Cited by 128Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsCerebrospinal fluid and hydrocephalus

Comparing the clinical utility and diagnostic performance of CSF P-Tau181, P-Tau217, and P-Tau231 Assays

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Leuzy, Antoine, Janelidze, Shorena, Mattsson-Carlgren, Niklas, Palmqvist, Sebastian, Jacobs, Dirk, Cicognola, Claudia, Stomrud, Erik, Vanmechelen, Eugeen +2 more·2021·Neurology

Abstract

BACKGROUND AND OBJECTIVES: Phosphorylated tau (p-tau) in CSF is considered an important biomarker in Alzheimer disease (AD) and has been incorporated in recent diagnostic criteria. Several variants exist, including p-tau at threonines 181 (p-tau181), 217 (p-tau217), and 231 (p-tau231). However, no studies have compared their diagnostic performance or association to β-amyloid (Aβ) and tau-PET. Understanding which p-tau variant to use remains an important yet answered question. We aimed to compare the diagnostic accuracy of p-tau181, p-tau217, and p-tau231 in CSF for AD and their association with Aβ and tau-PET. METHODS: ) and p-tau231, we also included p-tau181 measurements from 2 commonly used assays (Innotest and Elecsys). RESULTS: < 0.0001). DISCUSSION: seems to be more useful than other included p-tau assays in the workup of AD. Varied results across p-tau181 assays highlights the importance of anti-tau antibodies for biomarker performance. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that p-tau217 provides higher diagnostic accuracy for diagnosis of AD dementia than p-tau181 or p-tau231.

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Authors
Leuzy, A., Janelidze, S., Mattsson-Carlgren, N., Palmqvist, S., Jacobs, D., Cicognola, C., Stomrud, E., Vanmechelen, E., Dage, J. L., & Hansson, O.
Affiliations
  • Eli Lilly (United States) (US)
  • From the Clinical Memory Research Unit (A.L., S.J., N.M.-C., S.P., C.C., E.S., O.H.), Department of Clinical Sciences, Lund University, Malmö; Department of Neurology (N.M.-C.) and Memory Clinic (S.P., E.S., O.H.), Skåne University Hospital, Lund; Wallenberg Centre for Molecular Medicine (N.M.-C.), Lund University, Sweden; ADx NeuroSciences NV (D.J., E.V.), Ghent, Belgium; and Eli Lilly and Company (J.L.D.), Indianapolis, IN.
Corresponding author
  • Leuzy, Antoine
  • Hansson, Oskar
Venue
Neurology
Published
2021-10-26
Volume
97
Issue
17
Pages
e1681-e1694
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W3198098012
Cited by
128
References
16
Citations by year
2026: 21 · 2025: 25 · 2024: 28 · 2023: 24 · 2022: 28 · 2021: 2
FWCI
14.71
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Neurology (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Lund University Publications (Lund University) (submittedVersion)
  • IUScholarWorks (Indiana University) (submittedVersion, cc-by)
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
phosphorylated tau, p-tau181, p-tau217, p-tau231, cerebrospinal fluid biomarkers, Alzheimer's disease, diagnostic accuracy, anti-tau antibodies, amyloid-beta, tau PET, Elecsys, dementia diagnosis
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Female, Humans, Immunoassay, Male, Middle Aged, Sensitivity and Specificity, Sweden, Biomarkers, tau Proteins, Protein Isoforms

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