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Review
Research advances in multimodal MRI of the cerebellum in Parkinson's disease
GUO Rong  LIU Quanyuan  LIU Miaomiao  LI Minglong  LIU Wenxin  YANG Ping  QIAO Linjun  LI Xianglin 

DOI:10.12015/issn.1674-8034.2026.05.025.


[Abstract] Monitoring structural and functional abnormalities of the cerebellum in Parkinson's disease (PD) is of great significance for understanding disease mechanisms, guiding individualized treatment, and evaluating therapeutic efficacy. Multimodal MRI technology enables non-invasive and multi-dimensional assessment of cerebellar alterations in structure, function, and metabolism, providing crucial insights into the cerebellar pathological processes in PD. Based on recent advances in techniques such as structural MRI (sMRI), diffusion tensor imaging (DTI), blood oxygenation level-dependent functional MRI (BOLD-fMRI), quantitative susceptibility mapping (QSM), and magnetic resonance spectroscopy (MRS), this article systematically reviews the relationship between cerebellar structural and functional changes and clinical symptoms in PD. It focuses on characteristic manifestations including deep cerebellar nuclear atrophy, white matter microstructural damage, functional connectivity abnormalities, and metabolic disturbances, elaborates on the potential mechanisms of the cerebellum in both motor and non-motor symptoms of PD. This review identifies current limitations, such as insufficient analysis of functional heterogeneity within cerebellar subregions, low consistency across different imaging modalities, and a lack of longitudinal studies, and points out future research directions, including the integration of ultra-high field MRI and artificial intelligence techniques. The ultimate goal is to provide imaging evidence for early diagnosis, disease monitoring, and treatment evaluation of PD.
[Keywords] Parkinson's disease;cerebellum;magnetic resonance imaging;multimodal brain imaging;white matter microstructure;brain function

GUO Rong1   LIU Quanyuan2   LIU Miaomiao3   LI Minglong1   LIU Wenxin1   YANG Ping1   QIAO Linjun1   LI Xianglin1*  

1 School of Medical Imaging, Shandong Medical and Pharmaceutical University, Yantai 264003, China

2 Department of Radiology, Binzhou Medical University Hospital, Binzhou 256603, China

3 Department of Medical Imaging, Shandong University Affiliated Children's Hospital (Jinan Children's Hospital), Jinan 250022, China

Corresponding author: LI X L, E-mail: xlli@bzmc.edu.cn

Conflicts of interest   None.

Received  2026-01-16
Accepted  2026-04-19
DOI: 10.12015/issn.1674-8034.2026.05.025
DOI:10.12015/issn.1674-8034.2026.05.025.

