Evidence map›Paper›PMID 41481211›Full record

ArticleNeuromodulation : journal of the International Neuromodulation Society2026

Differential Gamma Responses to Transcutaneous Auricular Vagus Nerve Stimulation Revealed by Human Intracranial Recordings.

Kara M Donovan, Gansheng Tan, Jon T Willie, Peter Brunner, Eric C Leuthardt

Abstract read
In one paragraph

Article in Neuromodulation : journal of the International Neuromodulation Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

5 authors.

Kara M DonovanDepartment of Biomedical Engineering, Washington University, St. Louis, MO, USA; Division of Neurotechnology, Washington University School of Medicine, St. Louis, MO, USA.
Gansheng TanDepartment of Biomedical Engineering, Washington University, St. Louis, MO, USA; Division of Neurotechnology, Washington University School of Medicine, St. Louis, MO, USA.
Jon T WillieDepartment of Biomedical Engineering, Washington University, St. Louis, MO, USA; Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO, USA; Department of Psychiatry, Washington University School of Medicine, St. Louis, MO, USA; Department of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA; Department of Neurology, Washington University School of Medicine, St. Louis, MO, USA.
Peter BrunnerDepartment of Biomedical Engineering, Washington University, St. Louis, MO, USA; Division of Neurotechnology, Washington University School of Medicine, St. Louis, MO, USA; Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO, USA.
Eric C LeuthardtDepartment of Biomedical Engineering, Washington University, St. Louis, MO, USA; Division of Neurotechnology, Washington University School of Medicine, St. Louis, MO, USA; Department of Neurosurgery, Washington University School of Medicine, St. Louis, MO, USA; Department of Neuroscience, Washington University School of Medicine, St. Louis, MO, USA; Department of Mechanical Engineering and Materials Science, Washington University, St. Louis, MO, USA; Center for Innovation in Neuroscience and Technology, Washington University School of Medicine, St. Louis, MO, USA; Brain Laser Center, Washington University School of Medicine, St. Louis, MO, USA. Electronic address: leuthardte@wustl.edu.

Funding

Training and DisseminationP41EB018783 · NIBIB · WADSWORTH CENTER · PI Jonathan Rickel Wolpaw · 2014 to 2026
$15.4M
An Ecosystem of Technology and Protocols for Adaptive Neuromodulation Research in HumansU01NS128612 · NINDS · MAYO CLINIC ROCHESTER · PI Peter Brunner, Kai Miller · 2022 to 2026
$4.5M
BCI2000: Software Resource for Adaptive Neurotechnology ResearchU24NS109103 · NINDS · WASHINGTON UNIVERSITY · PI BRUNNER, PETER · 2019 to 2024
$2.8M
CRCNS: Processing speed in the human connectome across the lifespanR01MH122258 · NIMH · MAYO CLINIC ROCHESTER · PI HERMES, DORA · 2019 to 2023
$1.8M
Interdisciplinary Training in Cognitive, Computational and Systems Neuroscience (CCSN)T32NS115672 · NINDS · WASHINGTON UNIVERSITY · PI TODD S BRAVER, Camillo Padoa-Schioppa · 2020 to 2026
$1.8M
BCI2000+: A Software Platform for Adaptive NeurotechnologiesR01EB026439 · NIBIB · WASHINGTON UNIVERSITY · PI BRUNNER, PETER · 2018 to 2022
$1.5M
Dynamics and Causal Functions of Large-Scale Cortical and Subcortical NetworksU01NS108916 · NINDS · WADSWORTH CENTER · PI WOLPAW, JONATHAN RICKEL · 2018 to 2019
$1.4M
Translational Neuroscience and Neurotechnology Training (TNNT)T32NS126157 · NINDS · WASHINGTON UNIVERSITY · PI Daniel William Moran · 2022 to 2026
$776k
Non-invasive vagus nerve stimulation to mitigate subarachnoid hemorrhage induced inflammationR21NS128307 · NINDS · WASHINGTON UNIVERSITY · PI BRUNNER, PETER, LEUTHARDT, ERIC CLAUDE · 2023 to 2024
$428k
NIBIB NIH HHS P41 EB018783NIBIB NIH HHS R01 EB026439NIMH NIH HHS R01 MH122258NINDS NIH HHS R21 NS128307NINDS NIH HHS T32 NS115672NINDS NIH HHS T32 NS126157NINDS NIH HHS U01 NS108916NINDS NIH HHS U01 NS128612NINDS NIH HHS U24 NS109103
6 · The paper itself

Abstract

objectivesVagus nerve stimulation (VNS), along with noninvasive transcutaneous auricular VNS (taVNS), has been the focus of considerable research across numerous indications. However, although invasive VNS literature has explored ways stimulation amplitude influences both physiologic and behavioral outcomes, there is a less robust understanding of taVNS parameter-specific effects on central nervous system activity. The focus of this study was to better understand neurophysiologic responses to multiple taVNS intensities to inform future taVNS work with therapeutic applications. MATERIALS AND

methodsWe recorded stereotactic electroencephalography signals from ten patients (six male) with intractable epilepsy (N = 8 included for analysis, four male) while they underwent both active and sham taVNS. Both active and sham stimulation conditions were administered at 30-Hz frequency, 250-μs pulse width, 30-second train with 1-second intertrain interval, for a total duration of 1 minute. Active taVNS amplitudes included 0.5, 1.0, and 1.5 mA whereas sham taVNS was administered at 1.5 mA. High gamma power between 95 and 170 Hz was quantified as the primary indicator of local activity.

resultsHigh gamma activity was amplitude-dependent, with different taVNS amplitudes producing distinct effects. Active taVNS at 1.0- and 1.5-mA amplitudes caused increased high gamma activity. Furthermore, the increases in high gamma in the orbitofrontal cortex and insula were maintained for significantly greater durations during 1.5-mA active taVNS than during sham. In addition, 0.5-mA stimulation led to moderate suppression of high gamma in certain regions, although further research is needed to investigate brain responses to subthreshold stimulation.

conclusionstaVNS administered at 1.5-mA amplitude can elicit a sustained high gamma response throughout the course of stimulation in key brain areas implicated in the vagal afferent pathway. Our findings underscore the importance of parameter selection in taVNS protocols given different amplitudes can produce varied effects on brain activity.

Indexed as

BrainDrug Resistant EpilepsyElectrocorticographyGamma RhythmTranscutaneous Electric Nerve StimulationVagus Nerve StimulationAdolescentAdultElectroencephalographyFemaleHumansMaleYoung AdultElectrophysiologyneuromodulationstereotactic electroencephalographytaVNSvagus nerve

Identifiers

PMID41481211
PMCPMC13135851

What OpenQuestion holds

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Registered trials

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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.