Evidence map›Paper›PMID 38436939›Full record

ArticleBrain : a journal of neurology2024

The human subthalamic nucleus transiently inhibits active attentional processes.

Cheol Soh, Mario Hervault, Nathan H Chalkley, Cathleen M Moore, Andrea Rohl, Qiang Zhang, Ergun Y Uc, Jeremy D W Greenlee, Jan R Wessel

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06899022 (Investigating the Role of Attention in Perceptual and Cognitive Consequences of Parkinson's Disease), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.3field-weighted citation impact, top 8% 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.

NCT06899022 narecruitingnot on this mapstarted 2025, after this paper: background citation

Investigating the Role of Attention in Perceptual and Cognitive Consequences of Parkinson's Disease

TypeinterventionalSponsorUniversity of NebraskaRan2025 to 2028Enrolled138ConditionsEssential Tremor, Parkinson&#39, s Disease (PD), DystoniasArmsNormal therapeutic DBS, Reduced current DBS, Reduced frequency DBS
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 9 citations in OpenAlex.

  1. Review
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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 at 1 institution in 1 country.

Cheol SohDepartment of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0003-1397-3592
Mario HervaultDepartment of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, USA.
Nathan H ChalkleyDepartment of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, USA.
Cathleen M MooreDepartment of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, USA.
Andrea RohlDepartment of Neurosurgery, University of Iowa, Iowa City, IA 52242, USA.
Qiang ZhangDepartment of Neurology, University of Iowa, Iowa City, IA 52242, USA.
Ergun Y UcDepartment of Neurology, University of Iowa, Iowa City, IA 52242, USA.
Jeremy D W GreenleeDepartment of Neurosurgery, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0002-8481-8517
Jan R WesselDepartment of Psychological and Brain Sciences, University of Iowa, Iowa City, IA 52242, USA.ORCID 0000-0002-3489-7624
University of Iowa · US

Funding

The Role of a Neural Mechanism for Inhibitory Control in Cognitive FlexibilityR01NS102201 · NINDS · UNIVERSITY OF IOWA · PI WESSEL, JAN R · 2018 to 2022
$1.9M
NIH HHS R01 NS102201NINDS NIH HHS R01 NS102201
6 · The paper itself

Abstract

The subthalamic nucleus (STN) of the basal ganglia is key to the inhibitory control of movement. Consequently, it is a primary target for the neurosurgical treatment of movement disorders like Parkinson's disease, where modulating the STN via deep brain stimulation (DBS) can release excess inhibition of thalamocortical motor circuits. However, the STN is also anatomically connected to other thalamocortical circuits, including those underlying cognitive processes like attention. Notably, STN-DBS can also affect these processes. This suggests that the STN may also contribute to the inhibition of non-motor activity and that STN-DBS may cause changes to this inhibition. Here we tested this hypothesis in humans. We used a novel, wireless outpatient method to record intracranial local field potentials (LFP) from STN DBS implants during a visual attention task (Experiment 1, n = 12). These outpatient measurements allowed the simultaneous recording of high-density EEG, which we used to derive the steady state visual evoked potential (SSVEP), a well established neural index of visual attentional engagement. By relating STN activity to this neural marker of attention (instead of overt behaviour), we avoided possible confounds resulting from STN's motor role. We aimed to test whether the STN contributes to the momentary inhibition of the SSVEP caused by unexpected, distracting sounds. Furthermore, we causally tested this association in a second experiment, where we modulated STN via DBS across two sessions of the task, spaced at least 1 week apart (n = 21, no sample overlap with Experiment 1). The LFP recordings in Experiment 1 showed that reductions of the SSVEP after distracting sounds were preceded by sound-related γ-frequency (>60 Hz) activity in the STN. Trial-to-trial modelling further showed that this STN activity statistically mediated the sounds' suppressive effect on the SSVEP. In Experiment 2, modulating STN activity via DBS significantly reduced these sound-related SSVEP reductions. This provides causal evidence for the role of the STN in the surprise-related inhibition of attention. These findings suggest that the human STN contributes to the inhibition of attention, a non-motor process. This supports a domain-general view of the inhibitory role of the STN. Furthermore, these findings also suggest a potential mechanism underlying some of the known cognitive side effects of STN-DBS treatment, especially on attentional processes. Finally, our newly established outpatient LFP recording technique facilitates the testing of the role of subcortical nuclei in complex cognitive tasks, alongside recordings from the rest of the brain, and in much shorter time than peri-surgical recordings.

Indexed as

AttentionEvoked Potentials, VisualNeural InhibitionParkinson DiseaseSubthalamic NucleusAgedDeep Brain StimulationElectroencephalographyFemaleHumansImplantable NeurostimulatorsMaleMiddle AgedPhotic StimulationSoundTask Performance and Analysisattentiondeep brain stimulationinhibitory controlParkinson’s diseasesteady-state visual evoked potentialsubthalamic nucleus

Identifiers

PMID38436939
PMCPMC11370801
OpenAlexW4392381224

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.