Poster No:
163
Submission Type:
Abstract Submission
Authors:
Eva van Heese1, Max Laansma1, Ashni Ramesar2, Karin van Dijk3, Evelien Lemstra4, Miranda Ringnalda5, Julia de Groot3, Juliette van Alphen4, Odile van den Heuvel6, Ysbrand van der Werf6
Institutions:
1Amsterdam UMC, Amsterdam, NA, 2Amsterdam UMC, Amsterdam, Netherlands, 3Stichting Epilepsie Instellingen Nederland (SEIN), Sleep-Wake Centre, Heemstede, Netherlands, 4Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Neurology, Alzheimer Center Amsterdam, Amsterdam, Netherlands, 5Stichting Epilepsie Instellingen Nederland (SEIN), Sleep-Wake Centre, Zwolle, Netherlands, 6Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Anatomy and Neurosciences, Amsterdam, NA
First Author:
Co-Author(s):
Karin van Dijk
Stichting Epilepsie Instellingen Nederland (SEIN), Sleep-Wake Centre
Heemstede, Netherlands
Evelien Lemstra
Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Neurology, Alzheimer Center Amsterdam
Amsterdam, Netherlands
Miranda Ringnalda
Stichting Epilepsie Instellingen Nederland (SEIN), Sleep-Wake Centre
Zwolle, Netherlands
Julia de Groot
Stichting Epilepsie Instellingen Nederland (SEIN), Sleep-Wake Centre
Heemstede, Netherlands
Juliette van Alphen
Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Neurology, Alzheimer Center Amsterdam
Amsterdam, Netherlands
Odile van den Heuvel
Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Anatomy and Neurosciences
Amsterdam, NA
Ysbrand van der Werf
Amsterdam UMC, Vrije Universiteit Amsterdam, Department of Anatomy and Neurosciences
Amsterdam, NA
Introduction:
REM sleep behaviour disorder (RBD) is characterised by often violent dream enactments, following REM sleep without atonia. RBD is strongly linked to Lewy body diseases, including Parkinson's disease (PD; estimated prevalence of RBD: 30-50%) and dementia with Lewy bodies (DLB; 76%). Perivascular spaces (PVS), surrounding blood vessels, play a role in brain clearance by facilitating the removal of waste, including alpha-synuclein protein accumulations. When enlarged, PVS can be detected and segmented in MR images, as previously done in Parkinson's Disease (Chen et al., 2022; Kim et al., 2024; Ramirez et al., 2022) and Dementia with Lewy Bodies (Choe et al., 2022; Saji et al., 2024). While the mechanisms behind PVS enlargement remain unclear, it is suggested that it may reflect impaired brain clearance and is proposed as a relevant marker in the context of neurodegeneration (Bakker et al., 2016; van Veluw & Perosa, 2022). The current study aimed to optimise the segmentation of MR-visible perivascular spaces on 7T MRI in healthy controls, in preparation for further analysis in Lewy body diseases.
Methods:
Individuals with PD and DLB, as well as healthy controls from the openly available AHEAD dataset (Alkemade et al., 2020) were scanned on a Philips Achieva 7T MRI, with T1-weighted and T2* contrasts acquired using the same multi-echo magnetization-prepared rapid gradient echo (MP2RAGEME) sequence. White matter segmentation was performed on the T1-weighted image using FastSurfer (Henschel et al., 2020), while PVS were identified on the T2*-map using a Frangi filter (Frangi et al., 1998), with parameter optimization based on different sigma ranges, step size, and thresholds utilizing open-source Python code (github.com/hufsaim/pvsseg). The sigma range determines the size of PVS being detected, whereas the step size reflects the incremental progression between sigma values, determining the granularity of the PVS detection. Thresholding functions as a filter to isolate PVS of interest from noise and irrelevant features.
Results:
Initial testing of the Frangi filter for identifying PVS on T2*-map showed variability in PVS segmentation based on different filter parameters, including the sigmas and threshold. Both sigma ranges show very similar results, but the sigma 1-4 with step size 1 shows some more densely packed red regions, emphasising the small-scale structures, compared to the sigma 5-15 with step size 5. These differences between the filter settings are even less visible when the thresholding is increased (see Figure 1). The optimal filter settings were found with a sigma lower bound of 1, upper bound of 4, and steps of 1. Optimal thresholding settings varied by individual and were determined case by case, considering anatomy and imaging quality. This optimal set of parameters together were both sensitive and specific to PVS, based on visual inspection of the data.

