Aim: A high-frequency oscillation in the range of 600-900 Hz has been shown
to be a component of the somatosensory evoked potential (SEP) in humans. I
n the present communication, we studied these oscillation potentials in two
neurological disorders.
Subjects and methods: Subjects were 20 healthy volunteers, 17 patients with
Parkinson's disease (PD) and 3 with myoclonus epilepsy (ME). Median nerve
SEPs were recorded using filters set at 0.5 and 3000 Hz. Several peaks of o
scillation were obtained by digitally filtering raw SEPs from 500 to 1000 H
z, and their amplitudes and onset latencies were measured.
Results: In normal subjects, several oscillation potentials were observed a
t the latency of 0 to 8 ms after the onset of N20. In PD patients, the osci
llation potentials at normal latencies were significantly larger than those
of normal subjects. Moreover, in 7 of 17 PD patients, they were extremely
enlarged (>mean +/- 3 SD of normal values). In contrast, in patients with M
E, abnormally enlarged oscillation potentials were seen at longer latencies
(7-14 ms) in spite of normal-sized early oscillation potentials. Magnetoen
cephalographic analyses showed that any oscillation potentials originated f
rom the primary sensory cortex.
Conclusions: There are at least two mechanisms for producing the oscillatio
n potentials of SEP. Those around N20 have some relation with the basal gan
glia function and are enlarged in PD patients, the others around P25-N33 ar
e enhanced in ME patients. (C) 1999 Elsevier Science Ireland Ltd. All right
s reserved.