TY - JOUR
T1 - Brain symmetry and topographic analysis of laterized event-related potentials
AU - Oostenveld, R
AU - Stegeman, DF
AU - Praamstra, Peter
AU - Van Oosterom, A
PY - 2003/7/1
Y1 - 2003/7/1
N2 - Objective: We investigated the influence of symmetry assumptions implicit in the derivation and the use of event-related lateralized potentials (ERLs), such as the lateralized readiness potential (LRP). We describe these assumptions and demonstrate several alternative computational methods. Methods: Using analytical methods and forward simulations, we computed the error in the ERL topography that results from deviations in symmetry between homologous brain areas. Based on analytical considerations we show that, for source analysis, the ERL derivation provides no benefits compared to a single subtraction of the two (left-lateralized and right-lateralized) conditions underlying the ERL. Results: Relative errors of 10% in the ERL topography are found if the location of an active region in one hemisphere differs by 10 mm from the symmetric location as compared to the other hemisphere A difference of 30degrees in orientation results in a relative error of the ERL of 40%. Differences in source strength between hemispheres result in an ERL error that is half the size of the relative strength difference. Conclusions: We estimate that, due to violations of the symmetry assumption underlying the ERL, errors in the ERL topography of 10-40% can be expected. Source analysis does not benefit from the ERL. In topographic mapping and source analysis, the double subtraction of the ERL should be approached with caution and the single subtraction of the ERPs of two lateralized conditions should be first analyzed whenever possible. We suggest that analyses based on the topography of the ERL should only be performed after the assumption of symmetry has been validated. (C) 2003 International Federation of Clinical Neurophysiology. Published by Elsevier Science Ireland Ltd. All rights reserved.
AB - Objective: We investigated the influence of symmetry assumptions implicit in the derivation and the use of event-related lateralized potentials (ERLs), such as the lateralized readiness potential (LRP). We describe these assumptions and demonstrate several alternative computational methods. Methods: Using analytical methods and forward simulations, we computed the error in the ERL topography that results from deviations in symmetry between homologous brain areas. Based on analytical considerations we show that, for source analysis, the ERL derivation provides no benefits compared to a single subtraction of the two (left-lateralized and right-lateralized) conditions underlying the ERL. Results: Relative errors of 10% in the ERL topography are found if the location of an active region in one hemisphere differs by 10 mm from the symmetric location as compared to the other hemisphere A difference of 30degrees in orientation results in a relative error of the ERL of 40%. Differences in source strength between hemispheres result in an ERL error that is half the size of the relative strength difference. Conclusions: We estimate that, due to violations of the symmetry assumption underlying the ERL, errors in the ERL topography of 10-40% can be expected. Source analysis does not benefit from the ERL. In topographic mapping and source analysis, the double subtraction of the ERL should be approached with caution and the single subtraction of the ERPs of two lateralized conditions should be first analyzed whenever possible. We suggest that analyses based on the topography of the ERL should only be performed after the assumption of symmetry has been validated. (C) 2003 International Federation of Clinical Neurophysiology. Published by Elsevier Science Ireland Ltd. All rights reserved.
KW - event related potential
KW - lateralization
KW - symmetry
KW - lateralized readiness potential
UR - http://www.scopus.com/inward/record.url?scp=0038204684&partnerID=8YFLogxK
U2 - 10.1016/S1388-2457(03)00059-2
DO - 10.1016/S1388-2457(03)00059-2
M3 - Article
C2 - 12842715
VL - 114
SP - 1194
EP - 1202
JO - Clinical Neurophysiology
JF - Clinical Neurophysiology
IS - 7
ER -