Polysaccharide storage myopathy in Morgan, Arabian, and Standardbred related horses and Welsh-cross ponies.
Abstract: Polysaccharide storage myopathy is an equine neuromuscular disorder characterized by accumulation of glycogen-related polysaccharide inclusions within skeletal muscle fibers. The pathologic criteria for diagnosis of this disorder are somewhat controversial; however, periodic acid-Schiff-positive, amylase-resistant inclusions are considered pathognomonic. Although these inclusions are most often found in affected horses related to the Quarter Horse, draft horse, and Warmblood breeds, this report describes these characteristic inclusions in muscle of five horses from nonrelated breeds (two Morgans, one Arabian, one Arabian x Thoroughbred, and one Standardbred) and two Welsh cross ponies. Affected horses had histories of recurrent exertional rhabdomyolysis, and one developed progressive weakness leading to increased recumbency. The affected ponies were part of an unrelated research project and had no apparent clinical signs.
Publication Date: 2000-03-14 PubMed ID: 10714651DOI: 10.1354/vp.37-2-193Google Scholar: Lookup The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
- Journal Article
- Research Support
- Non-U.S. Gov't
- Arabian Horses
- Case Reports
- Clinical Findings
- Clinical Pathology
- Diagnosis
- Disease Diagnosis
- Disease Etiology
- Equine Diseases
- Equine Health
- Genetics
- Glycogen
- Horse Breeds
- Horses
- Muscle Fiber Types
- Musculoskeletal System
- Neuromuscular System
- Polysaccharide Storage Myopathy
- Ponies
- Recurrent Exertional Rhabdomyolysis
- Standardbred Horses
- Veterinary Medicine
Summary
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This research study focuses on a muscle disorder in horses known as polysaccharide storage myopathy, identifying it in horses and ponies of breeds where it is not usually found. The disorder is detected by looking for specific inclusions in muscle tissue, and can cause weakness, exercise-induced muscle damage, and in severe cases, increased time spent lying down.
About Polysaccharide Storage Myopathy
- Polysaccharide storage myopathy (PSSM) is a genetic muscle disorder in horses.
- The ailment is characterized by an excessive accumulation of glycogen-related polysaccharide inclusions within skeletal muscle fibers.
- This typically leads to symptoms such as muscle stiffness, pain, and difficulty moving after periods of rest or exertion.
Diagnostic Criteria
- Diagnosing this disease involves the identification of periodic acid-Schiff-positive, amylase-resistant inclusions. These are considered pathognomonic, meaning they are unique to and indicative of this disorder.
- The criteria for diagnosing this disorder are somewhat disputed, but these inclusions are usually a clear sign of the condition.
The Study’s Findings
- Polysaccharide storage myopathy is most commonly found in Quarter Horses, draft horses, and Warmblood breeds, but this study identified the disorder in other breeds as well.
- The study found PSSM in five horses of unrelated breeds – two Morgans, one Arabian, one Arabian x Thoroughbred, and one Standardbred.
- Two Welsh cross ponies were also found to have the disease.
- Moreover, the horses affected showed histories of recurrent exertional rhabdomyolysis, a condition causing muscle breakdown due to extreme physical exertion.
- One horse developed progressive weakness, leading to a rise in recumbency time, which means that the horse spent significantly more time lying down due to weakness.
- The ponies found with the disorder were part of an unrelated research project and displayed no noticeable symptoms.
Implications of the Study
- The findings expand the common perceptions about which horse and pony breeds can suffer from PSSM, suggesting the need for a broader approach to awareness and diagnosis.
- The absence of symptoms in the Welsh cross ponies indicates that the disease can be asymptomatic, highlighting the importance of regular checks in maintaining the health of horses and ponies.
Cite This Article
APA
Valentine BA, McDonough SP, Chang YF, Vonderchek AJ.
(2000).
Polysaccharide storage myopathy in Morgan, Arabian, and Standardbred related horses and Welsh-cross ponies.
Vet Pathol, 37(2), 193-196.
https://doi.org/10.1354/vp.37-2-193 Publication
Researcher Affiliations
- Department of Biomedical Sciences, College of Veterinary Medicine, Oregon State University, Corvallis 97331, USA. beth.valentine@orst.edu
MeSH Terms
- Amylases / chemistry
- Animals
- Breeding
- Carbohydrate Metabolism, Inborn Errors / genetics
- Carbohydrate Metabolism, Inborn Errors / pathology
- Carbohydrate Metabolism, Inborn Errors / veterinary
- Female
- Horse Diseases / diagnosis
- Horse Diseases / genetics
- Horse Diseases / pathology
- Horses
- Immunohistochemistry
- Male
- Muscle, Skeletal / metabolism
- Muscle, Skeletal / pathology
- Muscular Diseases / genetics
- Muscular Diseases / pathology
- Muscular Diseases / veterinary
- Periodic Acid-Schiff Reaction / veterinary
- Polysaccharides / analysis
- Polysaccharides / metabolism
- Rhabdomyolysis / veterinary
Citations
This article has been cited 6 times.- Lindsay-McGee V, Massey C, Li YT, Clark EL, Psifidi A, Piercy RJ. Characterisation of phenotypic patterns in equine exercise-associated myopathies. Equine Vet J 2025 Mar;57(2):347-361.
- Valberg SJ, McKenzie EC, Eyrich LV, Shivers J, Barnes NE, Finno CJ. Suspected myofibrillar myopathy in Arabian horses with a history of exertional rhabdomyolysis. Equine Vet J 2016 Sep;48(5):548-56.
- Naylor RJ, Livesey L, Schumacher J, Henke N, Massey C, Brock KV, Fernandez-Fuente M, Piercy RJ. Allele copy number and underlying pathology are associated with subclinical severity in equine type 1 polysaccharide storage myopathy (PSSM1). PLoS One 2012;7(7):e42317.
- El-Deeb WM, El-Bahr SM. Investigation of selected biochemical indicators of Equine Rhabdomyolysis in Arabian horses: pro-inflammatory cytokines and oxidative stress markers. Vet Res Commun 2010 Dec;34(8):677-89.
- Isgren CM, Upjohn MM, Fernandez-Fuente M, Massey C, Pollott G, Verheyen KL, Piercy RJ. Epidemiology of exertional rhabdomyolysis susceptibility in standardbred horses reveals associated risk factors and underlying enhanced performance. PLoS One 2010 Jul 14;5(7):e11594.
- McCue ME, Valberg SJ, Miller MB, Wade C, DiMauro S, Akman HO, Mickelson JR. Glycogen synthase (GYS1) mutation causes a novel skeletal muscle glycogenosis. Genomics 2008 May;91(5):458-66.
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