Evidence map›Paper›PMID 30418266›Full record

ArticleJournal of clinical neurophysiology : official publication of the American Electroencephalographic Society2019

Analysis of Movement-Related Beta Oscillations in the Off-Medication State During Subthalamic Nucleus Deep Brain Stimulation Surgery.

Ryan B Kochanski, Jay Shils, Leo Verhagen Metman, Gian Pal, Sepehr Sani

Abstract read
In one paragraph

Article in Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ryan B KochanskiDepartments of Neurosurgery and.
Jay ShilsAnesthesiology, Rush University Medical Center, Chicago, Illinois, U.S.A.
Leo Verhagen MetmanSection on Movement Disorders, Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, U.S.A.
Gian PalSection on Movement Disorders, Department of Neurological Sciences, Rush University Medical Center, Chicago, Illinois, U.S.A.
Sepehr SaniDepartments of Neurosurgery and.

Funding

Parkinson disease and DBS: cognitive effects in GBA mutation carriersK23NS097625 · NINDS · RUSH UNIVERSITY MEDICAL CENTER · PI PAL, GIAN D · 2017 to 2021
$936k
NINDS NIH HHS K23 NS097625
6 · The paper itself

Abstract

purposeLocal field potential recordings from deep brain stimulation (DBS) leads provide insight into the pathophysiology of Parkinson disease (PD). We recorded local field potential activity from DBS leads within the subthalamic nucleus in patients with PD undergoing DBS surgery to identify reproducible pathophysiological signatures of the disease.

methodsLocal field potentials were recorded in 11 hemispheres from patients with PD undergoing subthalamic nucleus-DBS. Bipolar recordings were performed off medication for 2 minutes at rest and another 2 minutes with continuous repetitive opening-closing of the contralateral hand. Spectral analysis and bicoherence were performed and compared between the two testing conditions.

resultsIn all hemispheres, predominance of the beta band frequency (13-30 Hz) was observed at rest and during movement. Beta peak energy was significantly (P < 0.05) increased during movement compared with rest in 6 of 10 hemispheres. Significant beta bicoherence was observed at rest and during movement in 5 of 10 hemispheres. The most robust local field potential recordings were observed at the DBS contact(s) independently chosen for programming in 9 of the 10 hemispheres.

conclusionsIn patients with PD, beta activity that increases with repetitive movement may be a signature of the "off" medication state. These findings provide new data on beta oscillatory activity during the Parkinsonian "off" state that may help further define the local field potential signatures of PD.

Indexed as

Deep Brain StimulationAgedBeta RhythmFemaleHandHumansIntraoperative Neurophysiological MonitoringMaleMiddle AgedMovementParkinson DiseaseSignal Processing, Computer-AssistedSubthalamic Nucleus

Identifiers

PMID30418266
PMCPMC6636622

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