Evidence map›Paper›PMID 37645954›Full record

ArticlebioRxiv : the preprint server for biology2023

TMS provokes target-dependent intracranial rhythms across human cortical and subcortical sites.

Ethan A Solomon, Jeffrey B Wang, Hiroyuki Oya, Matthew A Howard, Nicholas T Trapp, Brandt D Uitermarkt, Aaron D Boes, Corey J Keller

Registry-linked trialOpen access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07518745 (Mapping Transcrnial Magnetic Stimulation), which is not on this 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.

NCT07518745 naenrolling by invitationnot on this mapstarted 2025, after this paper: background citation

Mapping Transcrnial Magnetic Stimulation (TMS) Responses Within the Brain Using Intracranial Electrophysiological Monitoring Recordings

TypeinterventionalSponsorUniversity of PennsylvaniaRan2025 to 2029Enrolled10ConditionsEEG, TMSArmsSingle Pulse TMS
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Ethan A SolomonDept. of Psychiatry and Behavioral Sciences, Stanford University Medical Center, Palo Alto CA 94305.ORCID 0000-0003-0541-7588
Jeffrey B WangDept. of Psychiatry and Behavioral Sciences, Stanford University Medical Center, Palo Alto CA 94305.
Hiroyuki OyaDepartment of Neurosurgery, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242.ORCID 0000-0002-1733-5478
Matthew A HowardDepartment of Neurosurgery, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242.
Nicholas T TrappDepartment of Neurology, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242.
Brandt D UitermarktDepartment of Pediatrics, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242.
Aaron D BoesDepartment of Neurology, Carver College of Medicine, University of Iowa, Iowa City, IA, 52242.
Corey J KellerDept. of Psychiatry and Behavioral Sciences, Stanford University Medical Center, Palo Alto CA 94305.ORCID 0000-0003-0529-3490
University of Iowa · USStanford Medicine · USVA Palo Alto Health Care System · US

Funding

The Iowa Neuroscience Specialty Program in Research Education (INSPIRE)T32MH019113 · NIMH · UNIVERSITY OF IOWA · PI HANNA E STEVENS, John A Wemmie · 1991 to 2026
$5.6M
Investigating the neural mechanisms of repetitive brain stimulation with invasive and noninvasive electrophysiology in humansR01MH132074 · NIMH · STANFORD UNIVERSITY · PI Aaron D Boes, Corey J Keller · 2023 to 2026
$3.1M
Predicting Cognitive Outcomes from Stroke Based on Lesion LocationR01NS114405 · NINDS · UNIVERSITY OF IOWA · PI BOES, AARON D · 2020 to 2024
$2.1M
University of Iowa - Research 3T MRI Connectome UpgradeS10OD025025 · OD · UNIVERSITY OF IOWA · PI MAGNOTTA, VINCENT A · 2018 to 2018
$1.9M
Closing the loop: development of real-time, personalized brain stimulationR01MH126639 · NIMH · STANFORD UNIVERSITY · PI KELLER, COREY J · 2021 to 2024
$1.6M
CRCNS US-France Research Proposal: Probing the Dorsolateral Prefrontal Cortex and Central Executive Network for Improving Neuromodulation in DepressionR01MH129018 · NIMH · STANFORD UNIVERSITY · PI KELLER, COREY J · 2021 to 2025
$1.1M
Investigating the Effects of Transcranial Magnetic Stimulation with Intracranial EEG in HumansR21MH120441 · NIMH · UNIVERSITY OF IOWA · PI BOES, AARON D, OYA, HIROYUKI · 2019 to 2020
$425k
Whole-Brain Oscillatory and Behavioral Responses to Noninvasive Local Ketamine Uncaging in the Medial Prefrontal CortexF30MH119763 · NIMH · STANFORD UNIVERSITY · PI WANG, JEFFREY BOND · 2020 to 2021
$75k
NIH HHS S10 OD025025NIMH NIH HHS F30 MH119763NIMH NIH HHS R01 MH126639NIMH NIH HHS R01 MH129018NIMH NIH HHS R01 MH132074NIMH NIH HHS R21 MH120441NIMH NIH HHS T32 MH019113NINDS NIH HHS R01 NS114405
6 · The paper itself

Abstract

Transcranial magnetic stimulation (TMS) is increasingly deployed in the treatment of neuropsychiatric illness, under the presumption that stimulation of specific cortical targets can alter ongoing neural activity and cause circuit-level changes in brain function. While the electrophysiological effects of TMS have been extensively studied with scalp electroencephalography (EEG), this approach is most useful for evaluating low-frequency neural activity at the cortical surface. As such, little is known about how TMS perturbs rhythmic activity among deeper structures - such as the hippocampus and amygdala - and whether stimulation can alter higher-frequency oscillations. Recent work has established that TMS can be safely used in patients with intracranial electrodes (iEEG), allowing for direct neural recordings at sufficient spatiotemporal resolution to examine localized oscillatory responses across the frequency spectrum. To that end, we recruited 17 neurosurgical patients with indwelling electrodes and recorded neural activity while patients underwent repeated trials of single-pulse TMS at several cortical sites. Stimulation to the dorsolateral prefrontal cortex (DLPFC) drove widespread low-frequency increases (3-8Hz) in frontolimbic cortices, as well as high-frequency decreases (30-110Hz) in frontotemporal areas, including the hippocampus. Stimulation to parietal cortex specifically provoked low-frequency responses in the medial temporal lobe. While most low-frequency activity was consistent with brief evoked responses, anterior frontal regions exhibited induced theta oscillations following DLPFC stimulation. Taken together, we established that non-invasive stimulation can (1) provoke a mixture of low-frequency evoked power and induced theta oscillations and (2) suppress high-frequency activity in deeper brain structures not directly accessed by stimulation itself.

Identifiers

PMID37645954
PMCPMC10461914
OpenAlexW4385805601

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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.