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Updated: May 10, 2026

3D Modeling of the Lateral Ventricles and Histological Characterization of Periventricular Tissue in Humans and Mouse
Published on: May 19, 2015
Longitudinal MRI-based changes in intracranial volume and skull thickness observed in both metachromatic
Guus H J Vorst1, Nicole I Wolf1, David R van Nederpelt2
1Amsterdam Leukodystrophy Centre, Department of Child Neurology, Emma Children's Hospital, and Amsterdam Neuroscience, Amsterdam University Medical Center, Vrije Universiteit, Amsterdam 1105 AZ, the Netherlands.
Abstract:
Intracranial volume (ICV) is often used as normalization factor in volumetrics and considered to be stable in young adults. We noticed thick skulls on MRI scans of leukodystrophy patients, suggesting potentially changing skull morphology. In this study we aimed to quantify skull thickness and ICV in metachromatic leukodystrophy (MLD) patients and people with multiple sclerosis (pwMS). We retrospectively analyzed single-center cross-sectional and longitudinal MRI scans. Skull thickness and ICV were determined using automated segmentation techniques. Participants included MLD (n = 32, 11 male, scans = 136, median age first scan = 14.1 [IQR 7.9-25.7] years), MS (n = 232, 78 male, median age first scan = 47.3 [IQR 39.6-55.4] years, scans = 431), and controls (n = 139, 67 male, median age first scan = 30.7 [IQR 10.7-48.9] years, scans = 283). Both ICV and skull thickness showed natural growth in young controls. In young MLD participants, ICV decreased (-18.8 ± 22.4 mL/year, p < 0.001). Above age 20, ICV and skull thickness remained stable in controls. In comparison to controls, we observed ICV loss in MLD participants (-4.01 ± 8.29 mL/year, p < 0.001) and in pwMS (-2.99 ± 2.69 mL/year, p < 0.001), as well as skull thickening (MLD: 0.16 ± 0.14 mm/year, p < 0.001, pwMS: 0.04 ± 0.09 mm/year, p = 0.009). In adult patient groups, negative correlations were found between ICV and skull thickness (MLD: -19.24 mL/mm, p < 0.001, pwMS: -11.56 mL/mm, p < 0.001), but not in controls (p = 0.11). Despite limitations due to scanner variations, segmentation reliability and absence of validation against ground truth, these findings demonstrate a reduction in ICV in pathologies, already in young adulthood. Although the observed changes are small, they may lead to underestimations of atrophy when using ICV as a normalization factor.
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