Poster No:
91
Submission Type:
Abstract Submission
Authors:
Liuzhenxiong Yu1, Rong Ye2, Panpan Hu1
Institutions:
1The First Affiliated Hospital of Anhui Medical University, Hefei, Anhui Province, 2Anhui Medical University, Hefei, N/A
First Author:
Liuzhenxiong Yu
The First Affiliated Hospital of Anhui Medical University
Hefei, Anhui Province
Co-Author(s):
Rong Ye
Anhui Medical University
Hefei, N/A
Panpan Hu
The First Affiliated Hospital of Anhui Medical University
Hefei, Anhui Province
Introduction:
Cerebellar involvement in Parkinson's disease (PD) is heterogeneous across disease stages and sub-regions. The posterior vermis (PV) plays a crucial role in the PD-related gait disturbances. However, the specific contribution of these subdivisions remains unclear. This study investigated the relationship between structural and functional alterations in PV sub-regions across PD progression and their association with gait impairments in patients with predominant postural instability and gait difficulty (PD-PIGD).
Methods:
In retrospective cross-sectional study, we examined the structural and functional characteristics of the posterior vermis (PV) in patients with PD-PIGD across various disease stages defined by the Hoehn and Yahr (HY) scale. The study cohort comprised 94 patients with PD-PIGD, stratified by HY stage (HY1, n = 33; HY2, n = 30; HY3-4, n = 31). Additionally, 46 age- and sex-matched healthy controls (HC) were included for comparative analysis. Our focus was on the posterior superior vermis (PSV) and the posterior inferior vermis (PIV), the two primary anatomical subdivisions of the PV. Differences in PV volume and seed-based resting-state functional connectivity (FC) among the groups were assessed using one-way analysis of variance and general linear model approaches, respectively. Furthermore, Bonferroni (Bonf) correction and false discovery rate correction were applied during volumetric and FC analyses to mitigate the risk of false positives due to multiple comparisons. Spearman's correlation coefficients were utilized to explore the relationships among volumetric measurements, FC, gait impairments, and cognitive function. Mediation analyses were conducted to elucidate the potential pathways through which structural and functional alterations may influence gait impairments.
Results:
Patients at the HY1 stage exhibited significantly increased PSV volume when compared to HC (Cohen's d = 0.76, p_Bonf = 0.007). Conversely, patients at the HY3-4 stage displayed a marked decrease in PSV volume relative to those at the HY1 stage (Cohen's d = -0.94, p_Bonf = 0.001). FC analysis revealed significant alterations in the connections between the PSV and motor cortex, specifically involving the left paracentral lobule and right precentral gyrus, across different disease stages. Notably, no differences in structural or functional metrics were observed in the PIV. Moreover, both PSV volume and FC between the PSV and the left paracentral lobule were significantly correlated with gait impairments, as measured by PIGD scores, as well as with cognitive performance, assessed using the Mini-Mental State Examination (MMSE) and the Montreal Cognitive Assessment (MoCA), in patients with PD-PIGD. Mediation analysis further indicated that cognitive functioning serves as a mediator in the relationship between PSV alterations and gait impairments.

·Posterior vermis volume and correlation with both motor and cognitive functions

·Posterior superior vermis functional connectivity and correlation with both motor and cognitive functions
Conclusions:
Our underscored the critical role of the PSV in the pathophysiology of PD-PIGD. The dynamic changes in PSV volume and FC across disease stages suggested a complex interplay of compensatory adaptations and progressive neurodegeneration. The strong associations between PSV integrity, gait performance, and cognitive function highlighted the need for comprehensive management strategies. Targeted neuromodulation of the cerebellum emerged as a promising therapeutic approach. Additionally, longitudinal studies utilizing advanced neuroimaging techniques were deemed essential to further elucidate these complex relationships and to develop effective interventions for patients with PD-PIGD.
Disorders of the Nervous System:
Neurodegenerative/ Late Life (eg. Parkinson’s, Alzheimer’s) 1
Novel Imaging Acquisition Methods:
BOLD fMRI
Multi-Modal Imaging 2
Keywords:
Cerebellum
Cognition
FUNCTIONAL MRI
Motor
Movement Disorder
STRUCTURAL MRI
1|2Indicates the priority used for review
By submitting your proposal, you grant permission for the Organization for Human Brain Mapping (OHBM) to distribute your work in any format, including video, audio print and electronic text through OHBM OnDemand, social media channels, the OHBM website, or other electronic publications and media.
I accept
The Open Science Special Interest Group (OSSIG) is introducing a reproducibility challenge for OHBM 2025. This new initiative aims to enhance the reproducibility of scientific results and foster collaborations between labs. Teams will consist of a “source” party and a “reproducing” party, and will be evaluated on the success of their replication, the openness of the source work, and additional deliverables. Click here for more information.
Propose your OHBM abstract(s) as source work for future OHBM meetings by selecting one of the following options:
I am submitting this abstract as an original work to be reproduced. I am available to be the “source party” in an upcoming team and consent to have this work listed on the OSSIG website. I agree to be contacted by OSSIG regarding the challenge and may share data used in this abstract with another team.
Please indicate below if your study was a "resting state" or "task-activation” study.
Resting state
Healthy subjects only or patients (note that patient studies may also involve healthy subjects):
Patients
Was this research conducted in the United States?
No
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
NOTE: Any human subjects studies without IRB approval will be automatically rejected.
Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
NOTE: Any animal studies without IACUC approval will be automatically rejected.
Yes
Please indicate which methods were used in your research:
Functional MRI
Structural MRI
Behavior
Neuropsychological testing
For human MRI, what field strength scanner do you use?
3.0T
Which processing packages did you use for your study?
SPM
Other, Please list
-
SUIT, CONN
Provide references using APA citation style.
Basaia, S. (2022). Cerebro-cerebellar motor networks in clinical subtypes of Parkinson's disease. NPJ Parkinsons Dis, 8(1), 113. doi:10.1038/s41531-022-00377-w
Kerestes, R. (2023). Cerebellar Volume and Disease Staging in Parkinson's Disease: An ENIGMA-PD Study. Mov Disord, 38(12), 2269-2281. doi:10.1002/mds.29611
Li, T., Le, W. (2023). Linking the cerebellum to Parkinson disease: an update. Nature Reviews Neurology, 19(11), 645-654. doi:10.1038/s41582-023-00874-3
Maiti, B. (2020). Cognitive correlates of cerebellar resting-state functional connectivity in Parkinson disease. Neurology, 94(4), e384-e396. doi:10.1212/WNL.0000000000008754
Maiti, B. (2021). Functional Connectivity of Vermis Correlates with Future Gait Impairments in Parkinson's Disease. Mov Disord, 36(11), 2559-2568. doi:10.1002/mds.28684
O'Callaghan, C. (2016). Cerebellar atrophy in Parkinson's disease and its implication for network connectivity. Brain, 139(Pt 3), 845-855. doi:10.1093/brain/awv399
Pietracupa, S. (2024). Understanding the role of cerebellum in early Parkinson's disease: a structural and functional MRI study. NPJ Parkinsons Dis, 10(1), 119. doi:10.1038/s41531-024-00727-w
Riou, A. (2021). Functional Role of the Cerebellum in Parkinson Disease: A PET Study. Neurology, 96(23), e2874-e2884. doi:10.1212/WNL.0000000000012036
Wu, T.(2013). The cerebellum in Parkinson's disease. Brain, 136(Pt 3), 696-709. doi:10.1093/brain/aws360
No