[1]
OWENS-WALTON C, NIR T M, AL-BACHARI S, et al. A worldwide study of white matter microstructural alterations in people living with Parkinson's disease[J/OL]. NPJ Parkinson's Disease, 2024, 10(1): 151 [2026-01-16]. https://doi.org/10.1038/s41531-024-00758-3. DOI: 10.1038/s41531-024-00758-3.
[2]
BEN-SHLOMO Y, DARWEESH S, LLIBRE-GUERRA J, et al. The epidemiology of Parkinson's disease[J]. Lancet, 2024, 403(10423): 283-292. DOI: 10.1016/S0140-6736(23)01419-8.
[3]
TINAZZI M, GANDOLFI M, ARTUSI C A, et al. Advances in diagnosis, classification, and management of pain in Parkinson's disease[J]. Lancet Neurol, 2025, 24(4): 331-347. DOI: 10.1016/S1474-4422(25)00033-X.
[4]
MISHRA A K, DIXIT A. Dopaminergic Axons: Key Recitalists in Parkinson's Disease[J]. Neurochem Res, 2022, 47(2): 234-248. DOI: 10.1007/s11064-021-03464-1.
[5]
DEL-BEL E, BARROS-PEREIRA N, R P de MORAES, et al. A journey through cannabidiol in Parkinson's disease[J]. Int Rev Neurobiol, 2024, 177: 65-93. DOI: 10.1016/bs.irn.2024.04.015.
[6]
ALMIKHLAFI M A. The role of exercise in Parkinson's disease[J]. Neurosciences (Riyadh), 2023, 28(1): 4-12. DOI: 10.17712/nsj.2023.1.20220105.
[7]
THOME A D, WANG J, ATASSI F, et al. Peripheral monocyte transcriptional signatures of inflammation and oxidative stress in Parkinson's disease[J/OL]. Front Immunol, 2025, 16: 1571074 [2026-01-16]. https://www.frontiersin.org/articles/10.3389/fimmu.2025.1571074. DOI: 10.3389/fimmu.2025.1571074.
[8]
FENG Y, ZHANG W, XU Y, et al. Cerebellar contributions to cognitive deterioration in Parkinson's disease: insights from multi-omics and longitudinal data[J/OL]. Neurobiol Dis., 2026, 219: 107275 [2026-01-16]. https://doi.org/10.1016/j.nbd.2026.107275. DOI: 10.1016/j.nbd.2026.107275.
[9]
LI T, LE W, JANKOVIC J. Linking the cerebellum to Parkinson disease: an update[J]. Nat Rev Neurol, 2023, 19(11): 645-654. DOI: 10.1038/s41582-023-00874-3.
[10]
QIU T, LIU M, QIU X, et al. Cerebellar involvement in Parkinson's disease: pathophysiology and neuroimaging[J]. Chin Med J (Engl), 2024, 137(20): 2395-2403. DOI: 10.1097/CM9.0000000000003248.
[11]
GROBE-EINSLER M, BALJASNIKOWA V, FAIKUS A, et al. Cerebellar transcranial magnetic stimulation improves motor function in Parkinson's disease[J]. Ann Clin Transl Neurol, 2024, 11(10): 2673-2684. DOI: 10.1002/acn3.52183.
[12]
XUEYAN H, QI A, CHUNMING S, et al. Abnormalities of white matter network properties in middle-aged and elderly patients with functional constipation[J/OL]. Front Neurol, 2024, 15: 1357274 [2026-01-16]. https://doi.org/10.3389/fneur.2024.1357274. DOI: 10.3389/fneur.2024.1357274.
[13]
QIN J, WU H, WU C, et al. Robust computation of subcortical functional connectivity guided by quantitative susceptibility mapping: an application in Parkinson's disease diagnosis[J/OL]. NeuroImage, 2025, 314: 121256 [2026-01-16]. https://doi.org/10.1016/j.neuroimage.2025.121256. DOI: 10.1016/j.neuroimage.2025.121256.
[14]
ZHONG Y, LIU H, LIU G, et al. A review on pathology, mechanism, and therapy for cerebellum and tremor in Parkinson's disease[J/OL]. NPJ Parkinsons Dis, 2022, 8(1): 82 [2026-01-16]. https://doi.org/10.1038/s41531-022-00347-2. DOI: 10.1038/s41531-022-00347-2.
[15]
DUAN M, PAN R, GAO Q, et al. A rapid multi-parametric quantitative MR imaging method to assess Parkinson's disease: a feasibility study[J/OL]. BMC Med Imaging, 2024, 24(1): 58 [2026-01-16]. https://doi.org/10.1186/s12880-024-01229-0. DOI: 10.1186/s12880-024-01229-0.
[16]
OZGEN M N, SAHIN N E, ERTAN N, et al. Investigation of total cerebellar and flocculonodular lobe volume in Parkinson's disease and healthy individuals: a brain segmentation study[J]. Neurol Sci, 2024, 45(9): 4291-4298. DOI: 10.1007/s10072-024-07509-5.
