Evidence map›Paper›PMID 42749741›Full record

ArticleNPJ Parkinson's disease2026

Inconsistent subthalamic local field potential beta activity amid in- and antiphasic neuronal bursts.

Maximilian Scherer, Nina Wiedemann, Kai Bötzel, Matthias Löhle, Thomas Kriesen, Daniel Cantré, Jan Hinnerk Mehrkens, René Reese, Thomas Koeglsperger

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Adaptive Deep Brain Stimulation for Parkinson's Disease: Navigating the Roadblocks to Clinical Implementation.Movement disorders : official journal of the Movement Disorder Society · 2026
    Review
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

9 authors.

Maximilian SchererDepartment of Neurology, LMU University Hospital, LMU Munich, Munich, Germany. Maximilian.Scherer@med.uni-muenchen.de.
Nina WiedemannDepartment of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Kai BötzelDepartment of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.
Matthias LöhleDepartment of Neurology, Rostock University Medical Center, Rostock, Germany.
Thomas KriesenDepartment of Neurosurgery, Rostock University Medical Center, Rostock, Germany.
Daniel CantréInstitute and Policlinic of Radiology, Pediatric Radiology and Neuroradiology, Rostock University Medical Center, Rostock, Germany.
Jan Hinnerk MehrkensDepartment of Neurosurgery, LMU University Hospital, LMU Munich, Munich, Germany.
René Reese *Department of Neurology, Rostock University Medical Center, Rostock, Germany.
Thomas Koeglsperger *Department of Neurology, LMU University Hospital, LMU Munich, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Elevated subthalamic (STN) beta (12-32 Hz) local field potentials (LFP) are a hallmark of Parkinson's disease and closely tied to synchronized spiking. The biomarker guides deep brain stimulation (DBS) lead implantation and is under investigation to inform DBS programming and adaptive DBS, yet its prevalence has not been independently assessed. This study assesses the biomarkers prevalence and investigating its relationship to synchronized beta-bursting neurons. STN LFPs and spiking activity of n = 156 patients with Parkinson's disease from seven DBS centers recorded via microelectrodes were examined and spectral LFP peaks classified. The distribution of phase angles between beta LFP and beta-bursting neurons was explored. Beta LFPs were bilaterally expressed in 47.25% of patients (65.59% of hemispheres). LFP-synchronized neuronal spiking clustered in two peaks, 182.84° phase shifted. This applied on the group level and for individual patients. Beta-LFP-informed approaches mandate reliable biomarker expression, a requirement not met by 52.75% of patients. This is particularly troublesome for intraoperative guidance wherein the cause of biomarker absence, including DBS lead misplacement or a balanced ratio of phasic and antiphasic spiking neurons, cannot be determined. While STN-LFP beta remains a valuable biomarker, multiple biomarkers should be evaluated simultaneously to increase robustness.

Identifiers

PMID42749741
PMCPMC13582961

What Socratic holds

Textmetadata
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 Socratic graph.