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Neural consequences of post-exertion malaise in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome - Cook, Light +

Discussion in 'ME/CFS research' started by Sly Saint, Mar 9, 2018.

  1. Sly Saint

    Sly Saint Senior Member (Voting Rights)

    Messages:
    9,584
    Location:
    UK
    May 2017
    Neural consequences of post-exertion malaise in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome
    Dane B.CookabAlan R.LightcKathleen C.LightcGordonBroderickdMorgan R.ShieldsbRyan J.DoughertybJacob D.MeyerbStephanieVanRiperbAaron J.StegnerbLaura D.EllingsoneSuzanne D.Vernonf

    https://www.sciencedirect.com/science/article/pii/S088915911730051X?via=ihub#t0005
     
    Last edited: Mar 9, 2018
    Simon M, MEMarge, Joh and 13 others like this.
  2. JohnM

    JohnM Established Member (Voting Rights)

    Messages:
    53
    Thanks kindly for the bump @Sly Saint . You've saved me a job I was going to do later. On a brief read, seems that SMCI are ahead of the curve on this one, and seems to be the kind of approach many of us have been asking for?

    I'll look forward to reading comments from folks more qualified than me to do so .. do your thing s4me ;)

    Wishing everyone improved health and every happiness. John :)
     
    MEMarge, Missense, Jan and 6 others like this.
  3. Jan

    Jan Senior Member (Voting Rights)

    Messages:
    498
    30 minutes?? How do these patients manage it?
     
    MEMarge, MeSci, janice and 4 others like this.
  4. Dechi

    Dechi Senior Member (Voting Rights)

    Messages:
    552
    Yeah, really. 30 minutes of exercise is a whole lot for someone with ME. I’d be passed out long before that...
     
    MeSci, JohnM and Trish like this.
  5. Marco

    Marco Senior Member (Voting Rights)

    Messages:
    277
    While it's welcome to see research that appears to chime with personal experience (when subject to a stressor my brain turns to mush) unfortunately the results are open to interpretation that might support the BPS model. No criticism of the researchers - it's just the way it is.

    I could imagine that a BPS interpretation would see the cognitive deficits found (errors made) as reflecting either top down executive function or attentional processes leading to PWME excessively focusing on normal symptoms to the detriment of cognitive processes (too much bandwidth taken up attending to normal sensations).

    It may or may not be the case however that attentional processes in PWME's brains are overactivated because there is an earlier signalling problem (as per the Lights' work) that means they are being bombarded with sensory information. Unfortunately there's no way of telling from this study. We would need to show abnormal signalling at the pre-attentional level was driving the cognitive deficits and not some problem with top down control subject to 'conscious' control.

    PS - I've just skimmed this paper for apologies if these issues were addressed.

    Another small issue is that I do wish they wouldn't chuck in the kitchen sink when trying to make a case (e.g. 'white lesions' - barely relevant or Morris and Maes' 'feed- forward' theory - nice speculation I'm sure but hardly evidence). It just risks undermining their credibility.
     
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