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Diffusion tensor imaging of normal-appearing white matter in patients with neuromyelitis optica spectrum disorder and multiple sclerosis

Authors
Kim, SuhyunKwak, KichangHyun, Jae-wonJoung, AeranLee, Sang-hyunChoi, Yong-hoLee, Jong MinKim, Hojin
Issue Date
Jul-2017
Publisher
Blackwell Publishing Inc.
Keywords
diffusion tensor imaging; multiple sclerosis; neuromyelitis optica
Citation
European Journal of Neurology, v.24, no.7, pp 966 - 973
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
European Journal of Neurology
Volume
24
Number
7
Start Page
966
End Page
973
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/152025
DOI
10.1111/ene.13321
ISSN
1351-5101
1468-1331
Abstract
Background and purpose: The occult changes in normal-appearing white matter (NAWM) were investigated and compared amongst patients with neuromyelitis optica spectrum disorder (NMOSD), patients with multiple sclerosis (MS) and healthy controls (HCs) by applying tract-based spatial statistics to diffusion tensor imaging (DTI) data. Methods: Diffusion tensor imaging was performed with a 3-T scanner in 93 patients with NMOSD, 53 patients with MS and 43 HCs. Voxel-wise statistical analyses of the DTI data were performed using tract-based spatial statistics. Results: Compared to HCs, patients with NMOSD had significantly lower mean global fractional anisotropy, higher mean diffusivity and radial diffusivity, and no significant differences in axial diffusivity in their NAWM. Patients with MS demonstrated significantly lower mean global fractional anisotropy and higher mean diffusivity, axial diffusivity and radial diffusivity in the NAWM than did patients with NMOSD and HCs. Compared to patients with NMOSD, patients with MS had NAWM damage that was more extensive, particularly in the inferior cerebellar peduncle, external capsule, cingulum, superior fronto-occipital fasciculus and uncinate fasciculus. Conclusions: Using DTI, widespread occult damage was demonstrated in the NAWM of patients with NMOSD. However, the NAWM was less affected in patients with NMOSD than it was in patients with MS; specifically, the axonal injuries and diffusion abnormalities in the association fibers were more severe in patients with MS than they were in patients with NMOSD.
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