Evidence map›Paper›PMID 38631480›Full record

ArticleProgress in neurobiology2024

Prefrontal-subthalamic theta signaling mediates delayed responses during conflict processing.

Jeong Woo Choi, Mahsa Malekmohammadi, Soroush Niketeghad, Katy A Cross, Hamasa Ebadi, Amirreza Alijanpourotaghsara, Adam Aron, Ueli Rutishauser, Nader Pouratian

Open access · greenAbstract read
In one paragraph

Article in Progress in neurobiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.8field-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

6 citing papers in PubMed, 5 citations in OpenAlex.

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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 7 institutions in 1 country.

Jeong Woo ChoiDepartment of Neurological Surgery, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Mahsa MalekmohammadiDepartment of Neurosurgery, University of California, Los Angeles, CA 90095, USA.
Soroush NiketeghadDepartment of Neurosurgery, University of California, Los Angeles, CA 90095, USA.
Katy A CrossDepartment of Neurology, University of California, Los Angeles, CA 90095, USA.
Hamasa EbadiDepartment of Neurological Surgery, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Amirreza AlijanpourotaghsaraDepartment of Neurological Surgery, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Adam AronDepartment of Psychology, University of California, San Diego, CA 92093, USA.
Ueli RutishauserDepartments of Neurosurgery and Neurology, and Center for Neural Science and Medicine, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA; Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.
Nader PouratianDepartment of Neurological Surgery, UT Southwestern Medical Center, Dallas, TX 75390, USA. Electronic address: nader.pouratian@utsouthwestern.edu.
University of California, Los Angeles · USCedars-Sinai Medical Center · USNeurological Surgery · USSouthwestern Medical CenterSouthwestern Medical Center · USThe University of Texas Southwestern Medical Center · USUniversity of California San Diego · US

Funding

Invasive Approach to Model Human Cortex-Basal Ganglia Action-Regulating NetworksU01NS098961 · NINDS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI POURATIAN, NADER · 2016 to 2018
$3.9M
Modeling and Mapping Human Action Regulation NetworksU01NS132788 · NINDS · UT SOUTHWESTERN MEDICAL CENTER · PI Vasileios N Christopoulos, NADER POURATIAN · 2023 to 2026
$3.7M
NINDS NIH HHS U01 NS098961NINDS NIH HHS U01 NS132788
6 · The paper itself

Abstract

While medial frontal cortex (MFC) and subthalamic nucleus (STN) have been implicated in conflict monitoring and action inhibition, respectively, an integrated understanding of the spatiotemporal and spectral interaction of these nodes and how they interact with motor cortex (M1) to definitively modify motor behavior during conflict is lacking. We recorded neural signals intracranially across presupplementary motor area (preSMA), M1, STN, and globus pallidus internus (GPi), during a flanker task in 20 patients undergoing deep brain stimulation implantation surgery for Parkinson disease or dystonia. Conflict is associated with sequential and causal increases in local theta power from preSMA to STN to M1 with movement delays directly correlated with increased STN theta power, indicating preSMA is the MFC locus that monitors conflict and signals STN to implement a 'break.' Transmission of theta from STN-to-M1 subsequently results in a transient increase in M1-to-GPi beta flow immediately prior to movement, modulating the motor network to actuate the conflict-related action inhibition (i.e., delayed response). Action regulation during conflict relies on two distinct circuits, the conflict-related theta and movement-related beta networks, that are separated spatially, spectrally, and temporally, but which interact dynamically to mediate motor performance, highlighting complex parallel yet interacting networks regulating movement.

Indexed as

Conflict, PsychologicalDeep Brain StimulationMotor CortexParkinson DiseasePrefrontal CortexSubthalamic NucleusTheta RhythmAdultAgedDystoniaFemaleHumansMaleMiddle AgedNeural PathwaysAction regulationBasal-ganglia cortical networkConflict processingConflict-related theta networkIntracranial neural recordingsMovement-related beta network

Identifiers

PMID38631480
PMCPMC11149786
OpenAlexW4394824224

What OpenQuestion holds

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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 OpenQuestion graph.