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Prognostic value of cerebrospinal fluid biomarkers in mild cognitive impairment due to Alzheimer disease.

Authors :
López-Cuevas R
Baquero-Toledo M
Cuevas-Jiménez A
Martín-Ibáñez N
Pascual-Costa R
Moreno-Monedero MJ
Cañada-Martínez A
Peña-Bautista C
Ferrer-Cairols I
Álvarez-Sánchez L
Cháfer-Pericás C
Source :
Neurologia [Neurologia (Engl Ed)] 2020 Oct 31. Date of Electronic Publication: 2020 Oct 31.
Publication Year :
2020
Publisher :
Ahead of Print

Abstract

We performed a retrospective analysis of the patients assessed at our memory unit for whom Alzheimer disease (AD) cerebrospinal fluid biomarker results were available. We selected patients diagnosed with mild cognitive impairment due to AD (National Institute on Aging-Alzheimer's Association clinical criteria), confirmed neuropsychological deficit, a Global Deterioration Scale score of 3, and an abnormal profile of cerebrospinal fluid biomarkers. Of the 588 cases reviewed, 110 met the inclusion criteria. During follow-up, 50 cases (45.45%) progressed to dementia due to AD. Baseline levels of total and phosphorylated tau were higher in the group of patients that progressed to dementia than in those remaining with mild cognitive impairment. After adjusting for age, sex, history of hypertension, diabetes, and educational level, a 10% increase in total tau protein values was associated with a 7.60% increase in the risk of progression to dementia (hazard ratio: 2.22; 95% confidence interval, 1.28-3.84]; P = .004). Among patients with mild cognitive impairment due to AD and abnormal cerebrospinal fluid biomarker profiles, progressively higher concentrations of total or phosphorylated tau were associated with increased risk of progression to dementia.<br /> (Copyright © 2020 Sociedad Española de Neurología. Publicado por Elsevier España, S.L.U. All rights reserved.)

Details

Language :
English; Spanish; Castilian
ISSN :
2173-5808
Database :
MEDLINE
Journal :
Neurologia
Publication Type :
Academic Journal
Accession number :
33143865
Full Text :
https://doi.org/10.1016/j.nrl.2020.07.026