Evidence map›Paper›PMID 40660813›Full record

ArticleJournal of Alzheimer's disease : JAD2025

Alzheimer's disease classification using mutual information generated graph convolutional network for functional MRI.

Yinghua Fu, Li Jiang, John Detre, Ze Wang, Alzheimer's Disease Neuroimaging Initiative

Abstract read
In one paragraph

Article in Journal of Alzheimer's disease : JAD, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Advances in artificial intelligence for neuroimaging.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2026
    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

5 authors.

Yinghua FuDepartment of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Li JiangDepartment of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
John DetreNeurology and Radiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, USA.
Ze WangDepartment of Diagnostic Radiology and Nuclear Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Alzheimer's Disease Neuroimaging Initiative

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
Academic Industrial Partnership on Advanced Perfusion MRIR01EB031080 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI Yulin V Chang, JOHN A DETRE · 2022 to 2026
$2.7M
Diversity Supplement to Brain entropy mapping in Alzheimer's DiseaseR01AG070227 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, ZE · 2021 to 2024
$2.5M
Deep-Learning Enhanced ASL MRI For Early AD AssessmentR01AG081693 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI Ze Wang · 2024 to 2026
$2.3M
Automated Quality Evaluation and Harmonization for Multisite ASL MRI DataR21AG080518 · NIA · UNIVERSITY OF PENNSYLVANIA · PI DOLUI, SUDIPTO, WANG, ZE · 2023 to 2024
$453k
Assessing chronic pain using brain entropy mappingR21AG082345 · NIA · UNIVERSITY OF MARYLAND BALTIMORE · PI WANG, ZE · 2022 to 2022
$442k
NIA NIH HHS R01 AG070227NIA NIH HHS R01 AG081693NIA NIH HHS R21 AG080518NIA NIH HHS R21 AG082345NIA NIH HHS U01 AG024904NIBIB NIH HHS R01 EB031080
6 · The paper itself

Abstract

BackgroundHigh-order cognitive functions depend on collaborative actions and information exchange between multiple brain regions. These inter-regional interactions can be characterized by mutual information (MI). Alzheimer's disease (AD) is known to affect many high-order cognitive functions, suggesting an alteration to inter-regional MI, which remains unstudied.ObjectiveTo examine whether inter-regional MI can effectively distinguish different stages of AD from normal control (NC) through a connectome-based graph convolutional network (GCN).MethodsMI was calculated between the mean time series of each pair of brain regions, forming the connectome which was input to a multi-level connectome based GCN (MLC-GCN) to predict the different stages of AD and NC. The spatio-temporal feature extraction in MLC-GCN was used to capture multi-level functional connectivity patterns generating connectomes. The GCN predictor learns and optimizes graph representations at each level, concatenating the representations for final classification. We validated our model on 552 subjects from ADNI and OASIS3. The MI-based model was compared to models with several different connectomes defined by Kullback-Leibler divergence, cross-entropy, cross-sample entropy, and correlation coefficient. Model performance was evaluated using 5-fold cross-validation.ResultsThe MI-based connectome achieved the highest prediction performance for both ADNI2 and OASIS3 where it's accuracy/Area Under the Curve/F1 were 87.72%/0.96/0.88 and 84.11%/0.96/0.91 respectively. Model visualization revealed that prominent MI features located in temporal, prefrontal, and parietal cortices.ConclusionsMI-based connectomes can reliably differentiate NC, mild cognitive impairment and AD. Compared to other four measures, MI demonstrated the best performance. The model should be further tested with other independent datasets.

Indexed as

Alzheimer DiseaseBrainConnectomeMagnetic Resonance ImagingNeural Networks, ComputerAgedAged, 80 and overFemaleHumansMaleAlzheimer's diseasefunctional magnetic resonance imaginggraph convolutional networkmutual information

Identifiers

PMID40660813
PMCPMC12344501

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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.