16:00 |
0391. |
The physical basis of
inhomogeneous magnetization transfer
Scott D. Swanson1, David C. Alsop2,3,
and Dariya I. Malyarenko1
1Department of Radiology, University of
Michigan, Ann Arbor, MI, United States, 2Beth
Israel Deaconess Med. Ctr, Boston, MA, United States,3Radiology,
Harvard Medical School, Boston, MA, United States
Recent studies have shown that inhomogeneous
magnetization transfer (ihMT) can be created in white
matter and certain lipid systems by RF saturation at +/-
off-resonance frequencies. This work reports on
observation of MT and ihMT as a function of temperature
in model lipid systems. Our results show that the
structure and dynamics of lipids at low temperatures
create ihMT which decreases with increasing temperature
and is gradually converted into conventional MT by 65
°C. Both MT and ihMT disappear as the sample melts at
the 85 °C. A consistent theoretical explanation of ihMT
nature is provided in terms of selective dipolar
dynamics in model lipid systems.
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16:20 |
0392. |
Towards Understanding the
Anisotropy of Magnetization Transfer Parameters in Human
White Matter
André Pampel1, Henrik Marschner1,
Dirk K. Müller1, and Harald E. Möller1
1Max Planck Institute for Human Cognitive and
Brain Sciences, Leipzig, Germany
We examine the apparent dependence of qMT parameters, in
particular those of the T2 relaxation time of bound
protons, on the white matter fiber orientation. It is
found that those dependency results from parameter
fitting using the Super-Lorentzian lineshape, which
renders orientational dependency on other qMT
parameters. A novel RF absorption lineshape of the bound
pool considering the liquid-crystalline character of the
myelin sheath is derived that explains this dependence.
Data simulated using this lineshape were analyzed by
parameter fitting. A remarkable agreement was found in
the obtained parameters compared to those found in WM
regions with fractional anisotropy FA>0.7.
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16:40 |
0393. |
Combined NODDI and qMT for
full-brain g-ratio mapping with complex subvoxel
microstructure
Jennifer S.W. Campbell1, Nikola Stikov1,
Robert F. Dougherty2, and G. Bruce Pike1,3
1McConnell Brain Imaging Centre, McGill
University, Montreal, Quebec, Canada, 2Stanford
Center for Neurobiological Imaging, Stanford University,
Stanford, California, United States, 3Hotchkiss
Brain Institute, University of Calgary, Calgary,
Alberta, Canada
The myelin g-ratio is a fundamental metric that can be
computed from combined diffusion and quantitative
magnetization transfer (qMT) imaging. The g-ratio is a
function of the fiber volume fraction (FVF) and the
myelin volume fraction (MVF). The FVF may be obtained
from diffusion tensor imaging, but only in the case
where the MRI voxels contain a single fiber system with
parallel, straight fibers, making the FA an unsuitable
measure of FVF for full-brain quantitative maps. Here,
we apply the Neurite Orientation Dispersion and Density
Imaging (NODDI) model to obtain full brain g-ratio maps.
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17:00 |
0394. |
Quantifying the
contribution of white matter microstructure to frequency
contrast in gradient echo MRI
Samuel Wharton1 and
Richard Bowtell1
1Sir Peter Mansfield Magnetic Resonance
Centre, School of Physics and Astronomy, University of
Nottingham, Nottingham, United Kingdom
In most studies involving GE phase imaging, it is
assumed that the dominant source of phase contrast is
the variation in magnetic susceptibility across
different tissues. Recent studies have suggested that
white matter microstructure may be an additional source
of phase contrast. In this study, we quantify the
frequency contribution of white matter microstructure in
a small tissue phantom by using sophisticated simulation
techniques to model and remove the frequency
contribution of bulk isotropic and anisotropic magnetic
susceptibility. This approach also yields accurate
estimates of the isotropic (-82 ppb) and anisotropic (11
ppb) susceptibility of white matter.
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17:20 |
0395. |
A model for extra-axonal
diffusion spectra
Wilfred W Lam1, Saad Jbabdi1, and
Karla L Miller1
1FMRIB Centre, University of Oxford, Oxford,
Oxon, United Kingdom
Diffusion imaging has enormous potential for
quantitative measurements of geometric properties that
are directly relevant to brain function and pathology.
Most work has focused on intra-axonal diffusion, despite
the fact that significant signal contrast is expected to
arise from the extra-axonal space. White matter
diffusion models generally assume no frequency
dependence of the extra-axonal diffusion spectrum
measured with oscillating gradients. An empirical model
is proposed for the diffusion spectra of spins around
packed cylinders. Model predictions are compared with
Monte Carlo simulations. The model accurately captures
salient properties of the entire diffusion spectrum for
square, hexagonally, and randomly packed cylinders.
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17:40 |
0396.
|
Effects of realistic
vascular networks anisotropy on MR microvascular imaging
Nicolas Adrien Pannetier1,2, Thomas Christen3,
and Norbert Schuff1,2
1Department of Radiology and Biomedical
Imaging, University of California San Francisco, San
Francisco, CA, United States, 2Centre
for Imaging of Neurodegenerative Diseases, VA Medical
Center, San Francisco, CA, United States, 3Department
of Radiology, Stanford University, CA, United States
MRI microvasculature imaging is a powerful tool for
characterizing hemodynamic properties in vivo. However,
the structural complexity of the vasculature may
introduce inaccuracy in the estimation of the
microvasculature. Using full brain vasculature network
acquired with optical microscopy and simulation of the
MR signal, we characterized the impact of vascular
network anisotropy on the estimation of cerebral blood
volume (CBV) and vessel size index (VSI). We found an
intrinsic orientation dependent variability of about 20%
for CBV and VSI. This works indicates that variations in
the spatial distributions of vascular networks need to
be considered in microvascular MRI for accurate
estimations of hemodynamic properties.
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