ePoster

TRANSFORMER-BASED PROBABILISTIC MODELING OF PARKINSON’S DISEASE EYE MOVEMENTS FROM SACCADE-INDUCED OPTICAL FLOW

Maha Habibiand 2 co-authors

Philipps-University Marburg

FENS Forum 2026 (2026)
Barcelona, Spain
Board PS06-09PM-631

Presentation

Date TBA

Board: PS06-09PM-631

Poster preview

TRANSFORMER-BASED PROBABILISTIC MODELING OF PARKINSON’S DISEASE EYE MOVEMENTS FROM SACCADE-INDUCED OPTICAL FLOW poster preview

Event Information

Poster Board

PS06-09PM-631

Abstract

This study investigates whether saccades in Parkinson’s disease (PD) originate from a different action distribution compared to healthy controls. Participants were allowed to freely view videos with their head position stabilized using a chin rest. Unlike traditional deterministic control models, where a specific state corresponds to a single optimal action, we employ a probabilistic inverse optimal control framework (Rothkopf), in which behavior is characterized by a distribution over actions influenced by internal costs and sensorimotor factors uncertainty. We trained a Transformer model that encodes saccade-induced optical-flow patches, integrates them with a causal temporal Transformer, and predicts a Gaussian mixture over instantaneous saccadic velocity, yielding mixture weights (π), component means (μ), and variances (σ) as latent velocity regimes. A distance-to-goal signal was early-fused as an additional cue. The inferred velocity densities were predominantly unimodal; however, their structure varied across different groups. Trials involving PD exhibited a higher relative uncertainty (σ/|μ|) around the peak velocity and demonstrated increased mixture entropy, which is consistent with more variable action selection. At peak velocity, probability mass shifted across mixture components in PD, and component-mean distributions were more concentrated, suggesting a narrower set of effective velocity regimes. Within comparable peak-velocity ranges, group differences in component means persisted, indicating a distributional shift beyond simple amplitude differences. Model uncertainty was only weakly related to prediction error, supporting the interpretation that elevated uncertainty reflects intrinsic trial-to-trial motor variability rather than model unfamiliarity. These results motivate mixture-based oculomotor biomarkers that quantify changes in the full action distribution rather than relying on single summary statistics.

Recommended posters

Cookies

We use essential cookies to run the site. Analytics cookies are optional and help us improve World Wide. Learn more.