ArticleNeuroimage. Reports2026
Increased beta-HFO phase-amplitude coupling in the subthalamic nucleus during movement in Parkinson's disease.
Article in Neuroimage. Reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
In Parkinson's disease (PD), increased amplitude of high-frequency oscillations (HFO) has been confirmed to be coupled with the beta oscillations phase, resulting in increased phase-amplitude coupling (PAC) in the subthalamic nucleus (STN). This pathological coupling correlates with the severity of motor symptoms and is known to be modulated by therapeutic interventions. For example, dopaminergic medications and deep brain stimulation (DBS) were previously shown to reduce PAC, which changes in magnitude between states of rest and movement. However, PAC alterations during kinetic and static movements in the presence and absence of medications remain to be determined. Furthermore, there is little evidence on the relationship between PAC and clinical symptoms of PD. In this study, we investigated these two issues. We analyzed a publicly available dataset, which contained STN local field potential registrations (n = 20) and concurrent limb electromyography during resting, static, and kinetic movements with and without levodopa intake. We calculated the PAC within the STN during different conditions, and the PAC between the limb tremor and the ipsilateral LFP oscillations. Beta-HFO STN PAC was increased during the medication off period, especially during kinetic movement and was highly correlated with bradykinesia and negatively correlated with tremor. We observed no interaction between tremor frequency oscillation phase on electromyography and beta or HFO oscillation amplitude within the STN in either of the conditions. These results point out that beta-HFO PAC provides complementary information to beta power for electrophysiological localization during DBS implantation and during adaptive DBS.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.