Made this summary of the paper:
1) Trigger warning: suicide
This paper analyzed 505 entries on the National CFIDS Foundation memorial list.
These were people with ME/CFS who passed away. The messages summarize their life, illness and struggles. The researchers grouped these into several...
Thanks for doing this.
One issue I see is that we don't have a standardized measure of effect size to filter these. I suspect that in a lot of the things that come up like smoking, overall health and cognitive tests, the DNA has only very minor effects and that they only come up because these...
It seems that in this study the authors pre-selected only 22 traits because they have previously been implicated in ME/CFS and the brain/synapses was not included.
The full list is in table 1 in the online methods. Most did not reach high correlations. Migraine and IBS were already known to be...
Anyone has any updates on this?
No update or changes on the journal website yet from what I can see
https://onlinelibrary.wiley.com/doi/10.1002/hbm.70505
An addditional study by these authors, this time using GP records in 11 practices in Devon, UK.
They found that CFS patients had more GP consultations for various complaints in the 15 years before their diagnosis than controls with MS. This could point that CFS patients were never truly...
Excellent blog, clearly written, thanks!
Perhaps not very relevant but Jason also looked at seasonal onset in his Chicago cohort and found significantly more cases where onset was in January compared to other months. Seems likely to be due to chance in my opinion (it had a low sample size of...
Older 2-day CPET studies such as the one by Davenport also used the Fukuda criteria so that alone likely wouldn't explain the results.
Severe ME/CFS patients can't do these test so highly likely that these were mild-moderate patients just like in previous 2-day CPET studies.
The idea was that...
Hard to take anything useful from this paper...
Seems like all of Jason's studies are now based on that distinction between moderate ME/CFS and severe ME/CFS. But the latter is not actually severe ME/CFS, just patients that meet more than one case definition for ME/CFS.
They then conclude...
Looks like they failed to replicate the 2-day CPET results, although look forward to seeing the actual data.
The most replicated finding was workload at the ventilatory threshold which they don't report in this abstract.
An older study that I hadn't seen discussed much. It uses insurance data of the company Medical Sickness Group. Found 133 CFS cases and compared them to MS patients and non-claimant controls.
They could look at a median of 10 years before the claim of CFS. Results showed that ME/CFS patients in...
Trial data suggest that Coenzyme Q10 plus NADH supplementation is not an effective treatment for patients with myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)
Castro-Marrero and colleagues conducted a randomized controlled trial on 207 patients with myalgic encephalomyelitis/chronic...
The German ME/CFS Research Foundation also has registry where they list ME/CFS projects since 2019. It initially focused on Germany only but has expanded to a couple of other countries such as The Netherlands.
Research projects – ME/CFS Research Registry
I doubt that AI could do this, what I have seen is mostly people using existing PubMed tags or things mentioned in the abstract.
With a team it should be doable to screen all ME/CFS papers on PubMed: there are approximately 7700 at the moment. Many are short commentaries or letters. I (and many...
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