[17]
KERESTES R, LAANSMA M A, OWENS‐WALTON C, et al. Cerebellar Volume and Disease Staging in Parkinson's Disease: An ENIGMA-PD Study[J]. Mov Disord, 2023, 38(12): 2269-2281. DOI: 10.1002/mds.29611.
[18]
PIETRACUPA S, OJHA A, BELVISI D, et al. Understanding the role of cerebellum in early Parkinson's disease: a structural and functional MRI study[J/OL]. NPJ Parkinson's Disease, 2024, 10(1): 119 [2026-01-16]. https://doi.org/10.1038/s41531-024-00727-w. DOI: 10.1038/s41531-024-00727-w.
[19]
YUN J J, GAILLY DE TAURINES A, TAI Y F, et al. Anatomical abnormalities suggest a compensatory role of the cerebellum in early Parkinson's disease[J/OL]. NeuroImage, 2025, 310: 121121 [2026-01-16]. https://doi.org/10.1016/j.neuroimage.2025.121121. DOI: 10.1016/j.neuroimage.2025.121121.
[20]
SHIH Y C, TSENG W Y I, MONTASER-KOUHSARI L. Recent advances in using diffusion tensor imaging to study white matter alterations in Parkinson's disease: a mini review[J/OL]. Front Aging Neurosci, 2023, 14: 1018017 [2026-01-16]. https://doi.org/10.3389/fnagi.2022.1018017. DOI: 10.3389/fnagi.2022.1018017.
[21]
WANG M, LIU Y, HAN W, et al. White matter microstructural alterations and brain metabolism distributions in Parkinson's disease[J/OL]. Brain Imaging Behav, 2025 [2026-01-16]. https://link.springer.com/10.1007/s11682-025-01023-8. DOI: 10.1007/s11682-025-01023-8.
[22]
JIANG L, ZHUO J, FURMAN A, et al. Cerebellar functional connectivity change is associated with motor and neuropsychological function in early stage drug-naïve patients with Parkinson's disease[J/OL]. Front Neurosci, 2023, 17: 1113889 [2026-01-16]. https://doi.org/10.3389/fnins.2023.1113889. DOI: 10.3389/fnins.2023.1113889.
[23]
HE C, YANG R, RONG S, et al. Temporal evolution of microstructural integrity in cerebellar peduncles in Parkinson's disease: stage-specific patterns and dopaminergic correlates[J/OL]. NeuroImage Clin, 2024, 44: 103679. [2026-01-16]. https://doi.org/10.1016/j.nicl.2024.103679. DOI: 10.1016/j.nicl.2024.103679.
[24]
LIU Z, ZHANG Y, WANG H, et al. Altered cerebral perfusion and microstructure in advanced Parkinson's disease and their associations with clinical features[J]. Neurol Res, 2022, 44(1): 47-56. DOI: 10.1080/01616412.2021.1954842.
[25]
ZHENG Q, YUAN W, WEN J, et al. Arterial spin labeling MRI based perfusion pattern related to motor dysfunction and L-DOPA reactivity in Parkinson's disease[J/OL]. NeuroImage Clin, 2025, 46: 103776 [2026-01-16]. https://doi.org/10.1016/j.nicl.2025.103776. DOI: 10.1016/j.nicl.2025.103776.
[26]
ZHONG Y, LIU H, LIU G, et al. Cerebellar and cerebral white matter changes in Parkinson's disease with resting tremor[J]. Neuroradiology, 2023, 65(10): 1497-1506. DOI: 10.1007/s00234-023-03206-w.
[27]
BENARROCH E. What is the role of the dentate nucleus in normal and abnormal cerebellar function?[J/OL]. Neurology, 2024, 103(3): e209636 [2026-01-16]. https://doi.org/10.1212/WNL.0000000000209636. DOI: 10.1212/WNL.0000000000209636.
[28]
MENG H, ZHANG D, SUN Q. The applied value in brain gray matter nuclei of patients with early-stage Parkinson's disease : a study based on multiple magnetic resonance imaging techniques[J/OL]. Head Face Med, 2023, 19(1): 25 [2026-01-16]. https://doi.org/10.1186/s13005-023-00371-4. DOI: 10.1186/s13005-023-00371-4.
[29]
MITCHELL T, ARCHER D B, CHU W T, et al. Neurite orientation dispersion and density imaging (NODDI) and free‐water imaging in Parkinsonism[J]. Hum Brain Mapp, 2019, 40(17): 5094-5107. DOI: 10.1002/hbm.24760.
[30]
