Δημοσίευση

Progression of mild cognitive impairment to Alzheimer's disease: improved diagnostic value of the combined use of N200 latency and beta-amyloid(1-42) levels.

ΤίτλοςProgression of mild cognitive impairment to Alzheimer's disease: improved diagnostic value of the combined use of N200 latency and beta-amyloid(1-42) levels.
Publication TypeJournal Article
Year of Publication2009
AuthorsPapaliagkas, V. T., Anogianakis G., Tsolaki M. N., Koliakos G., & Kimiskidis V. K.
JournalDement Geriatr Cogn Disord
Volume28
Issue1
Pagination30-5
Date Published2009
ISSN1421-9824
Λέξεις κλειδιάAged, Alzheimer Disease, Amyloid beta-Peptides, Biological Markers, Cognition Disorders, Discrimination (Psychology), Disease Progression, Electroencephalography, Evoked Potentials, Auditory, Female, Humans, Male, Neuropsychological Tests, Peptide Fragments
Abstract

BACKGROUND/AIMS: The aim of this study was to investigate the role of cerebrospinal fluid beta-amyloid(1-42) levels and auditory event-related potentials (AERPs) in the progress of mild cognitive impairment (MCI) to Alzheimer's disease (AD).METHODS: In 53 MCI patients, lumbar puncture was performed and beta-amyloid(1-42) levels were determined. Twenty patients were reexamined after 11 months. During this period, 5 of them progressed to AD. Neuropsychological and ERP analyses were performed on all patients during both baseline and endpoint examinations.RESULTS: Compared to stable MCI patients, those that progressed to AD had significantly lower beta-amyloid(1-42) levels (Mann-Whitney test, Z = -2.952, p = 0.003; effect size r = -0.41) and significantly prolonged N200 latencies (Mann-Whitney test, Z = -3.561, p < 0.001, effect size r = -0.49). From ERP variables, only the N200 latency significantly correlated with beta-amyloid(1-42) levels (baseline examination: r(s) = -0.421, p = 0.002; follow-up examination: r(s) = -0.574, p = 0.008).CONCLUSIONS: The combined use of these two parameters enabled discrimination of stable MCI patients from those who developed AD, with 100% sensitivity and specificity. Therefore, this method could be of high diagnostic value for the early diagnosis of AD.

DOI10.1159/000229023
Alternate JournalDement Geriatr Cogn Disord
PubMed ID19628938

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