Movement Disorders (revue)

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Differential pattern of brain‐specific CSF proteins tau and amyloid‐beta in Parkinsonian syndromes

Identifieur interne : 001D48 ( Main/Exploration ); précédent : 001D47; suivant : 001D49

Differential pattern of brain‐specific CSF proteins tau and amyloid‐beta in Parkinsonian syndromes

Auteurs : Sigurd D. Süssmuth [Allemagne] ; Ingo Uttner [Allemagne] ; Bernhard Landwehrmeyer [Allemagne] ; Elmar H. Pinkhardt [Allemagne] ; Johannes Brettschneider [Allemagne] ; Axel Petzold [Royaume-Uni] ; Bernd Kramer [Allemagne] ; Jörg B. Schulz [Allemagne] ; Christian Palm [Allemagne] ; Markus Otto [Allemagne] ; Albert C. Ludolph [Allemagne] ; Jan Kassubek [Allemagne] ; Hayrettin Tumani [Allemagne]

Source :

RBID : ISTEX:E06A7675ED6F9BC2A578724A87C6A31F18A5977C

Descripteurs français

English descriptors

Abstract

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‐beta1–42 (Aβ1–42), Aβ1–40, 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 Aβ1–42 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 Aβ1–42 may indicate different protein processing in PSP patients and might, therefore, be relevant in the differentiation of PSP subtypes. © 2010 Movement Disorder Society

Url:
DOI: 10.1002/mds.22895


Affiliations:


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Le document en format XML

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<term>Adult</term>
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<div type="abstract" xml:lang="en">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‐beta1–42 (Aβ1–42), Aβ1–40, 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 Aβ1–42 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 Aβ1–42 may indicate different protein processing in PSP patients and might, therefore, be relevant in the differentiation of PSP subtypes. © 2010 Movement Disorder Society</div>
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