Prevalence of equine polysaccharide storage myopathy and other myopathies in two equine populations in the United Kingdom.
Abstract: The aim of this study was to determine the prevalence of equine polysaccharide storage myopathy (EPSM) in two populations of horses in the UK. Biopsy specimens from 94 horses presented to an abattoir (population 1), and 46 horses with neuromuscular disorders presented to a university referral hospital (population 2) were obtained over a period of 4years. Histological sections were examined by a veterinary pathologist for lesions including abnormal polysaccharide inclusions in myofibres. In population 1, a diagnosis of EPSM was made in 8% and non-specific myopathy in 33% of horses. In population 2, a diagnosis of EPSM was made in 22%, equine motor neurone disease (EMND) in 15% and non-specific myopathy in 37%. Within each population there was no difference in age, sex or breed distribution and muscle disease diagnosis. However, populations differed from each other in age and breed distributions and muscle disease diagnosis. EPSM was found in draft, Warmblood and related breeds and was diagnosed for the first time in cob-types. EMND was reported in 7/46 horses presented for neuromuscular disease and weakness, representing an important diagnosis in the UK. This study showed a high prevalence of EPSM and other myopathies in typical breeds of horses in the UK.
Publication Date: 2008-03-28 PubMed ID: 18375158DOI: 10.1016/j.tvjl.2008.01.008Google Scholar: Lookup
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- Journal Article
Summary
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This study is about determining the frequency of equine polysaccharide storage myopathy (EPSM) and other muscle diseases in two different horse populations in the UK.
Study Objective and Methodology
- The study aimed to recognize the prevalence of Equine Polysaccharide Storage Myopathy (EPSM), a muscle disease in horses, in two different UK horse populations.
- The researchers obtained biopsy specimens from 94 horses at an abattoir (population 1), and 46 horses with neuromuscular issues presented at a university referral hospital (population 2). The study period was four years.
- A veterinary pathologist examined these histological sections for signs including abnormal polysaccharide inclusions in the muscle fibers.
Study Findings
- From population 1, EPSM diagnosis was found in 8% and non-specific muscle disease occurred in 33% of the horses.
- In population 2, there were 22% EPSM diagnoses, 15% Equine Motor Neurone Disease (EMND), and 37% non-specific muscle disease.
- There was no significant difference in the distribution of age, sex, or breed, and muscle disease diagnosis within each population.
- However, the two populations differed in age, breed distributions and muscle disease diagnosis.
- EPSM was diagnosed in draft, Warmblood, and related breeds, including cob-types for the first time.
- EMND was reported in 7 out of 46 horses presented for neuromuscular disease and weakness, marking it an important diagnosis in the UK.
Study Conclusion
- Overall, the study revealed a high prevalence of EPSM and other muscle diseases in the typical breeds of horses in the UK.
Cite This Article
APA
McGowan CM, McGowan TW, Patterson-Kane JC.
(2008).
Prevalence of equine polysaccharide storage myopathy and other myopathies in two equine populations in the United Kingdom.
Vet J, 180(3), 330-336.
https://doi.org/10.1016/j.tvjl.2008.01.008 Publication
Researcher Affiliations
- Department of Equine and Small Animal Medicine, The University of Helsinki, P.O. Box 57, 00014, Helsinki, Finland. catherine.mcgowan@helsinki.fi
MeSH Terms
- Animals
- Female
- Horse Diseases / epidemiology
- Horses
- Male
- Muscular Diseases / epidemiology
- Muscular Diseases / veterinary
- Prevalence
- United Kingdom / epidemiology
Citations
This article has been cited 1 times.- Barrey E, Mucher E, Jeansoule N, Larcher T, Guigand L, Herszberg B, Chaffaux S, Guérin G, Mata X, Benech P, Canale M, Alibert O, Maltere P, Gidrol X. Gene expression profiling in equine polysaccharide storage myopathy revealed inflammation, glycogenesis inhibition, hypoxia and mitochondrial dysfunctions. BMC Vet Res 2009 Aug 7;5:29.
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