Hall D Tuesday 13:30-15:30
13:30
3058.
Whole Orbit Soft Tissue Deformation Acquired by Accelerated 3D CSPAMM
Tagging During Eye Motion
Computer 15
Marco
Piccirelli1,2, Andrea Kaspar Rutz1, Oliver
Bergamin2, Peter Boesiger1, Roger Luechinger1
1University
and ETH Zurich, Zurich, Switzerland; 2University Hospital Zurich,
Switzerland
In
complex orbital mechanical disorders, a better comprehension of ocular motion
dynamic is needed. The deformation pattern within extraocular muscles (EOM) and
orbital connective tissues has not been understood yet. In this work, an
accelerated truly three-dimensional tagging acquisition method is proposed
enabling the assessment of motion information with whole orbit coverage in a
scantime allowing good motion reproducibility. A reduced field-of-view method
was incorporated and 3D data sets were acquired sequentially with line tag
preparation in each of the three spatial dimensions. Data were post-processed
with 3D peak-combination HARP. Tissues within the orbit could be reliably
tracked and characterized.
14:00
3059.
Orthogonal TrueFISP Acquisitions Using Paired Reverse Centric Phase
Encoding
Computer 15
Jamal
Jon Derakhshan1,2, Mark A. Griswold1,2,
Jeffrey L. Sunshine2, Jeffrey L. Duerk,12
1Case
Western Reserve University, Cleveland, Ohio, USA; 2University
Hospitals Case Medical Center, Cleveland, Ohio, USA
Paired
reverse centric phase encoding is presented as a way to eliminate saturation
banding in interleaved orthogonal TrueFISP imaging. Simulation results
demonstrate significant (> 2x) reduction of orthogonal plane saturation
artifacts across various base resolutions, flip angles and tissue types.
Phantom imaging demonstrates the ability to eliminate both saturation and eddy
current artifacts by pairing the reverse centric lines. Human in vivo abdominal
scout imaging demonstrates the utility of the new acquisition strategy.
Application to interventional MRI is demonstrated by presenting three orthogonal
images acquired during real-time guidance of an RF electrode to the porcine
adrenal gland in vivo.
14:30
3060.
Artifact-Free Stimulated-Echo Acquisition Mode (STEAM) Cardiac Images
with Improved Signal-To-Noise Ratio (SNR)
Computer 15
Tamer
A. Basha1, ElSayed H. Ibrahim1, Nael F. Osman1
1Johns
Hopkins University, Baltimore, Maryland, USA
The
stimulated echo acquisition mode (STEAM) is currently used in a wide range of
applications for imaging tissue parameters. However, when applying STEAM in
cardiac imaging, signal loss of the myocardium has been reported due to the
intravoxel dephasing of the magnetization during the contraction (or
stretching) of the cardiac muscle. Despite of its intrinsically low SNR, STEAM
was quite appealing for the assessment of various cardiac functions. In this
work, we deal with the SNR and deformation artifactproblems in STEAM technique.
First, we introduce a SSFP acquisition technique to increase the SNR then we
propose a method for removing the deformation artifacts from the STEAM images.
Computer 15
Tim
P. DeMonte1, Jia-Hong Gao2, Dinghui Wang3,
Weijing Ma3, Michael L.G. Joy3
1Field
Metrica Inc., Toronto, Canada; 2University of Chicago, USA; 3University
of Toronto, Canada
Current
density imaging is an MRI technique used to measure current density vectors in
tissue. Human electro-muscular
incapacitation (HEMI) devices are becoming commonly used by law enforcement and
military. The ultimate goal of this work
is to achieve better understanding of the effects of HEMI on physiology for
enhancement of efficacy and safety. Specifically,
the relationship between applied current amplitude and measured current density
magnitude is investigated. This
relationship is expected to be linear over small ranges, but not well
understood for larger ranges. A small
range is investigated in an in-vivo pig to establish a method for future work.
