Evidence map›Paper›PMID 41107249›Full record

ArticleTranslational psychiatry2025

Modulation of brain oscillations by continuous theta burst stimulation in patients with insomnia.

Ximei Zhu, Lin Jiang, Le Shi, Fali Li, Qingqing Yang, Mingyue Zhang, Yinjiao Li, Qiuxuan Yu, Jie Chen, Xuejiao Gao and 5 more

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

15 authors.

Ximei Zhu *Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.
Lin Jiang *The Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.ORCID http://orcid.org/0000-0002-7892-118X
Le ShiPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.ORCID http://orcid.org/0000-0003-4827-4003
Fali LiThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.ORCID http://orcid.org/0000-0002-2450-4591
Qingqing YangThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China.
Mingyue ZhangPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.
Yinjiao LiPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.
Qiuxuan YuInstitute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Jie ChenPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.
Xuejiao GaoPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.
Zhong WangPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China.ORCID http://orcid.org/0000-0003-1055-4907
Yong WangDepartment of Rehabilitation Medicine, Zhujiang Hospital, Southern Medical University, Guangzhou, China.
Peng XuThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Lab for Neuroinformation, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, China. xupeng@uestc.edu.cn.
Lin LuPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China. linlu@bjmu.edu.cn.ORCID http://orcid.org/0000-0003-0742-9072
Jiahui DengPeking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, China. jiahuideng2012@bjmu.edu.cn.ORCID http://orcid.org/0000-0002-2025-0336

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82201646National Natural Science Foundation of China (National Science Foundation of China) 82271528
6 · The paper itself

Abstract

Continuous theta burst stimulation (cTBS) induces long-lasting depression of cortical excitability in motor cortex. In the present study, we explored the modulation of cTBS on resting state electroencephalogram (rsEEG) during wakefulness and subsequent sleep in patients with insomnia disorder. Forty-one patients with insomnia received three sessions active and sham cTBS in a counterbalanced crossover design. Each session comprised 600 pulses over right dorsolateral prefrontal cortex. Closed-eyes rsEEG were recorded at before and after each session. Effects of cTBS in subsequent sleep were measured by overnight polysomnography screening. Power spectral density (PSD) and phase locking value (PLV) were used to calculate changes in spectral power and phase synchronization after cTBS during wakefulness and subsequent sleep. Compared with sham cTBS intervention, PSD of delta and theta bands were increased across global brain regions with a cumulative effect after three active cTBS sessions. PLV of delta and theta bands were enhanced between stimulated frontal area and occipital areas. Efficiency of information communication within frontal-occipital networks was consistently improved through three active sessions. Increased theta power during wakefulness was positively related with that during the first sleep cycle. Active cTBS significantly enhanced the spectral power of delta and theta bands during wakefulness, with a cumulative effect observed over time. This modulation also extended to influence theta power during subsequent sleep onset period. Collectively, these findings provide a robust theoretical foundation for further investigating the therapeutic potential of long-term cTBS in the treatment of insomnia disorders.

Indexed as

Sleep Initiation and Maintenance DisordersTheta RhythmTranscranial Magnetic StimulationAdultCross-Over StudiesElectroencephalographyFemaleHumansMaleMiddle AgedPolysomnographyWakefulness

Identifiers

PMID41107249
PMCPMC12534500

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.