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This research introduces IID-GCN, a novel graph learning framework that decomposes fMRI data into redundancy, uniqueness, and synergy components to improve disease diagnosis. By moving beyond simple correlation metrics, the method captures how brain disorders reshape functional information organization rather than just connection strength. This approach offers an interpretable representation for rs-fMRI-based diagnosis, providing deeper insights into the neural mechanisms underlying various disorders.
Interpretable Information-Decomposed Brain Graph Learning for fMRI-based Disease Diagnosis
arXiv:2608.20380v1 Announce Type: cross Abstract: Resting-state functional magnetic resonance imaging (rs-fMRI) has enabled non-invasive mapping of functional brain interactions for computer-aided diagnosis, yet most existing approaches reduce inter-regional relationships to correlation-based edge weights. Such representations capture co-fluctuation strength but obscure how information is shared across brain regions. Because brain disorders may disrupt not only connectivity strength but also the organization of redundancy, uniqueness and synergy, traditional functional connectivity may miss disease-relevant information structures. Here we introduce IID-GCN, an interpretable graph learning framework that decomposes rs-fMRI interactions into redundancy, uniqueness and synergy graphs using partial entropy decomposition. These information-specific graphs separately characterize shared, region-specific and jointly emergent components of brain activity. A multi-channel graph convolutional network then integrates the decomposed graphs through edge recalibration, cross-information interaction, ROI-attention readout and channel-attentive fusion. Across three datasets, IID-GCN consistently captures complementary diagnostic information beyond traditional functional connectivity. The learned information profiles reveal disorder-specific patterns of altered redundancy, uniqueness and synergy, suggesting that brain diseases reshape functional information organization rather than merely changing connection strength. These results establish information-decomposed brain graphs as an interpretable representation for rs-fMRI-based diagnosis. Our code is available at https://github.com/Zdy12/IID-GCN.
Abstract:Resting-state functional magnetic resonance imaging (rs-fMRI) has enabled non-invasive mapping of functional brain interactions for computer-aided diagnosis, yet most existing approaches reduce inter-regional relationships to correlation-based edge weights. Such representations capture co-fluctuation strength but obscure how information is shared across brain regions. Because brain disorders may disrupt not only connectivity strength but also the organization of redundancy, uniqueness and synergy, traditional functional connectivity may miss disease-relevant information structures. Here we introduce IID-GCN, an interpretable graph learning framework that decomposes rs-fMRI interactions into redundancy, uniqueness and synergy graphs using partial entropy decomposition. These information-specific graphs separately characterize shared, region-specific and jointly emergent components of brain activity. A multi-channel graph convolutional network then integrates the decomposed graphs through edge recalibration, cross-information interaction, ROI-attention readout and channel-attentive fusion. Across three datasets, IID-GCN consistently captures complementary diagnostic information beyond traditional functional connectivity. The learned information profiles reveal disorder-specific patterns of altered redundancy, uniqueness and synergy, suggesting that brain diseases reshape functional information organization rather than merely changing connection strength. These results establish information-decomposed brain graphs as an interpretable representation for rs-fMRI-based diagnosis. Our code is available at this https URL.
Neurons and Cognition (q-bio.NC); Machine Learning (cs.LG)
arXiv:2608.20380 [q-bio.NC]
(or arXiv:2608.20380v1 [q-bio.NC] for this version)
https://doi.org/10.48550/arXiv.2608.20380 Focus to learn more arXiv-issued DOI via DataCite
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