Brain, Vol 121, Issue 6 1099-1108, Copyright © 1998 by Oxford University Press
PP Urban, T Vogt and HC Hopf
We investigated corticobulbar tract function by recording from the tongue
and orofacial muscles and using transcranial magnetic stimulation (TMS) in
30 patients with amyotrophic lateral sclerosis (ALS) in order to improve
the diagnostic yield in the detection of subclinical upper motor neuron
(UMN) dysfunction. A UMN lesion was assumed when the peripheral conduction
time and amplitude of the M-wave were within normal range and either the
response to cortical stimulation was absent, or the central conduction time
was delayed (> mean + 2.5 SD). Only two patients showed clinical
evidence of UMN involvement in the cranial nerves, while TMS demonstrated
corticobulbar tract dysfunction in the orofacial muscles in 17 patients
(57%) and to the tongue in 15 patients (50%). Following recording at both
sites, corticobulbar tract dysfunction was confirmed in 21 patients (70%).
Twelve out of 13 patients with bulbar symptoms had evidence of additional
subclinical corticobulbar tract involvement using TMS. In seven out of 15
patients with isolated limb involvement, subclinical corticobulbar tract
dysfunction was demonstrated. Our results indicate the presence of early
and, in most cases, subclinical corticobulbar tract involvement in the
pathways to the orofacial muscles and tongue in ALS.
ARTICLES
Corticobulbar tract involvement in amyotrophic lateral sclerosis. A transcranial magnetic stimulation study
Department of Neurology, University of Mainz, Germany.
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