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Distinct patterns of white matter hyperintensity and cortical thickness of CSF1Rrelated leukoencephalopathy compared with subcortical ischemic vascular dementiaopen access

Authors
Kim, Seung JooCho, WanzeeKim, Hee JinNa, Duk L.Seo, Sang WonJung, Na-YeonLee, Jae-HyeokLee, Myung JunKang, HeeyoungSeong, Joon-KyungKim, Eun-Joo
Issue Date
Oct-2024
Publisher
Public Library of Science
Citation
PLoS ONE, v.19, no.10 October
Indexed
SCIE
SCOPUS
Journal Title
PLoS ONE
Volume
19
Number
10 October
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/74481
DOI
10.1371/journal.pone.0308989
ISSN
1932-6203
1932-6203
Abstract
Background CSF1R-related leukoencephalopathy is a type of autosomal dominant leukodystrophy caused by mutations in the colony stimulating factor 1 receptor (CSF1R) gene. Subcortical ischemic vascular dementia (SIVaD), which is caused by cerebral small vessel disease, is similar to CSF1R-related leukoencephalopathy in that it mainly affects subcortical white matter. In this study, we compared the patterns of white matter hyperintensity (WMH) and cortical thickness in CSF1R-related leukoencephalopathy with those in SIVaD. Methods Fourteen patients with CSF1R-related leukoencephalopathy and 129 with SIVaD were retrospectively recruited from three tertiary medical centers. We extracted and visualized WMH data using voxel-based morphometry to compare the WMH distributions between the two groups. Cortical thickness was measured using a surface-based method. Statistical maps of differences in cortical thickness between the two groups were generated using a surface model, with age, sex, education, and intracranial volume as covariates. Results Predominant distribution of WMH in the CSF1R-related leukoencephalopathy group was in the bilateral frontal and parietal areas, whereas the SIVaD group showed diffuse WMH involvement in the bilateral frontal, parietal, and temporal areas. Compared with the SIVaD group, the CSF1R-related leukoencephalopathy group showed more severe corpus callosum atrophy (CCA) and widespread cortical thinning. Conclusions To our knowledge, this is the first study using the automated MR measurement to capture WMH, cortical thinning, and CCA with signal changes in CSF1R-related leukoencephalopathy. It provides new evidence regarding differences in the patterns of WMH distribution and cortical thinning between CSF1R-related leukoencephalopathy and SIVaD. Copyright: © 2024 Kim et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
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