Traditional Posters
: Diffusion & Perfusion - Neuro
|
Click on
to view the
abstract pdf and click on
to view the pdf of the poster viewable in the poster hall.
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Diffusion MR: Advanced Signal Models & Reconstruction
Monday May 9th
Exhibition Hall |
14:00 - 16:00 |
1911. |
A hierarchy of
analytic models for the diffusion MRI signal in
brain white matter
Eleftheria Panagiotaki1, Torben
Schneider1,2, Bernard Siow1,3,
Mark F Lythgoe3, Matt G Hall1,
and Daniel C Alexander1
1Centre for Medical Image Computing,
Dept. of Computer Science, University College
London, London, United Kingdom, 2Institute
of Neurology, University College London, 3Centre
for Advanced Biomedical Imaging, University
College London
This study aims to identify the minimum
requirements for an accurate model of the
diffusion MR signal in white matter of the
brain. We construct a hierarchy of
multi-compartment models of white matter from
combinations of simple models for the intra- and
the extra-axonal spaces. We devise a new
diffusion MRI protocol that provides
measurements with a wide range of parameters for
diffusion sensitization both parallel and
perpendicular to white matter fibres. We use the
protocol to acquire data from a fixed rat brain,
which allows us to fit, study and compare the
different models.
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1912. |
Statistical
Analysis of Apparent Fibre Density: Supra-threshold
clustering over space and orientation
David Raffelt1,2, J-Donald Tournier3,4,
Gerard Ridgway5, Stephen Rose6,
Robert Henderson7, Stuart Crozier2,
Alan Connelly3,4, and Olivier Salvado1
1The Australian E-Health Research
Centre, CSIRO, Brisbane, QLD, Australia, 2Biomedical
Engineering, School of ITEE, University of
Queensland, Brisbane, QLD, Australia, 3Brain
Research Institute, Florey Neuroscience
Institutes (Austin), Melbourne, VIC, Australia, 4Department
of Medicine, University of Melbourne, Melbourne,
VIC, Australia, 5Institute
of Neurology, University College London, London,
United Kingdom, 6Centre
for Advanced Imaging, University of Queensland,
Brisbane, QLD, Australia, 7Department
of Neurology, Royal Brisbane and Women's
Hospital, Brisbane, QLD, Australia
Apparent Fibre Density (AFD) is a new measure
based on information provided by Fibre
Orientation Distributions. AFD enables
voxel-based analysis to be performed over space
and orientation, and therefore population
differences may be attributed to a single fibre
within a voxel containing multiple fibres.
Performing comparisons over many orientations
within each voxel increases the number of
multiple comparisons. We present a method for
cluster-based inference of spatially extended
differences in AFD by identifying clusters of
contiguous supra-threshold directions using
neighbours defined in space and orientation. The
proposed method is demonstrated using a cohort
of Motor Neurone Disease and healthy subjects.
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1913. |
Rapid Diffusion
Spectrum Imaging with Partial q-Space Encoding
Anh Tu Van1, Rafael O'Halloran1,
Samantha Holdsworth1, and Roland
Bammer1
1Radiology, Stanford University,
Stanford, CA, United States
Despite its much richer information regarding
the microstructure of neuronal architectures
than other imaging techniques, such as diffusion
tensor imaging (DTI) and high angular resolution
diffusion imaging (HARDI), applications of
diffusion spectrum imaging (DSI) in in vivo
studies are limited due to its long total
acquisition time. The current study proposes to
significantly speed up DSI by using partially
encoding in q-space, similar to partial Fourier
encoding in traditional k-space domain. Both
phantom and in vivo experiments are done to show
the performance of the proposed method. For the
experiments presented, the achieved acquisition
speed-up was 44.4%.
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1914. |
Improved sampling
patterns for accelerated diffusion spectrum imaging
using compressed sensing
Marion Irene Menzel1, Jonathan
Immanuel Sperl1, Ek Tsoon Tan2,
Kedar Khare2, Kevin F King3,
Xiaodong Tao2, Christopher J Hardy2,
and Luca Marinelli2
1GE Global Research, Garching bei
München, Germany, 2GE
Global Research, Niskayuna, NY, United States, 3GE
Healthcare, Waukesha, WI, United States
The combination of undersampled acquisition and
reconstruction using compressed sensing enables
the acceleration of diffusion spectrum imaging,
bringing this application closer to clinical
practice. This work evaluates the performance of
compressed sensing as a function of data
reconstruction size, pattern pa-rameter and
specific realization of the random pattern.
Among the sampling pattern distributions we
tested both in simulations and in vivo data from
brains of healthy volunteers, our results
demonstrate that Gaussian undersampling
performed best. Especially for higher
acceleration factors and small matrix sizes the
appropriate realization of the sampling pattern
from the random distribution has to be chosen
carefully.
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1915. |
Sparsity
Characterisation of the Diffusion Propagator
Etienne Saint-Amant1, and Maxime
Descoteaux1
1Computer Science Department,
Université de Sherbrooke, Sherbrooke, Québec,
Canada
In a Compressed Sensing (CS) framework, we
focused on characterizing the sparsity of
diffusion propagator from Diffusion Spectrum
Imaging (DSI) data. We extensively analyzed the
performance of the 3D orthogonal wavelet basis
and biorthogonal wavelet basis. We answer
important questions such as: What is the best
basis? Is biorthogonality showing benefits over
orthogonality? What is the best thresholding
method? How does this apply in a real human
brain dataset?
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1916. |
Towards Automated
Modelling of Maxillofacial Musculature
Greg Daniel Parker1,2, Nicholas Drage3,4,
Paul L Rosin2, A David Marshall2,
Stephen Richmond4, John Evans1,
and Derek K Jones1
1CUBRIC, School of Psychology,
Cardiff University, Cardiff, United Kingdom, 2School
of Computer Science, Cardiff University,
Cardiff, United Kingdom, 3Cardiff
Vale NHS Trust, United Kingdom,4School
of Dentistry, Cardiff University, United Kingdom
Accurate in vivo estimates of muscle fibre
trajectory are desirable for evaluation of
subject-specific maxillofacial surgical
treatment options. While diffusion tensor MRI
provides adequatly reconstructs larger muscles
(e.g. calf), fibre crossing inherent to
maxillofacial musculature exposes well-known
limitations; necessitating alternative analysis
methodologies. Constrained spherical harmonic
deconvolution demonstrates potential, however
current data-driven calibration (optimized for
white matter) produce spurious peaks in the
fibre orientation density, adversely affecting
tractography. With clinical application in mind,
we demonstrate an automated tissue-specific
calibration which, for the first time,
successfully reconstructs complex muscle tissue
in vivo and include preliminary results of
unsupervised tract segmentation.
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1917. |
Interpolation of
DWI prior to DTI reconstruction, and its validation
Tim B. Dyrby1, Henrik M Lundell1,
Matthew G Liptrot1, Mark W Burke2,
Maurice Ptito1,3, and Hartwig R
Siebner1
1Danish Research Centre for MR,
Copenhagen University Hospital Hvidovre,
Hvidovre, Denmark, 2College
of Medicine, Howard University, Washington DC,
United States, 3School
of Optometry, University of Montreal, Montreal,
Canada
We hypothesise that super resolution (SR) of
HARDI DWI data can extract anatomical details
that are usually obscured by partial volume
effects and thus are currently only visible if
acquired at higher spatial resolutions. Here we
validate a simple SR approach, where DWI data
are interpolated prior to reconstruction. Using
8x SR interpolation of low resolution images,
acquired from an ex-vivo monkey brain, new
anatomical details matching those in a high
resolution dataset, became apparent. Higher
SR-factors introduced smoothing. Our preliminary
results suggest that HARDI DWI data contain
hidden anatomical detail that can be extracted
with this simple SR approach.
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1918. |
Fiber Continuity:
An Anisotropic Prior for ODF Estimation
Marco Reisert1, and Valerij Kiselev1
1Medical Physics, University Medical
Center Freiburg, Freiburg, Baden Württemberg,
Germany
The accurate and reliable estimation of fiber
orientation distributions based on
diffusion-sensitized magnetic resonance images
is a major prerequisite for tractography
algorithms or any other derived statistical
analysis. In this work we formulate the
principle of fiber continuity (FC), which is
based on the simple observation that the imaging
of fibrous tissue implies certain expectations
to the measured images. From this principle we
derive a prior for the estimation of fiber
orientation distributions based on high angular
resolution diffusion imaging (HARDI). We
demonstrate on simulated, phantom and in vivo
data the superiority of the proposed approach.
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1919. |
Non-Cartesian
Compressed Sensing for Diffusion Spectrum Imaging
Eric Aboussouan1, Luca Marinelli2,
and Ek Tsoon Tan2
1Barrow Neurological Institute,
Phoenix, AZ, United States, 2GE
Global Research, Niskayuna, NY, United States
Diffusion Spectrum Imaging (DSI) can be
accelerated the application of compressed
sensing (CS) in the three q-space dimensions.
