Limited sensitivity of somatosensory evoked potentials as disease monitoring biomarkers in hereditary spastic paraplegias

The neurophysiological progression of sensory long tract dysfunction is even slower than the progression of motor findings measured by COAs in HSP. The low sensitivity to change of SSEPs identified suggests that they should not be used as primary endpoints in future clinical trials for disease-modifying drugs.

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Publication Details

Journal
PLoS ONE
Published
2025-11-11
DOI
https://doi.org/10.1371/journal.pone.0335187
Primary Topic
Hereditary Neurological Disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Limited sensitivity of somatosensory evoked potentials as disease monitoring biomarkers in hereditary spastic paraplegias

Isabela Possebon Bevilacqua, Ana Luiza Rodrigues Louzada, Diana Maria Cubillos-Arcila, F Spengler et al.
PLoS ONE
Hereditary Neurological Disorders
article

Limited sensitivity of somatosensory evoked potentials as disease monitoring biomarkers in hereditary spastic paraplegias

Isabela Possebon Bevilacqua, Ana Luiza Rodrigues Louzada, Diana Maria Cubillos-Arcila, F Spengler, Samanta Ferraresi Brighente, Jonas Alex Morales Saute, Maria Mirian de Souza
article en

Abstract

The neurophysiological progression of sensory long tract dysfunction is even slower than the progression of motor findings measured by COAs in HSP. The low sensitivity to change of SSEPs identified suggests that they should not be used as primary endpoints in future clinical trials for disease-modifying drugs.

PLoS ONEVol. 20(11)
Universidade Federal do Rio Grande do Sul (BR), Hospital de Clínicas de Porto Alegre (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Hospital de Clínicas de Porto Alegre, Fundação Instituto de Pesquisas Econômicas
Openalex Percentile: Top 63%
Hereditary Neurological Disorders
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