Hall D Tuesday 13:30-15:30
13:30
3062.
Dark Blood BSSFP Imaging Using Magnetization Prepared Random Velocity
Encoding
Computer 16
Jamal
Jon Derakhshan1,2, Mark A. Griswold1,2,
Jeffrey L. Sunshine2, Jeffrey L. Duerk,12
1Case
Western Reserve University, Cleveland, Ohio, USA; 2University
Hospitals Case Medical Center, Cleveland, Ohio, USA
A
new method for generating steady state, short TR, dark blood bSSFP images based
on magnetization prepared TrueFISP is presented. Periodically, the
magnetization is returned to the z axis with an α/2 pulse. Thereafter,
magnetization preparation includes randomly scaled velocity encoding, similar
to RF-spoiling. Simulations demonstrate that flowing blood signal can be
reduced by > 95% while stationary tissue undergoes much lower loses (~ 24%)
based on T2 decay. Phantom imaging results demonstrate stationary and flowing
signals consistent with predictions. Human in vivo imaging demonstrates the
ability to null blood flow in a short TR magnetization prepared Cartesian bSSFP
sequence.
14:00
3063.
Enhanced Contrast in CEST MRI Via Intermolecular Double Quantum
Coherences
Computer 16
Shengchun
Zhang1, Huijun Sun1, Zhong Chen1, Congbo Cai1,
Jianhui Zhong2
1Xiamen
University, Xiamen, People's Republic of China; 2University of Rochester,
Rochester, New York, USA
A
CEST imaging technique based on intermolecular double quantum coherence (iDQC)
is proposed. Quantitative analysis and experiments in glucose agarose-gel
phantoms demonstrate that, in CEST MRI, iDQC signal is more sensitive to RF
saturation than the conventional SQC signal, and thus needs RF saturation
pulses of lower power to achieve similar CEST image contrast. Consequently, the
method can reduce the potential RF burning in clinic applications, and is
expected to facilitate the study of the CEST effect in the system with
exchangeable protons of low concentrations.
14:30
3064.
An Investigation of Optimizing and Translating Pulsed-Chemical Exchange
Saturation Transfer (CEST) Imaging to a 3 T Clinical Scanner
Computer 16
Phillip
Zhe SUN1, Thomas Benner1, Gregory Sorensen1
1A.
A. Martinos Center for Biomedical Imaging, Charlestown, Massachusetts, USA
Chemical
exchange saturation transfer (CEST) MRI provides a sensitive detection
mechanism that allows characterization of dilute labile protons usually
undetectable by MRI. Particularly, amide proton transfer (APT) imaging, a
variant of CEST MRI, has been shown capable of detecting ischemic tissue
acidosis, and may serve as a surrogate metabolic imaging marker. For
pre-clinical CEST imaging, long continuous-wave (CW) RF irradiation is often
applied so that the steady state CEST contrast can be reached. On clinical
scanners, however, specific absorption rate (SAR) limit and hardware design
preclude the use of CW irradiation, and instead require an irradiation scheme
of repetitive RF pulses (pulsed-CEST imaging). In this work, CW- and
pulsed-CEST MRI were systematically compared using a tissue-like pH phantom on
an imager capable of both CW and pulsed RF irradiation schemes. The results
showed that the maximally obtainable pulsed-CEST contrast is about 95% of
CW-CEST contrast, and their optimal RF irradiation powers are equal. Moreover,
the pulsed-CEST imaging sequence was translated to a 3 Tesla scanner and
detected minor pH difference of 0.6 pH unit using exchangeable amine groups
(1.9 ppm). Furthermore, pilot endogenous pulsed-APT imaging of control human
volunteers was demonstrated, warranting future APT MRI of stroke patients to
fully elucidate its diagnostic value.
15:00
3065.