Rather than sampling a subset of a Cartesian
q-space, we propose to further minimize coherent
aliasing by undersampling q-space according to a
non-Cartesian sampling pattern. Simulation and
preliminary in vivo results are shown suggesting
the validity of the approach.
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1920. |
Characterizing
Complex White Matter Structure from Cube and Sphere
Diffusion Imaging with a Multi-Fiber Model
(CUSP-MFM)
Benoit Scherrer1, and Simon K
Warfield1
1Radiology, Harvard Medical School,
Boston, Massachusetts, United States
Multi-tensor models are of great interest for
clinical applications because they enable the
assessment of the white matter microstructure in
addition to the brain connectivity. We propose a
novel acquisition scheme and a novel fitting
procedure for multi-fiber assessment. Our
acquisition scheme combines spherical and cubic
sampling. It enables multiple b-values to be
acquired with low geometric and intensity
distortion. Our optimization algorithm ensures
spatially smooth and consistent positive
definite tensors. We evaluate our CUSP-MFM
(CUbe+SPhere Multi-Fiber Model) on both
synthetic and clinical data. We demonstrate the
ability of CUSP-MFM to characterize complex
fiber structures from short duration
acquisitions.
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1921. |
Fibres at the
Magic Angle Generated by Inappropriate Calibration
(MAGIC)
Greg Daniel Parker1,2, and Derek K
Jones1
1CUBRIC, School of Psychology,
Cardiff University, Cardiff, United Kingdom, 2School
of Computer Science, Cardiff University,
Cardiff, United Kingdom
Constrained spherical-harmonic deconvolution
(CSD) provides resolution of intra-voxel
“crossing fibre” orientation through
deconvolution of an idealised (calibration)
response from spherical harmonics fit to the
target diffusion-weighted signal. Given a
single-fibre low anisotropy target,we observe
that, with high calibration anisotropies,
spurious peaks are observed in the resultant
deconvolution at elevations (relative to fibre
orientation) consistent with the zero crossing
(magic angle) and minima of the 2nd order
Legendre polynomial, adversely affecting
tractography. Bootstrap analysis however
indicates that azimuthal distribution of such
peaks appears uniform, allowing true “crossing
fibre” to be distinguished through measurement
of uncertainty.
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1922. |
Robustness of
diffusion scalar metrics when estimated with
Generalized Q-Sampling Imaging acquisition schemes
Marta Morgado Correia1, Guy B
Williams2, Frank Yeh3, Ian
Nimmo-Smith1, and Eleftherios
Garyfallidis1
1MRC Cognition and Brain Sciences
Unit, Cambridge, United Kingdom, 2Wolfson
Brain Imaging Centre, Cambridge, United Kingdom, 3Carnegie
Mellon University, Pittsburgh, United States
Generalized Q-Sampling Imaging (GQI) has
recently been introduced by Yeh and colleagues
and was shown to have comparable accuracy to
other well established q-space methods when it
comes to resolving crossing fibres. In this
study we compared the estimated values of MD, FA
and Quantitative Anisotropy (QA) obtained with
grid and shell GQI sampling schemes, in terms of
their precision and ability to differentiate
between different brain fibre populations. Our
results suggest that a grid sampling scheme
produces more robust results than a single shell
acquisition.
|
1923. |
Optimizing the
Metric for Brain White Matter Comparisons
Natasha Lepore*1, Caroline Brun*2,
Maxime Descoteaux3, Yi-Yu Chou4,
Greig de Zubicaray5, Katie McMahon5,
Margie Wright6, Nicholas Martin6,
James Gee2, and Paul Thompson *equal
contribution7
1Department of Radiology, Children's
Hospital, Los Angeles, Los Angeles, CA, United
States, 2Department
of Radiology, Penn Image Computing and Science
Laboratory, University of Pennsylvania,
Philadelphia, PA, United States, 3Université
de Sherbrooke, Canada, 4Laboratory
of NeuroImaging, UCLA, United States, 5University
of Queensland, Australia, 6Genetic
Epidemiology Lab, QIMR, Australia, 7Laboratory
of NeuroImaging, UCLA, Los Angeles, CA, United
States
Diffusion MRI is a popular tool used to compare
brain white matter structure between groups of
subjects. When this technique is used to compare
two populations, it is common practice to reduce
the sometimes-large number of diffusion
gradients to a univariate measure at each voxel,
such as the fractional anisotropy. However, we
and others have designed voxel-wise comparison
methods for HARDI data and used multivariate
measures for HARDI group comparisons. Here we
compare statistical power for two scalar and two
multivariate measures derived from the HARDI
signal.
|
1924. |
Compressive
Sensing Ensemble Average Propagator Estimation via
L1 Spherical Polar Fourier Imaging
Jian Cheng1,2, Sylvain Merlet2,
Aurobrata Ghosh2, Emmanuel Caruyer2,
Tianzi Jiang1, and Rachid Deriche2
1Institute of Automation, Chinese
Academy of Sciences, Beijing, Beijing, China,
People's Republic of, 2INRIA
Sophia Antipolis, Sophia Antipolis, Sophia
Antipolis, France
Since Diffusion Tensor Imaging (DTI) cannot
detect the fiber crossing, many new works beyond
DTI has been proposed to explore the q-space.
Most works, known as single shell High Angular
Resolution Imaging (sHARDI), focus on single
shell sampling and reconstruct the Orientation
Distribution Function (ODF). The ODF, which has
no radial information at all, is just one of
features of Ensemble Average Propagator (EAP).
Diffusion Spectrum Imaging (DSI) is a standard
method to estimate EAP via numerical Fourier
Transform (FT), which needs lots of samples and
is impractical for clinical study. Spherical
Polar Fourier Imaging (SPFI) [1,2] was proposed
to represent the signal using SPF basis, then
the EAP and the ODF have analytical closed
forms. So the estimation of the coefficients is
very important. In [1,2], the coefficients are
estimated based on a standard Least Square (LS)
with L2 norm regularization (L2-L2). In this
paper, we propose to estimate A using LS with L1
norm regularization (L2-L1), also named as Least
Absolute Selection and Shrinkage Operator
(LASSO). And we prove that the L2-L1 estimation
of the coefficients is actually the well known
Compressive Sensing (CS) method to estimate EAP,
which brings lots of Mathematical tools and
possibility to improve the sampling scheme in
q-space.
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1925. |
A Bayesian random
effects model for enhancing resolution in diffusion
MRI
Martin David King1, Daniel C
Alexander2, David G Gadian1,
and Chris A Clark1
1Institute of Child Health,
University College London, London, United
Kingdom, 2Computer
Science, University College London, London,
United Kingdom
Poor spatial resolution is a limitation in
various diffusion MRI applications, including
tractography. A Bayesian latent variables random
effects model has been developed for increasing
effective spatial resolution, based on a Markov
random field treatment in which intrinsic
Gaussian autoregressive priors are assigned to
the fibre spherical coordinates. The model is
used to separate crossing-fibres at the junction
between the cingulum and corpus callosum, using
diffusion MRI data acquired with a moderate
b-value and 20 directions. The analyses were
performed using Markov chain Monte Carlo
simulation. Results demonstrate that a
satisfactory separation of the crossing
components can be obtained.
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1926. |
A Riemannian
Framework for Ensemble Average Propagator Computing
Jian Cheng1,2, Aurobrata Ghosh1,
Tianzi Jiang2, and Rachid Deriche1
1INRIA Sophia Antipolis, Sophia
Antipolis, Sophia Antipolis, France, 2Institute
of Automation, Chinese Academy of Sciences,
Beijing, Beijing, China, People's Republic of
In Diffusion Tensor Imaging (DTI), Riemannian
framework (RF) has been proposed for processing
tensors, which is based on Information Geometry
theory. Recently RF also has been proposed for
Orientation Distribution Function (ODF)
computing. In this paper, we propose the RF for
EAPs and implement it via SPFI. We proved that
the RF for EAPs is diffeomorphism invariant,
which is the natural extension of affine
invariant RF for tensors. It could avoid the
so-called swelling effect for interpolating
EAPs, just like the RF for tensors. We also
propose the Log-Euclidean framework (LEF),
Affine-Euclidean framework (AEF), for fast
processing EAPs, and Geometric Anisotropy (GA)
for measuring the anisotropy of EAPs, which are
all the extensions of previous concepts in RM
for tensors respectively.
|
1927. |
Bessel Fourier
Orientation Reconstruction: Using Heat Equation and
Multiple Shell Acquisitions to Reconstruct Diffusion
Propagator
Ameer Pasha Hosseinbor1, Moo K. Chung2,
Yu-Chien Wu3, and Andrew L. Alexander4
1Medical Physics, University of
Wisconsin-Madison, Madison, Wisconsin, United
States, 2Biostatistics,
University of Wisconsin-Madison, 3Radiology,
University of Wisconsin-Madison, 4Medical
Physics, University of Wisconsin-Madison
We present a novel technique for analytical EAP
reconstruction from multiple q-shell
acquisitions. The solution is based on the heat
equation estimation of signal for each shell
acquisition.
