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a Department of
Clinical Neurology CHU Bordeaux, France, b Department of Clinical Neurophysiology
CHU Bordeaux, France
Correspondence to: Dr A Lagueny, Service de Neurologie, Hopital du Haut-Leveque, USN, Avenue de Magellan, 33604 Pessac, France. Telephone 0033 556 420; fax 0033 556 815.
Received 23 September 1997 and in revised form 25 November 1997;
Accepted 19 February 1998
OBJECTIVE
To study the
process of denervation-reinnervation in multifocal motor neuropathy
with persistent conduction blocks in clinically affected and unaffected muscles.
METHOD
Volitional
single fibre electromyography (SFEMG) was performed in the extensor
digitorum communis (EDC) of seven patients. The jitter, the fibre
density, and the mean interpotential interval were determined. The
results before and after treatment with intravenous immunoglobulin
(IVIg) between the unaffected EDC and affected EDC examined during the
same SFEMG session were also compared. In addition the values of
jitter, fibre density, and mean interpotential interval were analysed
for correlation with the strength score on the MRC scale, the duration
of the neuropathy, the number of IVIg treatment periods, and the radial
nerve conduction block values.
RESULTS
Mean jitter,
percentage of jitters>60 µs, and impulse blocking percentage, were
higher than normal in both the affected EDCs and to a lesser degree in
unaffected EDCs. Jitter decreased significantly after IVIg and
correlated only with the MRC score. Fibre density and mean
interpotential interval were higher than normal equally in the affected
EDC and unaffected EDCs, but no correlation was found with strength,
duration of the neuropathy, number of treatment periods, and conduction
block values.
CONCLUSION
The major
finding is the presence of SFEMG abnormalities in clinically unaffected
EDCs. This shows a process of denervation-reinnervation even in the
absence of clinical symptoms, probably more frequent than commonly
supposed in this neuropathy. The rapid clinical improvement after IVIg
infusions could be due to remyelination after demyelination and to an
interference of IVIg with the blocking effect of antibodies on the
Na+ channels at the motor nerve endings.
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