Evidence map›Paper›PMID 36345046›Full record

ArticleAlzheimer's research & therapy2022

Combining tau-PET and fMRI meta-analyses for patient-centered prediction of cognitive decline in Alzheimer's disease.

Davina Biel, Ying Luan, Matthias Brendel, Paul Hager, Anna Dewenter, Alexis Moscoso, Diana Otero Svaldi, Ixavier A Higgins, Michael Pontecorvo, Sebastian Römer and 8 more

Open access · goldAbstract read
In one paragraph

Article in Alzheimer's research & therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.7field-weighted citation impact, top 6% of its field
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

23 citing papers in PubMed, 28 citations in OpenAlex.

  1. Sex-specific brain reserve and progression from mild cognitive impairment to Alzheimer's disease dementia.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Multimodal Imaging of Hypoxia, Metabolism and pH in Feline Sarcoma Using HyperpolarizedAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
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  9. A systematic comparison of ATN biomarkers for monitoring longitudinal cognitive changes in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2025
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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

18 authors at 5 institutions in 4 countries.

Davina BielInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.ORCID 0000-0002-2597-1992
Ying LuanInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Matthias BrendelDepartment of Nuclear Medicine, University Hospital, LMU Munich, Munich, Germany.
Paul HagerInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Anna DewenterInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Alexis MoscosoWallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden.
Diana Otero SvaldiEli Lilly and Company, Indianapolis, IN, USA.
Ixavier A HigginsEli Lilly and Company, Indianapolis, IN, USA.
Michael PontecorvoAvid Radiopharmaceuticals, Philadelphia, PA, USA.
Sebastian RömerInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Anna StewardInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Anna RubinskiInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Lukai ZhengInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Michael SchöllWallenberg Centre for Molecular and Translational Medicine, University of Gothenburg, Gothenburg, Sweden.
Sergey ShcherbininEli Lilly and Company, Indianapolis, IN, USA.
Michael EwersInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany.
Nicolai FranzmeierInstitute for Stroke and Dementia Research (ISD), University Hospital, LMU Munich, 81377, Munich, Germany. Nicolai.Franzmeier@med.uni-muenchen.de.ORCID 0000-0001-9736-2283
Alzheimer’s Disease Neuroimaging Initiative
LMU Klinikum · DEEli Lilly (United States) · USGerman Center for Neurodegenerative Diseases · DEUniversity College London · GBUniversity of Gothenburg · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTau-PET is a prognostic marker for cognitive decline in Alzheimer's disease, and the heterogeneity of tau-PET patterns matches cognitive symptom heterogeneity. Thus, tau-PET may allow precision-medicine prediction of individual tau-related cognitive trajectories, which can be important for determining patient-specific cognitive endpoints in clinical trials. Here, we aimed to examine whether tau-PET in cognitive-domain-specific brain regions, identified via fMRI meta-analyses, allows the prediction of domain-specific cognitive decline. Further, we aimed to determine whether tau-PET-informed personalized cognitive composites capture patient-specific cognitive trajectories more sensitively than conventional cognitive measures.

methodsWe included Alzheimer's Disease Neuroimaging Initiative (ADNI) participants classified as controls (i.e., amyloid-negative, cognitively normal, n = 121) or Alzheimer's disease-spectrum (i.e., amyloid-positive, cognitively normal to dementia, n = 140), plus 111 AVID-1451-A05 participants for independent validation (controls/Alzheimer's disease-spectrum=46/65). All participants underwent baseline

resultsIn both amyloid-positive cohorts (ADNI [age = 75.99±7.69] and A05 [age = 74.03±9.03]), cognitive-domain-specific tau-PET outperformed global and temporal-lobe tau-PET for predicting future cognitive decline in episodic memory, language, executive functioning, and visuospatial abilities. Further, a tau-PET-informed personalized cognitive composite across cognitive domains enhanced the sensitivity to assess cognitive decline in amyloid-positive subjects, yielding lower sample sizes required for detecting simulated intervention effects compared to conventional cognitive endpoints (i.e., memory composite, global cognitive composite). However, the latter effect was less strong in A05 compared to the ADNI cohort.

conclusionCombining tau-PET with task-fMRI-derived maps of major cognitive domains facilitates the prediction of domain-specific cognitive decline. This approach may help to increase the sensitivity to detect Alzheimer's disease-related cognitive decline and to determine personalized cognitive endpoints in clinical trials.

Indexed as

Alzheimer DiseaseCognitive DysfunctionAgedAged, 80 and overAmyloidAmyloid beta-PeptidesBrainHumansMagnetic Resonance ImagingPatient-Centered CarePositron-Emission Tomographytau ProteinsAmyloidAmyloid beta-Peptidestau ProteinsAlzheimer’s diseaseCognitive declinefMRIPrecision medicineTau-PET

Identifiers

PMID36345046
PMCPMC9639286
OpenAlexW4308443965

What OpenQuestion holds

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LicenceCC BY
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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.