Scientific article
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English

Prognostic biomarkers in primary progressive multiple sclerosis : Validating and scrutinizing multimodal evoked potentials

Published inClinical neurophysiology, vol. 137, p. 152-158
Publication date2022-05
First online date2022-03-07
Abstract

Objective: To validate the prognostic value of multimodal evoked potentials (mmEP) in primary progressive multiple sclerosis (PPMS) and to determine the most predictive EP-modalities.

Methods: Thirty-nine patients with PPMS (expanded disability status scale (EDSS): 2.0-6.5; mean clinical follow-up: 2.8 years) had visual (VEP), upper and lower limb somatosensory (SEP) and motor EP (MEP) at baseline. Quantitative EP-scores for single (qVEP, qSEP, qMEP) and combined modalities were correlated to EDSS and compared to previously published data of 21 PPMS patients. Predictors of EDSS-change were analyzed in pooled data by linear regression.

Results: Samples were comparable. Except qVEP, all EP-scores were correlated to EDSS at baseline (Rho: 0.45-0.69; p < 0.01) and follow-up (Rho: 0.59-0.80; p < 0.001). Combined EP-modalities significantly predicted EDSS-change (R2 adj : 0.24), while EDSS and age did not. Tibial qSEP (R2 adj : 0.22) and qMEP (R2 adj : 0.26) were the best single modality predictors, outperformed by their combination (R2 adj : 0.32).

Conclusions: Quantitative EP-scores predict up to 32% of EDSS-change over three years. Modalities representing motor and long tract function carry the main prognostic information.

Significance: Replication of previous results corroborates the use of mmEP as a prognostic biomarker candidate in PPMS.

Keywords
  • Biomarker
  • Clinical trial design
  • Evoked Potentials
  • Prognosis
  • Progressive Multiple Sclerosis
  • Quantitative EP Score
Funding
  • Swiss Multiple Sclerosis Society
Citation (ISO format)
HARDMEIER, M et al. Prognostic biomarkers in primary progressive multiple sclerosis : Validating and scrutinizing multimodal evoked potentials. In: Clinical neurophysiology, 2022, vol. 137, p. 152–158. doi: 10.1016/j.clinph.2022.02.019
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Article (Published version)
Identifiers
Journal ISSN1388-2457
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Creation09/02/2025 16:26:21
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