Evaluation of CSF and plasma tau species as fluid surrogate candidates for tau PET in prodromal to moderate Alzheimer's disease

Abstract INTRODUCTION Positron emission tomography (PET) is a valuable tool for assessing tau pathology in Alzheimer's disease (AD), but it is not widely accessible. Clarifying the relationship between fluid tau species and tau PET in AD may allow for the identification of fluid biomarkers that could serve as more accessible surrogates for tau PET. METHODS Cerebrospinal fluid (CSF) and plasma tau species levels were assessed across prodromal to moderate AD subjects (CSF: n = 53, plasma: n = 181) via immunoassays and liquid chromatography‐mass spectrometry. Fluid measures were correlated with [ 18 F]GTP1 tau PET at baseline for head‐to‐head comparisons across analytes. RESULTS CSF C2N‐eMTBR‐tau243, tau phosphorylated at threonine 205 (p‐tau205), p‐tau217, and a peptide from the tau‐441 microtubule‐binding region (MTBR) (MTBR/243‐254) exhibited the highest correlations with [ 18 F]GTP1 standardized uptake value ratio. Plasma p‐tau181 and p‐tau217 demonstrated correlation rankings with tau PET similar to those observed with corresponding CSF analytes. DISCUSSION CSF C2N‐eMTBR‐tau243, MTBR/243‐254, p‐tau205, and p‐tau217 demonstrated comparable strong correlations with tau PET. These findings may guide future development of plasma biomarker surrogates for tau PET.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2026-06-29
DOI
https://doi.org/10.1002/alz.71604
Primary Topic
Alzheimer's disease research and treatments
Type
article
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article

Evaluation of CSF and plasma tau species as fluid surrogate candidates for tau PET in prodromal to moderate Alzheimer's disease

Veronica G. Anania, Anna Bayfield, Joel B. Braunstein, J Lee et al.
Alzheimer s & Dementia
Alzheimer's disease research and treatments
article

Evaluation of CSF and plasma tau species as fluid surrogate candidates for tau PET in prodromal to moderate Alzheimer's disease

Veronica G. Anania, Anna Bayfield, Joel B. Braunstein, J Lee, Anne Biever, Felix L. Yeh, Tobias Bittner, Emilia Calderon, Matthew R. Meyer, Melanie Mandl, Casper C Hoogenraad, Balazs Toth, Sandra M. Sanabria Bohórquez, Philip B. Verghese, Ellen Casavant, Venky Venkatesh, Cecilia Monteiro, Edmond Teng, Emily Olafson, Tim West, Stephen Schauer
article en

Abstract

Abstract INTRODUCTION Positron emission tomography (PET) is a valuable tool for assessing tau pathology in Alzheimer's disease (AD), but it is not widely accessible. Clarifying the relationship between fluid tau species and tau PET in AD may allow for the identification of fluid biomarkers that could serve as more accessible surrogates for tau PET. METHODS Cerebrospinal fluid (CSF) and plasma tau species levels were assessed across prodromal to moderate AD subjects (CSF: n = 53, plasma: n = 181) via immunoassays and liquid chromatography‐mass spectrometry. Fluid measures were correlated with [ 18 F]GTP1 tau PET at baseline for head‐to‐head comparisons across analytes. RESULTS CSF C2N‐eMTBR‐tau243, tau phosphorylated at threonine 205 (p‐tau205), p‐tau217, and a peptide from the tau‐441 microtubule‐binding region (MTBR) (MTBR/243‐254) exhibited the highest correlations with [ 18 F]GTP1 standardized uptake value ratio. Plasma p‐tau181 and p‐tau217 demonstrated correlation rankings with tau PET similar to those observed with corresponding CSF analytes. DISCUSSION CSF C2N‐eMTBR‐tau243, MTBR/243‐254, p‐tau205, and p‐tau217 demonstrated comparable strong correlations with tau PET. These findings may guide future development of plasma biomarker surrogates for tau PET.

Alzheimer s & DementiaVol. 22(7)
Roche (Switzerland) (CH), C2N Diagnostics (United States) (US), Clinical Insights (US), CS Diagnostics (DE), Statistical Service (CY)
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Openalex Percentile: Top 8%
Alzheimer's disease research and treatments
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