Evidence map›Paper›PMID 42251493›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2026

Age-related increase in plasma p-tau217 in amyloid-beta-negative cognitively unimpaired individuals affects diagnostic interpretation.

Anna E Mammel, Fernando Gonzalez-Ortiz, Ali Mousavi, Kelsey Hallett, Mary Encarnacion, Don Biehl, Pradip Gill, Sazan Ismael, Christopher Fowler, James D Doecke and 2 more

Abstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Anna E MammelNeurocode USA Inc, Bellingham, Washington, USA.
Fernando Gonzalez-OrtizNeurocode USA Inc, Bellingham, Washington, USA.
Ali MousaviBC Neuroimmunology Laboratory, Vancouver, British Columbia, Canada.
Kelsey HallettNeurocode USA Inc, Bellingham, Washington, USA.
Mary EncarnacionBC Neuroimmunology Laboratory, Vancouver, British Columbia, Canada.
Don BiehlNeurocode USA Inc, Bellingham, Washington, USA.
Pradip GillNeurocode USA Inc, Bellingham, Washington, USA.
Sazan IsmaelDivision of Neurology, Department of Medicine, University of British Columbia, Vancouver, British Columbia, Canada.
Christopher FowlerThe Florey Institute of Neuroscience and Mental Health, the University of Melbourne, Parkville, Victoria, Australia.
James D DoeckeThe Australian e-Health Research Centre, Commonwealth Scientific and Industrial Research Organisation, Brisbane, Queensland, Australia.
Larry WardThe Florey Institute of Neuroscience and Mental Health, the University of Melbourne, Parkville, Victoria, Australia.
Hans FrykmanNeurocode USA Inc, Bellingham, Washington, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe extent to which non-pathological aging influences plasma biomarkers remains unclear. Here, we investigate factors influencing plasma p-tau217 levels in cognitively unimpaired (CU), amyloid-beta-negative (Aβ-) individuals.

methodsPlasma p-tau217 was measured in CU Aβ- positron emission tomography-negative (PET-) participants using two immunoassays (ALZpath n = 360 and LUMIPULSE G1200 n = 73). Associations between p-tau217 and age groups (60-69, 70-79, and 80+ years), apolipoprotein E (APOE) genotype, and gender were evaluated.

resultsALZpath plasma p-tau217 showed a non-pathological age-related increase (p < 0.001), and increased percentage within the intermediate zone with age. Lumipulse p-tau217 showed an increase in the percentage of subjects with positive results with age, however, this trend was not significant (p > 0.05). Men had higher levels of p-tau217 only with the ALZpath assay (p = 0.02; Lumipulse: p = 0.81). No significant associations were found between p-tau217 and APOE genotype. DISCUSSION: Our results highlight the importance of incorporating age and sex into the interpretation of plasma p-tau217 particularly in preclinical stages.

Indexed as

AgingAmyloid beta-Peptidestau ProteinsAgedAged, 80 and overApolipoproteins EBiomarkersFemaleGenotypeHumansMaleMiddle AgedPositron-Emission TomographyAmyloid beta-PeptidesApolipoproteins EBiomarkerstau ProteinsAlzheimer's diseasebiomarkerscognitively normalnormal agingplasma p‐tau217

Identifiers

PMID42251493
PMCPMC13242609

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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.