Evidence map›Paper›PMID 40706726›Full record

ArticleNeuroImage2025

Oscillatory and evoked neural responses underlying gating in the primary somatosensory cortices: Evidence from optically-pumped magnetometry.

Yasra Arif, Elizabeth Heinrichs-Graham, Alexa M Wildy, Thomas W Ward, Augusto Diedrich, Christine M Embury, Maggie P Rempe, Ryan J Glesinger, Zhiying Shen, Kellen M McDonald and 5 more

Abstract read
In one paragraph

Article in NeuroImage, 2025. 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

15 authors.

Yasra ArifInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA. Electronic address: yasra.arif@boystown.org.
Elizabeth Heinrichs-GrahamInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Alexa M WildyInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA.
Thomas W WardInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Augusto DiedrichInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Christine M EmburyInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA.
Maggie P RempeInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; College of Medicine, University of Nebraska Medical Center (UNMC), Omaha, NE, 68198, USA.
Ryan J GlesingerInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA.
Zhiying ShenInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Kellen M McDonaldInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Peihan J HuangInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Seth BashfordInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA.
Brittany K TaylorInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Max J KurzInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.
Tony W WilsonInstitute for Human Neuroscience, Boys Town National Research Hospital, Boys Town, NE, 68010, USA; Department of Pharmacology & Neuroscience, Creighton University, Omaha, NE, 68178, USA.

Funding

Stress-Induced Aberrations in the Mitochondrial Redox Environment Impact Developing Neural Circuits Supporting Cognitive ControlP20GM144641 · NIGMS · FATHER FLANAGAN'S BOYS' HOME · PI Rachel K. Spooner · 2022 to 2026
$15.1M
Next-Generation MEG Imaging for Quantifying Cortical-Subcortical Dynamics in the Context of HIV and Cannabis UseR01DA059542 · NIDA · FATHER FLANAGAN'S BOYS' HOME · PI Tony W. Wilson · 2024 to 2026
$1.9M
Wearable magnetoencephalography (MEG): The next-generation of dynamic human neuroimagingS10OD032468 · OD · FATHER FLANAGAN'S BOYS' HOME · PI WILSON, TONY W · 2022 to 2022
$1.4M
Impact of HIV and Cannabis Use on Executive Brain Function and InflammationF31DA063403 · NIDA · FATHER FLANAGAN'S BOYS' HOME · PI Kellen M McDonald · 2025 to 2026
$100k
NIDA NIH HHS F31 DA063403NIDA NIH HHS R01 DA059542NIGMS NIH HHS P20 GM144641NIH HHS S10 OD032468
6 · The paper itself

Abstract

Sensory gating (SG) is a protective mechanism that prevents sensory overload by attenuating neural responses to repeated stimuli while allowing allocation of neural resources to salient inputs. While studies using conventional, cryogenic magnetoencephalography (MEG) have provided a foundational understanding of the neurophysiological spectro-temporal profile of sensory gating in somatosensory cortices, its utility in diverse populations is constrained by technical limitations, including movement restriction and a one-size-fits-all helmet design. Recent developments in optically pumped magnetometry (OPM) aim to overcome these constraints by providing greater tolerance to movement and customizable helmet sizes. A small number of studies have documented the reliability of OPM in mapping somatosensory responses to median nerve stimulation using OPM; however, none have examined SG. In this study, we utilized a whole-head 128-channel OPM system and a paired-pulse median nerve stimulation paradigm to examine somato-SG and map the precise spectro-temporal cortical dynamics in a group of 31 healthy adults. Neural responses per stimulation were imaged in both the time-frequency and time domains, and voxel time series data were extracted to quantify the dynamics of somato-SG. Robust gating effects were observed in the peak and average neural responses within the primary somatosensory cortices, in both the oscillatory and time domains. These findings underscore OPM's ability to precisely resolve the spatiotemporal neural dynamics of somato-SG and stress the utility of OPM in examining somatosensory processes across developmental trajectories extending down to infants, as well as in clinical populations.

Indexed as

Evoked Potentials, SomatosensoryMagnetoencephalographyMagnetometrySensory GatingSomatosensory CortexAdultFemaleHumansMaleMedian NerveYoung AdultBeamformerGammasLORETAThetaVirtual sensor

Identifiers

PMID40706726
PMCPMC12426474

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.