Eye movements may be key to chronic fatigue syndrome diagnosis


Senior Member
25 March 2022

Oculomotor testing in the lab.
A Monash Central Clinical School scientist has been awarded $180,000 over three years to develop a way to help diagnose myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS).

Associate Professor Joanne Fielding, from the Department of Neuroscience, is being funded by the Judith Jane Mason & Harold Stannet Williams Memorial Foundation (the Mason Foundation) through Equity Trustees to conduct a project identifying objective behavioural markers for this debilitating disorder. Associate Professor Fielding is working with Dr Scott Kolbe and Dr Meaghan Clough , both from the Department, and co-investigator Dr Chris Armstrong from the University of Melbourne on the project.

An enigmatic disorder, ME/CFS is characterised by extreme tiredness, pain and a range of other symptoms. Remarkably, there is currently no reliable way to diagnose it and to objectively monitor the effect of treatment in people with the disorder.

“You can’t directly measure ME/CFS at the moment. A clinician’s role is to essentially eliminate other potential causes for the constellation of symptoms,” Associate Professor Fielding said. “While there are some suggested diagnostic criteria there are no formal criteria.

“What we’re trying to do is generate a unique ME/CFS signature based on characteristic changes to eye movements, a behaviourial signature that is specific to the disorder that can be used to help diagnose it and monitor the effects of any treatments.”

Associate Professor Fielding and her team will develop the clinically useful test using ocular-motor, machine learning and neuroimaging techniques.

“We’re using video-oculography, which is basically high-powered cameras that record the eye movements in response to a set of simple stimuli on the screen.

“People with ME/CFS are typically extremely fatigued – we need something very quick that gives a snapshot of how they’re performing.”

Participants in the study can be tested in the lab or in their own homes with a portable eye-tracker – helpful to someone with such a disabling disorder.

Associate Professor Fielding said the research might also give the scientists clues about what might be happening neuropathologically in ME/CFS.

“Tentatively, what we’ve found already looks like a set of aberrant eye movements that suggest that something might be going on at the level of the brain stem – but it’s early days and that’s at best, speculative,” she said.



Senior Member
The problem is that it will probably turn out that PWME have some vision abnormalities, but generally different: one has blurry vision, one has convergence problems, another has jerkiness. I expect it will be "Yes, many PWME have abnormalities, but it's too inconsistent to form a diagnostic tool."
but generally different: one has blurry vision, one has convergence problems, another has jerkiness
thats not my sense of what they are looking at....I have autoimmune eye problems, will need cataract surgery someday, have lists of eye issues.

This is about exertion and neurological the brain fatiguing and I think its brilliant and very exciting.

As Cort described: (and thanks, @SlamDancin )....

"The tool may even be able to pick up the early fatigability and exertion intolerance that occurs as the eyes (and brains) of people with ME/CFS tire over time. Thus far, Armstrong is finding, in contrast to healthy controls, that the eyes of people with ME/CFS get worse over time at following that dot – leading to the possibility that the Ocular Motor Project could lead to the first easy test for exertion intolerance."
Is there nothing left untouched by this illness?!
Very aptly put as this illness seems to know no bounds.
If there is something to this concept, it would cause me to lean towards a hypothesis similar to the Midbrain Ascending Arousal Network which I believe was just recently posted.
Since ME/CFS may have numerous causes, perhaps a subset could be identified by this test.


Senior Member