Multiple Sclerosis Clinical Trial
Official title:
An Exploratory Study on Detection of Cortical Damage in Patients With Multiple Sclerosis Using Magnetic Resonance Imaging
This study will determine whether magnetic resonance imaging (MRI) can detect damage to
certain parts of the brain and analyze the thickness of the brain's outer surface in patients
with multiple sclerosis. MRI is a diagnostic test that uses a strong magnetic field and radio
waves to obtain images of body organs and tissues. It can sometimes permit diagnosis even
before symptoms develop.
MS is a disease of white matter, the fatty covering around the nerves in the brain and spinal
cord. The nerves themselves are called gray matter. Damage to white matter impairs nerve
function, leading to a variety of symptoms, such as weakness, vision problems, difficulty
walking, paralysis, and others. MRI can detect some changes in white matter, but changes that
may also appear in gray matter may be more difficult to find. This study will use new MRI
techniques to try to identify gray matter damage in patients with MS.
Healthy volunteers and people with MS or clinically isolated syndrome (an early stage of MS
in which the patient has had just one of the problems MS can cause) who are between 18 and 55
years of age may be eligible for this study. Candidates are screened with a medical history
and neurological examination, and blood and urine tests.
Within one month of the screening evaluation, participants undergo MRI scanning on a standard
1.5 Tesla machine to confirm their health status. (The power of the MRI scanner is measured
in Tesla; the higher the Tesla, the better the visualization.) For this procedure, the
subject lies on a table that moves into the scanner (a narrow cylinder with a magnetic
field), and wears earplugs to muffle loud knocking and thumping sounds that occur during the
scanning process. During the procedure, a contrast agent called Gadolinium is injected into
the blood stream to brighten the images. The test lasts about 2 hours, during which time the
subject must lie still for up to a few minutes at a time.
Within a month after the first MRI, participants repeat the test for a second time. The
procedure is identical to the first scan, except a 3.0 Tesla machine is used.
OBJECTIVE: Detection of cortical lesions in patients with multiple sclerosis (MS) using
magnetic resonance imaging (MRI) is challenging. Their identification might provide more
insight in explaining the level of disability in patients with MS.
Primary aim of the present study is identifying cortical lesions in patients with MS using
MRI. As a secondary aim, correlation between cortical lesions presence and clinical
disability score (i.e. Expanded Disability Status Score or EDSS scale) will be analyzed.
Tertiary aims will be provided by the relationships between the presence of cortical lesions
and reduction in cortical thickness and extent of remote white matter disease pathology.
Additionally, the role of white matter lesions in causing remote pathology will be studied.
To better characterize this damage, patients with previous stroke, presenting with a single
lesion on the pyramidal tract will be enrolled and diffusion-derived indices of white matter
remote tracts will be computed.
STUDY POPULATION: Fifty patients with definite MS or with a single attack and an MRI
suggestive of MS (i.e., clinically isolated syndrome) according to McDonald criteria, and 55
healthy volunteers will be enrolled. Fifteen patients with previous ischemic stroke and 15
age- and gender-matched healthy volunteers will also be enrolled.
DESIGN: After a clinical evaluation and an MRI at 1.5 Tesla, each individual will be imaged
once at 3.0 Tesla scan. Clinical MRI before and within 15 minutes after contrast injection
will be obtained in each patient at both 1.5 and 3 Tesla scans. In addition, 3 spoiled
gradient-echo sequence, diffusion tensor images and double inversion recovery sequences will
be acquired on the 3 Tesla MRI. Some healthy volunteers (up to 15) and patients (up to 15)
will be required to be imaged twice on the 3T magnet as to optimize the sequences of this
study. Additionally, 20 patients in whom cortical lesions will be identified using the
above-mentioned techniques and 20 healthy volunteers will undergo brain perfusion MRIs. This
may represent the third 3T MRI for the former in some instances.
OUTCOME MEASURES: In MS patients, the number of cortical lesions will be computed. The EDSS
score will serve for investigating the relationship between cortical lesions and clinical
disability. Effect of cortical or white matter lesions in causing remote degeneration will be
studied using diffusion tensor and magnetization transfer imaging in patients with both
stroke and MS.
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