Longitudinal cerebrospinal fluid biomarker trajectories along the Alzheimer's disease continuum in the BIOMARKAPD study.
Aged
Alzheimer Disease
/ cerebrospinal fluid
Amyloid beta-Peptides
/ cerebrospinal fluid
Apolipoproteins E
/ genetics
Biomarkers
/ cerebrospinal fluid
Chitinase-3-Like Protein 1
Cognitive Dysfunction
/ cerebrospinal fluid
Female
Humans
Longitudinal Studies
Male
Middle Aged
Neurofilament Proteins
/ cerebrospinal fluid
Peptide Fragments
Phosphorylation
tau Proteins
/ cerebrospinal fluid
Alzheimer
Amyloid
CSF
Inflammation
Neurofilaments
Tau
YKL-40
Journal
Alzheimer's & dementia : the journal of the Alzheimer's Association
ISSN: 1552-5279
Titre abrégé: Alzheimers Dement
Pays: United States
ID NLM: 101231978
Informations de publication
Date de publication:
06 2019
06 2019
Historique:
received:
27
08
2018
revised:
29
11
2018
accepted:
21
01
2019
pubmed:
11
4
2019
medline:
23
6
2020
entrez:
11
4
2019
Statut:
ppublish
Résumé
Within-person trajectories of cerebrospinal fluid (CSF) biomarkers in Alzheimer's disease (AD) are not well defined. We included 467 subjects from the BIOMARKAPD study with at least two serial CSF samples. Diagnoses were subjective cognitive decline (n = 75), mild cognitive impairment (n = 128), and AD dementia (n = 110), and a group of cognitively unimpaired subjects (n = 154) were also included. We measured baseline and follow-up CSF levels of total tau (t-tau), phosphorylated tau (p-tau), YKL-40, and neurofilament light (NfL). Median CSF sampling interval was 2.1 years. CSF levels of t-tau, p-tau, NfL, and YKL-40 were 2% higher per each year of baseline age in controls (P <.001). In AD, t-tau levels were 1% lower (P <.001) and p-tau levels did not change per each year of baseline age. Longitudinally, only NfL (P <.001) and YKL-40 (P <.02) increased during the study period. All four CSF biomarkers increase with age, but this effect deviates in AD for t-tau and p-tau.
Identifiants
pubmed: 30967340
pii: S1552-5260(19)30047-0
doi: 10.1016/j.jalz.2019.01.015
pii:
doi:
Substances chimiques
Amyloid beta-Peptides
0
Apolipoproteins E
0
Biomarkers
0
CHI3L1 protein, human
0
Chitinase-3-Like Protein 1
0
Neurofilament Proteins
0
Peptide Fragments
0
amyloid beta-protein (1-42)
0
tau Proteins
0
Types de publication
Journal Article
Multicenter Study
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
742-753Informations de copyright
Copyright © 2019 the Alzheimer's Association. Published by Elsevier Inc. All rights reserved.