IVCVLGJun 18, 2024

TADM: Temporally-Aware Diffusion Model for Neurodegenerative Progression on Brain MRI

arXiv:2406.12411v119 citations
Originality Incremental advance
AI Analysis

This work addresses the need for accurate prediction of future brain MRIs for clinicians to assess patient outcomes and disease progression, though it appears incremental as it builds on existing diffusion models with specific enhancements.

The paper tackles the problem of generating realistic brain MRI images to predict neurodegenerative progression by proposing TADM, a temporally-aware diffusion model that learns structural changes and combines them with baseline scans. The results show a 24% decrease in region size error and 4% improvement in similarity metrics on the OASIS-3 dataset.

Generating realistic images to accurately predict changes in the structure of brain MRI is a crucial tool for clinicians. Such applications help assess patients' outcomes and analyze how diseases progress at the individual level. However, existing methods for this task present some limitations. Some approaches attempt to model the distribution of MRI scans directly by conditioning the model on patients' ages, but they fail to explicitly capture the relationship between structural changes in the brain and time intervals, especially on age-unbalanced datasets. Other approaches simply rely on interpolation between scans, which limits their clinical application as they do not predict future MRIs. To address these challenges, we propose a Temporally-Aware Diffusion Model (TADM), which introduces a novel approach to accurately infer progression in brain MRIs. TADM learns the distribution of structural changes in terms of intensity differences between scans and combines the prediction of these changes with the initial baseline scans to generate future MRIs. Furthermore, during training, we propose to leverage a pre-trained Brain-Age Estimator (BAE) to refine the model's training process, enhancing its ability to produce accurate MRIs that match the expected age gap between baseline and generated scans. Our assessment, conducted on the OASIS-3 dataset, uses similarity metrics and region sizes computed by comparing predicted and real follow-up scans on 3 relevant brain regions. TADM achieves large improvements over existing approaches, with an average decrease of 24% in region size error and an improvement of 4% in similarity metrics. These evaluations demonstrate the improvement of our model in mimicking temporal brain neurodegenerative progression compared to existing methods. Our approach will benefit applications, such as predicting patient outcomes or improving treatments for patients.

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