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Veterinary pathology2005; 42(6); 823-827; doi: 10.1354/vp.42-6-823

Incidence of polysaccharide storage myopathy: necropsy study of 225 horses.

Abstract: Muscle samples were obtained at necropsy from 225 horses and ponies 1 year of age or older. Samples were processed in routine manner and were stained with hematoxylin and eosin and with periodic acid-Schiff for glycogen. Sections were examined for abnormal glycogen content and amylase-resistant complex polysaccharide and for chronic myopathic change (excessive fiber size variation, increase in number of internal nuclei). A total of 101 horses and ponies with lesions of polysaccharide storage myopathy were identified. Age of affected horses ranged from one to 30 years, with a mean of 14.7 years. Mean age of nonaffected horses was 12 years. Incidence of polysaccharide storage myopathy varied depending on breed; Thoroughbreds had the lowest (27%) and draft-related horses had the highest (86%) incidence. Chronic myopathic changes were more severe in polysaccharide storage myopathy-affected horses than in nonaffected horses. Results of this study indicate that polysaccharide storage myopathy is a common disorder of many breeds of horses and ponies.
Publication Date: 2005-11-23 PubMed ID: 16301580DOI: 10.1354/vp.42-6-823Google Scholar: Lookup
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  • Comparative Study
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

This research study investigated the incidence of polysaccharide storage myopathy (PSSM), a muscle disorder, in a sample of 225 horses and ponies. The researchers found that symptoms of PSSM were present in 101 of the sampled horses, varying in degree depending on the breed.

Methodology of the Study

  • The research work was carried out on muscle samples which were procured at necropsy (postmortem examination) from 225 horses and ponies that were at least one year old.
  • The samples were processed and stained with hematoxylin and eosin, and with periodic acid-Schiff which is a staining method used to detect glycogen.
  • The stained sections were examined for abnormal glycogen content, resistant complex polysaccharide, and chronic myopathic change—distinguished by an excessive difference in fiber size and an increase in the number of internal nuclei.

Key Findings

  • The research identified 101 horses and ponies with lesions characteristic of polysaccharide storage myopathy.
  • The age of the affected horses ranged from one to 30 years old, with an average age of 14.7 years, while the mean age of horses that were not affected was 12 years.
  • The study discovered that the incidence of polysaccharide storage myopathy varied depending on the breed: Thoroughbreds had the lowest incidence at 27%, while draft-related horses had the highest incidence at 86%.
  • Chronic myopathic changes were more severe in PSSM-affected horses than in horses that were not affected.

Conclusion

  • The results of the study indicate that polysaccharide storage myopathy is a prevalent disorder in many breeds of horses and ponies.

This study provides significant insights into the occurrence and implications of polysaccharide storage myopathy across various breeds of horses and ponies, highlighting the need for further research and perhaps breed-specific care guidelines.

Cite This Article

APA
Valentine BA, Cooper BJ. (2005). Incidence of polysaccharide storage myopathy: necropsy study of 225 horses. Vet Pathol, 42(6), 823-827. https://doi.org/10.1354/vp.42-6-823

Publication

ISSN: 0300-9858
NlmUniqueID: 0312020
Country: United States
Language: English
Volume: 42
Issue: 6
Pages: 823-827

Researcher Affiliations

Valentine, B A
  • Department of Biomedical Sciences, College of Veterinary Medicine, Magruder 142, Oregon State University, Corvallis, OR 97331, USA. Beth.Valentine@oregonstate.edu
Cooper, B J

    MeSH Terms

    • Animals
    • Carbohydrate Metabolism, Inborn Errors / epidemiology
    • Carbohydrate Metabolism, Inborn Errors / pathology
    • Carbohydrate Metabolism, Inborn Errors / veterinary
    • Female
    • Glycogen / metabolism
    • Horse Diseases / epidemiology
    • Horse Diseases / pathology
    • Horses
    • Incidence
    • Male
    • Muscle, Skeletal / pathology
    • Muscular Diseases / epidemiology
    • Muscular Diseases / pathology
    • Muscular Diseases / veterinary
    • Species Specificity

    Citations

    This article has been cited 6 times.
    1. Ellero N, Freccero F, Lanci A, Morini M, Castagnetti C, Mariella J. Rhabdomyolysis and Acute Renal Failure Associated with Oxytetracycline Administration in Two Neonatal Foals Affected by Flexural Limb Deformity.. Vet Sci 2020 Oct 22;7(4).
      doi: 10.3390/vetsci7040160pubmed: 33105842google scholar: lookup
    2. Valberg SJ, Finno CJ, Henry ML, Schott M, Velez-Irizarry D, Peng S, McKenzie EC, Petersen JL. Commercial genetic testing for type 2 polysaccharide storage myopathy and myofibrillar myopathy does not correspond to a histopathological diagnosis.. Equine Vet J 2021 Jul;53(4):690-700.
      doi: 10.1111/evj.13345pubmed: 32896939google scholar: lookup
    3. Williams ZJ, Bertels M, Valberg SJ. Muscle glycogen concentrations and response to diet and exercise regimes in Warmblood horses with type 2 Polysaccharide Storage Myopathy.. PLoS One 2018;13(9):e0203467.
      doi: 10.1371/journal.pone.0203467pubmed: 30183782google scholar: lookup
    4. 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.
      doi: 10.1371/journal.pone.0042317pubmed: 22860112google scholar: lookup
    5. 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.
      doi: 10.1186/1746-6148-5-29pubmed: 19664222google scholar: lookup
    6. 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.
      doi: 10.1016/j.ygeno.2008.01.011pubmed: 18358695google scholar: lookup