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Open Sweden: ME/CFS lactate, glucose and hypoxanthine

Discussion in 'Recruitment into current ME/CFS research studies' started by mango, Jul 27, 2021.

  1. mango

    mango Senior Member (Voting Rights)

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    An ad is currently being circulated in Swedish ME groups on social media, a research study led by prof Jonas Bergquist at Uppsala University that is currently recruiting.

    It's a study on altered energy metabolism in ME/CFS, focusing mainly on lactate, glucose and hypoxanthine.

    (I couldn't find any info about this study on the ME/CFS Collaborative Research Center at Uppsala University's website, nor on the OMF website's page on Uppsala's research that it redirects to.)

    They are inviting people mainly in Västa Götaland region, who have been diagnosed with ME/CFS according to the Canadian consensus criteria, and healthy controls too.

    They are offering home visits for the tests (blood tests + light physical & mental exertion challenge).

     

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    Last edited: Jul 28, 2021
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  2. mango

    mango Senior Member (Voting Rights)

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    I have received copies of all the documents from the Ethical Review Authority now, too :) Too many, too large to upload them all here, but feel free to ask if you want more details on something.

    Ethical approval was obtained on 21 July 2021.

    Other people involved in this project are: professor emeritus Ola Saugstad, Oslo, Norway (advisor) and Anders Tageson, MD (responsible for collecting the samples).
     
    Last edited: Jul 27, 2021
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  3. mango

    mango Senior Member (Voting Rights)

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    Some auto-translated bits:
    Original project title: Förändringar av laktat, glukos och hypoxantinnivåer i blod från patienter med myalgisk encefalomyelit (ME) under mental och lätt fysisk ansträngning.
     
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  4. Grigor

    Grigor Senior Member (Voting Rights)

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    Interesting. Thank you for sharing! Had never heard of hypoxanthine. Had it ever been tested in relation to ME?
     
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  5. mango

    mango Senior Member (Voting Rights)

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    I don't know if it has been researched in relation to ME before. Here's what the Background section in the ethics application says:
     
    Last edited: Jul 28, 2021
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  6. Grigor

    Grigor Senior Member (Voting Rights)

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    Thank you! Very interesting and I'm looking forward to the results.
     
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  7. Andy

    Andy Committee Member

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  8. mango

    mango Senior Member (Voting Rights)

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    From the Overview section of the ethics application:
     
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  9. Grigor

    Grigor Senior Member (Voting Rights)

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  10. Ravn

    Ravn Senior Member (Voting Rights)

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    The inclusion of elite athletes as controls is interesting. I wonder why they didn't also include sedentary healthy controls?
     
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  11. Andy

    Andy Committee Member

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  12. Marky

    Marky Senior Member (Voting Rights)

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    Interesting, I just found out via test that I have low xanthine. is that the same as hypoxanthine?
     
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  13. Marky

    Marky Senior Member (Voting Rights)

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    Maybe because we ME-patients work out metabolically all day he he
     
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  14. Kitty

    Kitty Senior Member (Voting Rights)

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    There was talk in the 90s about ME patients being in a sense comparable to highly trained athletes, in that both groups are functioning at the limits of their endurance.

    I don't know whether that comparison is meaningful or not, though.
     
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  15. Hutan

    Hutan Moderator Staff Member

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    So, the hypothesis is that hypoxanthine is increased.

    The McGregor study associated lower hypoxanthine with PEM.

    And Andy tells us this one found lower hypoxanthine in pwME.

    It's interesting. Hopefully the study will tell us more. Possibly it will take some careful stratification of participants, including determining whether they are in PEM or not.
     
  16. Ravn

    Ravn Senior Member (Voting Rights)

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  17. mango

    mango Senior Member (Voting Rights)

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  18. mango

    mango Senior Member (Voting Rights)

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  19. Ravn

    Ravn Senior Member (Voting Rights)

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    The programme is geofenced outside the EU/EEC so haven't watched myself but based on the English summaries in Anil's twitter thread below they found some interesting mitochondrial markers during very light physical exertion. Finding markers without having to put pwME through the whole 2-day CPET thing would be great.

    But where did the claim that ME is now sometimes labelled MS-CCD (Multisystem Complex Chronic Disease) come from? Haven't we enough names? Is MS-CCD a Swedish thing?
    https://twitter.com/user/status/1518661128997552132
     
  20. mango

    mango Senior Member (Voting Rights)

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    I doubt it. I've never heard of it. I tried googling a literal translation of the expression, but I got no results at all in Swedish.
     
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