TY - JOUR
T1 - Active brain changes after initiating fingolimod therapy in multiple sclerosis patients using individual voxel-based analyses for diffusion tensor imaging
AU - Senda, Joe
AU - Watanabe, Hirohisa
AU - Endo, Kuniyuki
AU - Yasui, Keizo
AU - Hawsegawa, Yasuhiro
AU - Yoneyama, Noritaka
AU - Tsuboi, Takashi
AU - Hara, Kazuhiro
AU - Ito, Mizuki
AU - Atsuta, Naoki
AU - Epifanio, Bagarinao
AU - Katsuno, Masahisa
AU - Naganawa, Shinji
AU - Sobue, Gen
PY - 2016
Y1 - 2016
N2 - Voxel-based analysis (VBA) of diffusion tensor images (DTI) and voxel-based morphometry (VBM) in patients with multiple sclerosis (MS) can sensitively detect occult tissue damage that underlies pathological changes in the brain. In the present study, both at the start of fingolimod and post-four months clinical remission, we assessed four patients with MS who were evaluated with VBA of DTI, VBM, and fluid-attenuated inversion recovery (FLAIR). DTI images for all four patients showed widespread areas of increased mean diffusivity (MD) and decreased fractional anisotropy (FA) that were beyond the highintensity signal areas across images. After four months of continuous fingolimod therapy, DTI abnormalities progressed; in particular, MD was significantly increased, while brain volume and high-intensity signals were unchanged. These findings suggest that VBA of DTI (e.g., MD) may help assess MS demyelination as neuroinflammatory conditions, even though clinical manifestations of MS appear to be in complete remission during fingolimod.
AB - Voxel-based analysis (VBA) of diffusion tensor images (DTI) and voxel-based morphometry (VBM) in patients with multiple sclerosis (MS) can sensitively detect occult tissue damage that underlies pathological changes in the brain. In the present study, both at the start of fingolimod and post-four months clinical remission, we assessed four patients with MS who were evaluated with VBA of DTI, VBM, and fluid-attenuated inversion recovery (FLAIR). DTI images for all four patients showed widespread areas of increased mean diffusivity (MD) and decreased fractional anisotropy (FA) that were beyond the highintensity signal areas across images. After four months of continuous fingolimod therapy, DTI abnormalities progressed; in particular, MD was significantly increased, while brain volume and high-intensity signals were unchanged. These findings suggest that VBA of DTI (e.g., MD) may help assess MS demyelination as neuroinflammatory conditions, even though clinical manifestations of MS appear to be in complete remission during fingolimod.
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U2 - 10.18999/nagjms.78.4.455
DO - 10.18999/nagjms.78.4.455
M3 - Article
AN - SCOPUS:84999041519
SN - 0027-7622
VL - 78
SP - 455
EP - 463
JO - Nagoya journal of medical science
JF - Nagoya journal of medical science
IS - 4
ER -