|
1928. |
A High Angular
Resolution Diffusion Imaging (HARDI) Template of the
Human Brain
Anna Varentsova1, Shengwei Zhang2,
and Konstantinos Arfanakis2
1Biological, Chemical and Physical
Sciences, Illinois Institute of Technology,
Chicago, IL, United States, 2Biomedical
Engineering, Illinois Institute of Technology,
Chicago, IL, United States
The present work is devoted to the development
of a high angular resolution diffusion imaging
(HARDI) template from 67 coregistered,
artifact-free datasets acquired with low angular
resolution diffusion imaging. Preliminary
results show that intravoxel fiber crossings can
be resolved from combination of the 67 datasets,
and that the information contained in the
resulting template is in agreement with
underlying fiber anatomy of the human brain.
|
1929. |
A framework for
modelling the regional variation of white matter
microstructure
Gemma L Morgan1, Hui Zhang1,
Brandon Whitcher2, and Daniel C
Alexander1
1Centre for Medical Image Computing,
Department of Computer Science, University
College London, London, United Kingdom, 2Clinical
Imaging Centre, GlaxoSmithKline, London, United
Kingdom
We present a new framework for modelling the
regional variation of tissue parameters
estimated from diffusion MRI across white matter
regions of interest. The method can be used to
compare differences in parameter variation
between groups and statistical tests allow the
localisation of significant differences. We
demonstrate the technique on the midsagittal
corpus callosum and are able to detect
significant differences in the genu of two
distinct age groups
|
1930. |
Real-time Rician
noise correction applied to real-time HARDI and HYDI
Véronique Brion1, Olivier Riff1,
Irina Kezele1, Maxime Descoteaux2,
Denis Le Bihan1, Jean-François Mangin1,
Cyril Poupon1, and Fabrice Poupon1
1NeuroSpin, CEA/I²BM, Gif-sur-Yvette,
France, 2Sherbrooke
University, Sherbrooke, Canada
We adressed the problem of the correction of the
Rician noise, corrupting diffusion-weighted
images at high b-values, in real-time. We
combined a Linear Minimum Mean Square Error
Estimator (LMMSE) together with a Kalman
framework in order to compute in real-time the
noise-free diffusion data, as well as the
diffusion maps stemming from any local high
angular resolution diffusion (HARDI) or hybrid
diffusion (HYDI) model. A feedback is
retropropagated from the Kalman filter to the
LMMSE, in order both to reinforce the influence
of the local structure onto the noise
correction, and to prevent smoothing effects.
The technique vas validated on synthetic and
real data acquired at low signal to noise ratio
(SNR) to assess its efficiency and the full
pipeline was tested on the computation of
orientation distribution functions.
|
1931. |
Multi-shelled
q-ball imaging without assuming inversion symmetry
Eizou Umezawa1, Masayuki Yamada1,
Chiaki Tsunetomi1, and Hirofumi Anno1
1Graduate School of Health Sciences,
Fujita Health University, Toyoake, Aichi, Japan
In diffusion MR analyses, the inversion symmetry
of the water molecule diffusion is often
assumed: the property of diffusion into a
direction is identical to that into the opposite
direction. Recently, a novel method,
multi-shelled q-ball imaging (MS-QBI), has been
proposed. In this study, we propose a method to
detect the inversion asymmetry of diffusion with
MS-QBI. We also perform the numerical simulation
of detecting the asymmetry and examine the
ability. MS-QBI will be able to detect the
inversion asymmetry if the asymmetry is large
enough. It is possible that MS-QBI can detect
the inversion asymmetry in the case of the small
voxel size realized by a high sensitivity coil
system such as the cryoprobe.
|
1932. |
Registration of
high b value diffusion images
Shani Ben Amitay1, Silvia De Santis2,
Derek Jones2, and Yaniv Assaf3
1Tel Aviv University, Tel Aviv,
Israel, 2CUBRIC,
School of Psychology, Cardiff University, Wales,
UK, United Kingdom, 3Tel
Aviv University, Israel
High b-value diffusion imaging has been
suggested to provide an enhanced contrast toward
different cellular components. However, they
suffer from low SNR, therefore, we suggest a
framework based on both experimental data (DTI)
and simulations (using CHARMED framework) to
register the high b-value diffusion images. We
inversely used the CHARMED model to generate
template images that simulated the contrast seen
in diffusion weighted images acquired at
different b-values and gradient directions in
the native image space of each subject. All high
b-value images were registered to the matching
templates. This approach makes motion correction
feasible for the first time.
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|
|
Traditional Posters
: Diffusion & Perfusion - Neuro
|
Click on
to view the
abstract pdf and click on
to view the pdf of the poster viewable in the poster hall.
|
Diffusion: DTI & ADC
Tuesday May 10th
Exhibition Hall |
13:30 - 15:30 |
1933. |
Size and Shape Matter:
Another Look at Tensor Statistics
Nicholas Lange1,2, and Peter J Basser3
1Departments of Psychiatry and Biostatistics,
Harvard University, Boston, MA, United States, 2Neurostatistics
Laboratory, McLean Hospital, Belmont, MA, United States, 3PPITS,
STBB, NICHD, National Institutes of Health, Bethesda,
MD, United States
More biological information may already be contained in
diffusion tensors measured typically by standard
protocols run on clinical scanners in addition to that
conveyed by their first-order size (e.g., mean, axial
and radial diffusivity), second-order shape (e.g., FA)
and third-order shape (skewness) coefficients. An
enriched understanding of the “size” and “shape” of a
tensor can be obtained by close inspection of its
associated covariance tensor. This tensor takes on a
variety of patterns whose complexity depends on the
tissue’s unknown symmetry class, which can be determined
by statistical methods, that may provide new insights in
typical and disordered brain circuitry.
|
1934. |
Robust and efficient white
matter analysis using tract shape modelling and principal
components analysis
Jonathan D Clayden1
1Institute of Child Health, University
College London, London, United Kingdom
Here we demonstrate how probabilistic neighbourhood
tractography (PNT) and principal component analysis
(PCA) may be used together to analyse properties of
white matter tracts in a robust and data-efficient
manner. PNT is a method for segmenting tracts in groups
using a shape model, while PCA allows common factors
across tracts to be identified. This approach can help
reduce the multiple comparisons problems widely faced in
the statistical analysis of magnetic resonance data.
|
1935. |
Generalizing Diffusion
Tensor Model using Probabilistic Inference in Markov Random
Fields
Cagatay Demiralp1, and David H. Laidlaw2
1Brown University, Providence, RI, United
States, 2Brown
University
We provide a proof of concept for modeling configuration
distributions in DTI and their practical estimations.
The power of the MAP-MRF framework comes from its
mathematical convenience in modeling prior distributions
and the fact that it results in a global optimization
driven by local patches (context).
|
1936. |
The Effect of Inflammation
on DTI Derived Axial and Radial Diffusivity: A Monte Carlo
Simulation Study
Yong Wang1, and Sheng-Kwei Song2
1Radiology, Washington University, Saint
Louis, MO, United States, 2Radiology,
Washington University in St. Louis, Saint Louis, MO,
United States
Diffusion tensor imaging (DTI) derived radial
diffusivity and axial diffusivity have been used to
detect myelin and axon integrity respectively in CNS
injury. Although it has been well recognized that
crossing fibers pose significant challenge in the
application of DTI derived directional diffusivity. It
is not clear how the inflammation caused vasogenic edema
and cell infiltration impact DTI findings. In this
study, Monte Carlo simulation is employed to demonstrate
the possible false assessment of axonal injury and/or
demyelination of a normal axon fiber bundle under the
influence of inflammation.
|
1937. |
The Relative Sensitvity of
Different White Matter Indices to Partial Volume Artefacts
Derek K Jones1
1CUBRIC, School of Psychology, Cardiff
University, Cardiff, Wales, United Kingdom
We characterise the relative sensitivity of different
white matter indices to the effects of partial volume
contamination by CSF. We show that mean diffusivity is
far more sensitivity than fractional anisotropy. The
sensitivity is also dependent on the b-value and the
anisotropy of the tensor.
|
1938. |
A New Robust Algorithm for
Diffusion Tensor Evaluation
Ivan I. Maximov1, Farida Grinberg1,
and Nadim Jon Shah1,2
1Institute of Neuroscience and Medicine 4,
Forschungszentrum Juelich, Juelich, Germany, 2Department
of Neurology, Faculty of Medicine, JARA, RWTH Aachen
University, Aachen, Germany
We propose a new algorithm for diffusion tensor
reconstruction based on the robust least median squares
estimator. The developed method allows one to determine
the outliers that may appear due to physiological noise
or other tissue-related singularities. This feature and
the stability of the least median squares to noise level
variation yield a new and very promising approach in
research and in clinical practice.
