Study Results
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Basic Information
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COMPLETED
NA
59 participants
INTERVENTIONAL
2019-01-31
2019-07-01
Brief Summary
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MRE-IA has already been demonstrated based on the use of existing, clinically approved MR imaging sequences, and once this capability has been established at the two centers, initial trials will be done to demonstrate the method's potential in liver and neurovascular imaging. In the case of the liver, this pilot project funding will be used to perform MRE-IA imaging in patients with chronic liver disease and focal liver lesions. Results will be analyzed to establish the relationship between the mechanical properties mentioned above and disease stage. In the neurovascular case, imaging will be conducted under basic visual and motor stimulus conditions in healthy subjects, and results compared non-stimulus control images to determine changes in the above properties based on brain function. In addition, MRE-IA images will be compared with BOLD imaging to investigate the role of fluid conductivity in fMRI results.
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Detailed Description
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Goals: The principal goal of this project is to establish Magnetic Resonance Elastography by Intrinsic Activation (MRE-IA) imaging methods at the imaging centers of the Centre de recherche du centre hospitalier universitaire de Sherbrooke (CRCHUS) and the Centre de recherche du centre hospitalier universitaire de Montréal (CRCHUM). Each imaging center will then focus on separate sub-goals: improving liver disease assessment with MRE-IA (CRCHUM) and evaluating the role of fluid conductivity and changes in elastic properties with mental tasks (CRCHUS).
Hypothesis: There are two main hypotheses underlying this project: (1) that internal activation provides an effective, robust displacement source for MRE image reconstruction that eliminates the problems of discomfort, high attenuation, artefact sensitivity, and low signal to noise associated with traditional extrinsic MRE methods; and (2) that the advanced material property maps provided by MRE-IA, such as viscoelastic damping, poroelastic effects and anisotropy, will lead to better classification and understanding of both diseased and healthy tissue states.
Methods: The image acquisition methodology for this project will be identical at both imaging centers. Intrinsic activation MRE displacement data will be obtained through the use the Q-Flow angiographic sequence available on the Philips 3T systems at both the CRCHUS and CRCHUM.
MRE-IA for diffuse and focal liver disease (CRCHUM): The objective of this study is to demonstrate the feasibility of MRE-IA imaging in the assessment of liver disease. MRE-IA will be performed in three populations (10 healthy volunteers, 25 patients with diffuse liver disease and 10 patients with focal liver lesions)
Intrinsic MRE: MRE-IA images are reconstructed from phase-contrast sequences that are currently available on MRI scanners at CHUM and CHUS. Post-processing of the images with finite element analysis (FEA) mechanical simulations allows calculation of poroviscoelasticity parameters (i.e. porosity, bulk modulus, storage modulus \[G'\], and loss modulus \[G''\]). These poroviscoelasticity parameters will be correlated with histopathological markers of disease severity (fibrosis, inflammation, fat) in patients with chronic liver disease and with the final diagnosis (type of liver lesion).
Cerebral function imaging via MRE-IA (CRCHUS): The objective of this study is to investigate the changes in mechanical properties during the performance of mental tasks and the role of inherent fluid conductivity in the BOLD imaging used in fMRI methods. Multiple imaging sessions will be performed to investigate changes to MRE-IA property maps to visual (V1) stimulation. Imaging sessions will be include either V1 (n=6) or non-stimulus (n=3) cases. Each case will include both MRE-IA and fMRI acquisitions.
Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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MRE-IA (no stimuli)
Additional sequencing only
No stimuli
Additional sequencing only
MRE-IA with stimuli
Visual stimulation while using additional sequencing
Stimuli
Visual stimulation while using additional sequencing
Interventions
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Stimuli
Visual stimulation while using additional sequencing
No stimuli
Additional sequencing only
Eligibility Criteria
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Inclusion Criteria
* Are able to comprehend and willingness to provide voluntary consent;
* Are able to have a MRI;
* Understand French or English;
* At CHUM:
* Healthy volunteers or;
* Have a diffuse liver disease (non alcoholic cirrhosis, hepatitis, NASH) and
* Are scheduled for liver biopsy as part of their standard of care
* Are scheduled for a MRI for clinical or research purpose, or;
* Have a focal liver lesion (e.g. hemangioma, hepatocellular carcinoma, cholangiocarcinoma, and metastases) and
* Are scheduled for clinical MRI as part of their standard of care for characterization of liver masses
* At CHUS:
* Healthy volunteers.
Exclusion Criteria
* Are pregnant or trying to become pregnant;
* Have a weight or girth preventing them from entering the MR magnet bore;
* Are unable to understand or unwilling to provide written informed consent for this study.
18 Years
100 Years
ALL
Yes
Sponsors
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Centre hospitalier de l'Université de Montréal (CHUM)
OTHER
Réseau de bio-imagerie du Québec (RBIQ)
UNKNOWN
Université de Sherbrooke
OTHER
Responsible Party
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Principal Investigators
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Van Houten Elijah, Ing., PhD
Role: PRINCIPAL_INVESTIGATOR
Centre hospitalier de l'Université de Sherbrooke
Locations
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CRCHUM
Montreal, Quebec, Canada
CRCHUS
Sherbrooke, Quebec, Canada
Countries
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Other Identifiers
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MEO-31-2019-7773
Identifier Type: -
Identifier Source: org_study_id
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