Serveur d'exploration autour de Joseph Jankovic

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CSF multianalyte profile distinguishes Alzheimer and Parkinson diseases.

Identifieur interne : 000143 ( PubMed/Corpus ); précédent : 000142; suivant : 000144

CSF multianalyte profile distinguishes Alzheimer and Parkinson diseases.

Auteurs : Jing Zhang ; Izabela Sokal ; Elaine. Peskind ; Joseph. Quinn ; Joseph Jankovic ; Christopher Kenney ; Kathryn. Chung ; Steven. Millard ; John. Nutt ; Thomas. Montine

Source :

RBID : pubmed:18343778

English descriptors

Abstract

The therapeutic imperative for Alzheimer disease (AD) and Parkinson disease (PD) calls for discovery and validation of biomarkers. Increased cerebrospinal fluid (CSF) tau and decreased amyloid (A) beta42 have been validated as biomarkers of AD. In contrast, there is no validated CSF biomarker for PD. We validated our proteomics-discovered multianalyte profile (MAP) in CSF from 95 control subjects, 48 patients with probable AD, and 40 patients with probable PD. An optimal 8-member MAP agreed with expert diagnosis for 90 control subjects (95%), 36 patients with probable AD (75%), and 38 patients with probable PD (95%). This MAP consisted of the following (in decreasing order of contribution): tau, brain-derived neurotrophic factor, interleukin 8, Abeta42, beta2-microglobulin, vitamin D binding protein, apolipoprotein (apo) AII, and apoE. This first large-scale validation of a proteomic-discovered MAP suggests a panel of 8 CSF proteins that are highly effective at identifying PD and moderately effective at identifying AD.

DOI: 10.1309/W01Y0B808EMEH12L
PubMed: 18343778

Links to Exploration step

pubmed:18343778

Le document en format XML

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<div type="abstract" xml:lang="en">The therapeutic imperative for Alzheimer disease (AD) and Parkinson disease (PD) calls for discovery and validation of biomarkers. Increased cerebrospinal fluid (CSF) tau and decreased amyloid (A) beta42 have been validated as biomarkers of AD. In contrast, there is no validated CSF biomarker for PD. We validated our proteomics-discovered multianalyte profile (MAP) in CSF from 95 control subjects, 48 patients with probable AD, and 40 patients with probable PD. An optimal 8-member MAP agreed with expert diagnosis for 90 control subjects (95%), 36 patients with probable AD (75%), and 38 patients with probable PD (95%). This MAP consisted of the following (in decreasing order of contribution): tau, brain-derived neurotrophic factor, interleukin 8, Abeta42, beta2-microglobulin, vitamin D binding protein, apolipoprotein (apo) AII, and apoE. This first large-scale validation of a proteomic-discovered MAP suggests a panel of 8 CSF proteins that are highly effective at identifying PD and moderately effective at identifying AD.</div>
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<RefSource>Mov Disord. 2004 Sep;19(9):1020-8</RefSource>
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<RefSource>Int Psychogeriatr. 1997;9 Suppl 1:173-6; discussion 177-8</RefSource>
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<RefSource>Ann Neurol. 2007 Feb;61(2):120-9</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Alzheimers Dis. 2006 Aug;9(3):293-348</RefSource>
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</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>J Alzheimers Dis. 2005 Apr;7(2):125-33; discussion 173-80</RefSource>
<PMID Version="1">15851850</PMID>
</CommentsCorrections>
<CommentsCorrections RefType="Cites">
<RefSource>Alzheimer Dis Assoc Disord. 2005 Oct-Dec;19(4):220-5</RefSource>
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