February 7, 2013
Safeguard horse health by educating yourself about genetic disease tests available through AQHA.
Thanks to decades of research, we now know that defects in inheritable genes are responsible for some of the diseases that afflict some American Quarter Horses. The effects of these diseases are wide-ranging, from mild and manageable to severe and terminal. Passing these diseases on to successive generations often causes unnecessary suffering and also leads to financial losses for breeders.
Fortunately, genetic tests have been developed to help breeders identify affected horses, allowing them to make better decisions and avoid perpetuating these traits. AQHA offers a panel test for five genetic diseases – glycogen branching enzyme deficiency, heredity equine regional dermal asthenia, hyperkalemic periodic paralysis, malignant hyperthermia and polysaccharide storage myopathy.
Here’s more about each of those diseases:
Glycogen Branching Enzyme Deficiency
- Disorder: An autosomal recessive disease caused by mutation in the GBE1 gene.
- Affects: Approximately 8-10 percent of American Quarter Horses are affected; Paints can be carriers. Appaloosas and other breeds that descend from the American Quarter Horse may be carriers. An estimated 3 or more percent of second- and third-term abortions are caused by GBED.
- Description: The mutation of the GBE1 gene reduces the function of the glycogen branching enzyme so that cardiac and skeletal muscle and the liver and the brain cannot store and mobilize glycogen. Because glycogen provides energy to the muscles, the inability to properly store and mobilize it leads to muscle weakness and eventually death.
GBED results in second- and third-term abortions and stillborn foals. Researchers think many aborted and stillborn foals whose cause of death was not previously identified might have had GBED. Foals that survive birth generally die or are euthanized within 8 weeks of age. Although a few foals have survived to the age of 4 months, GBED is always fatal.
Are you looking to learn more about equine diseases? With AQHA’s “Your Horse’s Health” DVD collection you’ll be guided by veterinatians Dr. Tom Lenz and Dr. Kenton Morgan on the basics of diseases such as strangles, West Nile Virus and more.
Hereditary Equine Regional Dermal Asthenia
- Disorder: An autosomal recessive disease caused by mutation in peptidyl-prolylisomerase B (PPIB) gene.
- Affects: Approximately 3.5 percent of American Quarter Horses are carriers.
- Description: Collagen makes up connective tissues (skin, bones, tissue, muscles and cartilage). The mutation in the PPIB gene results in defective collagen that causes the outer layer of the skin to split from the layer underneath. In some cases, the outer layer of skin sloughs off entirely, leaving raw wounds.
Young horses with HERDA might appear to have an unusual number of nicks and cuts on their skin, but the disease is most often noticed then the horse starts training under saddle. The pressure of the saddle on the back causes the skin to tear and separate, leaving raw areas. These areas are slow to heal, and many horses with HERDA are euthanized due to slow-healing injuries.
Hyperkalemic Periodic Paralysis
- Disorder: An autosomal dominant disease caused by point mutation in the SCN4A gene.
- Affects: Approximately 1.5 percent of all Quarter Horses and as many as 56 percent of all halter horses.
- Description: The mutation in the sodium channel gene causes dysfunction in a specific type of sodium ion channel. These channels are involved in generating electrical impulses associated with muscle contraction. The mutation disrupts the proper conduction of these impulses, causing muscle tremors and even temporarily paralysis in affected horses. In severe cases, HYPP can cause collapse or sudden death.
HYPP traces back to the stallion Impressive. HYPP was seen in Impressive’s sons and daughters, because to be expressed, the disease does not require two copies of the defective gene. However, successive generations of offspring that received two defective genes often show more severe versions of the disease.
- Disorder: An autosomal dominant disease caused by mutation in the ryanodine receptor 1 (RyR1).
- Affects: American Quarter Horses and several other breeds; the percentage of affected horses is unknown.
- Description: The mutation results in a malfunctioning calcium-release channel of the sarcoplasmic reticulum in skeletal muscle. The malfunction causes excessive calcium to be released into the myoplasm (the contractile part of a muscle cell). This can cause a hypermetabolic state (increases metabolism) and may result in death.
MH is triggered by the use of anesthetic halothane, the muscle relaxant succinylcholine and stress. Affected horses experience increased muscle metabolism, fever often exceeding 109 degrees F, excessive sweating, high heart rate, abnormal heart rhythm, shallow breathing, hypertension, muscle rigidity, breakdown of muscle tissue, muscle protein in the urine and/or death.
The “Your Horse’s Health” DVD collection is a must-have for youth groups, aspiring veterinarians and anyone interested in keeping their horses healthy and happy. Even the most veteran horse owner will learn something essential to keeping their horse in great health.
Polysaccharide Storage Myopathy
- Disorder: An autosomal dominant disease caused by mutation in the glycogen synthase 1 (GYS1) gene.
- Affects: Eleven percent of American Quarter Horses. PSSM also affects many other breeds.
- Description: PSSM is a common form of tying-up. The mutation in the GYS1 gene causes unregulated synthesis of glycogen, which results in excessive sugar in muscle cells. This leads to muscle pain and stiffness, sweating, exercise intolerance and weakness. Because of the pain and stiffness, horses are reluctant to move.
Research conducted at the University of Minnesota has identified two types of PSSM. Genetic testing determined that some horses with PSSM had a specific mutation in GYS1 (PSSM Type 1) while others did not have the mutation in the GYS1 gene (PSSM Type 2). Horses identified as having a moderate to severe form of the disease according to the muscle biopsy were more likely to have PSSM Type 1 than horses with a milder version of the disease. Researchers have not yet determined what causes PSSM Type 2.
When horse owners order an AQHA panel test, AQHA will send a DNA kit, and the owner will mail it to the Veterinary Genetics Laboratory at the University of California-Davis for testing. Once the tests are complete, AQHA will notify the owners and put the results on the horse’s record.
To order your test, call AQHA at 806-376-4811, or use our online form.