1. Patients launch $1.27 million crowdfunding campaign for ME/CFS gut microbiome study.
    Check out the website, Facebook and Twitter. Join in donate and spread the word!
9th Invest in ME International ME Conference, 2014 - Part 2: Pathogens and the Gut
Mark Berry continues his series of articles on the 9th Invest in ME International ME Conference in London, with the emphasis shifting from autoimmunity to pathogens and the gut ...
Discuss the article on the Forums.

Update on the ME/CFS Tissue and Post Mortem Tissue Bank | ME Association | 24 August 2012

Discussion in 'Latest ME/CFS Research' started by Aquila, Aug 24, 2012.

  1. Aquila

    Aquila

    Messages:
    43
    Likes:
    15
    UK
    http://www.meassociation.org.uk/?p=12558 This is in an interesting article posted by the Me association. It's quite short so I will copy and paste below I hope that's ok.

    The MEA receives regular queries about the initiative to set up a formal UK tissue and post-mortem tissue bank where muscle, gastrointestinal and nervous system tissue samples can be collected, stored and made available for research.
    The current situation is as follows:
    This work has been running in parallel with the ME Biobank, which is collecting and storing blood samples for research. Work on the first phase of the Biobank is now well underway at University College London/Royal Free Hospital and The MEA Ramsay Research Fund has committed £40,000 towards the joint charity costs of funding this work for a further year starting in November 2012.
    Plans to establish a tissue and post-mortem bank were initiated by setting up a steering group that looked at the complex ethical, legal, practical and financial issues that would be involved in establishing such a facility. A report of the work that was done by this group has been published in The Journal of Clinical Pathology.
    Exploring the feasibility of establishing a disease-specific post-mortem tissue bank in the UK: a case study in ME/CFS
    Eliana M Lacerda, Luis Nacul, Derek Pheby, Charles Shepherd, Peter Spencer J Clin Pathol doi:10.1136/jcp.2010.082032​
    The plan to set up a formal ‘bricks and mortar’ tissue and post-mortem facility are currently on hold – mainly due to the enormous cost of setting this up and then maintaining it.
    In the meantime, I am continuing to work with our consultant neuropathologist at Addenbrooke’s Hospital in Cambridge in arranging post mortems when we are notified that someone has died and the person has made it clear that they want to donate their body to ME/CFS research
    The MEA does not at present hold a database of people who want to donate body tissues. However, this is something that may now be incorporated into the blood sample donor database – which should be in operation before the end of the year.
    In the absence of a database, anyone who wants to donate post mortem tissues for ME research needs to make this clear in writing in a Statement of Intent which can be kept with their Will, or in a Codicil to their Will. Next of kin will need to know about this instruction and where it is kept.
    More information on this procedure, as well as a Statement of Intent, can be downloaded from the MEA website.
    One of the most important practical aspects in the whole process of post-mortem tissue collection is for someone (ie next of kin or solicitor) to notify The MEA as soon as possible after a death has occurred. This is because the sort of research that is being done at present requires removal and fixation of very specific tissues as soon as possible, preferably within 24 hours – and this obviously requires consent and co-operation from relatives, coroners, pathologists at a very sensitive tine.
    A number of post-mortems have now taken place and some interesting findings reported – including the presence of dorsal root ganglionitis (= inflammation in bundles of nerve cells in the nerve roots that transmit sensory information back to the brain via the spinal cord).
    Those of us who are involved in various stages of this post mortem process have produced a preliminary summary of the findings in the form of a conference abstract:
    Pathology of Chronic Fatigue Syndrome: Pilot Study of Four Autopsy Cases
    DG O’Donovan(1,2), T Harrower(3), S Cader(2), LJ Findley(2), C Shepherd(4), A Chaudhuri(2)

    (1) Addenbrooke’s Hospital Cambridge UK
    (2) Queen’s Hospital Romford Essex UK
    (3) Royal Devon & Exeter Hospitals UK
    (4) Honorary Medical Advisor to ME Association UK

