Evidence map›Paper›PMID 32889400›Full record

ArticleNeuroImage. Clinical2020

Identifying controllable cortical neural markers with machine learning for adaptive deep brain stimulation in Parkinson's disease.

Sebastián Castaño-Candamil, Tobias Piroth, Peter Reinacher, Bastian Sajonz, Volker A Coenen, Michael Tangermann

Open access · goldAbstract read
In one paragraph

Article in NeuroImage. Clinical, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 15% 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

13 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Neuroscientific therapies for subjective tinnitus.Journal of Zhejiang University. Science. B · 2026
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. Machine Learning in Spinal Cord Stimulation for Chronic Pain.Operative neurosurgery (Hagerstown, Md.) · 2023
    Article
  8. Review
  9. AnFrontiers in neuroscience · 2023
    Article
  10. Article
  11. Review
  12. Review
  13. Article
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 2 countries.

Sebastián Castaño-CandamilBrain State Decoding Lab (BrainLinks-BrainTools), Dept. of Computer Science at the University of Freiburg, Germany. Electronic address: sebastian.castano@blbt.uni-freiburg.de.
Tobias PirothKantonsspital Aarau, with the Faculty of Medicine at the University of Freiburg, and with the Dept. of Neurology and Neurophysiology at the University Medical Center, Freiburg, Germany.
Peter ReinacherFaculty of Medicine at the University of Freiburg, and with the Dept of Stereotactic and Functional Neurosurgery at the University Medical Center, Freiburg, Germany.
Bastian SajonzFaculty of Medicine at the University of Freiburg, and with the Dept of Stereotactic and Functional Neurosurgery at the University Medical Center, Freiburg, Germany.
Volker A CoenenFaculty of Medicine at the University of Freiburg, and with the Dept of Stereotactic and Functional Neurosurgery at the University Medical Center, Freiburg, Germany.
Michael TangermannBrain State Decoding Lab (BrainLinks-BrainTools) and Autonomous Intelligent Systems, Dept. of Computer Science at the University of Freiburg, Germany; Artificial Cognitive Systems Lab, Artificial Intelligence Dept., Donders Institute for Brain, Cognition and Behaviour, Faculty of Social Sciences, Radboud University, Nijmegen, The Netherlands. Electronic address: michael.tangermann@blbt.uni-freiburg.de.
University of Freiburg · DEBrain (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The identification of oscillatory neural markers of Parkinson's disease (PD) can contribute not only to the understanding of functional mechanisms of the disorder, but may also serve in adaptive deep brain stimulation (DBS) systems. These systems seek online adaptation of stimulation parameters in closed-loop as a function of neural markers, aiming at improving treatment's efficacy and reducing side effects. Typically, the identification of PD neural markers is based on group-level studies. Due to the heterogeneity of symptoms across patients, however, such group-level neural markers, like the beta band power of the subthalamic nucleus, are not present in every patient or not informative about every patient's motor state. Instead, individual neural markers may be preferable for providing a personalized solution for the adaptation of stimulation parameters. Fortunately, data-driven bottom-up approaches based on machine learning may be utilized. These approaches have been developed and applied successfully in the field of brain-computer interfaces with the goal of providing individuals with means of communication and control. In our contribution, we present results obtained with a novel supervised data-driven identification of neural markers of hand motor performance based on a supervised machine learning model. Data of 16 experimental sessions obtained from seven PD patients undergoing DBS therapy show that the supervised patient-specific neural markers provide improved decoding accuracy of hand motor performance, compared to group-level neural markers reported in the literature. We observed that the individual markers are sensitive to DBS therapy and thus, may represent controllable variables in an adaptive DBS system.

Indexed as

Deep Brain StimulationMachine LearningParkinson DiseaseSubthalamic NucleusHandHumansAdaptive deep brain stimulationBrain-computer interfaceDeep brain stimulationMachine learningNeural marker

Identifiers

PMID32889400
PMCPMC7479445
OpenAlexW3048522827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.