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Published on: October 13, 2016
Mirror movements in amyotrophic lateral sclerosis.
Mathias Wittstock1, Steffanie Meister, Uwe Walter
1Department of Neurology, University of Rostock, Rostock, Germany. matthias.wittstock@med.uni-rostock.de
Mirror movements (MM) in amyotrophic lateral sclerosis (ALS) patients indicate impaired transcallosal inhibition (TI). This suggests MM may serve as an early diagnostic biomarker for ALS, reflecting motor system degeneration.
Area of Science:
- Neuroscience
- Neurology
- Motor Neuron Diseases
Background:
- Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease affecting motor neurons.
- Mirror movements (MM) have been observed in ALS and linked to disrupted transcallosal inhibition (TI).
Purpose of the Study:
- To investigate the occurrence of MM in ALS patients.
- To assess the relationship between MM and TI.
- To explore the potential of MM as an early diagnostic biomarker for ALS.
Main Methods:
- Clinical assessment of MM in 26 ALS patients.
- Transcranial magnetic stimulation (TMS) to evaluate TI using the ipsilateral silent period.
Main Results:
- Mirror movements were present in 39% of ALS patients.
- A significant negative correlation was found between MM occurrence and the ALS Functional Rating Scale-Revised (ALSFRS-R).
- All patients with MM exhibited pathological TI in at least one hemisphere.
Conclusions:
- The presence of MM in ALS patients is associated with impaired transcallosal inhibition.
- MM may reflect the involvement of transcallosally projecting neurons in the ALS disease process.
- Mirror movements could represent an early diagnostic biomarker for amyotrophic lateral sclerosis.
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