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Induction of Paralysis and Visual System Injury in Mice by T Cells Specific for Neuromyelitis Optica Autoantigen Aquaporin-4
Published on: August 21, 2017
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Normal-Appearing Cerebellar Damage in Neuromyelitis Optica Spectrum Disorder
1From the Department of Radiology and Tianjin Key Laboratory of Functional Imaging (J.S., N.Z., Q.W., X.Z., W.Q., C.Y.).
AJNR. American Journal of Neuroradiology
|June 22, 2019
Summary
Subtle cerebellar damage in neuromyelitis optica spectrum disorder (NMOSD) is linked to spinal lesions or aquaporin-4 antibodies. Identifying these causes may help develop new imaging markers for NMOSD.
Area of Science:
- Neuroscience
- Neurology
- Neuroimmunology
Background:
- The cerebellum is crucial for motor and cognitive functions.
- The impact of neuromyelitis optica spectrum disorder (NMOSD) on the normal-appearing cerebellum is not well understood.
- Occult structural damage in the cerebellum of NMOSD patients requires investigation.
Purpose of the Study:
- To identify subtle structural damage within the cerebellum of NMOSD patients.
- To determine the potential causes of this cerebellar damage at the substructure level.
Main Methods:
- Compared normal-appearing gray matter volumes of cerebellar lobules and nuclei between NMOSD patients and healthy controls.
- Compared normal-appearing white matter volumes of cerebellar peduncles between NMOSD patients and healthy controls.
Main Results:
- Cerebellar damage in specific lobules (VI, VIII, X) and nuclei was associated with spinal lesions or aquaporin-4 antibodies.
- Mixed cerebellar damage in lobules V, IX, Crus I, and VIIb showed primary associations with spinal lesions or aquaporin-4 antibodies.
- Other cerebellar substructures did not exhibit significant damage.
Conclusions:
- Cerebellar damage in NMOSD involves normal-appearing white and gray matter.
- Damage is linked to aquaporin-4-mediated injury, secondary axonal degeneration from spinal lesions, or both.
- Substructure-specific etiologic classifications can aid in developing neuroimaging markers for NMOSD severity and treatment assessment.
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