Evidence map›Paper›PMID 27151601›Full record

ArticleBrain stimulation

Coordinated Reset Deep Brain Stimulation of Subthalamic Nucleus Produces Long-Lasting, Dose-Dependent Motor Improvements in the 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Non-Human Primate Model of Parkinsonism.

Jing Wang, Shane Nebeck, Abirami Muralidharan, Matthew D Johnson, Jerrold L Vitek, Kenneth B Baker

Open access · greenAbstract read
In one paragraph

Article in Brain stimulation. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
9.0field-weighted citation impact, top 2% of its field
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

74 citing papers in PubMed, 125 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Closing the loop in psychiatric deep brain stimulation: physiology, psychometrics, and plasticity.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Review
  12. Review
  13. Article
  14. Review
  15. Advances in Deep Brain Stimulation: From Mechanisms to Applications.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Review
  16. Article
  17. Article
  18. Journal of neural engineering · 2023
    Article
  19. Article
  20. Review

14 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Jing WangDepartment of Neurology, University of Minnesota, Minneapolis, MN 55455, USA.
Shane NebeckDepartment of Neurology, University of Minnesota, Minneapolis, MN 55455, USA.
Abirami MuralidharanDepartment of Neurology, University of Minnesota, Minneapolis, MN 55455, USA.
Matthew D JohnsonDepartment of Biomedical Engineering, University of Minnesota, Minneapolis, MN 55455, USA.
Jerrold L VitekDepartment of Neurology, University of Minnesota, Minneapolis, MN 55455, USA.
Kenneth B BakerDepartment of Neuroscience, Cleveland Clinic Lerner College of Medicine, Cleveland, OH 44195, USA. Electronic address: bakerk6@ccf.org.
University of Minnesota · USCleveland Clinic Lerner College of Medicine · US

Funding

Chronic physiologic and behavior changes induced by novel STN DBS patterns for PDR01NS092730 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI BAKER, KENNETH B · 2016 to 2020
$2.7M
NINDS NIH HHS R01 NS092730
6 · The paper itself

Abstract

backgroundNovel deep brain stimulation (DBS) paradigms are being explored in an effort to further optimize therapeutic outcome for patients with Parkinson's disease (PD). One approach, termed 'Coordinated Reset' (CR) DBS, was developed to target pathological oscillatory network activity. with desynchronizing effects and associated therapeutic benefit hypothesized to endure beyond cessation of stimulus delivery.

objectiveTo characterize the acute and carry-over effects of low-intensity CR DBS versus traditional DBS (tDBS) in the region of the subthalamic nucleus (STN).

methodsA within-subject, block treatment design involving the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) non-human primate model of parkinsonism was used. Each treatment block consisted of five days of daily DBS delivery followed by a one week minimum post-treatment observation window. Motor behavior was quantified using a modified rating scale for both animals combined with an objective, upper-extremity reach task in one animal.

resultsBoth animals demonstrated significant motor improvements during acute tDBS; however, within-session and post-treatment carry-over was limited. Acute motor improvements were also observed in response to low-intensity CR DBS; however, both within- and between-session therapeutic carry-over enhanced progressively following each daily treatment. Moreover, in contrast to tDBS, five consecutive days of CR DBS treatment yielded carry-over benefits that persisted for up to two weeks without additional intervention. Notably, the magnitude and time-course of CR DBS' effects on each animal varied with daily dose-duration, pointing to possible interaction effects involving baseline parkinsonian severity.

conclusionOur results support the therapeutic promise of CR DBS for PD, including its potential to induce carryover while reducing both side effect risk and hardware power consumption.

Indexed as

Subthalamic NucleusAnimalsBehavior, AnimalDeep Brain StimulationDisease Models, AnimalFemaleMacaca mulattaMPTP PoisoningParkinson Disease, SecondaryCoordinated resetDeep brain stimulationMPTPNeuromodulationRhesus macaque

Identifiers

PMID27151601
PMCPMC10226766
OpenAlexW2309909559

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.