Relaxometry Changes in a Gel Dosimetry Phantom Due to Continued RF
Exposure
Computer 16
Gary
Paul Liney1, Mark Godber2, Andrew D. Wilson2,
John W. Goodby3
1University
of Hull, Hull, UK; 2University of York, York, UK; 3University
of York, York, UK
To
quantify changes in transverse relaxometry, in phantoms used for MRI
gel-dosimetry, due to continued RF heating in the scanner, and to map the
distribution of these effects.
13:30
3066.
B1 Correction for Improved Bound Pool Fraction Maps
Computer 17
Nikola
Stikov1, Robert F. Dougherty1, John Mark Pauly1
1Stanford
University, Stanford, California , USA
The
bound pool fraction (f) is an
indicator of myelin content in the brain, and cross-relaxation imaging is an
efficient method of mapping the f
parameter in vivo. The first step in
cross-relaxation imaging is obtaining an accurate T1 map of the
brain, but B1 inhomogeneity makes this task difficult. We incorporated B1 correction in
our cross-relaxation procedure, and scanned three subjects with and without
this correction. Our procedure removed
variations in the T1 values of white matter across subjects, while
reducing the total cross-relaxation scan time.
14:00
3067.
FISPCEST: A Rapid, Acquisition for Dynamic Detection of CEST/PARACEST
Activity
Computer 17
Tejas
Shah1,2, Meser Ali1, Guanshu Liu1,
Mark D. Pagel1, Chris A. Flask1
1Case
Western Reserve University, Cleveland, Ohio, USA
We
have developed a new FISP Chemical Exchange Saturation Transfer (FISPCEST)
pulse sequence to sensitively detect effects. The FISPCEST technique provides
<3sec acquisition times which is an order of magnitude less than current
CEST techniques. The FISPCEST acquisition combines a single, ~2sec,
nonselective CEST preparation and a ~500ms FISP acquisition. The improved
temporal resolution is obtained with only a 15% loss in CEST sensitivity in
comparison to a spin echo CEST acquisition. The FISPCEST acquisition is
adaptable to both endogenous and exogenous (PARA)CEST applications and enables
the acquisition of CEST spectra maps and/or multislice CEST images in under 1
minute.
14:30
3068.
Tissue-Dependent Asymmetries in the SSFP Off-Resonance Profile
Computer 17
Karla
L. Miller1, Daniel P. Bulte1, Gwenaelle Douaud1,
Peter Jezzard1
1Oxford
University, Oxford, UK
The
SSFP signal is strongly sensitive to off-resonance, with a signal profile for
an isochromat population that is theoretically symmetric about the tissue
frequency ("on-resonance"). However, the existence of
frequency-shifted compartments may lead to an asymmetric profile. We demonstrate
this asymmetric response for tissues in the brain, finding a strongly
asymmetric response in white matter, a moderately asymmetric response in gray
matter and an approximately symmetric response in CSF. This response profile
may be useful as a novel marker for tissue content.
15:00
3069.
Dynamic Nuclear Polarization Using a Low Field Multi-Channel MR System
Computer 17
Eugeny
Krjukov1, Martyn Paley1
1University
of Sheffield, Sheffield, UK
Dynamic
nuclear polarisation has been investigated with the free radical
carbomyl-PROXYL using a low frequency (360kHz) multi-channel MR system.
Enhancement factors of up to 40 were found with 50W or ESR irradiation at
220MHz.
13:30
3070.
Contrast Enhancement by Feedback-Enhanced MRI
Computer 18
Sophia
Y. Yang1, Dennis W. Hwang1, Susie Y. Huang2,
Lian-Pin Hwang3, Yung-Ya Lin1
1UCLA,
Los Angeles, California , USA; 2Harvard Medical School, Boston,
Massachusetts, USA; 3National Taiwan University, Taipei, Taiwan
Feedback-enhanced
MRI yields robust image contrast that is sensitive to small differences in the
underlying microscopic frequency distributions. Important applications of this
method include improving the visualization of SPIO nanoparticles through
generation of positive contrast and distinguishing small changes in microscopic
susceptibility corresponding to tumor and normal tissue. Using an external
electronic device can significantly enhance the feedback field and open
opportunities for the design of novel imaging pulse sequences in which the
feedback interaction is controllable. Examples of in vitro and in vivo tumor
detection in human brain tissue and mouse models of lung adenocarcinoma with
active feedback will be demonstrated.
