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Detection of Mycotoxins In Patients With CFS (93% Positive), 2013, Brewer et al

Discussion in 'ME/CFS research' started by DigitalDrifter, Jun 6, 2021.

  1. DigitalDrifter

    DigitalDrifter Senior Member (Voting Rights)

    Messages:
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    https://pubmed.ncbi.nlm.nih.gov/23580077/

    I don't know what criteria they used but it seems interesting that such a high percentage tested positive for mould. Question is, is this a cause or an effect?
     
  2. Milo

    Milo Senior Member (Voting Rights)

    Messages:
    2,108
    Why didn’t they assess living family members of the patients, to compare the environmental exposure, someone in the same household that does not live with ME?

    Note: this is not a new paper, this is 2013
     
  3. Subtropical Island

    Subtropical Island Senior Member (Voting Rights)

    Messages:
    1,992
    the “control” was required to have no history of mold exposure. Probably no such requirement for CFS patients tested. Not a good control then.
     
    borko2100, Hutan and Peter Trewhitt like this.
  4. Subtropical Island

    Subtropical Island Senior Member (Voting Rights)

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    1,992
    Anyone know: Did Brewer et al go on to do more with this finding since? They’ve had a decade.
     
  5. dreampop

    dreampop Senior Member (Voting Rights)

    Messages:
    443
    Several responses to the paper....


    https://www.mdpi.com/2072-6651/8/11/322/htm

    Whatever the detection methods are, the results seem common in the general population.

    Human biomonitoring of multiple mycotoxins in the Belgian population: Results of the BIOMYCO study

    https://pubmed.ncbi.nlm.nih.gov/26233555/


    I have serious questions about the significance of mycotoxin testing, but don't really know enough to comment further.
     

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