Multiple Sclerosis Clinical Trial
Official title:
The Bladder and the Brain - Investigation of the Supraspinal Neural Control of Lower Urinary Tract Function in Healthy Subjects and Patients With Neurogenic and Non-neurogenic Bladder Dysfunction Using Advanced Neuroimaging Techniques
The purpose of this study is to provide profound insight into the supraspinal neuronal mechanisms and networks responsible for lower urinary tract (LUT) control and to verify, amend or adjust neuronal circuitry models established from findings in healthy subjects in the context of neurogenic and non-neurogenic LUT dysfunction.
The subject recruitment will be performed within the Neuro-Urology outpatient clinic at the
Balgrist University Hospital and in collaboration with the Departments of Neurology, Urology
and Gynecology at the University Hospital Zürich.
The following subject groups will be recruited: 1) healthy controls (n=22), Non-neurogenic
overactive bladder (NNOAB) patients (n=20), multiple sclerosis (MS) patients with OAB (n=15),
MS patients without OAB (n=15), spinal cord injury (SCI) patients with neurogenic detrusor
overactivity (n=24).
After inclusion, all subjects and patients will undergo one to two functional magnetic
resonance imaging (fMRI) sessions. NNOAB patients might undergo an additional fMRI session
after receiving overactive bladder (OAB) treatment (such as antimuscarinics, intradetrusor
injections of botulinum toxin type A). Spinal cord injury (SCI) patients with neurogenic
detrusor overactivity will undergo an additional fMRI session 5-7 weeks after intradetrusor
injections of botulinum toxin type A.
High-resolution anatomical images and functional blood-oxygen-level-dependent (BOLD)-signal
sensitive images will be acquired. In addition to the fMRI, diffusion tensor imaging (DTI)
sequences will be recorded after the anatomical scans to provide information about the
structural supraspinal connectivity.
Study endpoints are changes of the BOLD signal in regard to location and intensity,
structural and functional connectivity (FC) between previously described supraspinal centers
involved in LUT control, and statistical differences of changes in BOLD signals, structural
and functional connectivity between patients and healthy controls.
All acquired fMRI data will be transferred to an off-line workstation running BrainVoyager QX
or Statistical Parametric Mapping (SPM) Version 8. The functional data will be pre-processed
for motion correction, spatial smoothing, linear trend removal, and temporal high-pass
filtering. With both programs statistical analysis and graphical presentation of the results
can be performed.
The DTI records will be evaluated with SPM8, BrainVoyager QX or other programs like
Functional Magnetic Resonance Imaging of the Brain (FMRIB) Software Library (FSL) and
DTI-Studio. To estimate FC we will use SPM8 or the brain connectivity toolbox. Both softwares
allow the estimation of rest- and task-related connectivity on single subject and group level
with corrected statistical threshold.
Overall, 96 subjects for the main study are estimated to be sufficient to demonstrate
significant differences between groups.
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