Evidence map›Paper›PMID 40986433›Full record

Observational studyNeurology2025

Implication for Clinical Trials From Longitudinal Tau-PET Accumulation Across Biological Alzheimer Disease Stages.

Lydia Trudel, Joseph Therriault, Arthur C Macedo, Stijn Servaes, Seyyed Ali Hosseini, Gleb Bezgin, Etienne Aumont, Nesrine Rahmouni, Jaime Fernandez Arias, Yansheng Zheng and 13 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Predicting continuous amyloid PET levels with CSF and plasma brain-derived p-tau217.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  4. Visual versus quantitative tau-PET Braak staging in Alzheimer's disease using [European journal of nuclear medicine and molecular imaging · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Rates of clinical progression according to biological Alzheimer's disease stages.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
    Article
  9. Review
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

23 authors.

Lydia TrudelTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0009-0002-5593-7717
Joseph TherriaultTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0002-7826-4781
Arthur C MacedoTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0002-3957-0284
Stijn ServaesTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.
Seyyed Ali HosseiniTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0001-7542-7541
Gleb BezginTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.
Etienne AumontTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.
Nesrine RahmouniTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0009-0004-3081-8468
Jaime Fernandez AriasTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0002-6810-5920
Yansheng ZhengTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.
Yi-Ting Tina WangTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0002-9130-5461
Tevy ChanTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0009-0001-9134-5949
Brandon J HallTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0009-0007-4578-2033
Robert HopewellPET Unit, McConnell Brain Imaging Centre, Montreal, Quebec, Canada.
Chris Hung-Hsin HsiaoPET Unit, McConnell Brain Imaging Centre, Montreal, Quebec, Canada.
Pamela C L FerreiraDepartment of Psychiatry, School of Medicine, University of Pittsburgh, PA; and.
Bruna BellaverDepartment of Psychiatry, School of Medicine, University of Pittsburgh, PA; and.
Paolo VitaliTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0001-8953-1542
Jean-Paul SoucyDepartment of Neurology and Neurosurgery, McGill University, Montreal, Quebec, Canada.ORCID 0000-0001-6979-1259
Tharick A PascoalDepartment of Psychiatry, School of Medicine, University of Pittsburgh, PA; and.ORCID 0000-0001-9057-8014
Serge GauthierTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0003-4272-3330
Pedro Rosa-NetoTranslational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Montreal Neurological Institute, Quebec, Canada.ORCID 0000-0001-9116-1376
Alzheimer's Disease Neuroimaging Initiative

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectivesTau-PET is increasingly used in Alzheimer disease (AD) clinical trials, both for participant selection based on disease stage and as an outcome measure. However, the longitudinal patterns of tau accumulation according to AD stages remain unclear. We aimed to examine the patterns of tau-PET accumulation in different AD stages defined by the Alzheimer's Association Workgroup to inform trial design.

methodsThis was a retrospective analysis of data collected from participants in 2 longitudinal observational cohort studies: the Translational Biomarkers in Aging and Dementia (TRIAD) study from Montreal, Canada, and Alzheimer's Disease Neuroimaging Initiative (ADNI), a multisite study in North America. Amyloid-PET-positive participants were biologically staged as one of the following based on tau-PET uptake: A+T

resultsThe study included 542 participants (mean age: 67.9 ± 15.3 years; 56.3% female), comprising 321 non-AD controls and 221 individuals with AD. The baseline AD stage determined both the regional distribution and magnitude of tau accumulation. No significant accumulation occurred in A+T DISCUSSION: Stage-specific patterns of tau-PET change highlighted the importance of baseline biological AD staging for selecting outcome regions of interest. Statistical power analyses indicated that aligning outcome regions with disease stage reduced sample size estimates, suggesting potential gains in trial efficiency. While findings were consistent across 2 independent cohorts, differences in tracers and demographic composition represent key limitations.

Indexed as

Alzheimer DiseaseBrainPositron-Emission Tomographytau ProteinsAgedAged, 80 and overClinical Trials as TopicDisease ProgressionFemaleHumansLongitudinal StudiesMaleRetrospective Studiestau Proteins

Identifiers

PMID40986433
PMCPMC12459282

What OpenQuestion 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 OpenQuestion graph.