Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8274421 | Journal of the Neurological Sciences | 2016 | 5 Pages |
Abstract
Neuromyelitis optica spectrum disorder (NMOSD) has been differentiated from relapsing-remitting multiple sclerosis (RRMS) by clinical, laboratory, and pathological findings, including the presence of the anti-aquaporin 4 antibody. Measurement of evoked potentials (EPs) is often used for the diagnosis of RRMS, although the possibility of applying EPs to the diagnosis of NMOSD has not been investigated in detail. Eighteen patients with NMOSD and 28 patients with RRMS were included in this study. The patients' neurological symptoms and signs were examined and their EPs were recorded. Characteristic findings were absence of visual evoked potentials and absence of motor evoked potentials in the lower extremities in patients with NMOSD, and a delay in these potentials in patients with RRMS. Most patients with NMOSD did not present abnormal subclinical EPs, whereas many patients with RRMS did. None of the patients with NMOSD showed abnormalities in auditory brainstem responses. NMOSD can be differentiated from RRMS by EP data obtained in the early stages of these diseases.
Keywords
VEPAQP4-AbTMSCMCTSPMSPPMSNMOSDSEPRRMsABRMEPEDSSSomatosensory evoked potentialNeuromyelitis optica spectrum disorderMRILower extremityUpper extremityevoked potentialTranscranial magnetic stimulationMagnetic resonance imagingCentral motor conduction timeNeuromyelitis opticaExpanded Disability Status ScaleMotor evoked potentialMotor evoked potentialsprimary progressive multiple sclerosisrelapsing-remitting multiple sclerosisMultiple sclerosisVisual evoked potentialVisual evoked potentialsauditory brainstem responsesauditory brainstem response
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Authors
Keiko Ohnari, Kazumasa Okada, Toshiyuki Takahashi, Kosuke Mafune, Hiroaki Adachi,