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Prevalence of clinical signs and factors impacting expression of myosin heavy chain myopathy in Quarter Horse-related breeds with the MYH1 E321G mutation.

Authors :
Valberg SJ
Schultz AE
Finno CJ
Bellone RR
Hughes SS
Source :
Journal of veterinary internal medicine [J Vet Intern Med] 2022 May; Vol. 36 (3), pp. 1152-1159. Date of Electronic Publication: 2022 Apr 14.
Publication Year :
2022

Abstract

Background: The prevalence of clinical signs and factors triggering muscle atrophy and rhabdomyolysis associated with an MYH1 <superscript>E321G</superscript> mutation in Quarter Horses and related breeds (QH) remain poorly understood.<br />Hypothesis/objectives: Determine the prevalence and potential triggers of atrophy and stiffness in horses homozygous reference (N/N), heterozygous (My/N), and homozygous (My/My) for the MYH1 <superscript>E321G</superscript> mutation.<br />Animals: Two-hundred seventy-five N/N, 100 My/N, and 10 My/My QH.<br />Methods: A retrospective case-control study using a closed-ended questionnaire completed by clients of the Veterinary Genetics Laboratory at the University of California, Davis. History of clinical signs, disease, vaccination and performance were analyzed by genotype using contingency testing.<br />Results: Atrophy occurred in proportionately more horses with MYH1 <superscript>E321G</superscript> (My) than N/N QH and more frequently in My/My than My/N QH (P < .001; My/My 8/10 [80%], My/N 17/100 [17%], N/N 29/275 [11%]). More My/My horses had rapid atrophy (P < .001), with recurrence in 50%. Fewer My/My horses recovered versus My/N QH (P < .001). Stiffness was common across genotypes (P = .100; My/My 4/10 [40%], My/N 18/100 [18%], N/N 48/275 [17%]). Three months before the observed atrophy and stiffness, 47% of MYH1 <superscript>E321G</superscript> QH were vaccinated or had respiratory or gastrointestinal disease. Horses achieving 100% expected performance did not differ across genotypes (50% My/My, 71% My/N, 55% N/N), but, only 4/10 My/My QH were competing. My/N horses achieved national or world championships or both.<br />Conclusion and Clinical Importance: Approximately 20% of My/N QH develop rapid atrophy. Atrophy is more common (80%) in homozygous My/My QH and less likely to resolve. Inciting causes such as vaccination and infection are inapparent in over half of cases.<br /> (© 2022 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals LLC on behalf of American College of Veterinary Internal Medicine.)

Details

Language :
English
ISSN :
1939-1676
Volume :
36
Issue :
3
Database :
MEDLINE
Journal :
Journal of veterinary internal medicine
Publication Type :
Academic Journal
Accession number :
35426178
Full Text :
https://doi.org/10.1111/jvim.16417