UK ME/CFS Biobank
History[edit | edit source]
The UK ME/CFS Biobank was established in 2011 with joint grant from the UK charities ME Association, ME Research UK, and Action for ME, plus private donors. The ME Association's Ramsay Research Fund provides ongoing funding, with MEB aiming be financially self-sustaining by 2021.
By 2018, the UK ME/CFS Biobank held samples from 600 donors classified into the following groups:
- 350 patients with myalgic encephalomyelitis
- Patients with multiple sclerosis, acting as a comparison group
- Healthy controls
Severely ill patients[edit | edit source]
Patients with severe and very severe ME can receive home visits from UKMEB staff in order to donate samples to the biobank, but must live in England close to the biobank.
UK Biobank[edit | edit source]
Notable studies[edit | edit source]
Online presence[edit | edit source]
See also[edit | edit source]
Learn more[edit | edit source]
References[edit | edit source]
- "The UK ME/CFS Biobank – CureMe". London School of Hygiene and Tropical Medicine. Retrieved September 7, 2021.
- Lacerda, Eliana M.; Mudie, Kathleen; Kingdon, Caroline C.; Butterworth, Jack D.; O'Boyle, Shennae; Nacul, Luis (December 4, 2018). "The UK ME/CFS Biobank: A Disease-Specific Biobank for Advancing Clinical Research Into Myalgic Encephalomyelitis/Chronic Fatigue Syndrome". Frontiers in Neurology. 9. doi:10.3389/fneur.2018.01026. ISSN 1664-2295. PMC 6288193. PMID 30564186.
- "Research Projects". The ME Association. November 17, 2015. Retrieved September 7, 2021.