Plasma p-tau <sub>217</sub> correlates strongly with cerebrospinal fluid Aβ <sub>42</sub> and increases over a ten-year period in amyloid-positive, non-demented very old men

BackgroundPlasma phosphorylated tau<sub>217</sub> (p-tau<sub>217</sub>) is a robust biomarker of Alzheimer's disease (AD) pathology. However, its full potential as a dynamic marker has still not been verified in very old persons, i.e., those with the highest incidence of AD.ObjectiveTo examine the cross-sectional and longitudinal associations between plasma p-tau<sub>217</sub> concentration and cerebrospinal fluid (CSF) AD biomarkers. Further, to investigate the performance of p-tau<sub>217</sub> as a predictor of amyloid status in a cohort of very old men.MethodsCSF AD biomarkers were analyzed in thirty-five 89-year-old men. Amyloid-β (Aβ) positivity was defined according to CSF Aβ<sub>42</sub> level. Plasma p-tau<sub>217</sub> concentration was measured at the mean age of 82, 87, and 91. Incident dementia diagnoses in survivors were identified through medical records up to the age of 102.ResultsPlasma p-tau<sub>217</sub> strongly correlated with CSF Aβ<sub>42</sub> concentration in Aβ-positive (n = 16, Spearman <i>ρ</i>: rho = -0.63, <i>p</i> = 0.009) but not in Aβ-negative (n = 19, rho = 0.111, <i>p</i> = 0.652) men and predicted Aβ status (area under the curve, AUC 0.91). Plasma p-tau<sub>217</sub> increased over ten years in the Aβ-positive group, while it remained unchanged in the negative group (p = 0.018).ConclusionsOur findings indicate that plasma p-tau<sub>217</sub> is a predictor of brain Aβ deposition also in very old individuals.

Authors

Institutions

Publication Details

Journal
Journal of Alzheimer s Disease
Published
2025-10-29
DOI
https://doi.org/10.1177/13872877251390387
Primary Topic
Dementia and Cognitive Impairment Research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Plasma p-tau 217 correlates strongly with cerebrospinal fluid Aβ 42 and increases over a ten-year period in amyloid-positive, non-demented very old men

Martin Ingelsson, Vilma Veličkaitė, Bodil Weidung, Divya Bali et al.
Journal of Alzheimer s Disease
Dementia and Cognitive Impairment Research
article

Plasma p-tau 217 correlates strongly with cerebrospinal fluid Aβ 42 and increases over a ten-year period in amyloid-positive, non-demented very old men

Martin Ingelsson, Vilma Veličkaitė, Bodil Weidung, Divya Bali, Vilmantas Giedraitis, Oskar Hansson, Kristin Franzon, Henrik Zetterberg, Shorena Janelidze, Lena Kilander, Elisabeth Hellquist
article en

Abstract

BackgroundPlasma phosphorylated tau<sub>217</sub> (p-tau<sub>217</sub>) is a robust biomarker of Alzheimer's disease (AD) pathology. However, its full potential as a dynamic marker has still not been verified in very old persons, i.e., those with the highest incidence of AD.ObjectiveTo examine the cross-sectional and longitudinal associations between plasma p-tau<sub>217</sub> concentration and cerebrospinal fluid (CSF) AD biomarkers. Further, to investigate the performance of p-tau<sub>217</sub> as a predictor of amyloid status in a cohort of very old men.MethodsCSF AD biomarkers were analyzed in thirty-five 89-year-old men. Amyloid-β (Aβ) positivity was defined according to CSF Aβ<sub>42</sub> level. Plasma p-tau<sub>217</sub> concentration was measured at the mean age of 82, 87, and 91. Incident dementia diagnoses in survivors were identified through medical records up to the age of 102.ResultsPlasma p-tau<sub>217</sub> strongly correlated with CSF Aβ<sub>42</sub> concentration in Aβ-positive (n = 16, Spearman <i>ρ</i>: rho = -0.63, <i>p</i> = 0.009) but not in Aβ-negative (n = 19, rho = 0.111, <i>p</i> = 0.652) men and predicted Aβ status (area under the curve, AUC 0.91). Plasma p-tau<sub>217</sub> increased over ten years in the Aβ-positive group, while it remained unchanged in the negative group (p = 0.018).ConclusionsOur findings indicate that plasma p-tau<sub>217</sub> is a predictor of brain Aβ deposition also in very old individuals.

Journal of Alzheimer s DiseaseVol. 108(4)
Uppsala University (SE), University Health Network (CA), Karolinska University Hospital (SE), University of Wisconsin–Madison (US), Lund University (SE), Sahlgrenska University Hospital (SE), Occupational Cancer Research Centre (CA), UK Dementia Research Institute (GB), National Hospital for Neurology and Neurosurgery (GB), Ontario Brain Institute (CA), University College London (GB), University of Gothenburg (SE)
Openalex Percentile: Top 63%
Dementia and Cognitive Impairment Research
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.