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Published on: April 12, 2024
The interaction between metaplastic neuromodulation and fatigue in multiple sclerosis
Claire Xian1, Chiara Barbi2, Mitchell R Goldsworthy3
1Discipline of Physiology, School of Biomedicine, The University of Adelaide, S433, Helen Mayo South, Frome Rd, 5005, South Australia, Australia.
Cathodal transcranial direct current stimulation (tDCS) priming did not enhance anodal tDCS effects on corticospinal excitability in people with Multiple Sclerosis (MS). Fatigue levels were not significantly altered by tDCS in MS patients.
Area of Science:
- Neuroscience
- Rehabilitation Medicine
- Neurology
Background:
- Neuromuscular fatigue significantly impacts quality of life in Multiple Sclerosis (MS).
- Current treatments for MS-related fatigue have limited effectiveness.
- Transcranial direct current stimulation (tDCS) shows potential for managing fatigue by modulating corticospinal excitability.
Purpose of the Study:
- To investigate the effects of cathodal tDCS (ctDCS) priming on anodal tDCS (atDCS)-induced corticospinal excitability.
- To explore tDCS-mediated modulation of neuromuscular fatigue in people with MS (pwMS).
- To assess potential metaplasticity changes in pwMS using a primed tDCS protocol.
Main Methods:
- 15 pwMS and 15 healthy controls participated.
- Participants underwent fatiguing exercise with either ctDCS or sham (stDCS) primed atDCS to the motor cortex.
- Changes in contraction force and motor evoked potential (MEP) amplitude were measured over time.
Main Results:
- Primed atDCS induced MEP elevation in healthy controls but not in pwMS, suggesting impaired metaplasticity in pwMS.
- No significant change in the magnitude of fatigue was observed with tDCS in either group.
- These findings indicate that fatigue development in MS may not be solely dependent on corticospinal excitability changes.
Conclusions:
- The study highlights differences in tDCS effects between pwMS and healthy controls.
- Impaired metaplasticity may be a factor in tDCS response in pwMS.
- Findings contribute to understanding tDCS applications and MS pathophysiology.
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