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DOI 10.1016/j.clinph.2023.06.021

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2023

Neurophysiological correlates of non-motor symptoms in late premanifest and early-stage manifest huntington's disease.

Davis Marie-Claire, Hill Aron T, Fitzgerald Paul B, Bailey Neil W, Stout Julie C, Hoy Kate E

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To find sensitive neurophysiological correlates of non-motor symptoms in Huntington's disease (HD), which are essential for the development and assessment of novel treatments.

METHODS

We used resting state EEG to examine differences in oscillatory activity (analysing the isolated periodic as well as the complete EEG signal) and functional connectivity in 22 late premanifest and early stage people with HD and 20 neurotypical controls. We then assessed the correlations between these neurophysiological markers and clinical measures of apathy and processing speed.

RESULTS

Significantly lower theta and greater delta resting state power was seen in the HD group, as well as significantly greater delta connectivity. There was a significant positive correlation between theta power and processing speed, however there were no associations between the neurophysiological and apathy measures.

CONCLUSIONS

We speculate that these changes in oscillatory power and connectivity reflect ongoing, frontally concentrated degenerative and compensatory processes associated with HD.

SIGNIFICANCE: Our findings support the potential utility of quantitative EEG as a proximate marker of processing speed, but not apathy in HD.

Для цитирования: Davis Marie-Claire, Hill Aron T, Fitzgerald Paul B, Bailey Neil W, Stout Julie C, Hoy Kate E. Neurophysiological correlates of non-motor symptoms in late premanifest and early-stage manifest huntington's disease.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2023. DOI: 10.1016/j.clinph.2023.06.021.

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