4.6 Article

Differential Pattern of Brain-Specific CSF Proteins Tau and Amyloid-Beta in Parkinsonian Syndromes

期刊

MOVEMENT DISORDERS
卷 25, 期 9, 页码 1284-1288

出版社

WILEY
DOI: 10.1002/mds.22895

关键词

cerebrospinal fluid; biomarker; progressive supranuclear palsy; Richardson's syndrome; PSP-P; multiple system atrophy

资金

  1. European Union [OLG1-CT-2000-01262]
  2. Sanofi-Aventis
  3. CHDI Foundation
  4. Neurosearch
  5. Siena Biotech
  6. German Research Foundation (DFG)
  7. German Ministry of Research and Education (BMBF)
  8. Thyssen Foundation
  9. Santhera
  10. Takeda
  11. Merz
  12. Pfizer
  13. Lundbeck
  14. GlaxoSmithKline
  15. European commission (Anteprion, cNeurpro, NeuroTAS)
  16. foundation of the state Baden-Wurttemberg
  17. German Research Foundation (Deutsche Forschungsgemeinschaft)
  18. Boehringer Ingelheim
  19. F.Hoffmann La Roche
  20. Knopp Neurosciences
  21. ONO Pharma
  22. Teva
  23. Thierry Latran Foundation
  24. Bayer Vital GmbH
  25. Teva-Aventis

向作者/读者索取更多资源

To evaluate cerebrospinal fluid (CSF) proteins reflecting processes of neurodegeneration and glial activation in progressive supranuclear palsy (PSP; Richardson's syndrome, n = 20; PSP-Parkinsonism, n = 7) and multiple system atrophy (MSA, n = 25), we analyzed tau, phosphorylated tau, amyloid-beta(1-42) (A beta 1-42), A beta 1-40, glial fibrillary acidic protein (GFAP), and CSF routine variables. Individuals with PSP-Parkinsonism and MSA had elevated tau levels when compared with Richardson's syndrome, Parkinson's disease (PD), and age-matched controls (P <= 0.001). Ratios of P-tau/T-tau were significantly different in Parkinsonian syndromes. CSF A beta 1-42 was decreased only in patients with Richardson's syndrome. In a subset of Parkinsonian syndromes, we found elevated GFAP concentrations and increased CSF/serum albumin ratios. There were no correlations between biomarker concentrations and clinical scores in any of the diseases. In conclusion, this preliminary data show that changes in CSF tau and A beta 1-42 may indicate different protein processing in PSP patients and might, therefore, be relevant in the differentiation of PSP subtypes. (C) 2010 Movement Disorder Society

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