of gestation, the lateral trochlear ridge of the femur, medial malleolus of the tibia, and the cranial part of the distal intermediate ridge of the tibia, all OCD susceptible sites, were found to have the highest cartilage percentage compared to all other sites assessed.
  • Post-partum, high cartilage percentages continued to persist in common OCD sites like the medial malleolus of the tibia and the cranial part of the distal intermediate ridge of the tibia.

Conclusion

  • The study’s findings imply that CT and MRI images can provide a pivotal understanding of equine epiphyseal development.
  • The study provides additional evidence suggesting that an increased cartilage thickness at certain joint sites could contribute to the development of OCD in horses.

Cite This Article

APA
Fontaine P, Blond L, Alexander K, Beauchamp G, Richard H, Laverty S. (2013). Computed tomography and magnetic resonance imaging in the study of joint development in the equine pelvic limb. Vet J, 197(1), 103-111. https://doi.org/10.1016/j.tvjl.2013.03.049

Publication

ISSN: 1532-2971
NlmUniqueID: 9706281
Country: England
Language: English
Volume: 197
Issue: 1
Pages: 103-111
PII: S1090-0233(13)00167-6

Researcher Affiliations

Fontaine, Pascal
  • Comparative Orthopaedic Research Laboratory, Faculté de médecine vétérinaire, Université de Montréal, Québec, Canada.
Blond, Laurent
    Alexander, Kate
      Beauchamp, Guy
        Richard, Hélène
          Laverty, Sheila

            MeSH Terms

            • Animals
            • Animals, Newborn
            • Bone Development
            • Cartilage / physiology
            • Fetal Development
            • Hindlimb / growth & development
            • Horses / growth & development
            • Joints / growth & development
            • Osteogenesis

            Grant Funding

            • Canadian Institutes of Health Research

            Citations

            This article has been cited 3 times.
            1. Lemirre T, Santschi E, Girard C, Fogarty U, Chapuis L, Richard H, Beauchamp G, Laverty S. Maturation of the equine medial femoral condyle osteochondral unit.. Osteoarthr Cartil Open 2020 Mar;2(1):100029.
              doi: 10.1016/j.ocarto.2020.100029pubmed: 36474556google scholar: lookup
            2. Pinsard M, Laverty S, Richard H, Dubuc J, Schanne-Klein MC, Légaré F. Maturation of the Meniscal Collagen Structure Revealed by Polarization-Resolved and Directional Second Harmonic Generation Microscopy.. Sci Rep 2019 Dec 5;9(1):18448.
              doi: 10.1038/s41598-019-54942-0pubmed: 31804577google scholar: lookup
            3. Gorissen BM, Wolschrijn CF, van Vilsteren AA, van Rietbergen B, van Weeren PR. Trabecular bone of precocials at birth; Are they prepared to run for the wolf(f)?. J Morphol 2016 Jul;277(7):948-56.
              doi: 10.1002/jmor.20548pubmed: 27098190google scholar: lookup