    Chronic Fatigue Syndrome / Myalgic Encephalomyelitis is a disorder characterised by chronic exercise induced fatigue, cognitive dysfunction, sensory disturbances and often pain.The aetiology and pathogenesis are not understood.
    We report the post mortem pathology of four cases of CFS diagnosed by specialists.
    The causes of death were all unnatural and included: suicidal overdose, renal failure due to lack of food and water, assisted suicide and probable poisoning.
    Selected portions of tissue were made available by the various Coroners in the UK and with the assent of the persons in a qualifying relationship.
    The cases were 1 male, and 3 female. Ages (years) M32, F32, F43 & F31.
    One case showed a vast excess of corpora amylacea in spinal cord and brain of unknown significance but Polyglucosan Body Disease was not supported by clinicopathologial review.No ganglionitis was identified.
    One case showed a marked dorsal root ganglionitis and two other cases showed mild excess of lymphocytes with nodules of nageotte in the dorsal root ganglia.
    This raises the hypothesis that dysfunction of the sensory and probably also the autonomic nervous system may lead to abnormal neural activity eg hyperalgesia & allodynia rather than anaesthesia and may explain some of the symptoms of CFS / ME such as pain, hypotension, hyperacusis and photophobia. However, the syndrome may be heterogeneous.
    Nevertheless, the precise relationship of fatigue, which may be either peripheral or central, to abnormalities in the peripheral nervous system (PNS) needs to be studied.
    The differential diagnosis of ganglionitis should be investigated in CFS/ME patients hence Varicella Zoster, Lyme disease, HIV, Sjogren’s disease, paraneoplastic sensory ganglionopathy should be excluded by appropriate history and tests.
    Thorough histopathological study of cases coming to autopsy may help to confirm or refute the hypothesis, that CFS is a disease process, and whether the symptomatology may be explained by inflammation of the sensory and autonomic divisions of the PNS.​
    Summary prepared by:
    Dr Charles Shepherd, Hon Medical Adviser, ME Association
    24 August 2012
     
    Firestormm, taniaaust1 and Dolphin like this.
  2. lnester7

    lnester7 Seven

    Messages:
    1,262
    Likes:
    1,163
    USA
    Can somebody please give me the Body donation instructions for USA?
     
  3. Firestormm

    Firestormm Guest

    Messages:
    5,824
    Likes:
    5,982
    Cornwall England
    Thanks for this Aquila. It's about time I had this discussion with my family.
     
    Dolphin likes this.
  4. peggy-sue

    peggy-sue

    Messages:
    2,494
    Likes:
    2,875
    Scotland
    I've had the discussion and the codicil is already in my will. (smug wee git :p )
    But the official form is great - thank-you!
     
    Dolphin likes this.
  5. Firestormm

    Firestormm Guest

    Messages:
    5,824
    Likes:
    5,982
    Cornwall England
    Did you find the discussion an easy one Peggy-sue?
     
  6. peggy-sue

    peggy-sue

    Messages:
    2,494
    Likes:
    2,875
    Scotland
    Yes, (Once mother was dead. She always said she'd block any attempt by me to even leave organs for donation. She had this silly notion they'd encourage death in order to obtain organs.)
    No problem at all with my partner or sibling.:)
    In fact it wasn't really a discussion, I merely wrote the codicil, stuck it to my will and told Michael it's there. He doesn't have any problems with it at all and he will see to it that my wishes are carried out, just as I will carry out whatever any of his wishes are should he go first.
    My brother knows it's there too, has no problem with it - and we are all aware of the importance of things being in place beforehand, so that the body can be harvested as quickly and freshly as possible.
    I've been through a similar process with my Dad already - leaving his brain to an organ bank for studying non-Korsakov alcoholic dementia. (His organs and corneas were unsuitable for donation to somebody else). The organ bank was absolutely delighted to be given his brain.
    I feel this is a really fiting tribute to him too. He had been in-with-the-bricks in the formation of the Health Service, (a dentist), he truly believed in free, first class service for everybody in all aspects of medical care, he took part in all sorts of clinical trials over the years, wanting to further scientific knowledge for the benefit of all.

    And his legacy of giving to scientific knowledge goes on.:thumbsup:
     
    August59 and Firestormm like this.
  7. John H Wolfe

    John H Wolfe Senior Member

    Messages:
    220
    Likes:
    36
    London

See more popular forum discussions.

Share This Page