Plasma proteins predict conversion to dementia from prodromal disease.

TitlePlasma proteins predict conversion to dementia from prodromal disease.
Publication TypeJournal Article
Year of Publication2014
AuthorsHye A, Riddoch-Contreras J, Baird AL, Ashton NJ, Bazenet C, Leung R, Westman E, Simmons A, Dobson R, Sattlecker M, Lupton M, Lunnon K, Keohane A, Ward M, Pike I, Zucht HDieter, Pepin D, Zheng W, Tunnicliffe A, Richardson J, Gauthier S, Soininen H, Kłoszewska I, Mecocci P, Tsolaki M, Vellas B, Lovestone S
JournalAlzheimers Dement
Volume10
Issue6
Pagination799-807.e2
Date Published2014 Nov
ISSN1552-5279
KeywordsAged, Aged, 80 and over, Apolipoproteins E, Blood Proteins, Cohort Studies, Dementia, Disease Progression, Female, Humans, Immunoassay, Magnetic Resonance Imaging, Male, Mental Status Schedule, Mild Cognitive Impairment, Predictive Value of Tests, Prodromal Symptoms, ROC Curve, Statistics as Topic
Abstract

BACKGROUND: The study aimed to validate previously discovered plasma biomarkers associated with AD, using a design based on imaging measures as surrogate for disease severity and assess their prognostic value in predicting conversion to dementia.METHODS: Three multicenter cohorts of cognitively healthy elderly, mild cognitive impairment (MCI), and AD participants with standardized clinical assessments and structural neuroimaging measures were used. Twenty-six candidate proteins were quantified in 1148 subjects using multiplex (xMAP) assays.RESULTS: Sixteen proteins correlated with disease severity and cognitive decline. Strongest associations were in the MCI group with a panel of 10 proteins predicting progression to AD (accuracy 87%, sensitivity 85%, and specificity 88%).CONCLUSIONS: We have identified 10 plasma proteins strongly associated with disease severity and disease progression. Such markers may be useful for patient selection for clinical trials and assessment of patients with predisease subjective memory complaints.

DOI10.1016/j.jalz.2014.05.1749
Alternate JournalAlzheimers Dement
PubMed ID25012867
PubMed Central IDPMC4240530
Grant ListG0801464 / / Medical Research Council / United Kingdom
G0801464 / / Medical Research Council / United Kingdom

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