🤖 AI Summary
Existing self-supervised methods (e.g., MAE) lack temporal awareness, hindering effective modeling of disease progression dynamics in longitudinal medical imaging (e.g., OCT/MRI). To address this, we propose a Random Twin Masked Autoencoding framework that reformulates the MAE reconstruction objective as a conditional variational inference task—explicitly capturing the intrinsic uncertainty of disease evolution via random time-difference sampling and joint masked reconstruction. Our approach integrates Siamese Vision Transformers, MAE, and Conditional Variational Autoencoders (CVAEs), abandoning deterministic temporal contrastive paradigms. Evaluated on multi-visit OCT (late-stage age-related macular degeneration) and MRI (Alzheimer’s disease) datasets, the pre-trained model significantly outperforms temporal MAE baselines and general-purpose foundation models on progression prediction tasks, demonstrating effective learning of non-deterministic longitudinal representations.
📝 Abstract
Temporally aware image representations are crucial for capturing disease progression in 3D volumes of longitudinal medical datasets. However, recent state-of-the-art self-supervised learning approaches like Masked Autoencoding (MAE), despite their strong representation learning capabilities, lack temporal awareness. In this paper, we propose STAMP (Stochastic Temporal Autoencoder with Masked Pretraining), a Siamese MAE framework that encodes temporal information through a stochastic process by conditioning on the time difference between the 2 input volumes. Unlike deterministic Siamese approaches, which compare scans from different time points but fail to account for the inherent uncertainty in disease evolution, STAMP learns temporal dynamics stochastically by reframing the MAE reconstruction loss as a conditional variational inference objective. We evaluated STAMP on two OCT and one MRI datasets with multiple visits per patient. STAMP pretrained ViT models outperformed both existing temporal MAE methods and foundation models on different late stage Age-Related Macular Degeneration and Alzheimer's Disease progression prediction which require models to learn the underlying non-deterministic temporal dynamics of the diseases.