Poster No:
2004
Submission Type:
Abstract Submission
Authors:
Ina Drabløs1, Stener Nerland1, Wibeke Nordhøy2, Robin Bugge3, Ole Andreassen4, Ingrid Agartz1, Kjetil Jørgensen5, Dimitrios Andreou1
Institutions:
1Department of Psychiatric Research, Diakonhjemmet Hospital, Oslo, Norway, 2Department of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine, Oslo, Norway, 3Department of Diagnostic Physics, Division of Radiology and Nuclear Medicine, Oslo, Norway, 4NORMENT, Division of Mental Health and Addiction, Oslo University Hospital, Oslo, Norway, 5NORMENT, Institute of Clinical Medicine, University of Oslo, Oslo, Norway
First Author:
Ina Drabløs
Department of Psychiatric Research, Diakonhjemmet Hospital
Oslo, Norway
Co-Author(s):
Stener Nerland
Department of Psychiatric Research, Diakonhjemmet Hospital
Oslo, Norway
Wibeke Nordhøy
Department of Physics and Computational Radiology, Division of Radiology and Nuclear Medicine
Oslo, Norway
Robin Bugge
Department of Diagnostic Physics, Division of Radiology and Nuclear Medicine
Oslo, Norway
Ole Andreassen
NORMENT, Division of Mental Health and Addiction, Oslo University Hospital
Oslo, Norway
Ingrid Agartz
Department of Psychiatric Research, Diakonhjemmet Hospital
Oslo, Norway
Kjetil Jørgensen
NORMENT, Institute of Clinical Medicine, University of Oslo
Oslo, Norway
Dimitrios Andreou
Department of Psychiatric Research, Diakonhjemmet Hospital
Oslo, Norway
Introduction:
The cerebellum serves a crucial role in motor control and cognitive function (Buckner, 2013; Schmahmann, 2019) and has been implicated in psychiatric disorders such as schizophrenia, bipolar disorder, and autism (Phillips et al., 2015; Villanueva, 2012). Measuring cerebellar structures and analyzing potential brain changes in such disorders is dependent on accurate cerebellar segmentation. In the literature, various MRI-based segmentation methods are compared on different measures such as repeatability, reproducibility, and dice overlap to expert delineations, with varying results. (Carass et al., 2018; Sörös et al., 2021). In this study we compared the test-retest reliability of two different cerebellar segmentation methods, and determined the correlations between the segmented volumes.
Methods:
Test-retest reliability for cerebellar volumes was calculated on an independent sample of n = 10 healthy volunteers acquired on two separate MRI scanners. T1-weighted structural images were acquired from n = 9 of the individuals (mean age = 35.76 years; range = [26.31-59.70]; 55% male) on a 3T GE Discovery MR750 scanner, and n = 9 of the individuals (mean age = 35.8 years; range = [25.24-60.52]; 55% male) on a 3T GE SIGNA Premier scanner. On each MRI scanner, individuals were scanned twice per session with a repositioning between scans, and a two-week interval between sessions, resulting in a total of four scans each. Cerebellar volumes were estimated with two different segmentation methods; the Sequence Adaptive Multimodal SEGmentation (SAMSEG; Puonti et al., 2016) and the Automatic Cerebellum Anatomical Parcellation using U-net with Locally Constrained Optimization (ACAPULCO; Han et al., 2020). Intra-class correlations (ICC) and 95% confidence intervals (CI) were computed for each combination of segmented volume, scan platform and segmentation tool, resulting in four measures from SAMSEG (grey- and white matter for each hemisphere) and an additional 28 measures of the cerebellar lobules from ACAPULCO. Furthermore, mean overall volumes and standard deviations were calculated, with a subsequent analysis of Pearson correlations to establish agreement between the methods.
Results:
We found ICCs > 0.9 for both methods between all sessions and scans within MRI scanner, indicating excellent reliability, apart from three lobules from ACAPULCO: Left I-III (MR750: ICC = 0.79; CI = 0.54-0.94, Premier: ICC = 0.8; CI = 0.57-0.94), Right I-III (MR750: ICC = 0.73; CI = 0.46-0.92, Premier: ICC = 0.85; CI = 0.66-0.96), and Vermis X (MR750: ICC = 0.89; CI = 0.73-0.97, Premier: ICC = 0.96; CI = 0.9-0.99). Correlations for overall volumetric output between the segmentation methods were high for whole-, hemispheric-, and grey matter-volumes (r = 0.96-0.97). However, correlations for white matter volumes were lower (r = 0.37-0.42).
Conclusions:
Both methods showed high test-retest reliability for global cerebellum measures. The most notable difference was the estimation of white matter volumes, resulting in low correlation between approaches. The segmentation of white matter differs between SAMSEG and ACAPULCO, with the former including part of the pons and most white matter branches and the latter only isolating the white matter of the Corpus Medullare (Bogovic et al., 2013). Selecting an approach for volumetric analyses of the cerebellum should thus be made not only based on the reliability of the method, but also depending on the measure of interest.
Modeling and Analysis Methods:
Segmentation and Parcellation 1
Neuroanatomy, Physiology, Metabolism and Neurotransmission:
Cortical Anatomy and Brain Mapping
Neuroanatomy Other
Neuroinformatics and Data Sharing:
Brain Atlases
Novel Imaging Acquisition Methods:
Anatomical MRI 2
Keywords:
Cerebellum
Cortex
Segmentation
STRUCTURAL MRI
White Matter
1|2Indicates the priority used for review
Provide references using author date format
Bogovic, J. A. (2013). 'Approaching expert results using a hierarchical cerebellum parcellation protocol for multiple inexpert human raters', NeuroImage, vol. 64, pp. 616–629
Buckner, R. L. (2013). 'The Cerebellum and Cognitive Function: 25 Years of Insight from Anatomy and Neuroimaging', Neuron, vol. 80, no. 3, pp. 807–815
Carass, A. (2018). 'Comparing fully automated state-of-the-art cerebellum parcellation from magnetic resonance images', NeuroImage, vol. 183, pp. 150–172
Han, S. (2020). 'Automatic cerebellum anatomical parcellation using U-Net with locally constrained optimization', NeuroImage, vol. 218, 116819
Phillips, J. R. (2015). 'The cerebellum and psychiatric disorders', Frontiers in Public Health, vol. 3, 66
Puonti, O. (2016). 'Fast and sequence-adaptive whole-brain segmentation using parametric Bayesian modeling', NeuroImage, vol. 143, pp. 235–249
Schmahmann, J. D. (2019). 'The cerebellum and cognition', The Cerebellum in Health and Disease, vol. 688, pp. 62–75
Sörös, P. (2021). 'Replicability, Repeatability, and Long-term Reproducibility of Cerebellar Morphometry', The Cerebellum, vol. 20, no. 3, pp. 439–453
Villanueva, R. (2012). 'The cerebellum and neuropsychiatric disorders', Psychiatry Research, vol. 198, no. 3, pp. 527–532