Deep brain stimulation of the anterior nucleus of the thalamus increases slow wave activity in non‐rapid eye movement sleep

Author:

Buenzli Jana C.12,Werth Esther2,Baumann Christian R.23,Belvedere Anina2,Renzel Roland4,Stieglitz Lennart H.5,Imbach Lukas L.234ORCID

Affiliation:

1. Neural Control of Movement Lab, Department of Health Sciences and Technology ETH Zurich Zurich Switzerland

2. Department of Neurology University Hospital and University of Zurich Zurich Switzerland

3. Neuroscience Center Zurich University of Zurich and ETH Zurich Zurich Switzerland

4. Swiss Epilepsy Center Klinik Lengg Zurich Switzerland

5. Department of Neurosurgery University Hospital and University of Zurich Zurich Switzerland

Abstract

AbstractObjectivePrevious studies suggest that intermittent deep brain stimulation (DBS) of the anterior nucleus of the thalamus (ANT) affects physiological sleep architecture. Here, we investigated the impact of continuous ANT DBS on sleep in epilepsy patients in a multicenter crossover study in 10 patients.MethodsWe assessed sleep stage distribution, delta power, delta energy, and total sleep time in standardized 10/20 polysomnographic investigations before and 12 months after DBS lead implantation.ResultsIn contrast to previous studies, we found no disruption of sleep architecture or alterations of sleep stage distribution under active ANT DBS (p = .76). On the contrary, we observed more consolidated and deeper slow wave sleep (SWS) under continuous high‐frequency DBS as compared to baseline sleep prior to DBS lead implantation. In particular, biomarkers of deep sleep (delta power and delta energy) showed a significant increase post‐DBS as compared to baseline (36.67 ± 13.68 μV2 /Hz and 799.86 ± 407.56 μV2*s, p < .001). Furthermore, the observed increase in delta power was related to the location of the active stimulation contact within the ANT; we found higher delta power and higher delta energy in patients with active stimulation in more superior contacts as compared to inferior ANT stimulation. We also observed significantly fewer nocturnal electroencephalographic discharges in DBS ON condition. In conclusion, our findings suggest that continuous ANT DBS in the most cranial part of the target region leads to more consolidated SWS.SignificanceFrom a clinical perspective, these findings suggest that patients with sleep disruption under cyclic ANT DBS could benefit from an adaptation of stimulation parameters to more superior contacts and continuous mode stimulation.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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