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Clinical Article
Graph-theoretical comparison of brain network topology during motor imagery and motor execution
LIU Fengyu  WANG Yu  WANG Jiangguang  WANG Xingyue  KE Yougang  WU Dong  XIAO Rong  RAO Haibing  ZHENG Wenbin  GUO Yuelin 

DOI:10.12015/issn.1674-8034.2026.07.004.


[Abstract] Objective To compare the topological properties of brain networks during right-hand motor execution and motor imagery in healthy individuals, and to explore the neural mechanisms underlying the two motor conditions.Materials and Methods Forty right-handed healthy volunteers underwent task-based functional magnetic resonance imaging. Whole-brain functional connectivity matrices were constructed using the Schaefer 2018 atlas (17-network parcellation). The left somatomotor network and its subnetworks (A and B) were extracted. Graph-theoretical methods were used to calculate network density, global efficiency, nodal efficiency, clustering coefficient, and betweenness centrality at the module-internal and module-to-whole-brain levels. Paired t-tests were performed, with false discovery rate (FDR) correction applied for multiple comparisons.Results Compared with motor execution, motor imagery showed increased network density, global efficiency, and betweenness centrality among the module-to-whole-brain metrics in the left somatomotor network A (t = 4.272, 4.280, and 8.981; P = 0.004, 0.004, and < 0.001, respectively; FDR-corrected), and decreased nodal efficiency and clustering coefficient (t = -3.867 and -4.107; P = 0.009 and 0.005, respectively; FDR-corrected). In the left somatomotor network B, network density, global efficiency, and betweenness centrality among the module-to-whole-brain metrics were also increased during motor imagery (t = 3.403, 3.217, and 4.543; P = 0.022, 0.029, and 0.003, respectively; FDR-corrected).Conclusions Motor imagery and motor execution showed distinct brain network topological patterns within the left somatomotor network, and the left somatomotor networks A and B responded differently to the two task conditions. This finding may provide imaging evidence for understanding the differences in neural mechanisms between motor imagery and motor execution.
[Keywords] motor imagery;motor execution;graph-theoretical analysis;functional magnetic resonance imaging;brain network topology

LIU Fengyu1   WANG Yu1   WANG Jiangguang1   WANG Xingyue1   KE Yougang1, 2   WU Dong1, 2   XIAO Rong1, 2   RAO Haibing1, 3   ZHENG Wenbin4   GUO Yuelin1, 2*  

1 Shenzhen Clinical College of Integrated Chinese and Western Medicine, Guangzhou University of Chinese Medicine, Shenzhen 518104, China

2 Department of Radiology, Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine, Shenzhen 518104, China

3 Department of Ultrasonography, Shenzhen Hospital of Integrated Traditional Chinese and Western Medicine, Shenzhen 518104, China

4 Department of Radiology, the Second Affiliated Hospital of Shantou University Medical College, Shantou 515000, China

Corresponding author: GUO Y L, E-mail: lamsubmit@126.com

Conflicts of interest   None.

Received  2026-03-09
Accepted  2026-06-09
DOI: 10.12015/issn.1674-8034.2026.07.004
DOI:10.12015/issn.1674-8034.2026.07.004.

