Evidence map›Paper›PMID 42059057›Full record

Trial reportMovement disorders : official journal of the Movement Disorder Society2026

Temporal Interference Stimulation Modulates Resting State Functional Connectivity of Motor Circuit in Parkinson's Disease.

Yongxin Xu, Chenhao Yang, Yichao Du, Xiaonan Shen, Tingting Li, Yufeng Zhang, Zijun Lu, Jie Zhuang, Nan Chen, Yulian Zhu and 10 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Movement disorders : official journal of the Movement Disorder Society, 2026. 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

20 authors.

Yongxin XuKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.ORCID https://orcid.org/0009-0003-8088-5266
Chenhao YangKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.ORCID https://orcid.org/0000-0002-6540-5311
Yichao DuKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Xiaonan ShenKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Tingting LiKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Yufeng ZhangKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Zijun LuKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Jie ZhuangSchool of Psychology, Shanghai University of Sport, Shanghai, China.
Nan ChenDepartment of Rehabilitation, Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Yulian ZhuDepartment of Rehabilitation Medicine, Huashan Hospital, Fudan University, Shanghai, China.
Chencheng ZhangClinica Neuroscience Center, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Jiaojiao LüKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Lingyan HuangKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Lu LiKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Jianqiang LüKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Zhenyu QianKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.
Zhen WangSchool of Martial Arts, Shanghai University of Sport, Shanghai, China.ORCID https://orcid.org/0000-0001-7225-9095
Jian ZhangSchool of Psychology, Shanghai University of Sport, Shanghai, China.
Junhong ZhouHinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Roslindale, Massachusetts, USA.ORCID https://orcid.org/0000-0002-7931-7646
Yu LiuKey Laboratory of Exercise and Health Sciences of Ministry of Education, School of Exercise and Health, Shanghai University of Sport, Shanghai, China.ORCID https://orcid.org/0000-0001-8729-2701

Funding

National Natural Science Foundation of China 11932013National Natural Science Foundation of China 12472328National Natural Science Foundation of China 2021HBQZYCXY002
6 · The paper itself

Abstract

backgroundTranscranial temporal interference stimulation (TIs) targeting the subthalamic nucleus (STN) is a novel noninvasive neuromodulation approach with potential to improve motor symptoms in Parkinson's disease (PD). However, its underlying neuroimaging mechanisms remain unclear. Changes in functional connectivity (FC) of the STN and the cortical-basal ganglia-thalamic-cortical (CBTC) circuit are central to PD pathophysiology.

objectiveThis randomized, double-blind, crossover study aimed to examine the effects of STN-TIs on FCs of the STN and regions in the CBTC circuit in PD.

methods23 participants with mild-to-moderate PD received a 20-minute session of 130 Hz TIs targeting the STN of the contralateral hemisphere of the patient's severely affected side (or the dominant side in case of bilateral disturbance), and active sham stimulation in randomized order. Resting-state functional magnetic resonance imaging (fMRI) and Part III of Movement Disorder Society Unified Parkinson's Disease Rating Scale (MDS-UPDRS-III) were completed before and after stimulation. The STN and regions in the CBTC circuit were defined as regions of interest (ROI) for ROI-to-ROI FC analysis.

resultsCompared to sham stimulation, 130 Hz STN-TIs induced a connectivity-specific effect, including the decreased FCs between the targeted side of STN and putamen (P = 0.004-0.046) and caudate (P < 0.001), and increased FC between the targeted side of STN and M1 (P = 0.002-0.004). No severe side effects were reported.

conclusionsOur study provides preliminary but novel evidence for the potential modulatory effect of STN-TIs on resting-state neural activities in the motor circuit. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society. © 2026 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Parkinson DiseaseSubthalamic NucleusTranscranial Magnetic StimulationAgedBasal GangliaCross-Over StudiesDeep Brain StimulationDouble-Blind MethodFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeural PathwaysRestThalamusfunctional connectivityParkinson's diseasesubthalamic nucleustranscranial temporal interference stimulation

Identifiers

PMID42059057
PMCPMC13518268

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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.