Δημοσίευση

Predicting progression to dementia in persons with mild cognitive impairment using cerebrospinal fluid markers.

ΤίτλοςPredicting progression to dementia in persons with mild cognitive impairment using cerebrospinal fluid markers.
Publication TypeJournal Article
Year of Publication2017
AuthorsHandels, R. L. H., Vos S. J. B., Kramberger M. G., Jelic V., Blennow K., van Buchem M., van der Flier W., Freund-Levi Y., Hampel H., Rikkert M. Olde, Oleksik A., Pirtosek Z., Scheltens P., Soininen H., Teunissen C., Tsolaki M., Wallin A. K., Winblad B., Verhey F. R. J., & Visser P. Jelle
JournalAlzheimers Dement
Volume13
Issue8
Pagination903-912
Date Published2017 Aug
ISSN1552-5279
Λέξεις κλειδιάAged, Aged, 80 and over, Biomarkers, Cognitive Dysfunction, Dementia, Disease Progression, Educational Status, Female, Follow-Up Studies, Humans, Logistic Models, Magnetic Resonance Imaging, Male, Mental Status and Dementia Tests, Middle Aged, Prognosis, Risk Assessment, Temporal Lobe
Abstract

INTRODUCTION: We aimed to determine the added value of cerebrospinal fluid (CSF) to clinical and imaging tests to predict progression from mild cognitive impairment (MCI) to any type of dementia.METHODS: The risk of progression to dementia was estimated using two logistic regression models based on 250 MCI participants: the first included standard clinical measures (demographic, clinical, and imaging test information) without CSF biomarkers, and the second included standard clinical measures with CSF biomarkers.RESULTS: Adding CSF improved predictive accuracy with 0.11 (scale from 0-1). Of all participants, 136 (54%) had a change in risk score of 0.10 or higher (which was considered clinically relevant), of whom in 101, it was in agreement with their dementia status at follow-up.DISCUSSION: An individual person's risk of progression from MCI to dementia can be improved by relying on CSF biomarkers in addition to recommended clinical and imaging tests for usual care.

DOI10.1016/j.jalz.2016.12.015
Alternate JournalAlzheimers Dement
PubMed ID28216393

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