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The evolution of motor cortical dysfunction in amyotrophic lateral sclerosis.
- Source :
-
Clinical Neurophysiology . Jun2017, Vol. 128 Issue 6, p1075-1082. 8p. - Publication Year :
- 2017
-
Abstract
- Objective The present study aimed to investigate alterations in cortical function in amyotrophic lateral sclerosis (ALS) related to disease progression. Methods In total, clinical assessments were evaluated in 189 ALS patients, combined with assessment of cortical function utilising threshold tracking transcranial magnetic stimulation. Results were compared with disease stage. Disease stage was defined in three ways: (1) as a proportion of disease duration in deceased patients; (2) from the time of ALS onset; and (3) using the ALS rating scale-revised (ALSFRS-R). Results Prospective studies in ALS patients demonstrated decreased neurophysiological index ( p < 0.0001) and decreased compound muscle action potential (CMAP) ( p < 0.0001), combined with abnormalities of central function including prolonged central motor conduction time (CMCT) ( p < 0.05), increased motor evoked potential/CMAP amplitude ratio ( p < 0.0001) and decreased short interval intracortical inhibition (SICI) ( p < 0.001). SICI at 3 ms ( p < 0.05, β = −0.21) and averaged SICI ( p < 0.05, β = −0.21) decreased with disease progression, measured using proportion of disease duration. Alternatively, using time from disease onset, CMCT prolonged with disease progression ( p < 0.01, β = 0.25), while ALSFRS-R decline correlated with decreased SICI at 3 ms ( p < 0.01, β = 0.20). Conclusions Clinical measures combined with assessment of cortical function established that SICI decreased with disease progression. Significance These findings may suggest dysfunction of inhibitory interneurons with disease progression. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 13882457
- Volume :
- 128
- Issue :
- 6
- Database :
- Academic Search Index
- Journal :
- Clinical Neurophysiology
- Publication Type :
- Academic Journal
- Accession number :
- 123015123
- Full Text :
- https://doi.org/10.1016/j.clinph.2017.03.004