ArXiv TLDR

Learning Cross-Atlas Consistent Brain Disorder Representations via Disentangled Multi-Atlas Functional Connectivity Learning

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2605.07026

Minheng Chen, Chao Cao, Jing Zhang, Tianming Liu, Dajiang Zhu

q-bio.NCcs.AIcs.LG

TLDR

MADCLE learns cross-atlas consistent brain disorder representations from fMRI functional connectivity by disentangling disease-related factors from atlas-specific and covariate noise.

Key contributions

  • Introduces MADCLE, a multi-branch framework for joint encoding of FC from multiple brain atlases.
  • Learns atlas-wise disease representations and ensures cross-atlas consistency via distributional alignment.
  • Disentangles covariate-related and atlas-dependent factors using specific supervision and constraints.
  • Achieves competitive performance in disorder identification on ADNI and ADHD-200 datasets.

Why it matters

This paper addresses the critical issue of inconsistent brain disorder representations due to varying brain atlases in fMRI analysis. MADCLE provides a robust solution by disentangling disease-specific signals from atlas-dependent noise. This advancement could significantly improve the reliability and generalizability of FC-based diagnostics for neurological and psychiatric disorders.

Original Abstract

Functional connectivity (FC) derived from resting-state fMRI is widely used to characterize large-scale brain network alterations in neurological and psychiatric disorders. However, FC construction critically depends on the choice of brain atlas, and different parcellations may emphasize distinct organizational features, leading to heterogeneous and sometimes inconsistent representations. Existing multi-atlas approaches partially alleviate this issue but often fuse atlas-derived features or predictions at a relatively shallow level, while single-atlas disentanglement methods do not explicitly address cross-atlas heterogeneity. We propose Multi-Atlas Disentangled Connectivity LEarning (MADCLE), a multi-branch representation learning framework that jointly encodes FC matrices derived from different brain atlases. Rather than introducing a single explicitly shared latent variable across parcellations, MADCLE learns atlas-wise disease-related representations and encourages them to be cross-atlas consistent through distributional alignment. Meanwhile, covariate-related and atlas-dependent residual factors are modeled separately using covariate similarity supervision, atlas-specific reconstruction, and decorrelation constraints, thereby reducing the leakage of non-disease and parcellation-dependent information into the disease-related embeddings. Experiments on the ADNI and ADHD-200 datasets suggest that MADCLE achieves competitive or improved performance compared with single-atlas baselines, multi-atlas GNN/Transformer models, and recent multi-atlas consistency frameworks. These results support the potential value of structured disentanglement for FC-based disorder identification under heterogeneous parcellation schemes.

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