The paper says the study was registered:
The registration number given is not for a CFS study, but for a study of green tea therapy in rheumatoid arthritis: NCT03719469
Epstein Barr virus, infectious mononucleosis and associated diseases as contributors to the costs of intimate kissing
Ewald, Paul W.
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Abstract
When evaluating whether kissing is an evolutionary adaptation, fitness costs and benefits need to be considered. Any disease...
Moderation note
Some posts deleted in error when removing off-topic or rule breaching posts have been reinstated. Some posts discussing the deletions have been removed so as not to distract from the discussion.
I think it's almost certainly just a wrong unit since it's off by 1000 from the numbers you'd expect for count/uL. So probably should be baseline 100 count/uL in one patient and 125 count/uL in the other. I'm not sure what the plot can tell us, though.
There was discussion about NK cell counts correlating to response in multiple myeloma, with the caveat that I think those studies saw correlations based on bone marrow NK cells, as opposed to blood like in the Fluge study.
-...
I think it's that first each metric is considered a separate experiment with a threshold of p<.05 for the ANOVA comparing all groups at once. Then for each metric, they do 3 pairwise tests: ME/CFS-LC, ME/CFS-HC, LC-HC, so they divide the threshold by 3 to account for this.
But no multiple test...
It's a bit strange to me how consistent the results are for all five of the miRNAs they tested:
They seem to have used something called fractional rank as a measure of miRNA levels.
So they determine, for each participant, the rank of each miRNA. If a given miRNA species is the 25th...
"Us" in line three is referring to everyone trying to find an answer. "Support" is ambiguous if the second part isn't just about pwME. The support a researcher, or even a caregiver, needs is very unlike the support a bedbound patient needs, so I think the sentence would be too confusing with...
Maybe we could make an S4ME branded meme/image for sharing on social media. The message seems impactful and gets across both the problem of ME/CFS and what S4ME is focused on.
With slight change from:
To
"We" doesn't seem like it would work when talking about S4ME because there are people...
Exploring the effects of GLP-1 receptor agonists in fibromyalgia: a propensity-matched real-world cohort using TriNetX research platform
Nouran Eshak, Anushka Irani, Megan Sullivan
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Objectives
We aimed to evaluate the effects of GLP-1 receptor agonists (GLP-1RA) on symptom...
Response to the Comment by Steinkirchner et al. On the Article “Variation in Repeated Handgrip Strength Testing Indicates Submaximal Force Production in Patients With Myalgic Encephalomyelitis/Chronic Fatigue Syndrome”
Stoyan Popkirov
See article for full response.
Web | PDF
Comment on “Variation in Repeated Handgrip Strength Testing Indicates Submaximal Force Production in Patients With Myalgic Encephalomyelitis/Chronic Fatigue Syndrome”
Felix Steinkirchner, Viktoria Kimmerling, Christina Kaufmann, Elisabeth Schieffer, Michael Gruber, Alexander Dejaco
See...
Thread about paper for recovery rate in children and a bit of speculating similar to this thread: Long Term Follow up of Young People With Chronic Fatigue Syndrome Attending a Pediatric Outpatient Service, 2019, Rowe
Oh ok, thank you.
I think I would personally be much more annoyed at having to take pills four or more times a day than just sipping from a water bottle throughout the day, which I do anyway.
I'm not arguing for adopting CPET as an endpoint, but I'm not sure I understand your specific point here. Presumably, a decrease in metrics on day 2 is not analogous to weak grip strength, since the idea is that this is not something seen in deconditioning, so exercise alone should not improve...
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