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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
Quantitative 7T MRI does not detect occult brain damage in neuromyelitis optica
Baptiste Pasquier1, Nadja Borisow1, Ludwig Rasche1
1Neurologic Clinic and Policlinic (B.P., T.J.D., T.S.), Departments of Medicine, Clinical Research and Biomedical Engineering, University Hospital and University of Basel, Basel, Switzerland; NeuroCure Clinical Research Center (N.B., L.R., J.B.-S., F.P., T.S.), Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health; Department of Neurology (N.B., J.B.-S., K.R., F.P.), Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health; Experimental and Clinical Research Center (F.P.), Charité-Universitätsmedizin Berlin and Max Delbrück Center for Molecular Medicine; Clinical and Experimental Multiple Sclerosis Research Center (K.R., F.P.), Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health; Berlin Ultrahigh Field Facility (T.N.), Max Delbrück Center for Molecular Medicine in the Helmholtz Association, Germany; Medical Image Analysis Center AG (J.W., T.S.); and qbig (J.W.), Department of Biomedical Engineering, University of Basel, Basel, Switzerland.
Subtle brain damage in aquaporin-4 (AQP4) regions differs between neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS). NMOSD patients showed no significant T1 changes, unlike MS patients, suggesting focal pathology in NMOSD.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Neuromyelitis optica spectrum disorder (NMOSD) and multiple sclerosis (MS) are distinct inflammatory demyelinating diseases of the central nervous system.
- Aquaporin-4 (AQP4) antibodies are specific to NMOSD, targeting AQP4-rich periependymal regions.
- Subtle, occult white matter damage may precede overt lesions in these conditions.
Purpose of the Study:
- To compare occult damages in AQP4-rich periependymal regions between NMOSD patients, MS patients, and healthy controls (HCs).
- To investigate the utility of quantitative T1 mapping at 7 Tesla (T) for detecting subtle neuropathology.
Main Methods:
- A cross-sectional study involving 11 NMOSD patients, 7 MS patients, and 10 HCs.
- High-resolution 7T MRI including T2*-weighted imaging and MP2RAGE sequences for T1 mapping.
- Semiautomated segmentation of lesion-free periependymal areas around ventricles and cerebral aqueduct for T1 relaxation time measurement.
Main Results:
- No significant differences in T1 relaxation time were observed in periependymal regions between NMOSD patients and HCs.
- Patients with MS exhibited longer T1 relaxation times in periependymal regions compared to both NMOSD patients and HCs.
- These differences were statistically significant in several periventricular areas and the cerebral aqueduct.
Conclusions:
- Subtle T1 changes were not detected in the periependymal regions of NMOSD patients, contrasting with findings in MS patients.
- This suggests that brain pathology in NMOSD is predominantly focal rather than diffuse.
- Quantitative T1 mapping at 7T can differentiate between MS and NMOSD based on periependymal region involvement.
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