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Author Notes:

Correspondence: Dr. Aasef G. Shaikh, Department of Neurology, Case Western Reserve Un iversity, 11100 Euclid Avenue, Cleveland, OH44022; E-mail: aasefshaikh@gmail.com

Author Contributions: AS conceptualized the manuscript, collected, analyzed data, wrote and edited manuscript.

JJ and SF collected data and edited manuscript.

Disclosures: Stewart A. Factor reports honoraria from Neurocrine, Lundbeck, Auspex/Teva, Avanir, Cynapsus Therapeutics, Adamas, and UCB, grants from Ipsen, Medtronics, Teva, US World Meds, Pharm-Olam, Cynapsus Therapeutics, Solstice, Vaccinex, the CHDI Foundation, the Michael J. Fox Foundation, and the National Institutes of Health; and royalties from Demos, Blackwell Futura (for textbooks), and UpToDate.

Jorge L. Juncos reports support from the National Institutes of Health, the National Institute of Child Health and Development, the Michael J. Fox Foundation, Adamas, and World Meds and support for research through Emory University

Subject:

Research Funding:

Aasef G. Shaikh was supported by a Dystonia Medical Research Foundation Clinical Fellowship Award and a Dystonia Coalition/Dystonia Medical Research Foundation Career Development Award (NIH U54 TR001456).

Keywords:

  • brainstem
  • eye movement
  • parkinsonism
  • superior colliculus

Saccades in progressive supranuclear palsy - maladapted, irregular, curved, and slow.

Tools:

Journal Title:

Movement Disorders Clinical Practice

Volume:

Volume 4, Number 5

Publisher:

, Pages 671-681

Type of Work:

Article | Post-print: After Peer Review

Abstract:

Background and objectives: Slowed and curved rapid eye movements, saccades, are the well-known features of progressive supranuclear palsy (PSP). We hypothesized that the saccades in PSP are not only slow and curved, but they are also irregular and have timing deficits. Methods: We tested this hypothesis in 12 patients with PSP by measuring vertical and horizontal visually guided saccades using a limbus tracker. Results: Both, horizontal and vertical saccades were slow and had irregular trajectory and velocity profiles, but deficits were much more robust in vertical saccades. The irregularity in the saccade velocity was due to premature interruptions that either completely stopped the eyes, or moved the eyes at much slower velocity along or in the opposite direction of the ongoing saccade. The direction of the eyes' trajectory was often changed after the interruption. We simulated a conductance based single-compartment model of the burst neurons embedded in local feedback circuit for saccade generation. This model mimicked anatomical and physiological realism, while allowing the liberty to selectively change the activation of individual burst neurons or the pause neurons. The PSP saccades were comparable to the simulations during reduced activity of the inhibitory and excitatory burst neurons. Conclusion: PSP saccades are due to the paucity in burst generation at the excitatory and imprecise timing signal from the inhibitory burst neurons. Premature discharge of the inhibitory burst neuron further leads to breaks in the saccade trajectory, and maladaptive superior colliculus activity leading to aberrant saccades changing the intended trajectory of the ongoing saccade.

Copyright information:

© 2017 International Parkinson and Movement Disorder Society

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