|
1939. |
Bias in Diffusion
Tensor-Derived Quantities Depend on The Number of DWIs
Composing The DT-MRI Dataset
Firouzeh Tannazi1, Lindsay Walker1,
Michael Curry1, and Carlo Pierpaoli1
1STBB/PPITS/NICHD/NIH, Bethesda, MD, United
States
In this study we investigate the effects of the number
of images comprising the DTI data set on the statistical
properties of diffusion tensor eigenvalues and
anisotropy indices derived from them. The results of
Monte Carlo simulations along with the analysis of
phantom DTI data indicate an overall underestimation of
Eig3 and an overestimation of FA and Eig1 as the number
of images in DTI estimation is reduced.
|
1940. |
DTI Reconstruction:
K-space Average, Image-space Average, or No Average
Shu-Wei Sun1,2
1Biophysics and Bioengineering, Loma Linda
University, Loma Linda, CA, United States, 2Radiation
Medicine, Loma Linda University, Loma Linda, CA, United
States
Diffusion Tensor Imaging (DTI) is achieved by collecting
a series of Diffusion Weighted Images (DWI) with
different diffusion weighted vectors. For each DWI, it
is usually acquired with multiple repetitions to boost
the signal to noise ratio. On may perform k-space
average or image-space average to boost the signal to
noise ratio for each DWI. In this study, we compared DTI
maps of mouse brains in vivo using k-space average,
image-space average, and no average approaches. K-space
average provided the least contrast for presenting white
matter on RA maps.
|
1941. |
Diffusion Anisotropy
Corrections for Vessel Size and Microvessel Density Imaging
Jens H Jensen1
1Department of Radiology, New York University
School of Medicine, New York, NY, United States
The standard theories for vessel size imaging (VSI) and
microvessel density imaging (MDI) are based on an
assumption of isotropic water diffusion. Therefore, the
validity of applying these techniques to white matter
may be questioned. Here the corrections to the basic VSI
and MDI equations due to diffusion anisotropy are
explicitly calculated in terms of the diffusion tensor.
For the most anisotropic brain regions, the corrections
are found to be significant, although not large. These
results may relevant for application of VSI and MDI to
the assessment of angiogenesis in white tumors.
|
1942. |
Correcting the bias in the
ADC value due to local perturbation fields: a physically
informed model
Siawoosh Mohammadi1, Zoltan Nagy1,
Harald E Moeller2, David Carmichael3,4,
Mark Symms3, Oliver Josephs1, and
Nikolaus Weiskopf1
1Wellcome Trust Centre for Neuroimaging, UCL
Institute of Neurology, University College London,
London, United Kingdom, 2Max
Planck Institute for Human Cognitive and Brain Sciences,
Leipzig, Germany, 3Clinical
and Experimental Epilepsy, UCL Institute of Neurology,
London, United Kingdom, 4MRI
unit, National Society for Epilepsy, Chalfont St. Peter,
United Kingdom
Imaging artefacts, which perturb diffusion-weighted
images, can bias the estimated diffusion tensor.
Important sources of imaging artefacts in DTI are eddy
current fields, gradient nonlinearities or
mis-calibration of the gradient amplitude. They can be
modelled by introducing the concept of a local
perturbation field (LPF). In this study, we used
first-order perturbation theory to introduce a
physically-informed model that estimates and corrects
for the effect of LPFs. Using phantom and human DTI
measurements on two different scanners we were able to
estimate the LPFs and improve the quality of FA maps
without requiring vendor-specific information.
|
1943. |
Model-Based Reconstruction
of Undersampled DTI Data
Christopher L Welsh1,2, Edward W Hsu1,2,
and Edward VR DiBella1,2
1Bioengineering, University of Utah, Salt
Lake City, Utah, United States, 2UCAIR,
University of Utah, Salt Lake City, Utah, United States
Diffusion Tensor Imaging (DTI) is useful for
characterizing tissue microstructure, but suffers from
long scan time and low SNR. To allow faster acquisition,
a model-based strategy is presented to directly estimate
diffusion tensors from undersampled k-space data. Using
an acceleration factor of 2, different sampling schemes
were investigated and found to generally outperform
acquiring equivalent number of full-resolution scans.
Minor performance differences were also observed among
the schemes for estimating different DTI parameters.
These findings suggest the proposed strategy can be used
to reduce DTI scan time by half while incurring little
or no loss in the parameter estimation accuracy.
|
1944. |
Registration based
correction of DWI gradient orientations
Ben Jeurissen1, Maarten Naeyaert1,
Alexander Leemans2, and Jan Sijbers1
1Vision Lab, Dept. of Physics, University of
Antwerp, Antwerp, Belgium, 2Image
Sciences Institute, University Medical Center Utrecht,
Utrecht, Netherlands
Misalignment between diffusion weighted (DW) images and
the corresponding gradient orientations leads to
misinterpretation of rotationally variant diffusion
parameters and tractography results. We propose a method
to automatically correct for rigid misalignment of the
gradient orientations, using a registration metric based
on the average fiber trajectory length. Using
simulations we show that our method converges to the
'ground truth' orientations and that small 'angulation'
errors can still be detected, that are easily overlooked
by visual inspection. While the method uses diffusion
tensor tractography to calculate trajectory lengths, the
recovered gradient orientations can be applied in
general DWI post-processing.
|
1945. |
The anisotropic bias of
fractional anisotropy in anisotropically acquired DTI data
Sjoerd B Vos1, Max A Viergever1,
and Alexander Leemans1
1Image Sciences Institute, University Medical
Center Utrecht, Utrecht, Netherlands
In order to reduce DTI scan time, slice thickness is
often increased while maintaining a high in-plane
resolution. The resulting anisotropic voxel size means
that the orientation-dependent diffusion information is
sampled in a higher resolution in-plane than
through-plane. In this work we show that the bias in
fractional anisotropy, introduced by anisotropically
acquired DTI data, is dependent on the orientation of
the fiber bundle of interest. Furthermore, we
demonstrate that the diffusion bias is not solely
determined by the anisotropy of the voxel size, but
strongly depends on the relation between the fiber
bundle and the data grid as well.
|
1946. |
Diffusion tensor imaging
distortion correction with T1
KI SUENG CHOI1,2, Alexandre R. Franco2,
Paul E. Holtzheimer2, Helen S. Mayberg2,
and Xiaoping P. Hu1
1Bioengineering, Georgia Institute of
Technology / Emory University, Atlanta, GA, United
States, 2Psychiatry
and Behavioral Sciences, Emory University, Atlanta, GA,
United States
DW-EPI is very sensitive to B0 inhomogeneities that
produce geometric distortion, primarily along the
phase-encoding direction. As a result, artifacts degrade
the ability of using diffusion measures and diffusion
tractography. Several different techniques were
suggested for correcting susceptibility distortion.
However, to apply these correction techniques,
additional images (field map, T2) are required. In this
work, we examine susceptibility distortion correction
using image based non-linear registration along with
inverting the intensity of the T1 image. This method
exhibits better performance for geometrical distortion
correction in frontal region and an ability to analyze
clinical diffusion data without additional collection of
images.
|
1947. |
The effect of atlas
selection on voxel based analyses of DTI data
Wim Van Hecke1,2, Louise Emsell3,4,
Alexander Leemans5, Caroline Sage6,
Jelle Veraart7, Stefan Sunaert6,
Jan Sijbers7, and Paul M Parizel7
1University of Antwerp, Antwerp, Antwerp,
Belgium, 2University
of Leuven, Leuven, Leuven, Belgium, 3The
Murdoch Childrens Research Institute, Australia, 4NUI
Galway, Ireland, 5Image
Sciences Institute, Utrecht, Netherlands, 6University
of Leuven, Belgium, 7University
of Antwerp, Belgium
In this study, the effect of atlas selection on voxel
based analyses of DTI data is examined. To this end,
data sets of healthy subjects and multiple sclerosis
patients were aligned to a population-specific atlas, a
subject-based MNI template, and the ICBM-81 atlas.
|
1948. |
What is the component that
appears in diffusion-weighted imaging at low b values?
Kimihiro Ogisu1, Hidetsugu Sakai2,
and Toru Yamamoto2
1Graduate School of Medicine, Hokkaido
University, Sapporo, Japan, 2Graduate
School of Health Sciences, Hokkaido University
The signal from intravoxel incoherent motion (IVIM)
appears in diffusion-weighted imaging at low b values.
