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Bas Jasperse

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3 papers
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3

YNICL Journal 2024 Journal Article

Scanner-specific optimisation of automated lesion segmentation in MS

  • David R. van Nederpelt
  • Giuseppe Pontillo
  • Mar Barrantes-Cepas
  • Iman Brouwer
  • Eva M.M. Strijbis
  • Menno M. Schoonheim
  • Bastiaan Moraal
  • Bas Jasperse

BACKGROUND & OBJECTIVE: Automatic lesion segmentation techniques on MRI scans of people with multiple sclerosis (pwMS) could support lesion detection and segmentation in trials and clinical practice. However, knowledge on their reliability across scanners is limited, hampering clinical implementation. The aim of this study was to investigate the within-scanner repeatability and between-scanner reproducibility of lesion segmentation tools in pwMS across three different scanners and examine their accuracy compared to manual segmentations with and without optimization. METHODS: 30 pwMS underwent a scan and rescan on three MRI scanners. GE Discovery MR750 (3.0 T), Siemens Sola (1.5 T) and Siemens Vida (3.0 T)). 3D-FLuid Attenuated Inversion Recovery (3D-FLAIR) and 3D T1-weighted scans were acquired on each scanner. Lesion segmentation involved preprocessing and automatic segmentation using the Lesion Segmentation Toolbox (LST) and nicMSlesions (nicMS) as well as manual segmentation. Both automated segmentation techniques were used with default settings, and with settings optimized to match manual segmentations for each scanner specifically and combined for the three scanners. LST settings were optimized by adjusting the threshold to improve the Dice similarity coefficient (DSC) for each scanner separately and a combined threshold for all scanners. For nicMS the last layers were retrained, once with the multi-scanner data to represent a combined optimization and once separately for each scanner for scanner specific optimization. Volumes and counts were extracted. DSC was calculated for accuracy, and reliability was assessed using intra-class correlation coefficients (ICC). Differences in DSC between software was tested with a repeated measures ANOVA and when appropriate post-hoc paired t-tests using Bonferroni correction. RESULTS: Scanner-specific optimization significantly improved DSC for LST compared to default and combined settings, except for the GE scanner. NicMS showed significantly higher DSC for both the scanner-specific and combined optimization than default. Within-scanner repeatability was excellent (ICC>0.9) for volume and counts. Between-scanner ICC for volume between Vida and Sola was higher (0.94-0.99) than between GE MR750 and Vida or Sola (0.18-0.93), with improved ICCs for nicMS scanner-specific (0.87-0.93) compared to others (0.18-0.79). This was not present for Sola vs. Vida where all ICCs were excellent (>0.94). CONCLUSION: Scanner-specific optimization strategies proved effective in mitigating inter-scanner variability, addressing the issue of insufficient reproducibility and accuracy found with default settings.

YNICL Journal 2018 Journal Article

Automatic normative quantification of brain tissue volume to support the diagnosis of dementia: A clinical evaluation of diagnostic accuracy

  • Meike W. Vernooij
  • Bas Jasperse
  • Rebecca Steketee
  • Marcel Koek
  • Henri Vrooman
  • M. Arfan Ikram
  • Janne Papma
  • Aad van der Lugt

Objectives: To assesses whether automated brain image analysis with quantification of structural brain changes improves diagnostic accuracy in a memory clinic setting. Methods: = 4915, aged >45 years), and were expressed as age- and sex-specific percentiles. Experienced radiologists determined the most likely imaging-based diagnosis based on structural brain MRI using three strategies (visual assessment of MRI only, quantitative normative information only, or a combination of both). Diagnostic accuracy of each strategy was calculated with the clinical diagnosis as the reference standard. Results: Providing radiologists with only quantitative data decreased diagnostic accuracy both for AD and FTD compared to conventional visual rating. The combination of quantitative with visual information, however, led to better diagnostic accuracy compared to only visual ratings for AD. This was not the case for FTD. Conclusion: Quantitative assessment of structural brain MRI combined with a reference standard in addition to standard visual assessment may improve diagnostic accuracy in a memory clinic setting.

YNIMG Journal 2007 Journal Article

Regional brain atrophy development is related to specific aspects of clinical dysfunction in multiple sclerosis

  • Bas Jasperse
  • Hugo Vrenken
  • Ernesto Sanz-Arigita
  • Vincent de Groot
  • Stephen M. Smith
  • Chris H. Polman
  • Frederik Barkhof

Brain atrophy in multiple sclerosis (MS) is thought to reflect irreversible tissue damage leading to persistent clinical deficit. Little is known about the rate of atrophy in specific brain regions in relation to specific clinical deficits. We determined the displacement of the brain surface between two T1-weighted MRI images obtained at baseline and after a median follow-up time of 2. 2 years for 79 recently diagnosed, mildly disabled MS patients. Voxel- and cluster-wise permutation-based statistics were used to identify brain regions in which atrophy development was significantly related to Expanded Disability Status Scale (EDSS), Timed Walk Test (TWT), Paced Auditory Serial Addition Test (PASAT) and 9-Hole Peg Test (HPT). Clusters were considered significant at a corrected cluster-wise p-value of 0. 05. Worse EDSS change-score and worse follow-up EDSS were related to atrophy development of periventricular and brainstem regions and right-sided parietal, occipital and temporal regions. Worse PASAT at follow-up was significantly related to atrophy of the ventricles. A worse TWT change-score and worse follow-up TWT were exclusively related to atrophy around the ventricles and of the brainstem. Worse HPT change-score and worse follow-up HPT of either arm were significantly related to the atrophy of widely distributed peripheral regions, as well as atrophy of periventricular and brainstem regions. Our findings suggest that decline in ambulatory function is related to atrophy of central brain regions exclusively, whereas decline in neurologically more complex tasks for coordinated hand function is related to atrophy of both central and peripheral brain regions.

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