Computer 18
Robert
Henry Morris1, Martin Bencsik1, Marie-Pierre Krafft2,
Gilles Waton2, Nikolaus Nestlé3, Petrik Galvosas4,
Anil Vangala, Yvonne Perrie5
1Nottingham
Trent University, Nottingham, UK; 2Institut Charles Sadron,
Strasbourg, France; 3BASF Aktiengesellschaft, Ludwigshafen, Germany;
4University of Leipzig,
Leipzig, Germany; 5Aston Universit
MRI
manometry is performed in vitro using two alternative contrast agents comprised
of compressible microcapsules suspended in a liquid medium presenting high
viscosity with little reduction of the diffusion coefficient compared to that
of bulk water. The currently available contrast agent utilising standard lipid
coated gas microcapsules is shown to be highly unstable in typical clinically
relevant pressure conditions, whilst perfluorinated gas microcapsules coated
with a perfluoroalkylated lipid will allow in vivo measurements in the future.
14:30
3072.
Visualization of Viscoelastic Properties by Combining US Pulses and MRI
Computer 18
Ole
Benjamin Oehms1, Marcus Radicke1, Sarah Wrede1,
Meinert Lewerenz1, Andre Engelbertz1, Karl Maier1
1Friedrich
Wilhelms Universität, Bonn, Germany
The
irradiation of Ultrasound Pulses (30 ms, at 10 MHz) into a sample during a
diffusion sensitive MRI sequence leads to signal changes in liquids and tissue.
They are caused by the decrease of the acoustic radiation pressure due to
damping of the sound wave which leads to a movement in a liquid along the path
of sound propagation. This movement leads to a dephasation if it occurs while
the diffusion gradient is active which results in a signal diminishment in that
region. This diminishment depends on the viscoelastic properties of the sample.
First measurements on Water and Glycerine and on a piece of tissue will be
presented in the talk.
15:00
3073.
MR Imaging of Transient Shear Waves Induced by Ultrasonic Radiation
Force
Computer 18
Remi
Souchon1, Rares Salomir1, Olivier Beuf2, Denis
Lyonnet3, Jean-Yves Chapelon1, Olivier Rouviere3
1INSERM
U556, Lyon, France; 2CNRS UMR 5220, Lyon, France; 3Hospices
Civils de Lyon, France
This
study reports preliminary wave images and temperature measurements for
transient MR elastography (MRE) using ultrasound radiation force. Our initial
data suggest that an EPI MRE sequence is likely to provide elasticity images
while ensuring patient safety.
13:30
3074.
Improved MREIT Reconstruction Using Sodium MRI
Computer 19
Mark
Jason Hamamura1, L Tugan Muftuler1, Orhan Nalcioglu1
1University
of California, Irvine, California , USA
In
magnetic resonance electrical impedance tomography (MREIT), electrical currents
are injected into an object and the resulting magnetic flux density
distribution measured using MRI. These
MRI measurements are then used to reconstruct the conductivity distribution
within the object. In this study, we
investigated the incorporation of sodium MRI data into the MREIT reconstruction
algorithm. The results demonstrate that
this incorporation can improve the accuracy of the reconstructed conductivity
maps.
14:00
3075.
