π€ AI Summary
This study addresses the challenge of limited accessibility and high cost of Tau-PET imaging in Alzheimerβs disease diagnosis by proposing DisQ-HNet, a framework that synthesizes interpretable Tau-PET images from multimodal T1 and FLAIR MRI. The method integrates a partial information decomposition (PID)-guided vector quantization encoder with a Half-UNet decoder, augmented by edge-aware pseudo skip connections to preserve fine anatomical details while disentangling and attributing modality-specific contributions. Experimental results demonstrate that DisQ-HNet outperforms existing baselines in reconstruction fidelity, more effectively retains disease-relevant Tau signals, and significantly enhances downstream tasks such as Braak staging, Tau localization, and classification. Furthermore, the framework provides clear, modality-specific interpretability, offering valuable insights into the contribution of each MRI sequence to the synthesized Tau-PET output.
π Abstract
Tau positron emission tomography (tau-PET) provides an in vivo marker of Alzheimer's disease pathology, but cost and limited availability motivate MRI-based alternatives. We introduce DisQ-HNet (DQH), a framework that synthesizes tau-PET from paired T1-weighted and FLAIR MRI while exposing how each modality contributes to the prediction. The method combines (i) a Partial Information Decomposition (PID)-guided, vector-quantized encoder that partitions latent information into redundant, unique, and complementary components, and (ii) a Half-UNet decoder that preserves anatomical detail using pseudo-skip connections conditioned on structural edge cues rather than direct encoder feature reuse. Across multiple baselines (VAE, VQ-VAE, and UNet), DisQ-HNet maintains reconstruction fidelity and better preserves disease-relevant signal for downstream AD tasks, including Braak staging, tau localization, and classification. PID-based Shapley analysis provides modality-specific attribution of synthesized uptake patterns.