Cited by 26Alzheimer's disease research and treatmentsDementia and Cognitive Impairment ResearchCerebrospinal fluid and hydrocephalus

Validation of a prototype tau Thr231 phosphorylation CSF ELISA as a potential biomarker for Alzheimer's disease

Santos, Joana R. F., Bauer, Chris, Schuchhardt, Johannes, Wedekind, Dirk, Waniek, Katharina, Lachmann, Ingolf, Wiltfang, Jens, Vogelgsang, Jonathan·2019·Journal of Neural Transmission

Abstract

Alzheimer's disease (AD) is a progressive neurodegenerative disorder characterized by the presence of extracellular amyloid plaques (senile plaques) and intracellular neurofibrillary tangles formed by hyperphosphorylated tau protein. This process leads to neuronal degradation and neuronal death. Phosphorylation of tau protein at threonine 231 (p-tau231) has been shown to be characteristic in post-mortem brain tissue of patients with AD and it can be sensitively detected in cerebrospinal fluid (CSF). Therefore, it may serve as a biomarker to support the diagnosis of AD. In this study, we analysed how well p-tau231 could differentiate between patients suffering from dementia either due or not due to AD by a sandwich enzyme immunoassay. CSF p-tau231 was significantly higher in patients with dementia due to AD than in those with dementia due to other causes. In addition, we studied different factors affecting p-tau231 levels in CSF. We found that apolipoprotein E genotype influences p-tau231 CSF levels. Gender and age did not affect p-tau231 levels in CSF. Our findings indicate that p-tau231 levels in CSF can be a valuable marker for the clinical diagnosis of AD.

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Crossref · 10.1007/s00702-019-01982-5

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  • CSF p-tau231 has been widely reported as a biomarker to detect AD at both the MCI and dementia stages, but often it has been concluded that these changes are not different from CSF p-tau181 when directly compared.

    “CSF p-tau231 has been widely reported as a biomarker to detect AD at both the MCI and dementia stages of disease11,49, 50, 51, 52, 53 but often it has been concluded these changes are not different from CSF p-tau181 when directly compared.54”

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Authors
Santos, J. R. F., Bauer, C., Schuchhardt, J., Wedekind, D., Waniek, K., Lachmann, I., Wiltfang, J., & Vogelgsang, J.
Affiliations
  • Universitätsmedizin Göttingen (DE)
  • MicroDiscovery (Germany) (DE)
  • German Center for Neurodegenerative Diseases (DE)
Corresponding author
Vogelgsang, Jonathan
Venue
Journal of Neural Transmission
Published
2019-02-14
Volume
126
Issue
3
Pages
339-348
ISSN
  • 0300-9564 (ISSN-L)
  • 1435-1463
OpenAlex
W2915010166
Cited by
26
References
9
Citations by year
2026: 1 · 2025: 3 · 2024: 2 · 2023: 6 · 2022: 4 · 2021: 5 · 2020: 5
FWCI
2.40
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Neural Transmission (publishedVersion)
  • PubMed (publishedVersion)
  • DZNE Pub (submittedVersion)
Funders
  • European Commission
  • Ministério da Educação e Ciência
  • Fundação para a Ciência e a Tecnologia
  • European Regional Development Fund
Topics
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Cerebrospinal fluid and hydrocephalus
Keywords
Alzheimer's disease, tau phosphorylation, cerebrospinal fluid biomarkers, sandwich ELISA, dementia diagnosis, APOE genotype
MeSH terms
Aged, Alzheimer Disease, Enzyme-Linked Immunosorbent Assay, Female, Humans, Male, Middle Aged, Phosphorylation, Biomarkers, tau Proteins

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