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DOI 10.1016/j.clinph.2020.12.023

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2021

Deciphering the saccade velocity profile of progressive supranuclear palsy: A sign of latent cerebellar/brainstem dysfunction?

Terao Yasuo, Tokushige Shin-Ichi, Inomata-Terada Satomi, Fukuda Hideki, Yugeta Akihiro, Ugawa Yoshikazu

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To study whether the velocity profile of horizontal saccades could be used as an indicator of brainstem and cerebellar output dysfunction, depending on progressive supranuclear palsy (PSP) subtype.

METHODS

We compared the velocity profiles in 32 PSP patients of various subtypes with 38 age-matched normal subjects, including Richardson syndrome (RS), PSP-parkinsonism (PSPp), and pure akinesia (PAGF), and cerebellar subtypes of PSP (PSPc).

RESULTS

PSP patients showed reduced peak velocity along with increased duration, especially in the deceleration phase. This alteration was more prominent for larger target eccentricities (20-30 degrees), and correlated with disease severity. The changes were most pronounced in PSPc patients, with irregular increases and decreases in velocity profile, followed by RS patients, whereas the change was smaller in PSPp and normal in PAGF patients.

CONCLUSIONS

Saccade velocity profile can be an indicator of brainstem and/or cerebellar output. Altered velocity profile of PSP patients may reflect the pathology in the brainstem, but may also reflect cerebellar dysfunction, most prominently in PSPc.

SIGNIFICANCE: Saccade velocity profile may be used as an indicator of latent cerebellar/brainstem dysfunction.

Для цитирования: Terao Yasuo, Tokushige Shin-Ichi, Inomata-Terada Satomi, Fukuda Hideki, Yugeta Akihiro, Ugawa Yoshikazu. Deciphering the saccade velocity profile of progressive supranuclear palsy: A sign of latent cerebellar/brainstem dysfunction?. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2021. DOI: 10.1016/j.clinph.2020.12.023.

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