Cited by 194Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

Cerebrospinal Fluid Beta-Amyloid 42 Is Reduced before the Onset of Sporadic Dementia: A Population-Based Study in 85-Year-Olds

Skoog, I., Davidsson, P., Aevarsson, Ó., Vanderstichele, H., Vanmechelen, E., Blennow, K.·2003·Dementia and Geriatric Cognitive Disorders

Abstract

Deposition of β-amyloid (Aβ) is an early pathogenic event in Alzheimer’s disease (AD). We measured Aβ42 and Aβ40 in cerebrospinal fluid (CSF) in a population-based sample of 85-year-olds, 27 demented and 35 non-demented. During the following 3 years, 7 of the 35 non-demented individuals had developed dementia, while 28 remained non-demented. Reduced CSF levels of both Aβ42 (p = 0.001) and Aβ40 (p = 0.0001) were found in patients with manifest AD and vascular dementia at the age of 85. Non-demented individuals who developed dementia during follow-up had lower levels of CSF- Aβ42 (p = 0.003), but not CSF-Aβ40 (p = 0.96), than those who remained non-demented. The odds ratio for development of dementia was 8.2 (p = 0.027) for individuals in the lower 50th percentile of CSF-Aβ42, while none of those in the highest 33rd percentile of CSF-Aβ42 developed dementia during follow-up. There were no significant differences between carriers and non-carriers of the apolipoprotein E Ε4 allele regarding CSF-Aβ42or CSF-Aβ40.Our study suggests that low CSF-Aβ42 is found also in an unselected population-based sample of old demented patients and provides the first evidence of a disturbance in the metabolism of Aβ, specifically involving Aβ42, before the onset of clinical symptoms in AD.

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Crossref · 10.1159/000068478

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  • Cognitively unimpaired individuals with abnormal amyloid biomarkers have more rapid progression of atrophy, hypometabolism, and clinical/cognitive decline than individuals without biomarker evidence of Aβ deposition.

    “Numerous studies have shown that CU individuals with abnormal amyloid biomarkers have more rapid progression of atrophy, hypometabolism, and clinical/cognitive decline than individuals without biomarker evidence of Aβ deposition [13,33,80,93–99]”

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References 46 · Cited by 194

Authors
Skoog, I., Davidsson, P., Aevarsson, Ó., Vanderstichele, H., Vanmechelen, E., & Blennow, K.
Affiliations
  • Sahlgrenska University Hospital (SE)
  • Fujirebio (Belgium) (BE)
Venue
Dementia and Geriatric Cognitive Disorders
Publisher
S. Karger AG
Published
2003
Volume
15
Issue
3
Pages
169-176
ISSN
  • 1420-8008 (ISSN-L)
  • 1421-9824
OpenAlex
W1985262420
Cited by
194
References
46
Citations by year
2025: 3 · 2024: 4 · 2023: 1 · 2022: 4 · 2021: 7 · 2020: 9 · 2019: 4 · 2018: 8 · 2017: 6 · 2016: 5 · 2015: 19 · 2014: 12 · 2013: 12 · 2012: 12
FWCI
6.14
Type
journal article
Language
en
Open access
closed
Locations
  • Dementia and Geriatric Cognitive Disorders (publishedVersion)
  • PubMed (publishedVersion)
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 42, Aβ40, cerebrospinal fluid biomarkers, Alzheimer's disease, vascular dementia, preclinical dementia, amyloid metabolism, APOE ε4, dementia risk prediction
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Apolipoproteins E, Brain, Dementia, Female, Follow-Up Studies, Humans, Male, Peptide Fragments, Population Surveillance, Risk Factors, Sampling Studies, Amyloid beta-Peptides, Protein Isoforms

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