This low-b-value component is believed to reflect
capillary blood flow in tissue. However, the quantity of
the low-b-value component contradicts the data on
capillary blood volume in the literature. To determine
the origin of the low-b-value component, we investigated
the proton density and T2 value of the component. We
found that the low-b-value component has a larger T2
value than does blood and that this component exhibits
IVIM. Because the hydrostatic pressure and osmotic
pressure in capillaries drive interstitial fluid flow,
which has a large T2 value, we suggest that the
interstitial fluid mainly contributes to the low-b-value
component.
|
1949. |
Diffusion Tensor Imaging
tracks repair of Retinal Pigment Epithelium (RPE) layer
using Hematopoietic Stem Cells in mice
Saurav Chandra1, Sergio Caballero2,
Maria B Grant2, and John R Forder1,3
1Biomedical Engineering, University of
Florida, Gainesville, FL, United States, 2Pharmacology,
University of Florida, 3Radiology,
University of Florida
The study aims to restore visual function in mice
impaired by retinal degeneration by using hematopoietic
stem cells (HSCs) to repair the retinal pigment
epithelium (RPE) layer. HSCs expressing the gene RPE65
were successful in differentiating into RPE cells and
proliferating to the specific site to restore the RPE
layer. Diffusion tensor imaging successfully visualized
differences between repaired and unrepaired RPE layers
in mice. Fractional anisotropy (FA) was observed to
markedly higher in repaired retinas (as is the case in
any structured anatomy) compared to unrepaired retinas
which had a depleted RPE layer.
|
1950. |
High Angular Resolution
Diffusion Microscopy (HARDM) detects Retinal Disruption in
mice with Diabetic Retinopathy
Saurav Chandra1, Angelos Barmpoutis2,
Nicholas Simpson3, and John R Forder1,4
1Biomedical Engineering, University of
Florida, Gainesville, FL, United States, 2Computer
and Information Sciences Engineering, University of
Florida, 3College
of Medicine, University of Florida, Gainesville, FL,
United States, 4Radiology,
University of Florida, Gainesville, FL, United States
Diabetic retinopathy is the most common eye disease
affecting diabetics and a leading cause of blindness.
However, it cannot be diagnosed in its early stages. We
used High Angular Resolution Diffusion Microscopy (HARDM)
as a non-invasive tool to detect this disease at an
early stage in mice. HARDM of control eyes showed water
diffusion in the retina was restricted, reflecting an
organized structure within the retinal layers.
Comparison with control eyes showed the integrity of
these layers is compromised in eyes from diabetic
animals with elevated glucose levels. FA is also
significantly decreased in the diabetic retinas compared
to controls.
|
1951. |
Accounting for Changes in
Signal Variance in Diffusion Weighted Images Following
Interpolation for Motion and Distortion Correction
Mustafa Okan Irfanoglu1, Lindsay Walker2,
Raghu Machiraju3, and Carlo Pierpaoli2
1Computer Sciences and Engineering, The Ohio
State University, Columbus, OH, United States, 2NIH, 3The
Ohio State University
In this work, we propose a novel technique to account
for changes in signal variance in diffusion weighted
images due to interpolation artifacts related to image
registration based motion and distortion correction
steps. Our technique can model signal variance changes
due to sequential transformation applications and can
cope with all types of interpolation kernels. We show
our results as improvements in Chi-squared maps of
tensor fitting.
|
|
|
Traditional Posters
: Diffusion & Perfusion - Neuro
|
Click on
to view the
abstract pdf and click on
to view the pdf of the poster viewable in the poster hall.
|
Diffusion Acquisition & Pulse Sequences Methods
Wednesday May 11th
Exhibition Hall |
13:30 - 15:30 |
1952. |
High Resolution
Multiple Slice Composite Inner Volume Excitation Echo
Planar Diffusion Weighted imaging
Hing-Chiu Chang1,2, Tzu-Cheng Chao3,
Yi-Jui Liu4,5, Kuo-Fang Shao5,
Cheng-Chieh Cheng2, Chao-Chun Lin2,6,
and Hsiao-Wen Chung2,7
1Global Applied Science Laboratory, GE
Healthcare, Taipei, Taiwan, 2Institute
of Biomedical Electronics and Bioinformatics,
National Taiwan University, Taipei, Taiwan, 3Department
of Radiology, Brigham and Women's Hospital, Harvard
Medical School, Boston, Massachusetts, United
States, 4Department
of Automatic Control Engineering, Feng Chia
University, Taichung, Taiwan, 5Master's
Program in Biomedical Informatics and Biomedical
Engineering, Feng Chia University, Taichung, Taiwan, 6Department
of Radiology, China Medical University Hospital,
Taichung, Taiwan,7Department of
Radiology, Tri-Service General Hospital, Taipei,
Taiwan
Reduced field of view (rFOV) technique has been
known for its advance in shortening the read-out
train in MR imaging. With this excitation scheme,
high resolution Echo Planar Imaging (EPI) becomes
available with less geometric distortion. In this
work, a multiple slice rFOV sequence was proposed
with multiple sequential volume acquisition to
combine the rFOV images as a full FOV image with
appropriate intensity correction to compensate the
effect of RF profile imperfection during excitation.
And a high resolution in vivo EP-DTI dataset with
tractography result was demonstrated to confirm the
feasibility of this proposed scheme on clinical
research.
|
1953. |
Reduced-FOV
Single-Shot Diffusion-Weighted EPI: Extended Slice
Coverage with Tailored RF Pulse Design
Emine Ulku Saritas1, Ajit
Shankaranarayanan2, Greg Zaharchuk3,
and Dwight G Nishimura4
1Department of Bioengineering, University
of California, Berkeley, CA, United States, 2Applied
Science Laboratory, GE Healthcare, Menlo Park, CA,
United States, 3Department
of Radiology, Stanford University, Stanford, CA,
United States, 4Department
of Electrical Engineering, Stanford University,
Stanford, CA, United States
The use of a 2D echo-planar RF excitation has
recently been proposed for high-resolution
diffusion-weighted imaging (DWI) of targeted
regions. This method excites only the region of
interest, while providing inherent fat suppression
and contiguous multi-slice imaging. However, the
number of slices that can be acquired in a single TR
is limited due to the periodicity of the excitation
profile. In this work, we propose significant
improvements in RF pulse design to overcome this
limitation, and specifically demonstrate that the
coverage can be doubled without any SNR or scan time
penalty. We validate the proposed method with in
vivo high-resolution
axial DWI of the spinal cord.
|
1954. |
A 3D radial FSE-based
SPLICE sequence for MR diffusion imaging
Jiangsheng Yu1, Yiqun Xue1,
Mark A Rosen1, and Hee Kwon Song1
1Department of Radiology, University of
Pennsylvania School of Medicine, Philadelphia, PA,
United States
Currently, the gold standard technique for in vivo
diffusion imaging is single-shot diffusion-weighted
EPI (DW-EPI). However, DW-EPI is sensitive to
off-resonance effects, and artifacts are often
observed, particularly near air-tissue boundaries.
While FSE-based diffusion methods have also been
proposed, CPMG conditions can become easily
violated, particularly in the presence of motion
during diffusion sensitization. The SPLICE technique
was recently developed to overcome these artifacts.
In this work, we present preliminary results of a
hybrid 3D radial FSE SPLICE technique and
demonstrate improved ADC maps in both phantom and in
vivo experiments.
|
1955. |
Reduction of Image
Distortion in Non-Axial Diffusion-Weighted Imaging Using
Steer-PROP
Girish Srinivasan1,2, Novena Rangwala1,2,
and Xiaohong Joe Zhou1,3
1Center for MR Research, University of
Illinois Medical Center, Chicago, IL, United States, 2Department
of Bioengineering, University of Illinois Chicago,
Chicago, IL, United States, 3Departments
of Bioengineering, Radiology, Neurosurgery,
University of Illinois Medical Center, Chicago, IL,
United States
Severe image distortion is often seen in
diffusion-weighted single-shot EPI (SS-EPI) due to
strong concomitant gradient and other off-resonance
effects. A GRASE-based PROPELLER sequence,
Steer-PROP, is developed to reduce the image
distortion. Diffusion images were obtained from
non-axial planes on the human brain using the
Steer-PROP sequence, and showed substantially
reduced distortion when compared with SS-EPI. The
scan time of Steer-PROP was ~4-5 times longer than
that of SS-EPI, but 3-5 times faster than
conventional PROPELLER. With further improvement in
time efficiency, Steer-PROP can be a strong
contender for diffusion imaging in non-axial planes
where SS-EPI is problematic.
|
1956. |
A Sliding-Window
Re-Acquisition Scheme for Multi-Shot, Diffusion-Weighted
Imaging with 2D Navigator Correction
David Andrew Porter1, Keith Heberlein1,
and Robin Martin Heideman2
1Siemens Healthcare, Erlangen, Germany, 2Max
Planck Institute for Human Cognitive and Brain
Sciences, Leipzig, Germany
A number of sequences use a 2D navigator to correct
phase error in multi-shot, diffusion-weighted
imaging. The limited resolution of these 2D
navigators means that it is not possible to correct
high-spatial-frequency phase errors. Previous
studies have shown that navigator-based
re-acquisition can be used to re-measure these scans
and avoid artifacts in the final image, but the
techniques used were not suitable for acquiring
large volumes of data. This study describes the use
of a modified re-acquisition scheme with
diffusion-weighted, readout-segmented EPI to acquire
high resolution DTI with a 32 channel head coil.
|
1957. |
k-space and q-space:
Combining Ultra-High Spatial and Angular Resolution in
Diffusion Imaging using ZOOPPA at 7T
Robin Martin Heidemann1, Alfred Anwander1,
Thorsten Feiweier2, John Grinstead3,
Gabriele Lohmann1, Thomas R Knösche1,
and Robert Turner1
1Max Planck Institute for Human Cognitive
and Brain Sciences, Leipzig, Germany, 2Siemens
Healthcare, Erlangen, Germany, 3Siemens
Medical Solutions, Portland, United States
There is still a debate whether k-pace (high
resolution) or q-space (high angular resolution)
imaging is better to resolve crossing fibres. In the
current study we use a recently introduced
combination of zoomed imaging and parallel imaging
to obtain diffusion-weighted images with isotropic
high resolution and high angular resolution at
ultra-high field strength. The acquired data with 1
mm isotropic resolution has sufficient SNR to
resolve crossing fibres in the white matter.
