The Call for Opposition: Challenging the P2P and IOM Processes
In our second article on how to react to the publication of the draft P2P report, Gabby Klein provides her view of why she and a large group of advocates and patients are continuing their protest of the government’s ongoing control and manipulation of our disease via their processes...
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data on low O2 mechanisms in CFS?

Discussion in 'Latest ME/CFS Research' started by Sherlock, Jul 19, 2012.

  1. Sherlock

    Sherlock tart cherry etc. for joints, insomnia

    Czechosherlockia, USA
    Are there any studies on the mechanisms of why PWCs have such low O2 handling ability? Is it in the lungs, in the RBCs, in what? Thanks.
  2. merylg

    merylg Senior Member

    Sydney, NSW, Australia
    Hi Sherlock,
    You may be interested in exploring this thread
    which in part relates to inability to move Iron to bone marrow, leading to over-production of Zinc Protoporphyrins incorporating lead, at the expense of Hemoglobin production, leading to lowered ability of red blood cells to carry & deliver O2.
    Low Manganese...effect on ER stuctures. Accumulation & trapping of Iron & Copper in liver.
    Depleted B2 Riboflavin stores due to fortification of foods with Vitamins & dis-proportionate supplementation of Vitamins & Minerals, poor diet, lack of variety, lack of whole foods, malabsorption, eating foods that block absorption.
    Impact of low B2 Riboflavin on mitochondrial function...ATP production etc
    Production of proteins relying on functional liver

    Other things that I can think of are all things dealt with by Respiratory Physicians & Allergist/Immunologists. My Resp. Phys. for example said it's harder to breathe lying down. I have mild asthma, but major chemical sensitivities, food allergies & intolerances that impact on breathing. Vascular issues can also impact on breathing. How much O2 is in the air is also relevant. What noxious gases may be present? Do you have obstructive or central sleep apnoea? What metabolic issues are impacting breathing? Our general muscle weakness also impacts our ability to breathe.

    It's a good topic!!! The papers would be endless!
  3. oceanblue

    oceanblue Senior Member

    Hi Sherlock

    There's a separate thread on Deconditioning, and on balance most CFS patients - at least those well enough to attend outpatient clinics where most research takes place - have low but still normal VO2max levels, comparable with well-matched sedentary controls. See this post in particular. What does appear to be a consistent finding, however, is that CFS patients find exercise more exhausting (measured by the self-rated Borg RPE Exertion scale) than matched sedentary controls. Hope this helps.

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