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Atypical Myopathy Fact File

Atypical myopathy (sycamore myopathy) is a severe and often fatal muscle disorder caused by ingesting sycamore seeds, leaves or seedlings.

Sycamore seeds and leaves

It is fatal for around three quarters of affected horses. Some horses appear to be more susceptible than others, perhaps due to genetic differences.  Reports of cases began in the 1940s but there is evidence supporting a marked increase in recent years.

There are more than 25 species of Acer tree and and not all species have the HGA toxin. (Hypoglycin A).  HGA toxin concentrations vary between plant samples derived from different trees or seedlings from them. Understandably, horse owners and yard owners want to minimise the exposure to anything which is poisonous to horses. 

Download a copy of ºÚÁÏÉç's Owners' Fact File on Atypical Myopathy from the Comparative Neuromuscular Diseases Laboratory - Diagnostic Services page

As part of ºÚÁÏÉç’s ongoing commitment to scientific innovation - our teams are involved in research (supported by the Horse Trust) concerning the influence of genes on susceptibility and the impact of different treatments on the toxic effects of hypoglycin A. They are also establishing the reasons why different trees vary in their toxin production and other risk factors

Causes

Atypical myopathy is caused by horses eating sycamore seeds that fall onto pasture in Autumn and Winter, and their germinating seedlings in Spring.

Seeds and seedlings contain the toxin hypoglycin A (HGA) which slows or stops energy production in muscle and heart 

Some apparently unaffected horses have high concentrations of HGA in their blood suggesting that some horses are more susceptible to the toxin than others.

Clinical Signs

  • General weakness : horses struggle to walk, stand and breathe
  • Many horses develop heart problems. 
  • Horses appear depressed with low hanging heads
  • Muscle trembling
  • Signs of severe colic - yet, unlike colic,  they still have an appetite 
  • Brown or dark red urine 
  • Severely affected horses become unable to stand

Diagnosis

Vets consider the horse’s environment as well as symptoms reported and those observed during an examination.

Diagnosis requires a variety of tests available to referring vets from the ºÚÁÏÉç Comparative Neuromuscular Diseases Laboratory.

Treatment

As confirmation can take several days, vets often start treatment immediately and before official confirmation. Your horse may require admission to a specialist equine hospital for 24 hour advanced care. If horses survive the first few days of treatment they usually go on to recover completely, although this can take several months.

Prevention

The following steps can be taken to reduce horses' risk to atypical myopathy

  • Provide supplementary forage during Autumn
  • Clear fallen sycamore leaves and seeds from grazing areas 
  • Check neighbouring areas for high risk plants/seeds as some ‘helicopter’ seeds can travel up to 200 yards
  • Test for the presence of HGA in your own horses’ pastures

The ºÚÁÏÉç's Comparative Neuromuscular Diseases Laboratory offers horse owners and stable/yard owners a sycamore sample test for identifying plants that contain the HGA toxin known to cause atypical myopathy.

Key points

Diagnosis of atypical myopathy, despite its name, has become more common in recent years.

Evidence suggests it is caused by horses eating fallen sycamore seeds and their germinating seedlings.

It is a rapid onset disease affecting muscles, including the heart.

It is fatal for around three quarters of affected horses.

Some horses appear to be more susceptible than others, perhaps due to genetic differences

ºÚÁÏÉç provides diagnostic tests for referring vets dealing with suspected atypical myopathy cases

ºÚÁÏÉç provides atypical myopathy tests for horse owners & yard owners to establish if they have plants on their property which contain the HGA toxin

For information on testing (for vets and owners) see Comparative Neuromuscular Diseases Laboratory

Frequently asked questions

Our ºÚÁÏÉç's Owners' Fact File on Atypical Myopathy (available on this page) has a FAQ's section which should answer many of your queries.

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