The characteristics of pallidal low-frequency and beta bursts could help implementing adaptive brain stimulation in the parkinsonian and dystonic internal globus pallidus.


Journal

Neurobiology of disease
ISSN: 1095-953X
Titre abrégé: Neurobiol Dis
Pays: United States
ID NLM: 9500169

Informations de publication

Date de publication:
01 2019
Historique:
received: 03 08 2018
revised: 08 09 2018
accepted: 13 09 2018
pubmed: 19 9 2018
medline: 22 11 2019
entrez: 19 9 2018
Statut: ppublish

Résumé

Adaptive deep brain stimulation (aDBS) has been applied in Parkinson's disease (PD), based on the presence of brief high-amplitude beta (13-35 Hz) oscillation bursts in the subthalamic nucleus (STN), which correlate with symptom severity. Analogously, average low-frequency (LF) oscillatory power (4-12 Hz) in the internal globus pallidus (GPi) correlates with dystonic symptoms and might be a suitable physiomarker for aDBS in dystonia. Characterization of pallidal bursts could facilitate the implementation of aDBS in the GPi of PD and dystonia patients. We aimed to describe the bursting behaviour of LF and beta oscillations in a cohort of five GPi-DBS PD patients and compare their amplitude and length with those of a cohort of seven GPi-DBS dystonia, and six STN-DBS PD patients (n electrodes = 34). Furthermore, we used the information obtained to set up aDBS and test it in the GPi of both a dystonia and a PD patient (n = 2), using either LF (dystonia) or beta oscillations (PD) as feedback signals. LF and beta oscillations in the dystonic and parkinsonian GPi occur as phasic, short-lived bursts, similarly to the parkinsonian STN. The amplitude profile of such bursts, however, differed significantly. Dystonia showed higher LF burst amplitudes, while PD presented higher beta burst amplitudes. Burst characteristics in the parkinsonian GPi and STN were similar. Furthermore, aDBS applied in the GPi was feasible and well tolerated in both diseases. Pallidal LF and beta burst amplitudes have different characteristics in PD and dystonia. The presence of increased burst amplitudes could be employed as feedback for GPi-aDBS.

Identifiants

pubmed: 30227227
pii: S0969-9961(18)30391-7
doi: 10.1016/j.nbd.2018.09.014
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

47-57

Informations de copyright

Copyright © 2018 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

Dan Piña-Fuentes (D)

Department of Neurosurgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Department of Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Jonathan C van Zijl (JC)

Department of Neurosurgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Department of Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

J Marc C van Dijk (JMC)

Department of Neurosurgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Simon Little (S)

Sobell Department of Motor Neuroscience and Movement Disorders, Institute of Neurology, Queen Square, London, UK.

Gerd Tinkhauser (G)

Medical Research Council Brain Network Dynamics Unit and Nuffield Department of Clinical Neurosciences, University of Oxford, United Kingdom; Department of Neurology, Bern University Hospital and University of Bern, Bern, Switzerland.

D L Marinus Oterdoom (DLM)

Department of Neurosurgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Marina A J Tijssen (MAJ)

Department of Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Martijn Beudel (M)

Department of Neurology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands; Department of Neurology, Isala Clinics, Zwolle, The Netherlands. Electronic address: M.Beudel@umcg.nl.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH