4.7 Article

Changing the research criteria for the diagnosis of Parkinson's disease: obstacles and opportunities

期刊

LANCET NEUROLOGY
卷 12, 期 5, 页码 514-524

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/S1474-4422(13)70047-4

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资金

  1. Michael J Fox Foundation
  2. Bundesministerium fur Bildung und Forschung (BmBF)
  3. dPV (German Parkinson's disease association)
  4. Abbott
  5. Center of Integrative Neurosciences
  6. Internationale Parkinson Fonds
  7. Janssen
  8. TEVA
  9. UCB Pharma
  10. Canadian Institutes of Health Research
  11. Dystonia Medical Research Foundation
  12. National Parkinson Foundation
  13. Parkinson Society of Canada
  14. Ontario Problem Gambling Research Center
  15. Saunders
  16. Wiley-Blackwell
  17. Johns Hopkins Press
  18. Cambridge University Press
  19. Novartis
  20. Fonds de la Recherche en Sante du Quebec
  21. Webster Foundation
  22. Robert Bosch Foundation
  23. EU
  24. University of Tubingen
  25. Orion
  26. Lundbeck
  27. Pfizer
  28. Thieme publishers
  29. German Ministry of Education and Health
  30. Medtronic
  31. Cefalon Pharma
  32. Merck-Serono
  33. Boehringer Ingelheim
  34. Valeant Pharma
  35. Federal Ministry of Education and Research
  36. Helmholtz Association
  37. European Community
  38. German Ministry of Education and Research
  39. Spanish Science and Education Ministry
  40. European Union (REPLACES)
  41. AstraZeneca
  42. GlaxoSmithKline
  43. UCB
  44. Orion Pharma
  45. Merck Serono
  46. Merz Pharmaceuticals

向作者/读者索取更多资源

Recent findings question our present understanding of Parkinson's disease and suggest that new research criteria for the diagnosis of Parkinson's disease are needed, similar to those recently defined in Alzheimer's disease. However, our ability to redefine Parkinson's disease is hampered by its complexity and heterogeneity in genetics, phenotypes, and underlying molecular mechanisms; the absence of biochemical markers or ability to image Parkinson's disease-specific histopathological changes; the long prodromal period during which non-motor manifestations might precede classic motor manifestations; and uncertainty about the status of disorders diagnosed clinically as Parkinson's disease but without Lewy pathology. Although it is too early to confidently redefine Parkinson's disease, the time has come to establish a research framework that could lead to new diagnostic criteria. We propose the establishment of three tiers encompassing clinical features, pathological findings, and genetics or molecular mechanisms. Specific advances in each tier, bridged by neuroimaging and biochemical data, will eventually lead to a redefinition of Parkinson's disease.

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