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Extract and Refine Brain Subgraph for Disorder Analysis via Cross-Domain Learning

计算机科学 图形 瓶颈 子图同构问题 人工智能 机器学习 深度学习 突出 因子临界图 人工神经网络 理论计算机科学 功率图分析 图论 诱导子图同构问题 大数据 熵(时间箭头) 生物网络 知识抽取 人脑 复杂网络 特征学习
作者
Xuexiong Luo,Jia Wu,Shimin Zhang,Guangwei Dong,Shan Xue,Hao Peng,Jie Yang,Chuan Zhou,Wenbin Hu,Amin Beheshti
出处
期刊:IEEE Transactions on Big Data [IEEE Computer Society]
卷期号:12 (4): 1137-1150
标识
DOI:10.1109/tbdata.2026.3668682
摘要

Brain graphs (brain connectivity networks) play an important role in modeling the complex structure of the human brain. Furthermore, brain graph learning based on graph neural networks (GNNs) has recently attracted growing interest. Although existing methods have made great progress in brain disorder prediction and pathogenic analysis, there are two key problems: (1) They rarely utilize the pathogenic reason of brain disorders, that is, salient brain regions always lead to abnormal connections between brain regions, to extract critical brain graph information for disorder analysis; (2) Since most of the available brain graph data is limited, how can we improve the performance of brain graph learning models on insufficient training data? Thus, in this paper, we learn brain graph representations for disorder prediction and analyze disorder-specific brain regions and connections from the subgraph perspective. Besides, we introduce the cross-domain brain graph learning framework to alleviate the problem of poor model performance on limited data. To consider the pathogenic reason by brain subgraphs, we first propose the node entropy of brain graphs based on brain graph properties to extract important nodes. We then introduce subgraph information bottleneck to refine the critical subgraph from the rough subgraph generated by these important nodes, recognizing important connections related to disorders. To achieve a better model performance on limited data, we design a cross-domain brain graph learning framework to improve the subgraph extraction model by the meta-learning method. The subgraph extraction model is pre-trained on a large source training dataset and then quickly adapted to target task dataset. Besides, a simple yet effective feature alignment module is applied to mitigate the negative transfer problem for cross-domain datasets. Extensive experimental results, including disorder prediction and pathogenic analysis on real-world neuroimaging data, demonstrate the effectiveness of our method.
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