Eye movements and association with regional brain atrophy in clinical subtypes of progressive supranuclear palsy

Objective To investigate oculomotor impairment in subtypes of progressive supranuclear palsy (PSP) and its associations with clinical features and regional brain volumes in PSP. Methods We compared the video-oculography (VOG) findings of 123 PSP patients, consisting of 66 PSP-Richardson syndrome (PSP-RS), 28 PSP-parkinsonism (PSP-P), and 29 PSP-progressive gait freezing (PSP-PGF), along with 80 Parkinson's disease (PD) patients. We also investigated the associations of the VOG results with clinical features (disease duration, PSP rating scales [PSPRS] scores for dysphagia and postural stability) in the subtypes of PSP patients and with regional volumes in the brainstem, including the midbrain, pons, medulla, and the superior cerebellar peduncle (SCP), among the patients who had MRI images at the time of VOG (30 PSP). Results All of the three subtypes of PSP patients showed slower vertical saccades and smooth pursuit than that of the PD patients (adjustedp < 0.05). Among the PSP subtypes, saccadic peak velocity, saccadic accuracy, and pursuit gain were significantly decreased in patients with the PSP-RS compared to those with the PSP-PGF (adjustedp < 0.05). In multiple linear regression model, vertical saccadic velocity, latency, accuracy, and pursuit gain were associated with the PSPRS score for dysphagia (adjustedp < 0.05), and a decrease in vertical saccadic speed and accuracy was associated with SCP atrophy (correctedp < 0.05). Conclusions This study demonstrated the severity of oculomotor dysfunction in differentiating the subtypes of PSP and its significant relationships with the dysphagia symptom and SCP volume in PSP.

Automated summary

The study revealed that the severity of oculomotor dysfunction in PSP patients can differentiate between subtypes and is significantly related to dysphagia symptoms and SCP volume in PSP.