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Decoupling Alzheimer Disease Pathologic Abnormalities at PET with Improved Clinical Relevance by Interpretable

Cheng Tang1,2, Xun Sun1,3,4, Anqi Tang1,3,4

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This study introduces an interpretable deep-learning framework for Alzheimer disease (AD) PET imaging, creating personalized maps and an AI biomarker (ADAD score) that better correlate with clinical outcomes than traditional metrics.

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Area of Science:

  • Neuroimaging
  • Artificial Intelligence
  • Alzheimer Disease Research

Background:

  • Template-based PET metrics for Alzheimer disease (AD) amyloid-β (Aβ) and tau burden oversimplify data, potentially causing imaging-clinical discordance.
  • Current artificial intelligence (AI) methods offer richer patterns but often lack biological interpretability.
  • There is a need for interpretable AI biomarkers in AD diagnostics.

Purpose of the Study:

  • To develop and validate an interpretable deep-learning framework for PET imaging in Alzheimer disease.
  • To generate a clinically meaningful AI biomarker by separating AD-specific abnormalities from physiologic uptake using pathophysiologic constraints.
  • To enhance the understanding of disease heterogeneity and improve imaging-clinical correlations.

Main Methods:

  • Retrospective analysis of Aβ and tau PET scans from multiple cohorts (ADNI, AIBL, GAAIN, author's center).
  • Development of an adversarial decomposition learning (ADL) network to generate voxel-level pathologic maps and an AD adversarial decomposition (ADAD) score.
  • Evaluation of discriminatory performance using AUC and clinical relevance using cognitive, volumetric, CSF, and neuropathologic measures.

Main Results:

  • The ADL framework achieved high discriminatory performance with AUCs of 0.94 for Aβ and 0.98 for tau in external testing.
  • Interpretable pathologic attribution maps generated by ADL correlated well with expert rankings (Aβ: ρ=0.79, tau: ρ=0.63).
  • The ADAD score showed independent associations with cognitive outcomes and hippocampal atrophy, outperforming traditional metrics in clinical relevance.

Conclusions:

  • Pathophysiologically constrained ADL provides interpretable, personalized pathologic maps for AD.
  • The AI-derived ADAD score offers a clinically meaningful biomarker linking PET abnormalities to multimodal clinical measures.
  • This framework improves the interpretability and clinical utility of AI in Alzheimer disease neuroimaging.