%0 Journal Article
%T Multicentre assessment of motor and sensory evoked potentials in multiple sclerosis: reliability and implications for clinical trials
%A Christian Schindler
%A Fran£¿ois Jacques
%A Habib Bousleiman
%A Letizia Leocani
%A Martin Hardmeier
%A Peter Fuhr
%A Philipp Albrecht
%J Multiple Sclerosis Journal
%@ 2055-2173
%D 2019
%R 10.1177/2055217319844796
%X Motor and sensory evoked potentials (EP) are potential candidate biomarkers for clinical trials in multiple sclerosis. To determine test -retest reliability of motor EP (MEP) and sensory EP (SEP) and associated EP-scores in patients with multiple sclerosis. In three centres, 16 relapsing and five progressive multiple sclerosis patients had MEPs and SEPs 1¨C29 days apart. Five neurophysiologists independently marked latencies by central reading. By variance component analysis, we estimated the critical difference (absolute reliability) for cross-sectional group comparison, comparison of longitudinal group changes, within-subject minimal detectable change and defined within-subject improvement. Cortical SEP responses and cortico-muscular MEP latencies were more reliable than central conduction times. For comparison of 20 subjects per arm, cross-sectional group difference ranged from 0.7 to 3.9 ms and 1.1 to 1.7, group difference in longitudinal changes from 0.4 to 1.8 ms and 0.36 to 0.62, within-subject minimal detectable change from 1.2 to 5.8 ms and 1.2 to 2.0, within-subject improvement from 0.8 to 3.8ms and 0.8 to 1.3, for single EP modalities and EP scores, respectively. Multicentre EP assessment with central EP reading is feasible and reliable. The critical difference is reasonably low to detect significant group changes and to define responders. The results support the concept of using EP and EP-scores as candidate response biomarkers for quantification of disease progression and for studying remyelination in multiple sclerosis
%K Motor evoked potentials
%K sensory evoked potentials
%K biomarker
%K response biomarker
%K progressive MS
%K remyelination
%K test¨Cretest reliability
%K mean detectable change
%U https://journals.sagepub.com/doi/full/10.1177/2055217319844796