SPIO Acid Dissolution Kinetics with MR Susceptometry
Computer 19
Ludovic
de Rochefort1, Yi Wang1
1Weill
Medical College of Cornell University, New York, New York, USA
Superparamagnetic
iron oxides benefit from a very strong magnetic moment at low field due to
their superparamagnetic property. Here, we show the feasibility of monitoring
chemical reaction of SPIO dissolution by acids with MRI. The magnetic moment
destruction is measured continuously as a function of time with MR susceptometry.
14:30
3076.
A Quantitative Approach of Extracting Magnetic Moments in Small
Cylindrical Object
Computer 19
Ching-Yi
Hsieh1, Yu-Chung Norman Cheng1, Jaladhar Neelavalli1,
E. Mark Haacke1
1Wayne
State University, Detroit, USA
Our
goal is to quantify magnetic moments of a small in-vivo object such as veins in the brain from MR images, without
any a priori information. By summing
up MR signals within three concentric circles, the magnetic moment of the
object obtained from different complex data in the same image can be accurate
within 10% of its true value. To achieve this accuracy, a long echo time may be
needed. The simulations and experimental results are presented for the gel
phantom. The agreement between these two results indicates a promising
potential of this method.
15:00
3077.
In Vivo T1ρ-Weighted MR Imaging of Rat Brain Using a Surface Coil at 11.7 Tesla
Computer 19
Su
Xu1, Jehoon Yang1, Jun Shen1
1National
Institute of Mental Health, Bethesda, Maryland, USA
A
sech-based adiabatic spin-lock pulse sequence to obtain T 1ρ-weighted
MR images using a surface transceiver coil was optimized for enhancing tissue
contrast. The utility of this technique was demonstrated using in vivo rat brains after focal
bicuculline administration and an 11.7 Tesla 89 mm bore vertical microimager.
Signal intensity of the lesion in the T 11ρ-weighted images was
significantly elevated 50 minutes after administration of bicuculline.
13:30
3078.
Magnetization-Prepared Shells for Efficient T1-Weighted Brain Imaging
Computer 20
Yunhong
Shu1, Matthew A. Bernstein1
1Mayo
Clinic College of Medicine, Rochester, Minnesota, USA
To
maximize the contrast in MP-RAGE brain imaging, it is desirable to select a
k-space acquisition order that can sample the center of k-space compactly
during the peak contrast difference between WM and GM during the inversion
recovery curve. The shells trajectory is a non-Cartesian 3D trajectory with
high acquisition efficiency and an inherent centric nature. It provides the
flexibility required to synchronize the acquisition of the center of k-space to
the contrast maximum contrast. Here we theoretically and experimentally
demonstrate the feasibility of combining magnetization preparation with the
shells trajectory to achieve T1-weighted brain imaging efficiently.
14:00
3079.
Flow-Independent T2-Prepared Inversion Recovery Black Blood MR Imaging
Computer 20
Chia-Ying
Liu1,2, Oliver Wieben1, Jean H. Brittain2,
Scott Brian Reeder1
1University
of Wisconsin-Madison, Madison, Wisconsin, USA; 2GE Healthcare,
Madison, Wisconsin, USA
Black
blood prepared MRI is used extensively for cardiac and atherosclerotic plaque
imaging. Most black blood sequences employ double inversion recovery, which
relies on the inflow of nulled blood. As a result, double IR methods are less
effective in the presence of slow flow and in-plane flow. We present a new
black-black preparation scheme which employs a T2-prepared sequence in
combination with an inversion recovery pulse (T2Prep-IR). Excellent blood
suppression independent of flow was demonstrated in the heart and carotid
arteries of volunteers.
14:30
3080.
In Vivo Blood T1 Mapping Using Inversion Recovery TrueFISP
Computer 20
Wen-Chau
Wu1, Jiongjiong Wang1
1University
of Pennsylvania, Philadelphia, USA
In
the present study, we demonstrated the feasibility of in vivo blood T1 mapping
with an inversion recovery (IR) TrueFISP sequence. The IR TrueFISP signal has
been shown to vary with the flip angle, T1 and T2 of static tissue of interest.
