Heritability of recurrent exertional rhabdomyolysis in Thoroughbred racehorses.
Abstract: To determine the likely mode of inheritance and identify probable foundation horses for recurrent exertional rhabdomyolysis (RER) in Thoroughbred (TB) racehorses. Methods: 4 families of TB racehorses with a high prevalence of RER, consisting of 3 to 53 horses/family, were used to determine mode of inheritance. Sixty-two TB horses with RER and 34 control TB racehorses without RER were used to identify probable foundation horses for the RER trait. Methods: RER was diagnosed by a veterinarian and verified by detecting high serum creatine kinase activity. Pedigrees dating from 1930 for all horses were entered into a database. Pedigrees of horses in 4 families were visually inspected for a pattern of inheritance and used for calculation of foundation horse contributions and inbreeding coefficients. The Markov chain Monte Carlo technique was used to analyze pedigrees of the 62 affected and 34 control horses for the conditional probability of foundation genotypes. A dominant mode of inheritance with variable expression model was used. Results: Pedigree analysis supported an autosomal dominant mode of inheritance with variable expression. All affected horses from the 4 families shared a common ancestor. This ancestor and 5 other stallions had a conditional probability of 1.00 for being affected. All 6 stallions shared a common male ancestor within 3 to 5 generations. Conclusions: On the basis of this study, the RER trait has been in TB racehorses for more than 70 years and may be inherited as an autosomal dominant trait with variable expression.
Publication Date: 1999-02-27 PubMed ID: 10048561
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- Journal Article
- Research Support
- Non-U.S. Gov't
Summary
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This research aimed to determine the likely mode of inheritance for recurrent exertional rhabdomyolysis (RER), a muscle disorder, in Thoroughbred racehorses and identify potential original carrier horses. The study found that RER is likely passed through an autosomal dominant gene with variable expression, and all affected horses in the study shared a common ancestor.
Research Methods
- The researchers selected four families of Thoroughbred racehorses, each containing 3 to 53 horses, which exhibited a high prevalence of RER for their study.
- They also selected 62 Thoroughbred horses diagnosed with RER and 34 control Thoroughbred racehorses without RER to identify probable original carrier horses for RER.
- The diagnosis of RER was confirmed by a veterinarian and verified by detecting high serum creatine kinase activity, an indicator of muscle damage.
- The researchers collected and entered into a database the pedigree information of all the horses dating from 1930.
- The pedigrees of horses in the four selected families were visually inspected for a pattern of inheritance. They were also used for calculating the contributions of original carrier horses and inbreeding coefficients.
- The Markov chain Monte Carlo technique, a method used for making precise estimates, was used to analyze the pedigrees of the affected and control horses for the conditional probability of original carrier genotypes.
- A dominant mode of inheritance with variable expressivity model was used for the study.
Research Findings
- Based on the pedigree analysis of the four families, the researchers concluded that RER is likely inherited through an autosomal dominant gene with variable expression.
- It was discovered that all affected horses from the four families shared a common ancestor.
- This ancestor and five other stallions were found to have a conditional probability of 1.00 for being affected with RER, indicating they are very likely to be original carriers.
- These six stallions were found to share a common male ancestor within 3 to 5 generations.
Conclusions
- From this study, it can be inferred that the RER trait has been present in Thoroughbred racehorses for over 70 years.
- RER is likely inherited as an autosomal dominant trait with variable expression.
Cite This Article
APA
MacLeay JM, Valberg SJ, Sorum SA, Sorum MD, Kassube T, Santschi EM, Mickelson JR, Geyer CJ.
(1999).
Heritability of recurrent exertional rhabdomyolysis in Thoroughbred racehorses.
Am J Vet Res, 60(2), 250-256.
Publication
Researcher Affiliations
- Department of Clinical and Population Sciences, College of Veterinary Medicine, University of Minnesota, St Paul 55108, USA.
MeSH Terms
- Alleles
- Animals
- Creatine Kinase / blood
- Databases, Factual
- Female
- Genes, Dominant / genetics
- Horse Diseases / genetics
- Horses
- Inbreeding
- Male
- Markov Chains
- Monte Carlo Method
- Nuclear Family
- Parents
- Pedigree
- Physical Conditioning, Animal
- Recurrence
- Rhabdomyolysis / genetics
- Rhabdomyolysis / veterinary
Citations
This article has been cited 4 times.- Aldrich K, Velez-Irizarry D, Fenger C, Schott M, Valberg SJ. Pathways of calcium regulation, electron transport, and mitochondrial protein translation are molecular signatures of susceptibility to recurrent exertional rhabdomyolysis in Thoroughbred racehorses. PLoS One 2021;16(2):e0244556.
- Norton EM, Mickelson JR, Binns MM, Blott SC, Caputo P, Isgren CM, McCoy AM, Moore A, Piercy RJ, Swinburne JE, Vaudin M, McCue ME. Heritability of Recurrent Exertional Rhabdomyolysis in Standardbred and Thoroughbred Racehorses Derived From SNP Genotyping Data. J Hered 2016 Nov;107(6):537-43.
- Fritz KL, McCue ME, Valberg SJ, Rendahl AK, Mickelson JR. Genetic mapping of recurrent exertional rhabdomyolysis in a population of North American Thoroughbreds. Anim Genet 2012 Dec;43(6):730-8.
- 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.
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