MMCVLGApr 23, 2025

4D Multimodal Co-attention Fusion Network with Latent Contrastive Alignment for Alzheimer's Diagnosis

arXiv:2504.16798v17 citationsh-index: 10
Originality Incremental advance
AI Analysis

This work addresses the problem of early Alzheimer's diagnosis for medical researchers and clinicians by improving multimodal data fusion, though it appears incremental as it builds on existing integration methods.

The paper tackled the challenge of integrating heterogeneous neuroimaging data (sMRI and fMRI) for Alzheimer's disease diagnosis by proposing M2M-AlignNet, which uses a contrastive loss and co-attention module to align and fuse features, achieving enhanced diagnostic sensitivity as demonstrated in experiments.

Multimodal neuroimaging provides complementary structural and functional insights into both human brain organization and disease-related dynamics. Recent studies demonstrate enhanced diagnostic sensitivity for Alzheimer's disease (AD) through synergistic integration of neuroimaging data (e.g., sMRI, fMRI) with behavioral cognitive scores tabular data biomarkers. However, the intrinsic heterogeneity across modalities (e.g., 4D spatiotemporal fMRI dynamics vs. 3D anatomical sMRI structure) presents critical challenges for discriminative feature fusion. To bridge this gap, we propose M2M-AlignNet: a geometry-aware multimodal co-attention network with latent alignment for early AD diagnosis using sMRI and fMRI. At the core of our approach is a multi-patch-to-multi-patch (M2M) contrastive loss function that quantifies and reduces representational discrepancies via geometry-weighted patch correspondence, explicitly aligning fMRI components across brain regions with their sMRI structural substrates without one-to-one constraints. Additionally, we propose a latent-as-query co-attention module to autonomously discover fusion patterns, circumventing modality prioritization biases while minimizing feature redundancy. We conduct extensive experiments to confirm the effectiveness of our method and highlight the correspondance between fMRI and sMRI as AD biomarkers.

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