With continous inflow of flesh blood with undisturbed longitudinal
magnitization, the IR TrueFISP curve of blood pool signal approximated standard
T1 relaxation. The estimated blood T1 values at 3.0T match well with literature
results with minimal sensitivity to variations in flip angle.
15:00
3081.
Practical Optimum Experimental Designs for Fast T1 Relaxometry with SPGR
Sequences
Computer 20
Alexey
Samsonov1, Andrew L. Alexander1, Youngkyoo Jung1,
Aaron S. Field1
1University
of Wisconsin, Madison, Wisconsin, USA
Knowledge
of the longitudinal relaxation time T1 is required in many quantitative MRI
applications. T1 mapping using variable
flip angle SPGR acquisitions is an attractive choice due to its speed. In this work, we describe a method for
automatic selection of T1 mapping flip angles, which explicitly optimizes the
performance of T1 mapping for a wide range of T1 values. The method yielded 3 flip angle designs with
performance similar to the previously described 10 flip angle design. This development may allow more efficient T1
mapping optimized for wide range of tissue types.
Computer 21
Sean
CL Deoni1, Steven CR Williams2, Peter Jezzard1,
John Suckling3, Declan GM Murphy2, Derek K. Jones4
1University
of Oxford, Oxford, UK; 2Institute of Psychiatry, London, UK; 3University
of Cambridge, Cambridge, UK; 4Cardiff University Brain Research
Imaging Centre, Cardiff, UK
Multicentre
studies are becoming increasingly common as they facilitate the recruitment of
greater numbers of subjects while decreasing the economic cost and duration of
study. However, precise matching of
structural image quality, necessary to draw meaningful inferences from the data
particularly in regards to morphology, becomes difficult as the number and
diversity of imaging systems increases.
Here we report on the use of quantitative T1 and T2 imaging for
standardizing the structural imaging component of such studies, demonstrating
high reproducibility of the measures across different systems.
14:00
3083.
Combining Morphometry and T1 Relaxometry in a Single Imaging Protocol:
Measuring T1 with MPRAGE
Computer 21
Olivier
Mougin1, Penny Gowland1
1School
of Physics and Astronomy, Nottingham, UK
We
are using relaxation times to study normal and pathological brain development.
Acquisition times for T1 are generally long, so this study aims to make use of
the anatomical image that is acquired for morphological information into the
relaxometry protocol. Therefore we have optimized the Magnetization Preparation
followed by a RApid Gradient Echo (MPRAGE) sequence (which is routinely used
for morphology at our site) for the measurement of T1. Study on five subjects
at three different fields shows agreement with the literature and gold standard
sequences.
14:30
3084.
Fast T1 Mapping in Human Brain Using Inversion Recovery EPI with GRAPPA
at 3T and 7T
Computer 21
John
Grinstead1, William Rooney2
1Siemens
Medical Solutions USA, Inc., Portland, USA; 2Oregon Health &
Science University, Portland, USA
Quantitative
T1 techniques find a wide range of applications in biological NMR, but the
major drawback of these techniques is that they are slow. This is because the
sampling requirements are high, not only must the T1 recovery be well sampled,
but also spatial encoding is usually desired. This work investigates the
combination of inversion recovery echo-planar and parallel imaging techniques
for high-speed acquisition of quantitative T1 data sets in human brain at 3T
and 7T.
15:00
3085.
Measurement of R1 Dynamics Using a 3D FLASH Variable Flip Angle Sliding
Window Technique
Computer 21
Jessica
Schulz1,2, Eva Christina Wönne1, Arne Hengerer2,
Wolfhard Semmler1, Michael Bock1
1Deutsches
Krebsforschungszentrum (dkfz), Heidelberg, Germany; 2Siemens Medical
Solutions, Erlangen, Germany
A
3D FLASH variable flip angle method was combined with a sliding window
calculation to obtain the relaxation rates R1 dynamically with a temporal
resolution of 10 s. In a contrast agent study on tumor-bearing mice the
contrast agent-related changes in R1 could be mapped in tumors, and the R1
values were in excellent agreement with reference measurements.
