AMPLITUDE CHANGES OF TIBIAL NERVE CORTICAL SOMATOSENSORY-EVOKED POTENTIALS WHEN THE IPSILATERAL OR CONTRALATERAL EAR IS USED AS REFERENCE

Citation
M. Tinazzi et al., AMPLITUDE CHANGES OF TIBIAL NERVE CORTICAL SOMATOSENSORY-EVOKED POTENTIALS WHEN THE IPSILATERAL OR CONTRALATERAL EAR IS USED AS REFERENCE, Journal of clinical neurophysiology, 14(3), 1997, pp. 217-225
Citations number
32
Categorie Soggetti
Neurosciences,"Clinical Neurology
ISSN journal
07360258
Volume
14
Issue
3
Year of publication
1997
Pages
217 - 225
Database
ISI
SICI code
0736-0258(1997)14:3<217:ACOTNC>2.0.ZU;2-Z
Abstract
We performed topographical mapping of somatosensory evoked potentials (SEPs) to the posterior tibial nerve using earlobe references both ips ilateral and contralateral to the stimulation side. The voltage of the frontal contralateral N37 and P50 components was enhanced, while the voltage of the parietal ipsilateral P37 and N50 components was reduced when the contralateral earlobe was substituted by the ipsilateral ear lobe reference. Maps of the same data documented concomitant changes i n negative and positive potential fields, showing an expansion of the pre-Rolandic N37 toward the centrotemporal contralateral regions, and a tendency of the parietal ipsilateral P37, N50 components to be more focally distributed at the vertex. SEPs recorded at each earlobe (Cv6 reference) provided an explanation of these results: The contralateral earlobe detected a negative potential corresponding to the N37 potent ial recorded over the scalp, followed by a P50 potential that attenuat ed the contralateral responses and enhanced the ipsilateral ones. The ipsilateral earlobe had no significant effects on scalp SEPs, since it detected only a large N33 negativity. Current source density (CSD) ma ps were, of course, not influenced by the ear used as reference. Our r esults suggest that the ipsilateral ear reference is better than the c ontralateral one for recording ''genuine'' cortical SEPs. Therefore, i t can be recommended in the clinical domain for mapping studies of low er-limb cortical SEPs.