Bio - Marker: New research findings may shed... - Ramsays Disease

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Bio - Marker

Ian123 profile image
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New research findings may shed new light on the potential cause of Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME).

Researchers from Griffith University's National Centre for Neuroimmunology and Emerging Diseases (NCNED) -- part of the new Menzies Health Institute Queensland -- have uncovered significant factors contributing to the pathology of this illness.

The results reveal genetic changes in important receptors associated with immunological and cellular function and contribute to the development of this complex illness.

"These findings have been achieved through a team effort involving researchers, patients, funding bodies, clinicians and the support of Griffith University and the Queensland Government," say chief investigators Professor Sonya Marshall-Gradisnik and Professor Donald Staines.

Co-researcher and consultant immunologist Professor Pete Smith said that important signalling mechanisms are disrupted as a result of these genetic changes involving the detection and response to threats.

"These are primitive genes that are involved in many cellular signals in the brain, gut, cardiovascular and immune systems, as well as in the mediation of pain."

These research findings coincide with International Neuroimmune Awareness week commencing Monday 11 May.

The Griffith Health Centre on the university's Gold Coast campus is being lit up each evening from 10 -12 May to raise awareness of neurological conditions such as CFS/ME as well as other conditions such as Fibromyalgia and Gulf War Syndrome.

"The lighting up of the Griffith Health Centre signifies Griffith's commitment to the CFS patient community and our team approach to this research," says Pro-Vice Chancellor (Health) Professor Allan Cripps.

CFS/ME is a highly debilitating disorder characterized by profound fatigue, muscle and joint pain, cerebral symptoms of impaired memory and concentration, impaired cardiovascular function, gut disorder and sensory dysfunction such as noise intolerance and balance disturbance. Many cases can continue for months or years. It is believed to affect around 250,000 Australians.

The research findings are to be presented at an international conference in London later this month.

la-press.com/examination-of...

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Ian123 profile image
Ian123
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6 Replies
budgiefriend profile image
budgiefriend

Thank you, Ian, for posting more good research news! Nobody who is doing any quality biomedical research seems to be coming up with contradictory information from what we have believed is happening to us. This is always good to have reinforced.

I am a person who constantly doubts myself. Without validation, I sink into a sort of despair and wonder how and why I am so sick, if the doctor doesn't want to know about it or bother with me.

Ian123 profile image
Ian123 in reply to budgiefriend

Think the doctors experience some of that despair with no test that proves a diagnosis or treatment that cures.

Finding a bio marker that identifies patients will help us and the doctors that have their defences up against patients that keep coming back with more problems.

Stormchaser profile image
Stormchaser

Always followed a genetic element predisposing follows smaller genetic change makes Jen Brea Canary in a Coal Mine a standout warning

Halflife profile image
Halflife

Chimes on symptom signs listening into patients experience keep on.

slowmotion profile image
slowmotion

Not all my imagination yay

SNPs thought politics oops

RockRose profile image
RockRose

Encore !

Both to the findings and to everyone's responses !

Thanks for sharing invaluable info, Ian. :-)