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Globus pallidal deep brain stimulation for Tourette syndrome: Effects on cognitive function
Davide Cappon1, Mazda Beigi2, Zinovia Kefalopoulou3
1Unit of Functional Neurosurgery, Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, National Hospital for Neurology and Neurosurgery, London, UK; Berenson-Allen Center for Noninvasive Brain Stimulation, Division of Cognitive Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Bilateral deep brain stimulation of the anteromedial globus pallidus internus (GPiam-DBS) did not cause cognitive deficits in Tourette syndrome (TS) patients. Cognitive function remained stable, with some improvements noted in memory and set-shifting when GPiam-DBS was OFF.
Area of Science:
- Neuroscience
- Neurosurgery
- Psychiatry
Background:
- Tourette syndrome (TS) is a complex neurological disorder characterized by motor and vocal tics.
- Refractory TS cases often require advanced interventions when standard treatments fail.
- Deep brain stimulation (DBS) is an emerging therapy for severe, treatment-resistant TS.
Purpose of the Study:
- To evaluate the impact of bilateral deep brain stimulation of the anteromedial globus pallidus internus (GPiam-DBS) on cognitive function in patients with refractory Tourette syndrome.
- To determine if GPiam-DBS affects memory, executive function, attention, or other cognitive domains in TS patients.
- To assess potential adverse cognitive effects of GPiam-DBS in the context of tic reduction.
Main Methods:
- A double-blind randomized crossover trial involving 11 patients with refractory Tourette syndrome.
- Cognitive assessments including tests for memory, executive function, and attention were conducted at baseline and during periods of GPiam-DBS ON and OFF.
- Standardized neuropsychological tests such as the California Verbal Learning Test-II and Trail-making Test were utilized.
Main Results:
- GPiam-DBS did not result in significant global cognitive changes.
- Verbal episodic memory and set-shifting showed improvement when GPiam-DBS was OFF compared to baseline.
- No significant differences in cognitive test performance were observed between GPiam-DBS ON and OFF conditions.
Conclusions:
- GPiam-DBS does not appear to induce cognitive deficits in patients with Tourette syndrome.
- The findings support the safety of GPiam-DBS concerning cognitive function in refractory TS.
- Further research can explore the nuanced effects of GPiam-DBS on specific cognitive domains in TS.
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