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DOI 10.1016/j.clinph.2019.01.023

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

Vestibular evoked myogenic potentials and their clinical utility in patients with amyotrophic lateral sclerosis.

Liu Xiaoxuan, Zhang Shuo, Huang Xiao, Zhang Yingshuang, Fan Dongsheng

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

To evaluate the diagnostic value of vestibular evoked myogenic potentials (VEMPs) in the assessment of brainstem function integrity in patients with amyotrophic lateral sclerosis (ALS).

METHODS

This was a prospective case-control study including 30 definite or probable ALS patients divided into two groups (with or without brainstem involvement) and 30 healthy controls. Cervical (c-), masseter (m-) and ocular VEMP (o-VEMP) measurements were obtained for all the participants.

RESULTS

The c-VEMP mean p13 and n23 were significantly prolonged in the ALS patients. The interside peak differences in p13 and n23 of c-VEMP and in n10 and p15 of o-VEMP were significantly prolonged. The rates of alteration in c-VEMP, m-VEMP and o-VEMP in the ALS patients were 67%, 40%, and 45%, respectively. The ALS patients with brainstem involvement had a significantly higher percentage of VEMP abnormalities than did those without brainstem involvement (p = 0.027).

CONCLUSIONS

c-VEMP is a sensitive tool to detect lower levels of brainstem involvement. Impairments in o-VEMP and m-VEMP indicate involvement of the upper brainstem. The use of combined VEMPs may provide useful insights into the pathophysiological mechanism of ALS.

SIGNIFICANCE: VEMPs may be useful in the evaluation of brainstem dysfunction in ALS patients.

Для цитирования: Liu Xiaoxuan, Zhang Shuo, Huang Xiao, Zhang Yingshuang, Fan Dongsheng. Vestibular evoked myogenic potentials and their clinical utility in patients with amyotrophic lateral sclerosis.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2019. DOI: 10.1016/j.clinph.2019.01.023.

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