Cited by 59Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

No correlation between time‐linked plasma and CSF Aβ levels

Le Bastard, Nathalie, Aerts, Laetitia, Leurs, Judith, Blomme, Walter, De Deyn, Peter P., Engelborghs, Sebastiaan·2009·Neurochemistry International

Abstract

Plasma beta-amyloid protein (Abeta) isoforms are considered potential biomarkers for Alzheimer's disease (AD) and dementia. The relation between plasma and cerebrospinal fluid (CSF) levels of Abeta isoforms remains unclear. In order to identify possible correlations between Abeta levels in plasma and CSF we determined Abeta levels in time-linked plasma and CSF samples. Abeta concentrations in plasma (Abeta(1-42) and Abeta(N-42)) and CSF (Abeta(1-42)) samples from 49 AD patients, 47 non-Alzheimer's disease dementia (NONAD) patients, 39 MCI patients and 29 controls were determined using a multi-parameter fluorimetric bead-based immunoassay using xMAP((R)) technology (for plasma) and a conventional single-parameter ELISA (for CSF). Plasma Abeta(1-42) concentrations did not correlate with CSF Abeta(1-42) concentrations in the total study population, or in the different diagnostic groups. No correlations between plasma Abeta(N-42) and CSF Abeta(1-42) levels were found either. The CSF/serum albumin index did not show any significant differences between AD, NONAD, MCI and controls. These results suggest that the Abeta levels in plasma are independent of the Abeta levels in CSF both in dementia and controls. The fact that CSF and plasma Abeta do not correlate in patients as well as controls and no significant differences in plasma Abeta(1-42) or Abeta(N-42) between patients and controls can be detected hampers the diagnostic utility of the plasma Abeta levels as biomarkers for dement…

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Crossref · 10.1016/j.neuint.2009.08.006

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  • Previous studies have evaluated protein correlations between plasma and CSF biomarkers of AD.

    “Previous studies have evaluated protein correlations between plasma and CSF biomarkers of AD. 37 , 38 , 39 , 40 , 41 , 42 , 43”
  • Some previous studies indicate a poor correlation between plasma and CSF biomarkers, and some indicate a strong correlation.

    “Some of these studies indicate a poor correlation between plasma and CSF biomarkers, 39 and some indicate a strong correlation, 41”

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Authors
Le Bastard, N., Aerts, L., Leurs, J., Blomme, W., De Deyn, P. P., & Engelborghs, S.
Affiliations
University of Antwerp (BE)
Venue
Neurochemistry International
Publisher
Elsevier BV
Published
2009-12
Volume
55
Issue
8
Pages
820-825
ISSN
0197-0186 (ISSN-L)
OpenAlex
W2037239828
Cited by
59
References
1
Citations by year
2026: 2 · 2025: 1 · 2024: 3 · 2023: 2 · 2022: 2 · 2021: 4 · 2020: 6 · 2019: 1 · 2018: 4 · 2017: 3 · 2016: 4 · 2015: 4 · 2014: 3 · 2013: 5 · 2012: 5
FWCI
2.95
Type
journal article
Language
en
Open access
closed
Locations
  • Neurochemistry International (publishedVersion)
  • PubMed (publishedVersion)
  • Dépôt institutionnel de l'Université libre de Bruxelles (Université Libre de Bruxelles) (submittedVersion)
  • VUBIR (Vrije Universiteit Brussel) (submittedVersion)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
Keywords
amyloid-beta, cerebrospinal fluid amyloid, Alzheimer's disease, dementia, mild cognitive impairment, biomarkers, amyloid-beta 42
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Brain, Brain Chemistry, Enzyme-Linked Immunosorbent Assay, Female, Humans, Male, Neurochemistry, Peptide Fragments, Predictive Value of Tests, Sensitivity and Specificity, Time Factors, Biomarkers, Amyloid beta-Peptides, Fluorescence Polarization Immunoassay

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