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  1. hotblack

    SMPDL3B a novel biomarker and therapeutic target in myalgic encephalomyelitis, 2025, Moreau, Fluge, Mella et al

    The link appears to have become garbled in the matter transference process, here it is for others
  2. hotblack

    Uncovering the genetic architecture of ME/CFS: a precision approach reveals impact of rare monogenic variation, 2025, Birch, Younger et al

    Only just catching up with these posts but please don’t apologise. It’s great to have another researcher here discussing their work and wider aspects of ME/CFS. The more the better!
  3. hotblack

    UK House of Lords/ House of Commons - relevant people and questions

    Absolutely. Given we have prevention of future death reports, it seems like banging the drum to make hospitals at least safe for severe/v-severe patients is a clear obvious focus.
  4. hotblack

    Problems arising for pwME from additional diagnoses of MCAS, hEDS and POTS. Advocacy discussion.

    You are, in this paragraph, repeating what I see as a the problem. You do not blame patients directly but you do state that the reason to take action is because patients have been excluded from physician care and that has been contributed to by the actions of patients. My counter is this is an...
  5. hotblack

    Still to open Recruiting patients to provide details from existing genetic data for dissertation- any age, country, sex, gender etc.

    Here’s the researcher access page for DecodeME, it seems like the best possible, ready made, validated data set. https://institute-genetics-cancer.ed.ac.uk/decodeme-the-worlds-largest-mecfs-study/researcher-access Some data (like the summary information from the GWAS) is also freely available...
  6. hotblack

    Machine Learning-assisted Research on ME/CFS

    Have you got a complete list of the genes you are most interested in @mariovitali ? Apologies if you’ve already posted, thought it easier to ask the expert than search! And to play devil’s advocate, this is a view of successes, do we have a view of failures or at least of not yet confirmed...
  7. hotblack

    Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study, 2026, Missailidis et

    Yes, I think it’s just that this is all this paper shows us. It’s researchers being understandably cautious about wider speculation. Or at least drawing a distinction between speculation and evidence.
  8. hotblack

    Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study, 2026, Missailidis et

    Is this an entirely unique pathway for B cells, so is your expectation that this would only be seen in antigen+cytokine triggered b-cells? Or are the same pathways/mechanisms present elsewhere in different cell groups, perhaps used a bit differently as often seems to be the way! Wikipedia also...
  9. hotblack

    Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study, 2026, Missailidis et

    Can you elaborate? I don’t understand what this means (or how it would happen or manifest) so my head was very much in the ‘okay, lipids, mitochondria, phospholipid bilayer’ space.
  10. hotblack

    Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study, 2026, Missailidis et

    From the DecodeME candidate genes for PRDX6 (genecards link) This would support the idea of ‘stiff’ membranes from lipid build up wouldn’t it? Here’s the papers referenced https://www.sciencedirect.com/science/article/abs/pii/S0891584905000821...
  11. hotblack

    Problems arising for pwME from additional diagnoses of MCAS, hEDS and POTS. Advocacy discussion.

    Agreed. To me the question is how we approach that and the justification and arguments we use to do so. Maybe we can focus on the message of ‘this makes communicating the good new scientific discoveries (which yiu as a charity are supporting) harder’? Some of the other more grassroots patient...
  12. hotblack

    Problems arising for pwME from additional diagnoses of MCAS, hEDS and POTS. Advocacy discussion.

    The anecdotes and justification used for the action needed which keeps on accepting a false premise posited by medial professionals for their own failings and putting blame on patients. I’m sure it’s unintentional but that is how it can be perceived and it keeps on being repeated. I don’t...
  13. hotblack

    Problems arising for pwME from additional diagnoses of MCAS, hEDS and POTS. Advocacy discussion.

    On the POTS thing I officially have a POTS diagnosis, from one of the questionable ‘specialist cfs/me’ services and doctors, although on paper supported by a cardiology department. But I don’t think I have POTS, I don’t tend to say I do. But do have OI and something weird cardiovascular… Maybe...
  14. hotblack

    Problems arising for pwME from additional diagnoses of MCAS, hEDS and POTS. Advocacy discussion.

    No Jonathan I don’t believe ai have misunderstood your purpose. I think I share the goal, don’t doubt your intentions and am grateful for what you are trying to do. I have been very clear reading what you have said in this thread and in the past. I’ve also I think been clear in my position and...
  15. hotblack

    United Kingdom: ME Association news

    It’s incredibly disappointing to see. In this respect the MEA are acting as the useful fool rather than standing up for and representing the interests of patients. We’ve seen it with patient organisations and charities before, it reminds me of the path of the Sussex & Kent ME/CFS Society and...
  16. hotblack

    Multi-omics identifies lipid accumulation in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cell lines: a case-control study, 2026, Missailidis et

    Some of the questions going through my head. Sharing to aid discussion. Maybe get some answers, maybe more questions! Would this problem hit specific cell types or all cell types? If so why? Could it be present in all but showing up more in some or only affecting certain cell types? What could...
  17. hotblack

    Machine Learning-assisted Research on ME/CFS

    Can you tell us more about what this image is showing and what it means @mariovitali Is it it showing studies which have replicated genes/processes you have previously identified? Is this just the most recent studies? I look forward to hearing more about any discussion with Michal Tal too.
  18. hotblack

    Preprint Identification of Novel Reproducible Combinatorial Genetic Risk Factors for [ME] in [DecodeME Cohort] and Commonalities with [LC], 2025, Sardell+

    And I know the data is quite dense. So Here’s a hopefully fairly readable and overview of the clusters at k=5. There’s obviously been curation by me here but at this level the story seems to be about broad biological areas and systems which may be involved. Cluster 1 – Neuronal/synaptic...
  19. hotblack

    Preprint Identification of Novel Reproducible Combinatorial Genetic Risk Factors for [ME] in [DecodeME Cohort] and Commonalities with [LC], 2025, Sardell+

    With the above caveats, and while I don’t really have the biological grounding to interpret this well, a couple of things which popped up while reading all this. And may start some discussion We have the now familiar neuronal/synapse and immune signals being highlighted. And possibly some more...
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