Evidence map›Paper›PMID 42253606›Full record

ArticleImaging neuroscience (Cambridge, Mass.)

Stimulation priming and psychological state shape functional connectivity following prefrontal theta-burst stimulation.

Stefanie De Smet, Guo-Rong Wu, Debby C W Klooster, Beatriz Catoira, Sara De Witte, Lais B Razza, Vincent van de Ven, Alexander T Sack, Chris Baeken, Marie-Anne Vanderhasselt

Abstract read
In one paragraph

Article in Imaging neuroscience (Cambridge, Mass.). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

10 authors.

Stefanie De SmetGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.ORCID https://orcid.org/0000-0002-3764-3734
Guo-Rong WuKey Laboratory of Cognition and Personality, Faculty of Psychology, Southwest University, Chongqing, China.
Debby C W KloosterCare & Cure Lab of the Electromagnetics Group (EM4Care+Cure), Department of Electrical Engineering, Eindhoven University of Technology, Eindhoven The Netherlands.
Beatriz CatoiraGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.
Sara De WitteGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.
Lais B RazzaGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.
Vincent van de VenDepartment of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, The Netherlands.
Alexander T SackBrain Stimulation and Cognition (BSC) Lab, Department of Cognitive Neuroscience, Faculty of Psychology & Neuroscience, Maastricht University, Maastricht, The Netherlands.
Chris BaekenGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.
Marie-Anne VanderhasseltGhent Experimental Psychiatry (GHEP) lab, Faculty of Medicine and Health Sciences, Department of Head and Skin, Ghent University, Ghent, Belgium.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intermittent theta-burst stimulation (iTBS) is increasingly used to neuromodulate prefrontal brain regions, such as the dorsolateral prefrontal cortex (DLPFC), allowing to effectively change local excitability in research settings and to optimize therapeutic outcomes. However, response variability remains high, and its clinical efficacy is modest. Priming with theta-burst stimulation (TBS), in which a preconditioning TBS protocol precedes a test iTBS protocol, has been proposed to enhance stimulation efficacy and reduce inter-individual variability, particularly when combining protocols that are expected to induce different changes in cortical excitability. Yet, its underlying neurobiological effects remain unclear. In this within-subjects study, we investigated the effects of TBS priming on resting-state functional connectivity in 47 healthy subjects. Each participant completed four counterbalanced sessions, 1 week apart, receiving either a control condition with sham priming and sham test stimulation, an iTBS-alone condition (without priming), a priming condition where iTBS preceded iTBS, or a priming condition where continuous TBS (cTBS) preceded iTBS. Resting-state scans were acquired before and after each stimulation condition, alongside assessments of self-reported mood and perseverative thinking. Contrary to our expectations, priming prefrontal iTBS with cTBS resulted in reduced connectivity changes in both regions near the stimulation site and more distal temporal areas, and priming with iTBS significantly reduced connectivity changes in prefrontal regions, both relative to iTBS alone. Changes in perseverative thinking further moderated stimulation effects, with greater increases associated with stronger decreases in left prefrontal connectivity following cTBS-iTBS priming. These findings highlight the complex effects of prefrontal TBS priming and its interaction with psychological states, underscoring the importance of accounting for state dependency in neuromodulation research.

Indexed as

dorsolateral prefrontal cortex (DLPFC)functional magnetic resonance imaging (fMRI)resting-state connectivitystimulation primingtheta burst stimulation (TBS)

Identifiers

PMID42253606
PMCPMC13237992

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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.