|
1958. |
Distortion Free High
Resolution in vivo Whole Brain Diffusion Tensor Image on
7.0T MRI
Se-Hong Oh1, Jun-Young Chung1,
Sung-Yeon Park1, Joshua Haekyun Park1,
Dae-Hoon Kang1, Myung-Ho In2,
Maxim Zaitsev3, Oliver Speck2,
Young-Bo Kim1, and Zang-Hee Cho1
1Neuroscience Research Institute, Gachon
University of Medicine and Science, Incheon, Korea,
Republic of, 2Department
of Biomedical Magnetic Resonance, Institute for
Experimental Physics, Otto-von-Guericke University
Magdeburg, Magdeburg, Germany, 33
Department of Radiologic Research, Medical Physics,
University Hospital of Freiburg, Freiburg, Germany
Diffusion pulse sequences based on single-shot EPI
inherit virtually all of the artifacts associated
with EPI. For example, distortion caused by magnetic
susceptibility variations and B0 field inhomogeneity
is frequently observed in the frontal sinus. When
high resolution at higher magnetic field imaging
like 7.0T, diffusion weighted images severely suffer
from distortions due to susceptibility artifacts.
Therefore, to acquire high resolution DTI images at
7.0T UHF MRI, we should solve geometric distortion
problem. To correct geometric distortion use
distortion and non-distortion dimensional combined
PSF correction method. Then we can correct the
geometric distortion both compressed and stretched
area more accurately. These results show the
efficacy of distortion correction for the anatomical
accuracy of fiber tractography. With 7.0T distortion
free high-resolution DWI data, we are able to
visualize anatomically accurate fiber tractography
image as well as small fiber tractography image such
as mammillo thalamic tract, which not achievable at
low field MRI (i.e. 1.5T or 3.0T).
|
1959. |
Single-Shot
Diffusion-Weighted Spiral Imaging
Bertram Jakob Wilm1, Christoph Barmet1,
and Klaas Paul Pruessmann1
1Institute for Biomedical Engineering,
University and ETH Zurich, Zurich, Zurich,
Switzerland
We present a comprehensive approach to diffusion
weighted single-shot spiral imaging. On the basis of
field monitored data images are obtained by
higher-order reconstruction including static-B0correction
and parallel imaging. The Images with an in-plane
resolution of 1.4 mm do not show aliasing related
artifacts and are virtually free from B0 off-resonance
effects.
|
1960. |
Motion-Induced Phase
Error Correction in 3D Diffusion-Weighted Imaging
Anh Tu Van1, Diego Hernando1,
Joseph Holtrop2, and Bradley P Sutton2,3
1Electrical and Computer Engineering,
University of Illinois at Urbana-Champaign, Urbana,
IL, United States, 2Bioengineering,
University of Illinois at Urbana-Champaign, Urbana,
IL, United States,3Beckman Institute,
University of Illinois at Urbana-Champaign, Urbana,
IL, United States
A robust 3D motion-induced phase error estimation
and correction algorithm is introduced in the
present study to enable in vivo 3D
diffusion-weighted imaging. Parameters of the phase
error are estimated by nonlinear fitting of
navigator images to a motion-induced phase error
model and used to correct the k-space data. The
phase error parameter estimation is unbiased with
mean square errors approaching the Cramer-Rao lower
bound. The correction is time efficient with
performance independent of the 3D k-space trajectory
used. Simulation and in vivo results were obtained
to demonstrate the accuracy of the proposed method.
|
1961. |
Isotropic
High-Resolution 3D Diffusion Weighted SSFP Imaging with
Spiral Projection Imaging
Rafael Luis O'Halloran1, Murat Aksoy1,
Eun Soo Choi1, and Roland Bammer1
1Radiology, Stanford University, Palo
Alto, CA, United States
The Spiral projection readout is combined with
DW-SSFP to acquire 3D diffusion weighted images at
multiple diffusion directions in reasonable scan
times for whole brain coverage in a healthy human
volunteer. A retrospective cardiac gating technique
and iterative-SENSE reconstruction is used to
address reproducible phase errors caused by cardiac
motion and compared to a standard gridding
reconstruction. Images at multiple diffusion
encoding strengths are presented.
|
1962. |
Impact of the
point-spread function on parameters derived from
diffusion-weighted imaging: axial versus sagittal
acquisition
J-Donald Tournier1,2, Fernando Calamante1,2,
and Alan Connelly1,2
1Brain Research Institute, Florey
Neuroscience Institutes, Melbourne, Victoria,
Australia, 2Department
of Medicine, University of Melbourne, Melbourne,
Victoria, Australia
Diffusion-weighted imaging (DWI) data are typically
acquired using single-shot multi-slice EPI. Images
acquired with these sequences will inevitably have
differences in the point-spread function along the
different orientations (i.e. through-slice versus
in-plane). These differences can introduce errors in
the DW signal and derived parameters due to Gibbs
ringing in the immediate vicinity of high signal
areas (particularly CSF), which will depend on the
direction of the imaging slice with respect to the
direction of signal change. In this study, we
demonstrate this effect by comparing images acquired
using otherwise equivalent axial and sagittal DWI
protocols.
|
1963. |
The Deleterious Effect
of Concomitant Gradient Fields on Diffusion Imaging
Corey Allan Baron1, Robert Marc Lebel1,
Alan H Wilman1, and Christian Beaulieu1
1Biomedical Engineering, University of
Alberta, Edmonton, AB, Canada
Concomitant fields are small unavoidable magnetic
field components that exist during the application
of imaging gradients. They can usually be ignored
for common pulse sequences. However, in diffusion
tensor imaging, large gradients are required to
sensitize the MR signal to water diffusion, and
phase accrual from the concomitant fields can lead
to image artefacts. This is of particular concern
for eddy current cancelling diffusion preparations
used in combination with systems having large
gradients. We demonstrate that an erroneous increase
in apparent diffusion coefficient can occur in
phantom and human brain, and we propose and validate
a prospective correction.
|
1964. |
Crusher Gradient
Reversal to Eliminate Stimulated Echo Artifacts in Dual
Spin Echo Diffusion MRI
Gaohong Wu1, Sangwoo Lee1,
Xiaoli Zhao1, and Zhu Li1
1GE Healthcare, Waukesha, WI, United
States
A crusher gradient reversal method is proposed to
overcome the stimulated echo artifacts in dual spin
echo diffusion MRI. The polarity of crusher
gradients before and after the two refocusing pulses
is reversed according to the polarity of diffusion
gradients. The reversal allows the crusher gradients
and diffusion gradients to be added up, so that
there are always enough crushers to kill the
stimulated echo signal. The removal of stimulated
echo artifacts is not specific to certain b-values,
and does not have impact on sequence performance.
|
1965. |
Diffusion-limited
diffusion MRI and a universal optimum b-value
Van Wedeen1, and Guangping Dai1
1Radiology, Martinos Center/ MGH,
Charlestown, MA, United States
If we model q-space MRI as an imaging
micro-structure, its effective resolution is the sum
of two terms: “camera resolution” proportional to
q-1=( Gt)-1,
and blurring by the diffusion kernel, which if
Gaussian has width (2Dt)-1/2. Defining effective
resolution as the root-mean-square, setting t= =∆
and minimizing, the best-possible diffusion-limited
structural resolution is Rmin=√3(D/ G)1/3,
achieved with encoding time topt=D-1/3( G)-2/3
and bopt=(π2/6)D-1. In vivo, if observed
max(D-1)≈5Dwater-1 then bopt≈20,000s/mm-2. Thus, an
optimal b-value of q-space MRI depends only on
diffusivity and is gradient-independent; stronger
gradients improve structural resolution insofar as
they reduce diffusion encoding time at optimal b.
|
1966. |
Optimised Gradient
Waveform Spin-Echo sequence for Diffusion Weighted MR in
a Microstructure Phantom
Bernard M Siow1,2, Ivana Drobnjak1,
Mark F Lythgoe2, and Daniel C Alexander1
1Centre for Medical Image Computing, UCL,
London, United Kingdom, 2Centre
for Advanced Biomedical Imaging, UCL, London, United
Kingdom
Diffusion MRI has been used for probing tissue
microstructure and of particular interest is axon
radius distribution estimates. Abnormal
distributions are found in pathologies such as
amyotrophic lateral sclerosis and schizophrenia.
