Equine Health Update EHU Vol 21 Issue 01 | Page 26

EQUINE | Equine Disease Quarterly disease causing tying-up in Arabian horses. Advanced molecular techniques are also being applied to some disorders to determine exactly what goes wrong at the cellular level, to help define the basis of clinical signs and to better direct the development of effective genetic tests. Currently, the most clearly defined muscular disorders of athletic breeds are polysaccharide storage myopathy (PSSM), hyperkalemic periodic paralysis (HYPP), and glycogen branching enzyme deficiency (GBED), because the cellular nature of these diseases and the underlying causative genetic mutations are largely defined. PSSM is common in Quarter horses and related breeds, and typically causes signs of tying-up. It is also linked to high body condition, which can be desirable in those breeds. HYPP causes weakness and paralysis and, occasionally, death. It is also associated with high muscle mass, and therefore became prevalent due to positive selection pressure for this trait. GBED is an inevitably fatal disorder of Quarter Horses and Paints, causing weakness and death in the first days to weeks of life. It is uncommon, and association with a positive trait is not recognized. All three of these disorders can be readily tested for on hair or blood. Standardbred and Thoroughbred horses appear to share a disorder causing tying-up during training, with clinical signs rarely or never seen during actual racing exercise. This disease is referred to as recurrent exertional rhabdomyolysis (RER). It appears to be more common in faster horses because it might permit more rapid muscular processes at the cellular level, hence there has been positive selection pressure on this disease. The genetics of RER have proven frustrating to define despite many years of work. Warmblood and Arabian horses might also share a disorder recently coined as “myofibrillar myopathy” (MFM). Signs of this disease appear to consist of tying-up in Arabian horses, and poor performance and poorly defined movement 26 abnormalities in Warmblood horses. The genetic cause of MFM is not known and no scientifically validated genetic tests exist for MFM or RER. In summary, muscular disorders are common in athletic horses, and can be frustrating and even fatal under some circumstances. Association with specific positive traits has contributed to the prevalence of some of these diseases. Genetic testing is available for many heritable equine diseases, and it is likely that testing for less clearly defined disorders will be developed in the coming years. Genetic stewardship relies on breeders being educated about heritable disorders, and performing proactive breeding selection processes to produce horses that are not only high performers but also genetically sound. CONTACT: Erica McKenzie, BSc, BVMS, PhD, DACVIM, DACVSMR [email protected] (541) 737-2858 Carlson College of Veterinary Medicine Oregon State University Corvallis, OR Equine Renal Disease Renal function is an important component of overall health in any species. The kidneys perform several important functions, including waste removal, electrolyte balance, blood pressure maintenance, a calcium source for bone health and production of factors for red blood cell stimulation, to name a few. In addition, the kidneys receive substantial blood flow— approximately 25% of the cardiac output. Therefore, changes in blood flow, either increased or decreased, can have a significant impact on renal health. Equine necropsy cases submitted to the University of Kentucky Veterinary Diagnostic Laboratory (UKVDL) • Equine Health Update •