Evidence map›Paper›PMID 41848292›Full record

Observational studyAnnals of neurology2026

Association between Plasma P-tau217 and Alzheimer's Copathology and Cognitive Decline in Parkinson's Disease.

Thomas F Tropea, Patricia Aldea Stevenson, Matthew Flitter, David Meehan, Amanda Morris, Ming Lu, Leonardo Iaccarino, Emily C Collins, Michael E Hodsdon, David Irwin and 11 more

Abstract readObservational Study
In one paragraph

Observational study in Annals of neurology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Thomas F TropeaDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Patricia Aldea StevensonEli Lilly and Company.
Matthew FlitterEli Lilly and Company.
David MeehanEli Lilly and Company.
Amanda MorrisEli Lilly and Company.
Ming LuEli Lilly and Company.
Leonardo IaccarinoEli Lilly and Company.
Emily C CollinsEli Lilly and Company.ORCID 0009-0005-7065-7395
Michael E HodsdonEli Lilly and Company.
David IrwinDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-5599-5098
Meredith SpindlerDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Andres DeikDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Nabila DahodwalaDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Katheryn A Q CousinsDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0003-1879-2766
David A WolkDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Leslie ShawDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA.ORCID 0000-0002-7650-1210
Daniel WeintraubDepartment of Psychiatry, University of Pennsylvania, Philadelphia, PA.
Edward B LeeDepartment of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA.
Alice Chen-PlotkinDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.
Mark MintunEli Lilly and Company.
Andrew SiderowfDepartment of Neurology, University of Pennsylvania, Philadelphia, PA.

Funding

UPenn ADCC Biomarker CoreP30AG010124 · NIA · UNIVERSITY OF PENNSYLVANIA · PI WOLK, DAVID A · 1991 to 2020
$35.1M
Research Education ComponentP30AG072979 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DAVID A WOLK · 2021 to 2026
$24.8M
Project IV: "Alpha-Synuclein Strains & Diverse Synucleinopathies"P50NS053488 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI TROJANOWSKI, JOHN Q. · 2007 to 2017
$20.9M
Understanding Environmental Contributions to Heterogeneity in bvFTD.P01AG066597 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Lauren M Massimo · 2020 to 2026
$18.8M
Project IV "Tackling Heterogeneity of Cognitive Trajectory in LBD"U19AG062418 · NIA · UNIVERSITY OF PENNSYLVANIA · PI TROJANOWSKI, JOHN Q. · 2019 to 2023
$18.1M
Project IV: In Vivo Dissection of Genetic Modifiers on Different Stages of SynucleinopathyP01AG084497 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Kelvin C Luk · 2024 to 2026
$15.2M
Understanding biomarkers of cognitive decline in Lewy body diseasesR37NS115139 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI ALICE S CHEN-PLOTKIN · 2024 to 2026
$2.2M
The Role of Alzheimer's Disease Genetic Risk in Predicting Parkinson's Disease DementiaK23NS114167 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI TROPEA, THOMAS FRANCIS · 2020 to 2024
$985k
NIA NIH HHS P01 AG084497NIH HHS K23NS114167NIH HHS P01AG066597NIH HHS P01AG084497NIH HHS P30AG010124NIH HHS P30AG072979NIH HHS P50NS053488NIH HHS U19AG062418NINDS NIH HHS R37 NS115139
6 · The paper itself

Abstract

objectiveClinically relevant Alzheimer's disease co-pathology is common in Lewy body disorders. Plasma P-tau217 is a sensitive biomarker for amyloid and tau pathology in Alzheimer's disease. The objective was to determine if plasma P-tau217 associates with Alzheimer's disease co-pathology and cognition in Lewy body disorders.

methodsParticipants had (1) a clinicopathological diagnosis of Parkinson's disease or dementia with Lewy bodies in the pathology series, or (2) a clinical diagnosis of Parkinson's disease in the clinical series and were followed as part of the longitudinal, observational cohort study at the University of Pennsylvania between 2007 and 2024. Plasma concentration of P-tau217 was measured in previously collected samples.

resultsNeuropathology cases included 46 Parkinson's disease and 10 dementia with Lewy bodies, and clinical cases included 173 Parkinson's disease, and 64 controls. P-tau217 was greater in cases with (median, 0.3 [interquartile range (IQR), 0.2-0.4]) versus without (median, 0.1 [IQR, 0.1-0.2]) Alzheimer's disease co-pathology (p < 0.01) and discriminates Lewy body disorders participants with Alzheimer's disease co-pathology (area under curve, 0.84). Parkinson's disease participants with incident cognitive impairment had greater increases in serial P-tau217 than those who remained cognitively stable (group × time interaction β = -0.010, p = 0.0027). Higher baseline P-tau217 concentrations associated with longitudinal change in dementia rating scale (group × time interaction β = -4.947, p = 0.0166) and higher risk for cognitive progression (hazard ratio = 1.597, p = 0.003).

interpretationPlasma P-tau217 detects Alzheimer's disease co-pathology in Lewy body disorders and predicts cognitive decline. Future studies will evaluate associations between plasma P-tau217 and imaging and clinical outcomes, in consideration for use of amyloid-targeting therapies in Lewy body disorders. ANN NEUROL 2026;99:1428-1437.

Indexed as

Alzheimer DiseaseCognitive DysfunctionParkinson Diseasetau ProteinsAgedAged, 80 and overBiomarkersCohort StudiesFemaleHumansLewy Body DiseaseLongitudinal StudiesMaleBiomarkersMAPT protein, humantau Proteins

Identifiers

PMID41848292
PMCPMC13206273

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.