用专家混合机制提升自闭症诊断与脑标志物发现能力
ASDFormer: A Transformer with Mixtures of Pooling-Classifier Experts for Robust Autism Diagnosis and Biomarker Discovery
- 设计多分支池化分类专家,结合注意力机制捕捉脑区连接模式
- 在ABIDE数据集上达到最优诊断准确率,识别出关键异常连接
- 适合脑科学与临床辅助诊断研究者使用
自闭症谱系障碍(ASD)是一种复杂的神经发育障碍,表现为大脑连接网络的紊乱。功能磁共振成像(fMRI)通过测量全脑血氧水平依赖(BOLD)信号,为大规模神经动态提供了非侵入性观测窗口。这些信号可建模为感兴趣区域(ROIs)之间的交互,而这些区域按其在脑功能中的作用被划分为功能社区。最新研究表明,这些社区内部及之间的连接模式对ASD相关改变尤为敏感。有效捕捉这些模式并识别偏离典型发育的交互,对于改善自闭症诊断和推动生物标志物发现至关重要。本文提出ASDFormer,一种基于Transformer的架构,引入了池化-分类专家混合模型(MoE),以捕获与自闭症相关的神经特征。通过集成多个专用专家分支并结合注意力机制,ASDFormer能够自适应强调与自闭症相关的不同脑区及连接模式,从而实现更优的分类性能和更具可解释性的异常标志物识别。在ABIDE数据集上的实验表明,ASDFormer实现了当前最优的诊断准确率,并揭示了与自闭症相关的功能连接紊乱的稳健线索,展示了其作为生物标志物发现工具的巨大潜力。
原文摘要 · Abstract (English)
Autism Spectrum Disorder (ASD) is a complex neurodevelopmental condition marked by disruptions in brain connectivity. Functional MRI (fMRI) offers a non-invasive window into large-scale neural dynamics by measuring blood-oxygen-level-dependent (BOLD) signals across the brain. These signals can be modeled as interactions among Regions of Interest (ROIs), which are grouped into functional communities based on their underlying roles in brain function. Emerging evidence suggests that connectivity patterns within and between these communities are particularly sensitive to ASD-related alterations. Effectively capturing these patterns and identifying interactions that deviate from typical development is essential for improving ASD diagnosis and enabling biomarker discovery. In this work, we introduce ASDFormer, a Transformer-based architecture that incorporates a Mixture of Pooling-Classifier Experts (MoE) to capture neural signatures associated with ASD. By integrating multiple specialized expert branches with attention mechanisms, ASDFormer adaptively emphasizes different brain regions and connectivity patterns relevant to autism. This enables both improved classification performance and more interpretable identification of disorder-related biomarkers. Applied to the ABIDE dataset, ASDFormer achieves state-of-the-art diagnostic accuracy and reveals robust insights into functional connectivity disruptions linked to ASD, highlighting its potential as a tool for biomarker discovery.
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