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Rethinking chronic fatigue syndrome (The Saturday Paper, Australia)

Kati

Patient in training
Messages
5,497
A sympathetic article from Australia which includes patient experience and recent research from the Staines/Marshall-Gradisnik research

https://www.thesaturdaypaper.com.au/2016/08/06/rethinking-chronic-fatigue-syndrome/14704056003560

Exerpt:
One of the main pieces of ME/CFS research to come out of Australia recently is a series of papers by the team led by Staines and co-director Professor Sonya Marshall-Gradisnik, showing abnormalities in the genetic make-up and function of the immune systems of people with ME/CFS.

In research published during the past 12 months, the team found genetic mutations in the “threat receptors” of certain white blood cells in ME/CFS patients, and changes in the functions that these receptors control, such as energy production inside the cell. They also confirmed that immune cells affected by these changes fail to fight infection and cancer as well as they should.

The discovery of these faulty receptors may also have wider implications. “Nerve cells, muscle cells, pancreatic cells, intestinal cells, you name it, they all have these receptors in them,” he says. “And if these same changes [that are happening in white blood cells] are happening in every cell in the body, then the whole body is going to respond abnormally.” This could explain the complex and varied symptoms of ME/CFS “a huge amount”, says Staines. The team is in discussion with companies about producing a diagnostic test for the illness based on their findings.
 

Snow Leopard

Hibernating
Messages
5,902
Location
South Australia
Does anyone know the name of these "threat receptors"?

The studies that were done were gene-candidate studies, which are well, junk studies and the results are not statistically significant when controlling for multiple comparisons, and so I don't find any of these genetic findings exciting, but...

Here are the recent genetic studies from this team:
http://www.ncbi.nlm.nih.gov/pubmed/27346947
http://www.ncbi.nlm.nih.gov/pubmed/27099524
http://www.ncbi.nlm.nih.gov/pubmed/27245705
http://www.la-press.com/examination...rphisms-snps-in-transient-recep-article-a4824
http://www.la-press.com/examination...rphisms-in-acetylcholine-recept-article-a4862
http://www.la-press.com/genotype-fr...astatin-m3-ion-article-a5387?trendmd-shared=0

Mostly Transient receptor potential ion channels, acetylcholine receptor...
 

taniaaust1

Senior Member
Messages
13,054
Location
Sth Australia
great article.

I note the author of that article also does documentaries. Im thinking about contacting her to ask her if she's ever thought of doing one on people in Australia who have severe ME/CFS. I'd like to contact her and tell her that I've gone to jail at times due to not coping at home and being unable to get the support I needed for the ME (I now have an abusive support coordinator who appears doesnt believe in this illness).

I think a mind blowing documentary on the aussie situation could be made starting from some of the Aussie ME history with Alison Hunter.. and how people here today arent being given support.