Visual event-related potential changes in two subtypes of multiple system atrophy, MSA-C and MSA-P.

Published

Journal Article

We investigated the visual event-related potentials (ERPs) in two subtypes of multisystem atrophy (MSA) in 15 MSA-C patients, 12 MSA-P patients, and 21 normal control (NC) subjects. We used a visual oddball task to elicit ERPs. No significant changes were seen in N1 or N2 latency, in either MSA-C or MSA-P, compared with the NC group. An early stage of visual information process related to N1 and a visual discrimination process related to N2 might be preserved in both MSA-C and MSA-P. The P3a peak was more frequently undetectable in MSA than in the NC group. Significant P3a amplitude reduction in both MSA-C and MSA-P suggests impairment of the automatic cognitive processing in both MSA-C and MSA-P. Significant difference was found in P3b latency and P3b amplitude only in MSA-C, compared with the NC group. The result suggests the impairment of the controlled cognitive processing after the visual discrimination process in the MSA-C group. We further investigated the correlation between visual ERP changes and magnetic resonance imaging (MRI) data. Quantitative MRI measurements showed reduced size of the pons, cerebellum, perisylvian cerebral area, and deep cerebral gray matter in both MSA-C and MSA-P, and of the corpus callosum only in MSA-P, as compared to NC group. In both MSA-C and MSA-P, P3b latency was significantly correlated with the size on MRI of the pons and the cerebellum. P3b latency in the whole MSA group was also significantly correlated with the size of the pons and the cerebellum. These results indicate that P3b latency changes in parallel with the volume of the pons and the cerebellum in both MSA-C and MSA-P.

Full Text

Duke Authors

Cited Authors

  • Kamitani, T; Kuroiwa, Y; Wang, L; Li, M; Suzuki, Y; Takahashi, T; Ikegami, T; Matsubara, S

Published Date

  • August 2002

Published In

Volume / Issue

  • 249 / 8

Start / End Page

  • 975 - 982

PubMed ID

  • 12195440

Pubmed Central ID

  • 12195440

International Standard Serial Number (ISSN)

  • 0340-5354

Digital Object Identifier (DOI)

  • 10.1007/s00415-002-0764-7

Language

  • eng

Conference Location

  • Germany