Spinal Cord Injury Clinical Trial
Official title:
PET in Evaluating Cerebral Glucose Metabolism and Functional Change for Patients With Spinal Cord Injury
Background: Spinal cord injury (SCI) results in dysfunction of motor and sensory system and
the hormonal secretion. Not only the change of peripheral hormonal organs, the central
neurotransmitters were also affected. We consider there are some changes in cerebral
physiology, anatomy or function after SCI.
Objective: Use PET imaging to investigate the brain functional difference among the SCI and
control group.
Spinal cord injury (SCI) results in dysfunction of motor and sensory system and the hormonal
secretion. Not only the change of peripheral hormonal organs, the central neurotransmitters
were also affected. We consider there are some changes in cerebral physiology, anatomy or
function after SCI. Transcranial magnetic stimulation, magnetic coil or EEG were used to
study the phenomenon of cortical reorganization in post-injury of spinal cord. Now
functional imaging render the researcher easier to understand adaptive changes of cerebral
cortex in patients with SCI. Due to the development of positron emission tomography (PET)
and adequate supply of 18-F-deoxyglucose (FDG), the cerebral glucose metabolism and blood
flow were approached in easier way. PET was used in patients with cervical compressive
myelopathy to evaluate the glucose metabolic rate. Standardized uptake value of FDG and its
association with neurological status of pre- and post-operation had been studied. PET was
also used to assess the effect of a transverse cord lesion on cerebral energy metabolism in
view of sensorimotor reorganization. In addition to FDG, 15O-H2O was applied to evaluate the
activation adaptation of post-SCI cerebrum. 13N-NH3 was also used to study the cerebral
blood flow by its concentration in brain tissue. Recently the alteration of regional
cerebral blood flow was visualized by brain SPECT. We want to know the impact of spinal
lesion and function impairment on brain activation in patients with SCI. 6-[18F]fluorodopa
(18F-FDOPA) is indicator of brain presynaptic dopaminergic function, which can be used to
evaluate the changes of brain dopamine. WE will use 18F-FDOPA-PET to investigate its
difference among the SCI and control group.
In our three-year study, 40 men with SCI will be recruited each year, 40 age-matched men as
control. In the first year study, FDG-PET will be used to assess the cerebral metabolism,
then the glucose metabolic rate of cerebrum and spinal cord will be analyzed. The mechanism
of cerebral adaptation after SCI may be clarified. 13N-NH3 will be used in the second year
to evaluate the cerebral blood flow in the period of attempted and true action, then their
difference will be analyzed by statistical parametric mapping. The picture of activated
brain area will be compared between study and control group to investigate the
reorganization of cerebral cortex after SCI. In the third year, we will use 18F-FDOPA to
evaluate the brain presynaptic dopaminergic function among SCI and control group. Thus, we
will delineate the effect of SCI on cerebral function by PET.
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Observational Model: Case Control, Time Perspective: Prospective
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