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ORIGINAL RESEARCH article

Front. Vet. Sci.

Sec. Veterinary Neurology and Neurosurgery

Volume 12 - 2025 | doi: 10.3389/fvets.2025.1555889

Survival and deterioration time of walking abilities in dogs homozygous for the SOD1 gene mutation with and without thoracolumbar intervertebral disc protrusion

Provisionally accepted
Péter Sebestyén Péter Sebestyén 1*Malwina Ewa Kowalska Malwina Ewa Kowalska 2,3Lorenzo Golini Lorenzo Golini 1*
  • 1 Section of Neurology, Department of Small Animals, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland
  • 2 Section of Epidemiology, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland
  • 3 Section of Ophthalmology, Equine Department, Vetsuisse Faculty Zurich, University of Zurich, Zurich, Switzerland

The final, formatted version of the article will be published soon.

    Introduction: Dogs homozygous for the SOD1 gene mutation with presumptive degenerative myelopathy (DM) can develop concurrent intervertebral disc protrusion (IVDP). The impact of IVDP on the progression of SOD1-related clinical signs is unknown. The aim of this study was to describe a population of dogs with SOD1 mutation and to compare survival and time to non-ambulation between dogs with and without IVDP.Methods: This single-center exploratory cohort study was preregistered and retrospectively included dogs with the SOD1 gene mutation, compatible clinical signs, and available spinal magnetic resonance imaging (MRI). Dogs were divided into two groups based on the presence (IVDP+) or absence (IVDP-) of IVDP affecting the T3-L3 spinal cord segment. The primary outcomes were time to euthanasia from onset of clinical signs (neurological deficits) and from diagnosis (genetic testing and MRI). The secondary outcome was time to non-ambulatory status. Data were analyzed using descriptive statistics and survival analysis.Results: A total of 39 dogs were enrolled in the study, with a mean age of 115 months and a mean weight of 29 kg at the time of diagnosis. The most common breed was the German Shepherd (n = 9/39). In the IVDP-group (n = 28/39), the median survival time was 13 months (95% CI, 9-18 months) from the onset of clinical signs, and 6 months (95% CI, 5-11 months) from the time of diagnosis. In the IVDP+ group (n = 11/39), the median survival time was 11 months (95% CI, 9-∞ months) from the onset of clinical signs, and 7 months (95% CI, 5-∞ months) from the diagnosis. Cox regression analysis indicated that dogs with IVDP had a hazard ratio of 1.20 for euthanasia (95% CI: 0.58-2.49, P = 0.6), which was not statistically significant compared to dogs without IVDP.Discussion: Based on this retrospective cohort, dogs with SOD1 mutation appear to have similar disease progression and survival, regardless of the presence of concurrent IVDP.

    Keywords: canine, Magnetic Resonance Imaging, Spinal cord disease, Degenerative myelopathy, Kaplan-Meier survival analysis

    Received: 05 Jan 2025; Accepted: 24 Mar 2025.

    Copyright: © 2025 Sebestyén, Kowalska and Golini. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Péter Sebestyén, Section of Neurology, Department of Small Animals, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland
    Lorenzo Golini, Section of Neurology, Department of Small Animals, Vetsuisse Faculty, University of Zurich, Zurich, Switzerland

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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