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  1. ME/CFS Science Blog

    The missing heritability question is now (mostly) answered

    Counterpoint is this recent paper in Nature, which suggests that we simply need bigger sample sizes and more detailed measurements of all SNPs, including rare ones. Estimation and mapping of the missing heritability of human phenotypes | Nature
  2. ME/CFS Science Blog

    The missing heritability question is now (mostly) answered

    I thought they compared identical with non-identical twins, so that environmental confounders are substracted (as they are present in both pairs of twins).
  3. ME/CFS Science Blog

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Another increasing issue is AI-created summaries on social media. Researchers often oversell their findings in the paper, and it seems that AI then inflates this even further. Don't have an issue with using AI per se (it can be useful in many situations), but the LLMs people use don't think...
  4. ME/CFS Science Blog

    Should we initiate development of a new, short questionnaire to identify PEM (to aid diagnosis)?

    Researchers from the University of Vienna are developing a new PEM questionnaire. https://www.soscisurvey.de/V-PEM-AQ_english/ Shared by Rob Wust on Twitter:
  5. ME/CFS Science Blog

    Digitally Assessed Long COVID Symptomatology Is Associated With Lymphocyte Mitochondrial Dysfunction and Altered Immune Potential, 2025, Sularea+

    Probably not much to see here. The study has a small sample size (27 LC patients) and the authors measured mitochondrial mass and membrane potential in 9 different immune cell types. That's 18 different comparisons, and it looks as if no correction was done for multiple testing. So it should...
  6. ME/CFS Science Blog

    Association between chronic fatigue syndrome/myalgic encephalomyelitis and cardiovascular disease, 2025, Denu+

    Some questions were raised about the NHIS survey data in this thread: https://www.s4me.info/threads/cdc-data-brief-myalgic-encephalomyelitis-chronic-fatigue-syndrome-in-adults-united-states-2021%E2%80%932022-2023-vahratian-unger-et-al.36480/post-566066 In the 2023 NHIS survey, the prevalence of...
  7. ME/CFS Science Blog

    Hypothesis Hypothesis: A Mechanical Basis: Brainstem Dysfunction as a Potential Etiology of ME/CFS and Long COVID, 2025, Jeff Wood, Kaufman et al.

    "The authors declare no competing interests." Jeff Wood's website: "I now work as a consultant to chronically ill patients, as well as to researchers and MDs who serve the chronically ill community." https://www.explorewithjeff.com/
  8. ME/CFS Science Blog

    Epstein-Barr virus reprograms autoreactive B cells as antigen-presenting cells in systemic lupus erythematosus, Younis et al., 2025

    See what you mean. They show that lupus patients have an increased number of these EBV-infected B cells, that these are reprogrammed, for example, to remain active, and present antigens, that they respond to antinuclear antigens, and that they can activate T-cells. But the smoking seems to be...
  9. ME/CFS Science Blog

    Germany's "National Decade Against Post-Infectious Diseases"

    Great news! I wonder what they mean with post-infectious disease: is it ME/CFS and Long Covid, or other diseases as well?
  10. ME/CFS Science Blog

    Review The Clinical Relevance of Mast Cell Activation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome, 2025, Rohrhofer et al

    Looks like this is just based on self-reported questionnaires. Don't think one can study MCAS by just asking patients if they report certain symptoms or responses to treatment.
  11. ME/CFS Science Blog

    Integrated immune, hormonal, and transcriptomic profiling reveals sex-specific dysregulation in long COVID patients with ME/CFS, 2025, Shahbaz et al.

    Here's the link to that previous study: Upregulation of olfactory receptors and neuronal-associated genes highlights complex immune and neuronal dysregulation in Long COVID patients - ScienceDirect Looks like in other disorders such as schizophrenia, reeling has mostly been found to be...
  12. ME/CFS Science Blog

    Integrated immune, hormonal, and transcriptomic profiling reveals sex-specific dysregulation in long COVID patients with ME/CFS, 2025, Shahbaz et al.

    Should we have a closer look at reelin? Both the blood marker and gene expression were increased in patients. This team has reported this before in LC. Here's the wikipedia description:
  13. ME/CFS Science Blog

    Preprint Virus Genome Sequences in the Blood of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome Patients, 2025, Davis et al

    Do less viruses in the blood of ME/CFS patients mean something about their immune system or is the most likely explanation less contact with other people and therefore less exposure to viruses?
  14. ME/CFS Science Blog

    How do we stop charities and influencers spreading bio-babble about ME/CFS?'

    Think it might help if people are outspoken about this on social media. For example, regarding the 'ME is not CFS' debate, there is this sense that patient organisations and researchers conflate the two out of opportunism. And that the non-severe patients don't get the difference and are happy...
  15. ME/CFS Science Blog

    Severe and very severe ME/CFS - useful resources for clinicians and carers

    Hermisson et al. Pflegeanleitung für schwer- und schwerstkranke ME/CFS-Patient:innen Resource for severe ME/CFS in German (including automatic translation in English) Document | Thread
  16. ME/CFS Science Blog

    Preprint Hyperbaric oxygen therapy improves clinical symptoms and functional capacity and restores thalamic connectivity in ME/CFS, 2025, Kim, Scheibenbogen+.

    Suspect it was normalized. Either way, they report the minimal clinically significant improvement to be 10 points. So the mean improvement was lower than this, despite having no control group.
  17. ME/CFS Science Blog

    Book - Psychology's Quiet Conservatism, 2025, Brian Hughes

    Made a brief summary of David Tuller's interview with Prof. Hughes: 1) Interesting interview of Prof. Brian Hughes by David Tuller. In his new book Hughes argues that psychology is not woke but that its methods are essentially conservative because it focuses on an individualistic view and...
  18. ME/CFS Science Blog

    What can the science on the impact of acute infections on cognition tell us about ME/CFS?

    Perhaps a bit off-topic, but was wondering if ME/CFS is like sickness behavior, why we don't see more loss of appetite.
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