YANG L, CHENG Y, SUN Y, et al. Combined application of quantitative susceptibility mapping and diffusion kurtosis imaging techniques to investigate the effect of iron deposition on microstructural changes in the brain in Parkinson's disease[J/OL]. Front Aging Neurosci, 2022, 14: 792778 [2026-01-16]. https://doi.org/10.3389/fnagi.2022.792778. DOI: 10.3389/fnagi.2022.792778.
[31]
MOGUILNER S, BAEZ S, HERNANDEZ H, et al. Brain clocks capture diversity and disparities in aging and dementia across geographically diverse populations[J]. Nat Med, 2024, 30(12): 3646-3657. DOI: 10.1038/s41591-024-03209-x.
[32]
GARDONI A, AGOSTA F, SARASSO E, et al. Cerebellar alterations in Parkinson's disease with postural instability and gait disorders[J]. J Neurol, 2023, 270(3): 1735-1744. DOI: 10.1007/s00415-022-11531-y.
[33]
CAVALLO A, KÖHLER R M, BUSCH J L, et al. Differential modulation of movement speed with state-dependent deep brain stimulation in Parkinson's disease[J/OL]. Sci Adv, 2025, 11(37): eadx6849 [2026-01-16]. https://doi.org/10.1126/sciadv.adx6849. DOI: 10.1126/sciadv.adx6849.
[34]
WANG J, SHU Z, WANG Y, et al. A signature combining brain functional connectivity with executive and motor function for general cognitive decline in Parkinson's disease[J/OL]. Front Neurol, 2025, 16: 1434733 [2026-01-16]. https://doi.org/10.3389/fneur.2025.1434733. DOI: 10.3389/fneur.2025.1434733.
[35]
CIERI F, GIRIPRAKASH P P, NANDY R, et al. Functional connectivity differences of the olfactory network in Parkinson's disease, mild cognitive impairment and cognitively normal individuals: a resting-state fMRI study[J]. Neuroscience, 2024, 559: 8-16. DOI: 10.1016/j.neuroscience.2024.08.031.
[36]
SU D, JI L, CUI Y, et al. Altered visuomotor network dynamics associated with freezing of gait in Parkinson's disease[J/OL]. Mov Disord, 2025: mds.30146 [2026-01-16]. https://doi.org/10.1002/mds.30146. DOI: 10.1002/mds.30146.
[37]
LI G, JIANG M, CHEN X, et al. Clinical and Functional Connectivity Markers in Prediction of Hallucinations in Parkinson's Disease[J/OL]. CNS Neurosci Ther, 2025, 31(6): e70432 [2026-01-16]. https://doi.org/10.1111/cns.70432. DOI: 10.1111/cns.70432.
[38]
SAVOIE F A, ARPIN D J, VAILLANCOURT D E. Magnetic resonance imaging and nuclear imaging of Parkinsonian disorders: where do we go from here?[J]. Curr Neuropharmacol, 2024, 22(10): 1583-1605. DOI: 10.2174/1570159X21666230801140648.
[39]
BORGHAMMER P. The brain-first vs. body-first model of Parkinson's disease with comparison to alternative models[J]. J Neural Transm (Vienna), 2023, 130(6): 737-753. DOI: 10.1007/s00702-023-02633-6.
[40]
CHURCHILL L, CHEN Y C, LEWIS S J G, et al. Understanding REM Sleep Behavior Disorder through Functional MRI: A Systematic Review[J]. Movement Disorders, 2024, 39(10): 1679-1696. DOI: 10.1002/mds.29898.
[41]
LIU J. Altered regional homogeneity and connectivity in cerebellum and visual-motor relevant cortex in Parkinson's disease with rapid eye movement sleep behavior disorder[J]. Sleep Med, 2021, 82: 125-133. DOI: 10.1016/j.sleep.2021.03.041.
[42]
FIRBANK M J, PASQUINI J, BEST L, et al. Cerebellum and basal ganglia connectivity in isolated REM sleep behaviour disorder and Parkinson's disease: an exploratory study[J]. Brain Imaging Behav, 2024, 18(6): 1428-1437. DOI: 10.1007/s11682-024-00939-x.
[43]
CAO Y, SI Q, TONG R, et al. Abnormal dynamic functional connectivity changes correlated with non-motor symptoms of Parkinson's disease[J/OL]. Front Neurosci, 2023, 17: 1116111. [2026-01-16]. https://doi.org/10.3389/fnins.2023.1116111. DOI: 10.3389/fnins.2023.1116111.
[44]
