Cited by 80Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsParkinson's Disease Mechanisms and Treatments

Plasma Phospho‐Tau Identifies Alzheimer's Co‐Pathology in Patients with Lewy Body Disease

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Hall, Sara, Janelidze, Shorena, Londos, Elisabet, Leuzy, Antoine, Stomrud, Erik, Dage, Jeffrey L., Hansson, Oskar·2021·Movement Disorders

Abstract

Background: Alzheimer's disease co‐pathology is common in dementia with Lewy bodies and Parkinson's disease with dementia (Lewy body disease) and can reliably be detected with positron emission tomography (PET) or cerebrospinal fluid (CSF) biomarkers. Recently developed blood biomarkers are more accessible and less expensive alternatives. Objective: To investigate if plasma phospho‐tau217 and phospho‐tau181 can detect Alzheimer's pathology in Lewy body disease with dementia. Methods: In this cross‐sectional study we investigated plasma phospho‐tau217 and phospho‐tau181 in 35 patients with Lewy body disease with dementia. Patients underwent tau‐PET imaging ( 18 F‐RO948). Results: Plasma phospho‐tau217 correlated with plasma phospho‐tau181, CSF phospho‐tau217 (r s = 0.68, P < 0.001), and negatively with CSF β‐amyloid 42/40 (r s = −0.52, P = 0.001). Plasma phospho‐tau217 and phospho‐tau181 correlated with tau‐PET signal in the temporal cortex (r s > 0.56, P < 0.001) and predicted abnormal tau‐PET status and β‐amyloid status (area under the curve > 0.78 and > 0.81, respectively). Conclusion: Plasma phospho‐tau might be a useful marker for Alzheimer's co‐pathology in Lewy body disease with dementia. © 2020 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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  • Plasma tau has emerged as a marker of neuronal distress and appears in several neurodegenerative diseases, including preclinical AD.

    “Like NfL (neurofilament light chain), plasma tau has emerged as a marker of neuronal distress. It appears in several different neurodegenerative diseases, including importantly even preclinical AD patients (76–85).”

    From All the Tau We Cannot See (2023) · cites this paper as [80]

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Authors
Hall, S., Janelidze, S., Londos, E., Leuzy, A., Stomrud, E., Dage, J. L., & Hansson, O.
Affiliations
  • Lund University (SE)
  • Eli Lilly (United States) (US)
Corresponding author
  • Hall, Sara
  • Hansson, Oskar
Venue
Movement Disorders
Publisher
Wiley
Published
2020-12-07
Volume
36
Issue
3
Pages
767-771
ISSN
  • 0885-3185 (ISSN-L)
  • 1531-8257
OpenAlex
W3111319985
Cited by
80
References
26
Citations by year
2026: 13 · 2025: 15 · 2024: 18 · 2023: 12 · 2022: 17 · 2021: 5
FWCI
6.20
Type
journal article
Language
en
Open access
Locations
  • Movement Disorders (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion, cc-by)
Funders
  • Alzheimerfonden
  • Knut och Alice Wallenbergs Stiftelse
  • Marianne and Marcus Wallenberg Foundation
  • Parkinsonfonden
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Neurology › Parkinson's Disease Mechanisms and Treatments
Keywords
Alzheimer's disease co-pathology, Lewy body disease, dementia with Lewy bodies, Parkinson's disease dementia, blood biomarkers, tau PET imaging, cerebrospinal fluid biomarkers, temporal cortex
MeSH terms
Alzheimer Disease, Cross-Sectional Studies, Humans, Plasma, Biomarkers, Amyloid beta-Peptides, tau Proteins, Lewy Body Disease

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