[1]
PAVLOVIC D, PEKIC S, STOJANOVIC M, et al. Traumatic brain injury: neuropathological, neurocognitive and neurobehavioral sequelae[J]. Pituitary, 2019, 22(3): 270-282. DOI: 10.1007/s11102-019-00957-9.
[2]
LEFEVRE-DOGNIN C, COGNÉ M, PERDRIEAU V, et al. Definition and epidemiology of mild traumatic brain injury[J]. Neurochirurgie, 2021, 67(3): 218-221. DOI: 10.1016/j.neuchi.2020.02.002.
[3]
ALMEIDA S R M, STEFANO FILHO C A, VICENTINI J, et al. Modeling functional network topology following stroke through graph theory: functional reorganization and motor recovery prediction[J/OL]. Braz J Med Biol Res, 2022, 55: e12036[2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/35976269/. DOI: 10.1590/1414-431x2022e12036.
[4]
TANAMACHI K, KUWAHARA W, OKAWADA M, et al. Relationship between resting-state functional connectivity and change in motor function after motor imagery intervention in patients with stroke: a scoping review[J/OL]. J Neuroeng Rehabil, 2023, 20(1): 159 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/37980496/. DOI: 10.1186/s12984-023-01282-w.
[5]
SU H L, ZHAN G G, LIN Y F, et al. Analysis of brain network differences in the active, motor imagery, and passive stoke rehabilitation paradigms based on the task-state EEG[J/OL]. Brain Res, 2025, 1846: 149261 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/39396567/. DOI: 10.1016/j.brainres.2024.149261.
[6]
BAUMANN A, GLESS C A, KNUTZEN A, et al. Kinaesthetic motor imagery in writer's cramp dystonia reveals writing specific abnormalities in the occipital lobe[J/OL]. Neuroscience, 2025, 589: 221-229 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/41022349/. DOI: 10.1016/j.neuroscience.2025.09.042.
[7]
DEKLEVA B M, CHOWDHURY R H, BATISTA A P, et al. Motor cortex retains and reorients neural dynamics during motor imagery[J]. Nat Hum Behav, 2024, 8(4): 729-742. DOI: 10.1038/s41562-023-01804-5.
[8]
KANG H. Sample size determination and power analysis using the G*Power software[J/OL]. J Educ Eval Health Prof, 2021, 18: 17 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/34325496/. DOI: 10.3352/jeehp.2021.18.17.
[9]
BONDI E, DING Y D, ZHANG Y S, et al. Investigating the neurovascular coupling across multiple motor execution and imagery conditions: a whole-brain EEG-informed fMRI analysis[J/OL]. Neuroimage, 2025, 317: 121311 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/40484327/. DOI: 10.1016/j.neuroimage.2025.121311.
[10]
MEHTA K, SALO T, MADISON T J, et al. XCP-D: a robust pipeline for the post-processing of fMRI data[J/OL]. Imaging Neurosci, 2024, 2: imag-2-00257 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/40800264/. DOI: 10.1162/imag_a_00257.
[11]
SCHAEFER A, KONG R, GORDON E M, et al. Local-global parcellation of the human cerebral cortex from intrinsic functional connectivity MRI[J]. Cereb Cortex, 2018, 28(9): 3095-3114. DOI: 10.1093/cercor/bhx179.
[12]
MORISHIMA Y, VAN DEN HEUVEL M, STRIK W, et al. Neurobiologically informed graph theory analysis of the language system[J]. Netw Neurosci, 2025, 9(2): 504-521. DOI: 10.1162/netn_a_00443.
[13]
THEIS N, RUBIN J, CAPE J, et al. Threshold selection for brain connectomes[J]. Brain Connect, 2023, 13(7): 383-393. DOI: 10.1089/brain.2022.0082.
[14]
HAN L, CHAN M Y, AGRES P F, et al. Measures of resting-state brain network segregation and integration vary in relation to data quantity: implications for within and between subject comparisons of functional brain network organization[J/OL]. Cereb Cortex, 2024, 34(2): bhad506 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/38385891/. DOI: 10.1093/cercor/bhad506.
[15]
FRANSSON P, STRINDBERG M. Brain network integration, segregation and quasi-periodic activation and deactivation during tasks and rest[J/OL]. NeuroImage, 2023, 268: 119890 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/36681135/. DOI: 10.1016/j.neuroimage.2023.119890.
[16]
CHEN J, KAN W W, LIU Y, et al. Frequency-specific equivalence of brain activity on motor imagery during action observation and action execution[J]. Int J Neurosci, 2021, 131(6): 599-608. DOI: 10.1080/00207454.2020.1750394.
[17]
MUSTILE M, KOURTIS D, EDWARDS M G, et al. Neural correlates of motor imagery and execution in real-world dynamic behavior: evidence for similarities and differences[J/OL]. Front Hum Neurosci, 2024, 18: 1412307 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/38974480/. DOI: 10.3389/fnhum.2024.1412307.
[18]
KIM E, LEE W H, SEO H G, et al. Deciphering functional connectivity differences between motor imagery and execution of target-oriented grasping[J]. Brain Topogr, 2023, 36(3): 433-446. DOI: 10.1007/s10548-023-00956-x.
