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Mapping macrostructural and microstructural brain alterations in patients with neuronal intranuclear inclusion disease.
Lv, Shan; Tai, Hongfei; Sun, Jun; Zhuo, Zhizheng; Duan, Yunyun; Liu, Shaocheng; Wang, An; Zhang, Zaiqiang; Liu, Yaou.
  • Lv S; Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
  • Tai H; Tiantan Image Research Center, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Sun J; Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
  • Zhuo Z; China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Duan Y; Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
  • Liu S; Tiantan Image Research Center, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Wang A; Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
  • Zhang Z; Tiantan Image Research Center, China National Clinical Research Center for Neurological Diseases, Beijing, China.
  • Liu Y; Department of Radiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
Neuroradiology ; 66(8): 1373-1382, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38866958
ABSTRACT
BACKGROUND AND

PURPOSE:

Neuronal intranuclear inclusion disease (NIID) is a rare complex neurodegenerative disorder presents with various radiological features. The study aimed to investigate the structural abnormalities in NIID using multi-shell diffusion MR. MATERIALS AND

METHODS:

Twenty-eight patients with adult-onset NIID and 32 healthy controls were included. Volumetric and diffusion MRI measures, including volume, fractional anisotropy (FA), mean diffusivity (MD), intracellular volume fraction (ICVF), orientation dispersion index (ODI), and isotropic volume fraction (ISOVF) of six brain structures, including cortex, subcortical GM, cerebral WM, cerebellar GM and WM, and brainstem, were obtained and compared between NIID and healthy controls. Associations between MRI measures and clinical variables were investigated.

RESULTS:

Brain lesions of NIID included corticomedullary junction lesions on DWI, confluent leukoencephalopathy, lesions on callosum, cerebellar middle peduncle, cerebellar paravermal area and brainstem, and brain atrophy. Compared to healthy controls, NIID showed extensive volume loss of all the six brain regions (all p < 0.001); lower FA in cerebral WM (p < 0.001); higher MD in all WM regions; lower ODI in cortex (p < 0.001); higher ODI in subcortical GM (p < 0.001) and brainstem (p = 0.016); lower ICVF in brainstem (p = 0.001), and cerebral WM (p < 0.001); higher ISOVF in all the brain regions (p < 0.001). Higher MD of cerebellar WM was associated with worse cognitive level as evaluated by MoCA scores (p = 0.011).

CONCLUSIONS:

NIID patients demonstrated widespread brain atrophy but heterogeneous diffusion alterations. Cerebellar WM integrity impairment was correlated with the cognitive decline. The findings of the current study offer a sophisticated picture of brain structural alterations in NIID.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Neurodegenerativas / Imagen de Difusión por Resonancia Magnética / Cuerpos de Inclusión Intranucleares Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Neurodegenerativas / Imagen de Difusión por Resonancia Magnética / Cuerpos de Inclusión Intranucleares Límite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article