·Figure 1
Conclusions:
We have successfully optimized the parameters to apply a Frangi filter for PVS segmentation on this 7T MR dataset of healthy controls. Based on the different Frangi filter settings, we conclude that medium thresholding suppresses subtle differences caused by sigma and step size variations. Moving forward, this method will be applied to the Lewy body diseases cohort (n≈80) to investigate PVS in the context of neurodegeneration. Future analyses will focus on exploring correlations between PVS volume and clinical measures of cognition and sleep, with the goal of understanding the role of enlarged MR-visible PVS in Lewy body diseases.
Disorders of the Nervous System:
Neurodegenerative/ Late Life (eg. Parkinson’s, Alzheimer’s) 1
Modeling and Analysis Methods:
Methods Development
Segmentation and Parcellation 2
Neuroanatomy, Physiology, Metabolism and Neurotransmission:
Anatomy and Functional Systems
Keywords:
Aging
Cerebro Spinal Fluid (CSF)
Data analysis
Degenerative Disease
HIGH FIELD MR
Segmentation
Sleep
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 do not want to participate in the reproducibility challenge.
Please indicate below if your study was a "resting state" or "task-activation” study.
Other
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.
Not applicable
Please indicate which methods were used in your research:
Structural MRI
Neuropsychological testing
For human MRI, what field strength scanner do you use?
7T
Which processing packages did you use for your study?
AFNI
SPM
FSL
Free Surfer
Provide references using APA citation style.
1. Alkemade, A., et al., & Forstmann, B. U. (2020). The Amsterdam Ultra-high field adult lifespan database (AHEAD): A freely available multimodal 7 Tesla submillimeter magnetic resonance imaging database. NeuroImage, 221(117200), 117200.
2. Bakker, E. N. T. P., et al., & Carare, R. O. (2016). Lymphatic clearance of the brain: Perivascular, paravascular and significance for neurodegenerative diseases. Cellular and Molecular Neurobiology, 36(2), 181–194.
3. Chen, H., et al., & Wang, Y. (2022). Perivascular space in Parkinson’s disease: Association with CSF amyloid/tau and cognitive decline. Parkinsonism & Related Disorders, 95, 70–76.
4. Choe, Y. M., et al., & Lee, D. Y. (2022). Association between enlarged perivascular spaces and cognition in a memory clinic population. Neurology, 99(13), e1414–e1421.
5. Frangi, A. F., Niessen, W. J., Vincken, K. L., & Viergever, M. A. (1998). Multiscale vessel enhancement filtering. In Medical Image Computing and Computer-Assisted Intervention — MICCAI’98 (pp. 130–137). Springer Berlin Heidelberg.
6. Henschel, L., Conjeti, S., Estrada, S., Diers, K., Fischl, B., & Reuter, M. (2020). FastSurfer - A fast and accurate deep learning based neuroimaging pipeline. NeuroImage, 219(117012), 117012.
7. Kim, S., Na, H. K., Sun, Y., Yoon, Y. J., Chung, S. J., Sohn, Y. H., Lyoo, C. H., & Lee, P. H. (2024). Regional burden of enlarged perivascular spaces and cognition and neuropsychiatric symptoms in drug-naive patients with Parkinson disease. Neurology, 102(12), e209483.
8. Ramirez, J., Berberian, S. A., Breen, D. P., Gao, F., Ozzoude, M., Adamo, S., Scott, C. J. M., Berezuk, C., Yhap, V., Mestre, T. A., Marras, C., Tartaglia, M. C., Grimes, D., Jog, M., Kwan, D., Tan, B., Binns, M. A., Arnott, S. R., Bartha, R., … ONDRI Investigators. (2022). Small and large magnetic resonance imaging-visible perivascular spaces in the basal ganglia of Parkinson’s disease patients. Movement Disorders: Official Journal of the Movement Disorder Society, 37(6), 1304–1309.
9. Saji, N., Kinjo, Y., Murotani, K., Niida, S., Takeda, A., & Sakurai, T. (2024). High pulse wave velocity is associated with enlarged perivascular spaces in dementia with Lewy bodies. Scientific Reports, 14.
10. van Veluw, S. J., & Perosa, V. (2022). The perivascular space race: Understanding their role in brain clearance. Neurology, 98(3), 95–96.
No