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DOI 10.1016/j.clinph.2012.05.027

Медицинская библиотека · Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2012

Blink reflex in patients with postparalytic facial syndrome and blepharospasm: trigeminal and auditory stimulation.

Akalin M A, Kiziltan M E, Benbir G

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Аннотация

OBJECTIVE

The enhancement of blink reflex (BR) excitability was shown in patients with postparalytic facial syndrome (PFS) and essential blepharospasm (EB). We prospectively investigated patients with PFS and EB whether BR alterations demonstrated by trigeminal stimulation will similarly be observed upon auditory stimulation.

METHODS

Fifteen patients with PFS, 15 patients with EB, and 30 healthy volunteers were involved. Electrically stimulated trigeminal BR and auditory BR were studied bilaterally.

RESULTS

The mean R2 amplitude and duration values were highest in EB patients, being significantly higher than PFS patients (p < 0.05) and control group (p < 0.01). The mean R2 duration in PFS patients were also significantly longer in compared to control group (p = 0.025). EB patients showed a higher mean R (auditory) amplitude and duration than PFS patients (p < 0.05) and controls (p < 0.04). The mean R (auditory) duration was longer on symptomatic side of PFS patients in compared to controls (p = 0.05).

CONCLUSIONS

We observed that there is an enhanced excitability of BR circuit in postparalytic facial syndrome and essential blepharospasm, which could be evoked by auditory stimulation in addition to trigeminal stimulation.

SIGNIFICANCE: The enhanced excitability in patients with EB and PFS probably originates from the final common pathway of BR circuit, namely facial motor or premotor neurons.

Для цитирования: Akalin M A, Kiziltan M E, Benbir G. Blink reflex in patients with postparalytic facial syndrome and blepharospasm: trigeminal and auditory stimulation.. Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology. 2012. DOI: 10.1016/j.clinph.2012.05.027.

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