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DOI 10.1016/j.clinph.2018.12.009

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2019

Assessing blink reflex circuits by three different afferent routes in Parkinson's disease.

Weise David, Pargac Clemens, Pelz Johann Otto, Rumpf Jost-Julian, Fricke Christopher, Classen Joseph

СтатьяНаблюдательное исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

Degeneration of nuclei of the brainstem, especially parts of the vagal nuclei complex and the reticular formation, in Parkinson's disease (PD) may in part be responsible for nonmotor signs like obstipation, cardiac dysfunction and rapid eye movement sleep behavior disorder (RBD). The aim of the study was to establish a new blink reflex (BR) variant involving the vagal nuclei complex and the reticular formation and to investigate BR comprehensively using 3 different afferent routes in PD.

METHODS

In this cross-sectional observational study in 30 PD patients and 30 age and sex matched healthy controls, BR was elicited by stimulation of the auricular branch of the vagus nerve (ABVN) and compared to conventional BR variants evoked by the trigeminal and median nerve.

RESULTS

BRs could be elicited reliably by stimulation of ABVN in both groups. In none of the three BR variants, latencies or amplitudes differed between PD patients and controls. In PD, BR parameters were not related to cognition or presence of RBD.

CONCLUSION

The present study did not provide evidence for malfunctioning of neural circuits subserving BRs elicited by three different afferents in PD.

SIGNIFICANCE: Brainstem circuits mediating these BR variants may be spared from neurodegeneration in PD.

Для цитирования: Weise David, Pargac Clemens, Pelz Johann Otto, Rumpf Jost-Julian, Fricke Christopher, Classen Joseph. Assessing blink reflex circuits by three different afferent routes in Parkinson's disease.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2019. DOI: 10.1016/j.clinph.2018.12.009.

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