PGSE sequences have been traditionally used for
diffusion weighting and optimised protocols that use
these sequences have been used to provide reliable
axon radius estimates >5µm. Recently, an in
silico study
optimised the shape of the gradient waveforms for
particular axon radii and showed that protocols that
used these optimised waveforms provided improved
axon radii estimates <5µm. In this study, we
implement these optimised gradient waveform
protocols on a pre-clinical scanner. These protocols
were used to study microcapillary phantoms that have
pore radii of 1-10 µm. A good agreement between
simulated and measured signal was found, giving a
strong indication that these sequences can be
practically implemented in
vitro and in
vivo. Potentially, these protocols can provide
extra sensitivity to microstructural features <5µm.
|
1967. |
On the Diffusion
Sensitivity of 2D- and 3D-Turbo Spin Echo Sequences
Matthias Weigel1, and Jürgen Hennig1
1Dept. of Radiology, Medical Physics,
University Medical Center Freiburg, Freiburg,
Germany
The present work investigates the diffusion
sensitivity of 2D- and 3D-TSE sequences; for
variants with low constant or variable refocusing
flip angles in particular. The performed simulations
using realistic protocol settings are based on an
extended phase graph (EPG) approach that was
published recently. It is found that especially
novel 3D-TSE sequences with extended echo trains and
variable low flip angles – usually known as SPACE or
CUBE – exhibit a notable diffusion weighting that
should not be neglected.
|
1968. |
Simulation of
Diffusion Weighted SSFP: Time to Reach the Steady State
and Effects on Anisotropic Diffusion
Eun Soo Choi1, Rafael O'halloran2,
Ernesto Staroswiecki2, and Roland Bammer2
1Stanford University, Stanford,
California, United States, 2Department
of Radiology, Stanford University, Stanford,
California, United States
Diffusion-weighted SSFP imaging offers high
diffusion contrast with low spin preparation time,
but requires an initial period to reach steady
state. It is important to know how long this initial
period is so that data collection can begin after
steady state is achieved. Here, the time to reach
steady state is investigated in three simulated
brain tissue types using the extended phase graph
simulation. The dependence of the time to steady
state on multiple parameters such as TR, flip angle,
and diffusion coefficient is explored. Additionally
the effect of switching the diffusion gradient
direction on the steady state is investigated. The
time to return to steady state after the switch has
implications for diffusion tensor imaging of
anisotropic diffusion
|
1969. |
Analysis of
Diffusion-Weighted SSFP Signal with Computer Simulation
Eun Soo Choi1, Rafael O'halloran2,
Ernesto Staroswiecki2, and Roland Bammer2
1Stanford University, Stanford,
California, United States, 2Department
of Radiology, Stanford University, Stanford,
California, United States
Increasingly, diffusion weighted (DW) imaging is
being performed with higher numbers of diffusion
directions and is moving toward isotropic 3D
acquisition. DW SSFP imaging has the potential to
meet these challenges due to its increased scan time
efficiency compared with conventional spin echo DWI.
A major factor limiting widespread adoption of DW
SSFP is that the signal depends not only on pulse
timing and geometry but also upon the physical
parameters, T1, T2, and diffusion coefficient. Here
we present Bloch simulations of the pulsed gradient
DW-SSFP sequence and compare it to the extended
phase graph simulation as well as to the approximate
analytical solution of Wu and Buxton.
|
|
|
Traditional Posters
: Diffusion & Perfusion - Neuro
|
Click on
to view the
abstract pdf and click on
to view the pdf of the poster viewable in the poster hall.
|
Perfusion/Permeability: DSC Methods
Thursday May 12th
Exhibition Hall |
13:30 - 15:30 |
1970. |
Quantitative perfusion
imaging by USPIO bolustracking: the Maximum Slope Model
Peter Roland Seevinck1,2, Mark J Bouts1,
Annette van der Toorn1, and Rick Martin
Dijkhuizen1
1Biomedical MR Imaging and Spectroscopy,
Image Sciences Institute, University Medical Center
Utrecht, Utrecht, Utrecht, Netherlands, 2Physics
of MRI, Image Sciences Institute, University Medical
center Utrecht, Utrecht, Netherlands
Absolute quantification of perfusion parameters
critically contributes to the accuracy of
characterizing tissue status, predicting lesion
outcome, as well as monitoring therapy in
experimental and clinical stroke studies. In this
work we investigated the use of USPIO for perfusion
imaging, instead of Gd-DTPA, which would enable the
simultaneous assessment of vascular architecture
(e.g. angiogenesis) by ssCE-MRI. The signal time
course typical for USPIO bolus tracking motivated us
to apply an alternative method for absolute
quantification of perfusion parameters, i.e. the
maximum slope model. This model was demonstrated to
provide realistic values for CBV and CBF in rats in
vivo.
|
1971. |
An improved
quantification method to characterize cerebral
hemodynamic changes after carotid endarterectomy
surgery: a dynamic susceptibility contrast MRI study.
David E Crane1, Bradley J MacIntosh1,2,
Ediri Sideso3, James Kennedy3,
Ashok Handa4, Manus J Donahue5,
and Peter Jezzard5
1Heart and Stroke Foundation Centre for
Stroke Recovery, Sunnybrook Research Institute,
Toronto, ON, Canada, 2Medical
Biophysics, University of Toronto, Toronto, ON,
Canada, 3Nuffield
Department of Medicine, University of Oxford,
Oxford, United Kingdom, 4Nuffield
Department of Surgery, University of Oxford, Oxford,
United Kingdom, 5Clinical
Neurology, FMRIB Centre, University of Oxford,
Oxford, United Kingdom
A method of calculating quantitative DSC, thereby
permitting longitudinal comparison, is demonstrated
and applied to patients undergoing carotid
endarterectomy surgery. Quantification was performed
with the “bookend” technique, where T1-weighted
steady-state measurement of CBV is used to scale
DSC-derived absolute CBF values. Subcortical grey
matter CBF results agreed with reported values and
age trends. Comparison of pre vs. post surgery
showed low inter-session variability and significant
surgery effects. Thus, the DSC-bookend approach may
be useful in characterizing the interaction between
hemodynamics and CEA effects thereby helping to
identify patients most likely to benefit from
surgery.
|
1972. |
Spin-echo and
Gradient-echo PWI CBF vs. ASL CBF: An Initial
Comparison.
Matus Straka1, Heiko Schmiedeskamp1,
Greg Zaharchuk1, Jalal B Andre1,
Jean-Marc Olivot2, Nancy J Fischbein1,
Maarten G Lansberg2, Michael E Moseley1,
Gregory W Albers2, and Roland Bammer1
1Radiology, Stanford University,
Stanford, CA, United States, 2Stanford
Stroke Center, Stanford University, Stanford, CA,
United States
Novel SAGE DSC-MRI sequence delivers both spin- and
gradient-echo PWI CBF maps that provide information
about both microcapillary and macrovascular brain
perfusion. A comparison of the SAGE-derived CBF
values with reference ASL CBF is presented. 10
initial SAGE cases were acquired, postprocessed by
deconvolution to obtain CBF, and after
coregistration with ASL CBF, voxel-wise comparison
of CBF values was executed. A scaling factor of 4.8
was found between GRE and SE-based CBF values. It
was observed that SE-based CBF maps correlate with
ASL CBF better that those from GRE, but contrast in
SE CBF and ASL CBF is not identical.
|
1973. |
Low-Resolution
Cartesian Compressed Sensing MRI: Application to Dynamic
Susceptibility MRI
David S Smith1,2, Thomas E Yankeelov1,2,
and Christopher Chad Quarles1,2
1Radiology and Radiological Sciences,
Vanderbilt University, Nashville, TN, United States, 2Institute
of Imaging Science, Vanderbilt University,
Nashville, TN, United States
We show that using Compressed Sensing MRI to
accelerate low-resolution, 2-D Cartesian Dynamic
Susceptibility MRI by up to a factor of two has no
significant influence on the derived hemodynamic
parameters.
|
1974. |
Flow Heterogeneity as
a Potential Biomarker of Vascular Normalisation in
Tumour Studies
John David Dickson1, Richard E Ansorge1,
and Stephen Price2
1Department of Physics, Cambridge
University, Cambridge, Cambridgeshire, United
Kingdom, 2Medical
School, Cambridge University
Recent research has shown that the success of
anti-angiogenic treatment can be due to a process
known as vascular normalisation. The need to track
the effectiveness of anti-angiogenic treatment has
therefore created a demand for effective biomarkers
of vascular normalisation. One proposed biomarker is
the radii of vessels present, however vessel size
imaging requires intravenous injection of Iron Oxide
contrast agents. We propose that effective
information on normalisation of vascular morphology
may be attainable using only Gadolinium-based
tracers by measuring intravoxel heterogeneity in
flow rate.
|
1975. |
Use of the
relationship between phase and magnetic susceptibility
for assessment of assumed contrast agent distributions
in vivo: Application to R2*
maps in dynamic susceptibility contrast MRI
Emelie Lindgren1, Linda Knutsson1,
Danielle van Westen2, Freddy Ståhlberg1,3,
and Ronnie Wirestam1
1Dept. of Medical Radiation Physics, Lund
University, Lund, Sweden, 2Radiology,
Skane University Hospital, Lund, Sweden, 3Dept.