SHEN B, YAO Q, LI W, et al. Dynamic cerebellar and sensorimotor network compensation in tremor-dominated Parkinson's disease[J/OL]. Neurobiol Dis, 2024, 201: 106659 [2026-01-16]. https://doi.org/10.1016/j.nbd.2024.106659. DOI: 10.1016/j.nbd.2024.106659.
[45]
HUANG S, DE BRIGARD F, CABEZA R, et al. Connectivity analyses for task-based fMRI[J]. Physics of Life Reviews, 2024, 49: 139-156. DOI: 10.1016/j.plrev.2024.04.012.
[46]
CHEN K, WANG S, WEN Q, et al. Rehabilitation response in tremor‐ and non‐tremor‐dominant Parkinson disease: a task‐fMRI study[J/OL]. Brain and Behavior, 2024, 14(10): e70102. [2026-01-16]. https://doi.org/10.1002/brb3.70102. DOI: 10.1002/brb3.70102.
[47]
SARASSO E, GARDONI A, ZENERE L, et al. Neural correlates of bradykinesia in Parkinson's disease: a kinematic and functional MRI study[J/OL]. NPJ Parkinsons Dis, 2024, 10(1): 167 [2026-01-16]. https://doi.org/10.1038/s41531-024-00783-2. DOI: 10.1038/s41531-024-00783-2.
[48]
HANNAWAY N, LAO-KAIM N P, MARTÍN-BASTIDA A, et al. Longitudinal changes in movement-related functional MRI activity in Parkinson's disease patients[J]. Parkinsonism Relat Disord, 2021, 87: 61-69. DOI: 10.1016/j.parkreldis.2021.04.025.
[49]
NI C, CHEN L, LIN R, et al. Diffusion tensor image analysis along the perivascular space and quantitative susceptibility mapping in the diagnosis and severity assessment of Parkinson's disease[J]. Quant Imaging Med Surg, 2025, 15(2): 1411-1424. DOI: 10.21037/qims-24-1605.
[50]
GAURAV R, LEJEUNE F X, SANTIN M D, et al. Early brain iron changes in Parkinson's disease and isolated rapid eye movement sleep behaviour disorder: a four-year longitudinal multimodal quantitative MRI study[J/OL]. Brain Commun, 2025, 7(3): fcaf212 [2026-01-16]. https://doi.org/10.1093/braincomms/fcaf212. DOI: 10.1093/braincomms/fcaf212.
[51]
ZHANG Y, HUANG P, WANG X, et al. Visualizing the deep cerebellar nuclei using quantitative susceptibility mapping: an application in healthy controls, Parkinson's disease patients and essential tremor patients[J]. Hum Brain Mapp, 2023, 44(4): 1810-1824. DOI: 10.1002/hbm.26178.
[52]
ZHANG Y, YANG M, WANG F, et al. Histogram analysis of quantitative susceptibility mapping for the diagnosis of Parkinson's disease[J]. Acad Radiol, 2022, 29: S71-S79. DOI: 10.1016/j.acra.2020.10.027.
[53]
JOKAR M, JIN Z, HUANG P, et al. Diagnosing Parkinson's disease by combining neuromelanin and iron imaging features using an automated midbrain template approach[J/OL]. NeuroImage, 2023, 266: 119814 [2026-01-16]. https://doi.org/10.1016/j.neuroimage.2022.119814. DOI: 10.1016/j.neuroimage.2022.119814.
[54]
LEE G, JUNG W, SAKAIE K E, et al. An optimized framework of QSM mask generation using deep learning: QSMmask-net[J/OL]. NMR Biomed, 2025, 38(6): e70057 [2026-01-16]. https://doi.org/10.1002/nbm.70057. DOI: 10.1002/nbm.70057.
[55]
GUAN J T, ZHENG X, LAI L, et al. Proton magnetic resonance spectroscopy for diagnosis of non-motor symptoms in Parkinson's disease[J/OL]. Front Neurol, 2022, 13: 594711. [2026-01-16]. https://doi.org/10.3389/fneur.2022.594711. DOI: 10.3389/fneur.2022.594711.
[56]
PELLICANO C, VECCHIO D, GIOVE F, et al. Contribution of cerebellar glutamatergic and GABAergic systems in premotor and early stages of Parkinson's disease[J/OL]. Int J Mol Sci, 2025, 26(21): 10754 [2026-01-16]. https://doi.org/10.3390/ijms262110754. DOI: 10.3390/ijms262110754.
[57]
HONG C T, YANG C C, CHEN D Y T, et al. Cerebellar structural and N-acetylaspartate, choline, and creatine metabolic profiles in Parkinson's disease and essential tremor[J/OL]. Diagnostics (Basel), 2024, 14(21): 2430 [2026-01-16]. https://doi.org/10.3390/diagnostics14212430. DOI: 10.3390/diagnostics14212430.

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