[19]
WANG G Y, JIANG L, SONG X P, et al. Enhancing neural representations of motor imagery through action-specific brain connectivity patterns[J/OL]. IEEE Trans Neural Syst Rehabil Eng, 2025, 33: 3555-3564 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/40902051/. DOI: 10.1109/TNSRE.2025.3605612.
[20]
OGAWA T, SHIMOBAYASHI H, HIRAYAMA J I, et al. Asymmetric directed functional connectivity within the frontoparietal motor network during motor imagery and execution[J/OL]. Neuroimage, 2022, 247: 118794 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/34906713/. DOI: 10.1016/j.neuroimage.2021.118794.
[21]
HAY S I, ONG K L, SANTOMAURO D F, et al. Burden of 375 diseases and injuries, risk-attributable burden of 88 risk factors, and healthy life expectancy in 204 countries and territories, including 660 subnational locations, 1990–2023: a systematic analysis for the Global Burden of Disease Study 2023[J]. Lancet, 2025, 406(10513): 1873-1922. DOI: 10.1016/S0140-6736(25)01637-X.
[22]
FEIGIN V L, BRAININ M, NORRVING B, et al. World stroke organization: global stroke fact sheet 2025[J]. Int J Stroke, 2025, 20(2): 132-144. DOI: 10.1177/17474930241308142.
[23]
DORSEY E R, OKUN M S, BLOEM B R. A PLAN to address the Parkinson pandemic[J]. J Park Dis, 2025, 15(8): 1322-1336. DOI: 10.1177/1877718x251378115.
[24]
CLARK B, WHITALL J, KWAKKEL G, et al. The effect of time spent in rehabilitation on activity limitation and impairment after stroke[J/OL]. Cochrane Database Syst Rev, 2021, 2021(10) [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/34695300/. DOI: 10.1002/14651858.cd012612.pub2.
[25]
POLO-FERRERO L, TORRES-ALONSO J, SÁNCHEZ-GONZÁLEZ J L, et al. Motor imagery for post-stroke upper limb recovery: a meta-analysis of RCTs on fugl-Meyer upper extremity scores[J/OL]. J Clin Med, 2025, 14(21): 7891 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/41227288/. DOI: 10.3390/jcm14217891.
[26]
MEHRHOLZ J, THOMAS S, KUGLER J, et al. Electromechanical-assisted training for walking after stroke[J/OL]. Cochrane Database Syst Rev, 2020, 10(10): CD006185 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/33091160/. DOI: 10.1002/14651858.CD006185.pub5.
[27]
LEE M, KIM Y H, LEE S W. Motor impairment in stroke patients is associated with network properties during consecutive motor imagery[J]. IEEE Trans Biomed Eng, 2022, 69(8): 2604-2615. DOI: 10.1109/TBME.2022.3151742.
[28]
NICOLELIS M A L. Brain-machine-brain interfaces as the foundation for the next generation of neuroprostheses[J/OL]. Natl Sci Rev, 2022, 9(10): nwab206 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/36196121/. DOI: 10.1093/nsr/nwab206.
[29]
MA Z Z, WU J J, CAO Z, et al. Motor imagery-based brain-computer interface rehabilitation programs enhance upper extremity performance and cortical activation in stroke patients[J/OL]. J NeuroEngineering Rehabil, 2024, 21(1): 91 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/38812014/. DOI: 10.1186/s12984-024-01387-w.
[30]
LI X J, YU C X, ZHAO C J, et al. Research progress of fMRI in brain plasticity during the rehabilitation period of hemiplegia after stroke[J]. Chin J Magn Reson Imaging, 2025, 16(2): 135-141. DOI: 10.12015/issn.1674-8034.2025.02.022.
[31]
ZHU L, LIU Y Y, LIU R H, et al. Decoding multi-brain motor imagery from EEG using coupling feature extraction and few-shot learning[J/OL]. IEEE Trans Neural Syst Rehabil Eng, 2023, 31: 4683-4692 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/37995161/. DOI: 10.1109/TNSRE.2023.3336356.
[32]
OGANESIAN L L, SHANECHI M M. Brain-computer interfaces for neuropsychiatric disorders[J]. Nat Rev Bioeng, 2024, 2(8): 653-670. DOI: 10.1038/s44222-024-00177-2.
[33]
WU D R, JIANG X, PENG R M. Transfer learning for motor imagery based brain-computer interfaces: a tutorial[J/OL]. Neural Netw, 2022, 153: 235-253 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/35753202/. DOI: 10.1016/j.neunet.2022.06.008.
[34]
WANG A X, TIAN X, JIANG D, et al. Rehabilitation with brain-computer interface and upper limb motor function in ischemic stroke: a randomized controlled trial[J/OL]. Med, 2024, 5(6): 559-569.e4 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/38642555/. DOI: 10.1016/j.medj.2024.02.014.
[35]
ZHU H, FORENZO D, HE B. On the deep learning models for EEG-based brain-computer interface using motor imagery[J/OL]. IEEE Trans Neural Syst Rehabil Eng, 2022, 30: 2283-2291 [2026-03-08]. https://pubmed.ncbi.nlm.nih.gov/35951573/. DOI: 10.1109/TNSRE.2022.3198041.

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