About
ME/CFS has various neurological symptoms, such as mood swings, lack of energy and problems with sleep and concentration. Despite initial evidence of brain involvement in ME/CFS, little is known about possible molecular and cellular changes in the brain. In this project, brain tissue will be collected through a ME/CFS donor programme. The brain tissue will be used to investigate systems that deal with stress response, immunity and energy metabolism.
Goal
ME/CFS is often thought of as a brain disease because of its neurological symptoms. However, little is still known about changes in the brain of ME/CFS patients. By collecting brain tissue through a brain donor programme, this can be studied. This leads to more knowledge about the mechanisms and possible origins of this disease and can thus help improve diagnosis and treatment, which is relevant for patients, doctors and researchers.
Approach
Brain tissue from people with ME/CFS is currently not available for scientific research. To change this, this project sets up a brain donor programme to collect and study brain tissue from ME/CFS patients. The collected brain tissue will be made available for research. The aim is to find 200 donors to then be able to do 5 autopsies a year. So far, 25 ME/CFS donors have already been registered in the Netherlands Brain Bank (NBB). The study focuses on brain tissue changes in patients. It also looks at the Hypothalamic–pituitary–adrenal (HPA) stress axis, inflammatory cells and energy metabolism.
(Description adapted from project website: see link above)
ME/CFS according to Canadian Consensus Criteria (CCC).
Patients enrolled: 200
Age group: 18 - 65 years (Adults)