Evidence map›Paper›PMID 42494087›Full record

ReviewMovement disorders clinical practice2026

Acute and Chronic Local Field Potential Recordings in Dystonia-A Systematic Review.

Jack Horan, Eoghan Donlon, Aoibheann Gill, Rosalyn Moran, Conor Fearon, Richard A Walsh, Catherine Moran

Abstract readReview
In one paragraph

Review in Movement disorders clinical practice, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Jack HoranDepartment of Neurosurgery, Beaumont Hospital, Dublin, Ireland.
Eoghan DonlonDublin Neurological Institute, Mater Misericordiae University Hospital, Dublin, Ireland.ORCID https://orcid.org/0000-0003-2962-0943
Aoibheann GillDublin Neurological Institute, Mater Misericordiae University Hospital, Dublin, Ireland.
Rosalyn MoranKing's College London, London, UK.
Conor FearonDublin Neurological Institute, Mater Misericordiae University Hospital, Dublin, Ireland.
Richard A WalshDublin Neurological Institute, Mater Misericordiae University Hospital, Dublin, Ireland.
Catherine MoranDepartment of Neurosurgery, Beaumont Hospital, Dublin, Ireland.

Funding

Royal College of Surgeons in Ireland 24225A010
6 · The paper itself

Abstract

Dystonia is a hyperkinetic movement disorder increasingly conceptualized as a disorder of distributed network dysfunction involving the basal ganglia, cortex and cerebellum. Local field potentials (LFPs) recorded from deep brain stimulation (DBS) electrodes provide a unique opportunity to characterize the electrophysiological signatures underlying this network. We performed a systematic review of acute and chronic LFP recordings in dystonia to define common oscillatory patterns and propose a pathophysiological framework. Ninety three studies including 862 patients were analyzed, comprising predominantly globus pallidus internus (GPi) recordings, alongside subthalamic nucleus (STN) and other network nodes. Across dystonia subtypes, increased low-frequency oscillatory activity (approximately 3-12 Hz) was the most consistent finding, particularly within the GPi, where it often correlated with clinical severity and demonstrated coherence with cortical and muscle activity. Raised activity across other frequencies were inconsistently observed and appeared to reflect specific disease states or phenotypes rather than a unifying biomarker. Oscillatory abnormalities extended beyond the pallidum to include the GPe, STN and cortex, supporting a model of widespread network dysfunction. Both acute and chronic DBS studies demonstrated that stimulation can modulate low-frequency activity and network coherence, although these changes do not consistently parallel clinical improvement. Emerging chronic sensing technologies highlight temporal variability and longer-term network dynamics not captured in acute recordings. Overall, dystonia is characterized by abnormal low-frequency synchronization across distributed motor networks rather than a single pathological oscillation. Chronic-sensing provides a unique opportunity to study long-term network dynamics and may support biomarker development for personalized stimulation strategies in dystonia.

Indexed as

chronic LFPdystoniaLFP programminglocal field potential (LFP)sensing capable

Identifiers

PMID42494087
PMCPMC13396684

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.