Pilot Study of Acute Behavioral Effects of Pallidal Burst Stimulation in Parkinson's Disease.

Parkinson's disease burst stimulation deep brain stimulation

Journal

Movement disorders : official journal of the Movement Disorder Society
ISSN: 1531-8257
Titre abrégé: Mov Disord
Pays: United States
ID NLM: 8610688

Informations de publication

Date de publication:
15 Jul 2024
Historique:
revised: 30 05 2024
received: 31 01 2024
accepted: 26 06 2024
medline: 15 7 2024
pubmed: 15 7 2024
entrez: 15 7 2024
Statut: aheadofprint

Résumé

Burst-patterned pallidal deep brain stimulation (DBS) in an animal model of Parkinson's disease (PD) yields significantly prolonged therapeutic benefit compared to conventional continuous DBS, but its value in patients remains unclear. The aims were to evaluate the safety and tolerability of acute (<2 hours) burst DBS in PD patients and to evaluate preliminary clinical effectiveness relative to conventional DBS. Six PD patients were studied with DBS OFF, conventional DBS, and burst DBS. Unified Parkinson's Disease Rating Scale III (UPDRS-III) and proactive inhibition (using stop-signal task) were evaluated for each condition. Burst and conventional DBS were equally tolerated without significant adverse events. Both stimulation patterns provided equivalent significant UPDRS-III reduction and increased proactive inhibition relative to DBS OFF. This pilot study supports the safety and tolerability of burst DBS, with acute effects similar to conventional DBS. Further larger-scale studies are warranted given the potential benefits of burst DBS due to decreased total energy delivery. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Sections du résumé

BACKGROUND BACKGROUND
Burst-patterned pallidal deep brain stimulation (DBS) in an animal model of Parkinson's disease (PD) yields significantly prolonged therapeutic benefit compared to conventional continuous DBS, but its value in patients remains unclear.
OBJECTIVES OBJECTIVE
The aims were to evaluate the safety and tolerability of acute (<2 hours) burst DBS in PD patients and to evaluate preliminary clinical effectiveness relative to conventional DBS.
METHODS METHODS
Six PD patients were studied with DBS OFF, conventional DBS, and burst DBS. Unified Parkinson's Disease Rating Scale III (UPDRS-III) and proactive inhibition (using stop-signal task) were evaluated for each condition.
RESULTS RESULTS
Burst and conventional DBS were equally tolerated without significant adverse events. Both stimulation patterns provided equivalent significant UPDRS-III reduction and increased proactive inhibition relative to DBS OFF.
CONCLUSIONS CONCLUSIONS
This pilot study supports the safety and tolerability of burst DBS, with acute effects similar to conventional DBS. Further larger-scale studies are warranted given the potential benefits of burst DBS due to decreased total energy delivery. © 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Identifiants

pubmed: 39007445
doi: 10.1002/mds.29928
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NINDS NIH HHS
ID : F31NS127483
Pays : United States
Organisme : NINDS NIH HHS
ID : R01NS104835
Pays : United States
Organisme : NINDS NIH HHS
ID : R35NS132213
Pays : United States
Organisme : The Michael J. Fox Foundation

Informations de copyright

© 2024 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Références

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Auteurs

Saar Kariv (S)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Jeong Woo Choi (JW)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Koorosh Mirpour (K)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Ann M Gordon (AM)

Department of Neurology, UT Southwestern Medical Center, Dallas, Texas, USA.

Amirreza Alijanpourotaghsara (A)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Mohsen Benam (M)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Ruwayd Abdalla (R)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Sahil Chilukuri (S)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Jianwen W Gu (JW)

Boston Scientific Neuromodulation, Valencia, California, USA.

Hemant Bokil (H)

Boston Scientific Neuromodulation, Valencia, California, USA.

Shruti Nanivadekar (S)

Neuroscience Institute, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
School of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.

Aryn H Gittis (AH)

Neuroscience Institute, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania, USA.

Nader Pouratian (N)

Department of Neurological Surgery, UT Southwestern Medical Center, Dallas, Texas, USA.

Classifications MeSH