Evidence map›Paper›PMID 42337598›Full record

Trial reportAlzheimer's research & therapy2026

Clinico-biological trajectories stratified by combined tau biomarkers in preclinical Alzheimer's disease.

Miguel A Labrador-Espinosa, Nicolai Franzmeier, Stamatia Karagianni, Alexis Moscoso, Michael Schöll

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Alzheimer's research & therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

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

5 authors.

Miguel A Labrador-EspinosaDepartment of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Wallinsgatan 6, Mölndal, Sweden.
Nicolai FranzmeierDepartment of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Wallinsgatan 6, Mölndal, Sweden.
Stamatia KaragianniDepartment of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Wallinsgatan 6, Mölndal, Sweden.
Alexis MoscosoDepartment of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Wallinsgatan 6, Mölndal, Sweden.
Michael SchöllDepartment of Psychiatry and Neurochemistry, University of Gothenburg, Sahlgrenska University Hospital, Wallinsgatan 6, Mölndal, Sweden. michael.scholl@neuro.gu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTau pathology biomarkers provide prognostic indicators of neurodegeneration and cognitive decline in Alzheimer's disease (AD), making them crucial to early patient stratification for disease-modifying interventions. Plasma p-tau217 indexes early tau pathophysiology, whereas FDA/EMA-approved [

methodsWe included 330 cognitively unimpaired Aβ-PET-positive participants (72.2 ± 4.8 years; 58% female; 48% randomized to receive solanezumab) from the A4 Study, who underwent plasma p-tau217 and tau-PET at baseline. Plasma positivity (T

resultsAt baseline, 57% were negative-concordant (T

conclusionsIntegrating plasma p-tau217 with tau-PET visual assessment reveals clinically meaningful tau-biomarker heterogeneity in preclinical AD. Our findings highlight the value of combining these biomarkers to refine early risk prediction and support prioritization strategies for prevention trials. The frequency of discordance also motivates refining tau-PET visual assessments beyond binary classification (e.g., ordinal/semi-quantitative staging) to better capture subtle early tau signal.

Indexed as

Alzheimer Diseasetau ProteinsAgedAmyloid beta-PeptidesAntibodies, Monoclonal, HumanizedBiomarkersBrainCognitive DysfunctionDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMalePositron-Emission TomographyAmyloid beta-PeptidesAntibodies, Monoclonal, HumanizedBiomarkersMAPT protein, humansolanezumabtau ProteinsAlzheimer’s diseaseAmyloid-βCognitive declineMRIPETPreclinical ADP-tau217Tau

Identifiers

PMID42337598
PMCPMC13292533

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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 Socratic graph.