Shared Resources & Quality Control
Hall D Tuesday 13:30-15:30
13:30
3086.
The Neuroimaging Informatics Tools and Resources Clearinghouse (NITRC)
Computer 22
David
N. Kennedy1, Robert Buccigrossi2, Jeff Grethe, Christian
Haselgrove, Nina Preuss, Keith Wagner, Mark Ellisman
1MGH,
Charlestown, Massachusetts, USA; 2Turner Consulting Group, USA
NITRC,
a new neuroimaging knowledge environment, is now online (www.nitrc.org). We encourage
the fMRI community to try it out and provide feedback on its design, tools,
resources, and content. NITRC is a knowledge environment for the fMRI community
where tools and resources are presented in a coherent and synergistic
environment for the advancement of MRI-based neuroscience research.
14:00
3087.
PAQAP: A Quality Assessment Protocol for MRI
Computer 22
Pieter
Vandemaele1, Rik Achten1, Yves De Deene1
1Ghent
University Hospital, Ghent, Belgium
Quality
assessment in MR imaging provides clinician and researchers with objective
measures of the performance of their MR scanner and scan protocols. PAQAP (Pieter’s Automated Quality
Assurance Protocol) is a combination of a standard QA phantom and an elaborate
software program for full automatic data analysis and report generation. PAQAP
provides an easy way to acquire and process QA data on a regular basis with
minimal interaction and within a limited time frame by an MR technologist. The
system will be implemented and systematically used in a QA program at the
experimental MR site of the Ghent University Hospital.
14:30
3088.
MR Image Quality Evaluation Using Weighted Perceptual Difference Model
(Case-PDM)
Computer 22
Jun
Miao1, Wilbur C. K. Wong1, David L. Wilson1,2
1Case
Western Reserve University, Cleveland, USA; 2University Hospital of
Cleveland, Cleveland, USA
The
perceptual difference model (Case-PDM) is being used to quantify image quality
of fast, parallel MR acquisitions and reconstruction algorithms by comparing to
slower, full k-space, high quality reference images. In this paper, we create
an alternative metric weighted to image features to improve the linear
correlation coefficient between human ratings and weighted Case-PDM, across a
large set of MR reconstruction test images of varying quality. Our method is
robust across subjects and anatomy; that is, scores maintain a high correlation
with human ratings even if the test dataset is different from the training
dataset.
15:00
3089.
A Novel SNR Estimation Technique Applicable to Clinical Parallel MR
Images: Triple Band-Width Single Acquisition Method (TriSAM)
Computer 22
Yoshio
Machida1, Hiroshi Kusahara1, Yoshimori Kassai1
1Toshiba
Medical Systems Corporation, Otawara, Japan
We
have developed a new technique gTriple band-width Single Acquisition Methodh
(TriSAM) in which noise maps can be obtained with originally intended target
images with no extra scan time. Application of this technique with parallel
imaging to the head images on a volunteer provides the misregistration free
noise images. The TriSAM is considered to be one of the most practical SNR
estimation approaches for clinical images.
Hall D Tuesday 13:30-15:30
Computer 23
Vasily
L. Yarnykh1
1University
of Washington, Seattle, Washington, USA
A
recently developed Actual Flip-angle Imaging (AFI) method allows fast B1
mapping based on the spoiled steady-state principle. This study presents
theoretical and experimental examination of conditions required for optimal
spoiling in the AFI sequence. It was found that the spoiling behavior of the
AFI sequence is different from a traditional spoiled gradient echo sequence. To
achieve optimal spoiling, appropriate combinations of an RF phase increment and
spoiler gradient areas need to be used. The sequence design providing highly
accurate B1 measurements and possible sources of errors are described.
