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Published on: May 31, 2016
Subthalamic nucleus stimulation and levodopa-resistant postural instability in Parkinson's disease
Jasper E Visser1, John H J Allum, Mark G Carpenter
1Dept. of Neurology (HP 935), Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Subthalamic nucleus stimulation did not improve levodopa-resistant balance issues in Parkinson's disease patients. Pre-existing axial motor symptoms correlated with worse outcomes, suggesting STN stimulation is not effective for this specific patient group.
Area of Science:
- Neurology
- Neurosurgery
- Movement Disorders
Background:
- Parkinson's disease (PD) often involves levodopa-resistant postural instability.
- Subthalamic nucleus (STN) deep brain stimulation (DBS) is a treatment for PD motor symptoms.
- The efficacy of STN DBS for levodopa-resistant balance impairment remains unclear.
Purpose of the Study:
- To investigate the effect of bilateral STN stimulation on levodopa-resistant postural instability in Parkinson's disease patients.
- To assess whether STN stimulation improves quantitative measures of balance control.
Main Methods:
- 14 Parkinson's disease patients and 18 controls underwent quantitative posturography.
- Patients were tested with STN stimulators ON and OFF after levodopa administration.
- Backward directed perturbations were used to assess instability.
Main Results:
- Parkinson's disease patients (stimulators OFF) showed greater instability than controls during backward perturbations.
- STN stimulation did not significantly improve overall postural instability in the patient group.
- A significant inter-individual variability in response to STN stimulation was observed.
- Pre-operative levodopa-resistant axial motor symptoms correlated with a negative treatment effect.
Conclusions:
- Bilateral STN stimulation does not alleviate levodopa-resistant postural instability in Parkinson's disease.
- Pre-existing severe axial motor symptoms may predict a poor response to STN DBS for balance.
- Further research is needed to identify predictors of treatment response in PD.
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