Organization:European Huntington's Disease Network

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European Huntington's Disease Network
European Huntington's Disease Network (logo).png
AbbreviationEuro-HD Network, EHDN
Formation2003
TypeInternational Network
Legal statusConstitution
Purpose"to advance knowledge of Huntington's disease"[1]
HeadquartersUlm, Germany
Region served
Europe
Official language
English & 13 others
President
Prof G Bernhard Landwehrmeyer
Affiliations
Websiteehdn.org

The European Huntington's Disease Network (Euro-HD or EHDN) is a Europe-wide network of professionals and people affected by Huntington's disease, who collaborate to organise and perform research into the condition, and improve the care of HD-affected individuals.[2]

Huntington's disease (HD) is an incurable, genetically inherited degenerative brain condition that causes progressive impairment of motor function and cognitive decline and psychiatric symptoms.

EHDN was founded in 2003 and is financially supported by the CHDI Foundation.[2]

EHDN provides an infrastructure for multi-national observational studies and interventional clinical trials in HD; organises biannual plenary meetings attended by professionals and HD family members; supports a range of working groups focusing on aspects of the disease; and provides endorsement and seed funding for individual research projects.[2] At December 2011, EHDN had over 1000 regular members in 26 countries.[3] EHDN's activities are governed by an elected Scientific and Bioethics Advisory Committee and an Executive Committee.[2]

The core project of EHDN is the REGISTRY study, a multi-national observational project that aims to study the natural history of HD and expedite recruitment of suitable volunteers into clinical trials.[4] At December 2011, REGISTRY had enrolled over 7700 subjects in 145 sites,[5] and generated nine peer-reviewed publications.[6][7][8][9][10][11][12][13][14] The MermaiHD study of pridopidine and HORIZON study of latrepirdine in Huntington's disease were coordinated in Europe by EHDN.[15][16]

References

  1. ↑ "Constitution". EHDN. http://www.euro-hd.net/html/network/project/constitution/article1. Retrieved 19 December 2011. 
  2. ↑ 2.0 2.1 2.2 2.3 "About EHDN". EHDN. http://www.euro-hd.net/html/network/project. Retrieved 19 December 2011. 
  3. ↑ "Membership". EHDN. http://www.euro-hd.net/html/network/project/membership. Retrieved 19 December 2011. 
  4. ↑ "REGISTRY study: description". EHDN. http://www.euro-hd.net/html/registry/about/description. Retrieved 19 December 2011. 
  5. ↑ "REGISTRY study: enrolment". EHDN. http://www.euro-hd.net/html/registry/about/enrolment. Retrieved 19 December 2011. 
  6. ↑ Saft, C; Epplen, JT; Wieczorek, S; Landwehrmeyer, GB; Roos, RA; de Yebenes, JG; Dose, M; Tabrizi, SJ et al. (Oct 4, 2011). "NMDA receptor gene variations as modifiers in Huntington disease: a replication study". PLoS Currents 3: RRN1247. doi:10.1371/currents.RRN1247. PMID 21989477.  open access
  7. ↑ Quarrell, OW; Handley, O; O'Donovan, K; Dumoulin, C; Ramos-Arroyo, M; Biunno, I; Bauer, P; Kline, M et al. (January 2012). "Discrepancies in reporting the CAG repeat lengths for Huntington's disease". European Journal of Human Genetics 20 (1): 20–6. doi:10.1038/ejhg.2011.136. PMID 21811303. 
  8. ↑ López-Sendón, JL; Royuela, A; Trigo, P; Orth, M; Lange, H; Reilmann, R; Keylock, J; Rickards, H et al. (July 2011). "What is the impact of education on Huntington's disease?". Movement Disorders 26 (8): 1489–95. doi:10.1002/mds.23385. PMID 21432905. 
  9. ↑ Vaccarino, AL; Anderson, K; Borowsky, B; Duff, K; Giuliano, J; Guttman, M; Ho, AK; Orth, M et al. (April 2011). "An item response analysis of the motor and behavioral subscales of the unified Huntington's disease rating scale in huntington disease gene expansion carriers". Movement Disorders 26 (5): 877–84. doi:10.1002/mds.23574. PMID 21370269. 
  10. ↑ Busse, M; Al-Madfai, DH; Kenkre, J; Landwehrmeyer, GB; Bentivoglio, A; Rosser, A; European Huntington's Disease Network (Jan 21, 2011). "Utilisation of Healthcare and Associated Services in Huntington's disease: a data mining study". PLoS Currents 3: RRN1206. doi:10.1371/currents.RRN1206. PMID 21304753.  open access
  11. ↑ Orth, M; European Huntington's Disease Network; Handley, OJ; Schwenke, C; Dunnett, S; Wild, EJ; Tabrizi, SJ; Landwehrmeyer, GB (December 2011). "Observing Huntington's disease: the European Huntington's Disease Network's REGISTRY". Journal of Neurology, Neurosurgery, and Psychiatry 82 (12): 1409–12. doi:10.1136/jnnp.2010.209668. PMID 21097549. PMC 2947793. http://discovery.ucl.ac.uk/240946/1/240946.pdf. 
  12. ↑ Orth, M; Handley, OJ; Schwenke, C; Dunnett, SB; Craufurd, D; Ho, AK; Wild, E; Tabrizi, SJ et al. (Sep 28, 2010). "Observing Huntington's Disease: the European Huntington's Disease Network's REGISTRY". PLoS Currents 2: RRN1184. doi:10.1371/currents.RRN1184. PMID 20890398.  open access
  13. ↑ Boustany, Jr, CW; Murphy, GW; Hicks, Jr, GL (June 1991). "Mitral valve replacement in idiopathic hypereosinophilic syndrome". Annals of Thoracic Surgery 51 (6): 1007–9. doi:10.1016/0003-4975(91)91034-S. PMID 2039298. 
  14. ↑ Aziz, NA; Jurgens, CK; Landwehrmeyer, GB; EHDN Registry Study Group; van Roon-Mom, WM; van Ommen, GJ; Stijnen, T; Roos, RA (Oct 20, 2009). "Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease". Neurology 73 (16): 1280–5. doi:10.1212/WNL.0b013e3181bd1121. PMID 19776381. 
  15. ↑ de Yebenes, JG; Landwehrmeyer, B; Squitieri, F; Reilmann, R; Rosser, A; Barker, RA; Saft, C; Magnet, MK et al. (December 2011). "Pridopidine for the treatment of motor function in patients with Huntington's disease (MermaiHD): a phase 3, randomised, double-blind, placebo-controlled trial". Lancet Neurology 10 (12): 1049–1057. doi:10.1016/S1474-4422(11)70233-2. PMID 22071279. 
  16. ↑ "HORIZON Study". EHDN. http://www.euro-hd.net/html/projects/horizon. Retrieved 19 December 2011. 

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