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Variability of cortically evoked motor responses in multiple sclerosis
T C Britton1, B U Meyer, R Benecke
1Department of Neurology, University of Düsseldorf, F.R.G.
Electroencephalography and Clinical Neurophysiology
|June 1, 1991
Summary
This study investigated motor cortex stimulation in multiple sclerosis (MS) patients. Increased central motor conduction time and onset latency variability in electromyography responses are key indicators of pyramidal tract dysfunction in MS.
Area of Science:
- Neuroscience
- Clinical Electrophysiology
- Neurology
Background:
- Multiple Sclerosis (MS) is a demyelinating disease affecting the central nervous system.
- Pyramidal tract dysfunction is a common clinical manifestation in MS.
- Electromyography (EMG) is used to assess peripheral nerve and muscle function.
Purpose of the Study:
- To investigate central motor conduction time (CMCT) and onset latency variability (MCD) in the first dorsal interosseous (FDI) muscle following magnetic motor cortex stimulation.
- To compare neurophysiological findings in normal subjects and patients with MS.
- To correlate electrophysiological abnormalities with clinical signs of pyramidal tract dysfunction.
Main Methods:
- Magnetic motor cortex stimulation was applied to 20 normal subjects and 21 MS patients.
- Electromyographic (EMG) responses of the first dorsal interosseous (FDI) muscle were recorded.
- Central motor conduction time (CMCT) and onset latency variability (mean consecutive difference; MCD) were calculated.
Main Results:
- CMCT was prolonged in 19 out of 42 muscles (12 patients) in the MS group.
- Increased onset latency variability (MCD) was observed in 20 out of 42 muscles (14 patients) with MS.
- Abnormal onset latency variability correlated with impaired fine finger movements and increased finger jerks in MS patients.
Conclusions:
- This study confirms prolonged CMCT in MS patients.
- Abnormal onset latency variability is a significant neurophysiological finding in MS.
- Onset latency variability may serve as a valuable measure of pyramidal tract function in MS.