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This research introduces IBAHGT, a novel framework that unifies high-order correlations and long-range dependencies in brain networks using the information bottleneck principle for improved disease diagnosis. By adaptively learning message-passing weights and integrating global attention mechanisms, the model effectively reduces information redundancy to extract maximally informative biomarkers. The approach demonstrates superior performance over existing methods, offering a robust tool for clinical applications in neuroscience.
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Information Bottleneck-Guided Adaptive Hypergraph Transformer for Brain Disease Diagnosis

arXiv3 min de cititArticolul și perspectiva sunt în engleză.

arXiv:2609.37220v1 Announce Type: new Abstract: Exploring high-order correlations and long-range dependencies in brain networks holds significant value for both neuroscience research and clinical diagnosis. However, previous studies have lacked a unified integration of high-order and long-range dependency information in brain networks, and there is substantial redundancy behind various types of information. These issues limit their effectiveness in the diagnosis of brain diseases. To address this, we propose an Information Bottleneck-Guided Adaptive HyperGraph Transformer (IBAHGT). By incorporating the information bottleneck (IB) principle, this approach enables adaptive learning of high-order correlations and both short- and long-range dependencies within a unified framework for brain network analysis, achieving high-precision brain disease diagnosis. IBAHGT consists of three key components: an information bottleneck-guided adaptive hypergraph convolution, which introduces a novel hypergraph information bottleneck (HIB) principle to adaptively learn hypergraph message-passing weights between nodes and hyperedges, optimizes information flow and captures high-order information in brain networks that is maximally informative and minimally redundant (MIMR). The Transformer encoder captures global information within brain networks through the attention mechanism, specifically modeling short- and long-range dependencies. An information bottleneck-guided node-level adaptive fusion employs the IB principle to learn independent weights for each node, facilitating the fine-grained integration of high-order information and global information to obtain an efficient representation for downstream tasks. Extensive experiments demonstrate that the proposed method outperforms current state-of-the-art methods and can identify biomarkers for clinical applications.

Abstract:Exploring high-order correlations and long-range dependencies in brain networks holds significant value for both neuroscience research and clinical diagnosis. However, previous studies have lacked a unified integration of high-order and long-range dependency information in brain networks, and there is substantial redundancy behind various types of information. These issues limit their effectiveness in the diagnosis of brain diseases. To address this, we propose an Information Bottleneck-Guided Adaptive HyperGraph Transformer (IBAHGT). By incorporating the information bottleneck (IB) principle, this approach enables adaptive learning of high-order correlations and both short- and long-range dependencies within a unified framework for brain network analysis, achieving high-precision brain disease diagnosis. IBAHGT consists of three key components: an information bottleneck-guided adaptive hypergraph convolution, which introduces a novel hypergraph information bottleneck (HIB) principle to adaptively learn hypergraph message-passing weights between nodes and hyperedges, optimizes information flow and captures high-order information in brain networks that is maximally informative and minimally redundant (MIMR). The Transformer encoder captures global information within brain networks through the attention mechanism, specifically modeling short- and long-range dependencies. An information bottleneck-guided node-level adaptive fusion employs the IB principle to learn independent weights for each node, facilitating the fine-grained integration of high-order information and global information to obtain an efficient representation for downstream tasks. Extensive experiments demonstrate that the proposed method outperforms current state-of-the-art methods and can identify biomarkers for clinical applications.

Artificial Intelligence (cs.AI)

arXiv:2609.37220 [cs.AI]

(or arXiv:2609.37220v1 [cs.AI] for this version)

https://doi.org/10.48550/arXiv.2609.37220 Focus to learn more arXiv-issued DOI via DataCite (pending registration)

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