of Diagnostic Radiology, Lund University, Lund,
Sweden
Magnetic susceptibility quantification by
deconvolution of measured phase maps is an
interesting approach, although the method
constitutes an ill-posed inverse problem to which an
ideal solution is presently lacking. An interesting
intermediate step is to compare measured phase maps
(reflecting true local susceptibility) with
artificial phase maps calculated by convolution of
an assumed susceptibility distribution. Delta_R2*
maps were assumed to represent contrast agent
concentration (i.e., proportional to
susceptibility), as is traditionally the case in
DSC-MRI. Differences between measured and artificial
phase maps were observed, not inconsistent with
different T2* relaxivities in different
compartments, as predicted by previously published
simulation studies.
|
1976. |
Improving CBF Image
Contrast with Frequency Extrapolation for DSC-MRI during
Acute Stroke
Matthew Ethan MacDonald1,2, Micheal
Richard Smith1,3, and Richard Frayne2,3
1Departments of Electrical and Biomedical
Engineering, University of Calgary, Calgary, AB,
Canada, 2Seaman
Family MR Research Centre, Foothills Medical Centre,
Calgary, AB, Canada,3Departments of
Radiology and Clinical Neurosciences, University of
Calgary, Calgary, AB, Canada
DSC-MRI is can provide estimates of the tissue
perfusion in the early onset of stroke. CBF is a
perfusion parameter that has been suggested for
detecting regions of tissue that are affected by
ischemia and may still be salvageable with
treatment. The calculation of CBF from raw perfusion
data requires deconvolution, which has been shown to
have MTT-dependent bias. In this work, frequency
domain extrapolation is introduced during the
deconvolution process to correct for this bias. The
algorithm is tested across ten ischemic stroke
patient data sets, and compared with follow up
imaging, ROC analysis is used to determine
detection.
|
1977. |
Determination of
Collateral Supply Patterns Using Conventional Dynamic
Susceptibility Contrast Perfusion Imaging
Cihat Eldeniz1, Yueh Lee2,
Jeffrey Keith Smith2, Tyler B. Jones2,
Weili Lin2,3, Sten Solander2,
James Faber4, and Hongyu An2
1Biomedical Engineering, University of
North Carolina, Chapel Hill, NC, United States, 2Department
of Radiology, University of North Carolina, Chapel
Hill, NC, United States, 3Department
of Neurology, University of North Carolina, Chapel
Hill, NC, United States, 4Department
of Cell and Molecular Physiology, University of
North Carolina, Chapel Hill, NC, United States
In this study, we have shown that an integration of
CBF, MTT and Tmax obtained from DSC data can be
utilized in detecting collateral supply to ischemic
tissue. Our findings are in agreement with the gold
standard DSA assessment in human stroke patients.
|
1978. |
A patient-specific
global residue function improves reproducibility in
longitudinal monitoring of perfusion changes in
low-grade gliomas
Atle Bjornerud1,2, Kim Mouridsen3,
and Kyrre Eeg Emblem4,5
1Interventional Centre, Oslo Univeristy
Hospital, Oslo, Norway, 2Dept.
of Physics, Univ. of Oslo, Oslo, Norway, 3Center
for Functionally Integrative Neuroscience, Aarhus
University Hospital, Denmark, 4A.
A. Martions Center for Biomedical Imaging,
Massachusetts General Hospital, 5Oslo
Univeristy Hospital, Norway
We present a method for improved reproducibility of
DSC-MRI based perfusion measurements through the
generation of a global patient specific tissue
residue function obtained at a single time-point
using an automatically generated AIF. The global
scan-specific tissue response is then combined with
the global residue function and the initial AIF to
reconstruct a scan-specific AIF used to derive
perfusion parameters at each time-point. The method
was tested in the analysis of unaffected brain
tissue in glioma patients undergoing multiple
longitudinal scans and was found to significantly
improve reproducibility of perfusion measurements
compared to using scan-specific AIFs.
|
1979. |
Prediction of clinical
outcome in glioma patients using a combination of
epidermal growth factor receptor (EGFR) and relative
cerebral blood volume (rCBV) measured by dynamic
susceptibility-weighted contrast-enhanced magnetic
resonance imaging
Marcel Oei1, Albert Idema1,
Pieter Vos1, Sandra Boots-Sprenger1,
Judith Jeuken1, and Mathias Prokop1
1Radboud University Nijmegen Medical
Centre, Nijmegen, Gelderland, Netherlands
Problem: Good prediction of clinical outcome is
important for determining therapy in glioma tumors.
Aim: Evaluate the combination of rCBV and EGFR to
predict clinical outcome in glioma patients.
Methods: rCBV was measured from DSC-MR images in 44
patients. EGFR copy numbers of 18 tumor samples were
derived using MLPA. Statistical analyses were used
to determine correlation, ROC curves and
Kaplan-Meier Survival curves. Results: A strong
significant correlation was found between rCBV and
EGFR. Patients with rCBV < 5.45 and normal EGFR had
significant longer survival. Conclusion: The
addition of EGFR improved the prediction of clinical
outcome of rCBV.
|
1980. |
Correlation of DSC
parameters with histopathological complex
microvasculature in GBM patients
Emma Essock-Burns1,2, Joanna J Phillips3,4,
Janine M Lupo2, Soonmee Cha2,5,
Susan M Chang5, and Sarah J Nelson1,6
1UCSF/UCB Joint Graduate Group in
Bioengineering, University of California San
Francisco, San Francisco, California, United States, 2Department
of Radiology and Biomedical Imaging, University of
California San Francisco, San Francisco, California,
United States, 3Department
of Pathology, University of California San
Francisco, 4Department
of Laboratory Medicine, University of California San
Francisco, San Francisco, California, United States, 5Department
of Neurological Surgery, University of California
San Francisco, San Francisco, California, United
States, 6Department
of Bioengineering and Therapeutic Sciences,
University of California San Francisco, San
Francisco, California, United States
Glomeruloid vasculature, a hallmark of GBM tumors,
is associated with breakdown of the blood-brain
barrier. During DSC-imaging this results in
extravasation of contrast, causing challenges for
accurate perfusion assessment. 35° flip angle DSC
acquisition is one strategy for mitigating this
competing effect. This study correlated complex
vasculature from 22 GBM biopsies to DSC-perfusion
parameters acquired with either 35° or 60° flip
angle. Percent signal recovery inversely correlated
with presence of complex vasculature across the
study population and for the subset of data acquired
with 35° flip angle. This study supports that
complex vasculature can be well studied with 35°
DSC-imaging.
|
1981. |
MULTIPARAMETRIC
CLASSIFICATION OF HYPEROXIA CHALLENGE AND DYNAMIC
SUSCEPTIBILITY CONTRAST MAPS: STUDY OF THE HEALTHY BRAIN
Moran Artzi1,2, Orna Aizenstein3,
Talma Hendler1,2, Rinat Abramovitch4,
and Dafna Ben Bashat1
1Functional Brain Center, Wohl institute
for Advanced Imaging, Tel Aviv Sourasky Medical
Center, Tel-Aviv, Israel, 2Sackler
Faculty of Medicine, Tel Aviv University, Tel-Aviv,
Israel, 3Radiology
Department, Tel Aviv Sourasky Medical Center,
Tel-Aviv, Israel, 4The
Goldyne Savad Institute for Gene Therapy, Hadassah
Hebrew University Medical Center, Jerusalem, Israel
The aim of this study was to use unsupervised
multimodal classification method on a combined data
obtained from hyperoxia challenge and
dynamic-susceptibility-weighted imaging, in order to
characterize brain tissue vascularity in the healthy
brain. Three brain clusters were defined and
classified as white matter, gray matter and dura&blood
vessels. Significant differences between the
clusters and between brain lobes were detected with
a trend of higher vascularity in the right versus
the left hemisphere. This combination of methods
provides comprehensive knowledge which may be used
by future studies to improve characterization of the
hemodynamic features of the healthy and pathological
brain.
|
1982. |
Dynamic susceptibility
contrast imaging study of the healthy brain using
multiparametric classification
Moran Artzi1,2, Orna Aizenstein3,
Talma Hendler1,2, and Dafna Ben Bashat1
1Functional Brain Center, Wohl institute
for Advanced Imaging, Tel Aviv Sourasky Medical
Center, Tel-Aviv, Israel, 2Sackler
Faculty of Medicine, Tel Aviv University, Tel-Aviv,
Israel, 3Radiology
Department, Tel Aviv Sourasky Medical Center,
Tel-Aviv, Israel
The characterization and quantification of dynamic
susceptibility contrast (DSC) imaging is important
for clinical interpretation, though this calls for a
reliable healthy reference. In this study, an
unsupervised multiparametric method was used to
classify brain tissue and a defined brain vascular
territories template was used to study perfusion
parameters in 25 healthy subjects. Three brain
clusters were defined and classified as white
matter, gray matter and major blood vessels.
Perfusion parameters were significantly different
between tissue types and between vascular
territories. The unsupervised clustering method
enabled tissue classification and may have a wide
range of clinical applications.
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