Opinion The impact of COVID-19 on the understanding, management and treatment of post-viral conditions, 2024, Tate et al

Discussion in 'ME/CFS research' started by Dolphin, Oct 3, 2024.

Tags:
  1. Dolphin

    Dolphin Senior Member (Voting Rights)

    Messages:
    5,884
    Free fulltext:
    https://esmed.org/MRA/mra/article/view/5644


    The impact of COVID-19 on the understanding, management and treatment of post-viral conditions


    Warren Perry Tate
    Department of Biochemistry, School of Biomedical Sciences; Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand
    Katie Peppercorn
    Department of Biochemistry, School of Biomedical Sciences
    Bryn W.C Griffiths
    Department of Biochemistry, School of Biomedical Sciences
    Sayan Sharma
    Department of Pathology, Dunedin School of Medicine, University of Otago, Dunedin, New Zealand

    Abstract

    The COVID-19 pandemic was unprecedented in the number of people affected from all cultures and countries.

    It posed immediate challenges of how to counter the Severe Acute Respiratory Syndrome-Coronovirus-2 that was causing fatalities, overburdening hospitals, and to develop effective vaccines and antivirals to complement the public health measures.

    The ribonucleic acid technology used to develop a novel class of vaccines proved highly successful in reducing the severe case numbers and fatalities.

    More challenging were the secondary long lasting effects from the viral infection in a relatively high proportion of patients now estimated to be in the range of 5-15%.

    The post viral condition, termed publicly Long COVID, and clinically Post Acute Sequelae of COVID-19 surprised many clinicians with its intractability.

    However, it mirrored previous experiences of patients suffering from ongoing post-viral (stressor) conditions, covered by the umbrella term, Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome.

    From over 775 million worldwide COVID-19 infections reported to date there has arisen an estimated 60 million cases of Long COVID.

    Long COVID is a hetergeneous condition with ~50% having a classic Myalgic Encephalomyelitis/Chronic Fatigue Syndrome-like syndrome with over 200 similar symptoms to those reported for this syndrome, but in addition ~25% are debilitated following the specific acute effects of the virus on body organs like the lungs, heart, and kidneys.

    This heterogeneity highlights the challenges of developing future management strategies, and treatments for the group as a whole to at least lessen the burden for all, and to reverse the fatigue syndrome post-viral condition for those with that clinical phenotype.

    Opportunities to understand Long COVID as a model of post-viral conditions are possible because the condition has arisen with such a large number of cases specific from this single stressor at the same time.

    Meaningful longitudinal patient studies can now be initiated and its immediacy and frequency has caught the attention of clinicians and scientists worldwide.

    Myalgic Encephalomyelitis/Chronic Fatigue Syndrome cases by contrast have arisen constantly as a ‘drip feed’ in small numbers from boutique infectious outbreaks like the first Severe Acute Respiratory Syndrome virus epidemic in 2003 where there were only ~ 9000 infections, or from endemic viruses like Epstein-Barr virus (glandular fever) from which ~5-10% develop a post-viral condition, but additionally from other major stressors.

    Widespread interest and investment in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome research has been lacking.

    Long COVID has now many talented scientists and clinicians researching its pathophysiology, and there has been significant investment, spearheaded in the United States through the ‘Recover Initiative’.

    It is hoped promising treatments can now be developed and tested in clinical trials.

    This gives hope for the ‘missing millions’ of Myalgic Encephalomyelitis/Chronic Fatigue Syndrome patients worldwide, many of whom have had their condition neglected for decades.

    Beyond the core symptoms that define the clinical case definitions for both Long COVID and Myalgic Encephalomyelitis/Chronic Fatigue Syndrome it is becoming clear the broader symptoms of an individual patient can not only reflect their previous health histories and co-morbidities, but also their specific genetic background.

    The major challenge ahead is there will likely need an individual-focused treatment strategy to improve the quality of life for these patients.

    Fundamental advances are still needed like simple accessible diagnostic tests based on molecular markers that can rapidly confirm the condition, follow its progress, and identify those at risk.

    TATE, Warren Perry et al. The impact of COVID-19 on the understanding, management and treatment of post-viral conditions. Medical Research Archives, [S.l.], v. 12, n. 9, sep. 2024. ISSN 2375-1924. Available at: <https://esmed.org/MRA/mra/article/view/5644>. Date accessed: 03 oct. 2024. doi: https://doi.org/10.18103/mra.v12i9.5644.

     
    oldtimer, Hutan and Sasha like this.
  2. Hutan

    Hutan Moderator Staff Member

    Messages:
    29,697
    Location:
    Aotearoa New Zealand
    Screen Shot 2024-11-23 at 6.45.55 am.png
    Figures 2b and 2c
    B. the results reported by Dass et al [53] using a new combinatorial platform together with a Genome Wide association Scree with ME/CFS patient samples
    C. Frequencies of three of the most abundant SNPs in small cohorts of ME/CFS, LC and healthy controls (Griffiths and Tate unpublished)

    I can't copy text from the pdf. This part of the paper notes that Dass et al found fifteen clusters of 3-5 SNPs linked to 14 genes could account for 91% of the samples from ME/CFS patients in the UK Biobank and that a followup paper of Long Covid cohorts were linked to 9 of the genes identified in the ME/CFS study. Tate and Griffiths looked at the 5 most frequently found SNPs reported in that Dass et al ME/CFS study in a very small study of 5 ME/CFS, 5 LC and 4 healthy controls. The results for 'the three most abundant SNPs' are shown in that Figure 2c.
     
    oldtimer and wigglethemouse like this.
  3. wigglethemouse

    wigglethemouse Senior Member (Voting Rights)

    Messages:
    1,037
    rs6832769 is a very common gene variant (35% Alelle freq, 58% genotype frequency). With such a low number of samples the 3rd column in figure 2c could easily be chance. DecodeME should answer this question.
     
    Hutan, oldtimer and Trish like this.
  4. Hutan

    Hutan Moderator Staff Member

    Messages:
    29,697
    Location:
    Aotearoa New Zealand
    In the third column, the ME/CFS and Long Covid cohorts don't really look different to the healthy controls (the bottom four rows). Yeah, the samples are way too small to conclude anything (although that doesn't stop people concluding things). Looking forward to DecodeME.
     
    wigglethemouse and Trish like this.

Share This Page