Evidence map›Paper›PMID 42465696›Full record

ArticleFrontiers in aging neuroscience2026

A multi-view graph neural network framework for Parkinson's disease identification based on dynamic functional connectivity.

Meili Lu, Xiangyu Zhao, Xile Wei

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 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

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Meili LuSchool of Information Technology Engineering, Tianjin University of Technology and Education, Tianjin, China.
Xiangyu ZhaoSchool of Information Technology Engineering, Tianjin University of Technology and Education, Tianjin, China.
Xile WeiTianjin Key Laboratory of 5 Process Measurement and Control, School of Electrical and Information Engineering, Tianjin University, Tianjin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a common neurodegenerative disorder, and accurate diagnosis is crucial for timely intervention. Dynamic functional connectivity (DFC) analysis of resting-state functional magnetic resonance imaging (rs-fMRI) can capture the time-varying characteristics of brain networks, offering a new perspective for PD identification. However, traditional clustering-based DFC methods suffer from issues such as the loss of continuous temporal information. Existing machine learning approaches struggle to effectively integrate the temporal dynamics of DFC with inter-subject differences in functional connectivity patterns and are further limited by the poor generalizability and opaque decision-making processes inherent to the small sample sizes typical of neuroimaging data. Here, we propose a DFC analysis framework based on a multi-view graph convolutional network (GCN). This method independently constructs inter-subject similarity networks for each sliding time window, forming multi-view graph-structured inputs. It employs a shared-weight GCN to extract node embeddings from each window, which are then fused for classification. Furthermore, the gradient-weighted class activation mapping (Grad-CAM) algorithm is incorporated to provide visual interpretability of the model's decisions. Our method outperforms traditional static functional connectivity and clustering-based approaches in classification accuracy. Concurrently, it achieves superior classification performance compared to other benchmark models. Grad-CAM-based interpretability analysis further reveals that the frontal and parietal lobes contribute most significantly to the classification decisions, providing computational evidence for understanding the brain network mechanisms underlying PD.

Indexed as

DFCGCNGrad-CAMinterpretabilityPDRS-fMRIsimilarity networks

Identifiers

PMID42465696
PMCPMC13372981

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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.