Multiple Sclerosis Clinical Trial
Official title:
Multimodel MRI to Explore the Pathophysiology of Multiple Sclerosis and Neuromyelitis Optica Spectrum Disorders
To investigate multimodel MRI exploring the pathophysiology of multiple sclerosis and
neuromyelitis optica spectrum disorders.
The investigators use multimodel MRI to evaluate the extent of blood-brain barrier and white
matter fiber tracts destruction , iron deposition and cerebral blood flow of associated
regions in multiple sclerosis and neuromyelitis optica spectrum disorders using
contrast-enhanced magnetic resonance imaging , quantitative susceptibility mapping,
diffusion tension imaging, and arterial spin labeling with post labeling delay of 2.0
seconds. Transfer constant volume , magnetic susceptibility, cerebral blood flow and
fractional anisotropy(FA) value were measured in lesion and normal appearing white matter.
Patients:
Patients with multiple sclerosis and neuromyelitis optica spectrum disorders were included.
clinical characteristics such as disease duration, expanded disability status scale(EDSS)
score, age, associated laboratory examination(autoantibodies directed to aquaporin-4 and
oligoclonal bands in serum as well as cerebrospinal fluid)were recorded.
Imaging scan were conducted at admission, six months and one year after admission
Imaging protocols:
MRI scan protocols: T2 weighted image, T1 weighted image, Diffusion weighted image(DWI),
fluid-attenuated inversion recovery(FLAIR), dynamic contrast-enhanced magnetic resonance
imaging(DCE-MRI) , diffusion tension imaging(DTI) ,quantitative susceptibility mapping(QSM)
, arterial spin labeling(ASL) with post labeling delay(PLD) of seconds, sagittal CUBE Fluid
Attenuation Inversion Recovery (FLAIR) images, sagittal 3-dimensional Fast Spoiled Gradient
Echo(3D-FSPGR).
Contrast agent:
Omniscan 0.1mmol/kg, Inject rateļ¼2ml/s
Imaging evaluation:
Transfer constant volume value measured by DCE-MRI indicates the extent of blood-brain
barrier destruction.
Magnetic susceptibility manifests iron deposition in lesions and normal appearing white
matter.
Diffusion tension imaging demonstrates the extent of white matter fiber tracts destruction.
Arterial spin labeling(ASL) with post labeling delay(PLD)of seconds shows cerebral blood
flow in associated regions.
;
Observational Model: Case Control, Time Perspective: Prospective
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