14:00
3091.
In-Vivo Assessment of a STEAM Sequence for B1-Mapping
Computer 23
Rudolf
Stollberger1, Thomas Birngruber2
1Graz
University of Technology, Graz, Austria; 2Medical University of
Graz, Austria
RF
field inhomogeneities are a main source for image inhomogeneities, spatial
dependent SNR and CNR and systematic errors in quantification of MRI data. A
STEAM sequences was evaluated in-vivo at 3T for B1-determination in
quantitative studies. It could be shown that the sequence is robust and
sufficiently accurate for the application in most regions. Some problems occur
in the chest from motion artefacts. The acquisition time for a scanning matrix
of 128*64 was 47s for TR=800ms and 78s for TR=1300.
14:30
3092.
Impact of the Correction of B1 Inhomogeneities for Dynamic
Contrast-Enhanced Imaging at 3 Tesla
Computer 23
Robert
Merwa1, Franz Ebner2, Rudolf Stollberger1
1Graz
University of Technology, Graz, Austria; 2Medical University of
Graz, Graz, Austria
This
study was performed in order to evaluate the influence of the B1-inhomogenities
for dynamic contrast-enhanced MRI at 3 T. The active RF-field was measured with
a stimulated echo sequence whereas the actual flip angle distribution is
determined. Using a reference scan and a perfusion scan particular parameters
as temporal T1 relaxation time, concentrations and arterial input function can
be calculated. The results obtained with the correction of the flip angles show
a significant improvement compared to the results obtained without correction.
All the measurements were performed on a 3 T System (Siemens Magnetom Trio a
Tim System)
15:00
3093.
Rapid RF Flip Angle Imaging
Computer 23
Daniel
Kim1, Sohae Chung1, Daniel K. Sodickson1, Leon
Axel1
1New
York University, New York, New York, USA
The
transmit radiofrequency (RF) filed (B1) uniformity plays an important role in
determining the image quality in MRI, particularly at high field strengths
(&[ge] 3T). Accurate B1 or flip angle maps are needed to compensate for B1
variations through different compensation strategies. Among the existing
methods for in vivo B1 mapping, the double angle method (DAM) is most
straightforward. However, its image acquisition efficiency is very low due to a
need to set TR &[ge] 5 T1s. The purpose of this study is to develop a rapid
in vivo B1 mapping method based upon three single-shot image acquisitions.
Image Registration & Alignment
Hall D Wednesday 13:30-15:30
13:30
3094.
Validation of 3D Non-Rigid Whole Body MR Image Registration
Computer 15
Xia
Li1, Thomas Yankeelov, Todd Peterson, John Gore, Benoit Dawant
1Vanderbilt
University, Nashville, Tennessee, USA
The
automatic registration of whole body MR images, which requires non-rigid
registration techniques for the
articulated
structures, remains a challenge. Although we proposed a promising registration
method that permits the automatic registration of MR images for both intra- and
inter-subject, one weakness is found in this algorithm: bones can be deformed
incorrectly because of the surrounding structures. A modified method was
proposed to constrain the deformation of bony structures. However, complete
validation is required. In this study, quantitative validation results show the
accuracy of our algorithm.
14:00
3095.
Breast MR Registration for Evaluation of Neoadjuvant Chemotherapy
Response
Computer 15
Ruparani
Chittineni1,2, Min-Ying Su1, Orhan Nalcioglu1
1University
of California, Irvine, Irvine, USA
The
deformable nature of breast tissue results in significant shape differences
between serial studies, making it challenging to chalk out a clear trajectory
of the corresponding tumor locations. These studies correspond to MR-based
monitoring of chemotherapy for therapy response evaluation. In this abstract we
demonstrate the use of constraint based free-form deformations for registration
of serial breast MR studies. The algorithm is especially useful in patients
with multi-centric or multi-focal lesions. Also, differentiating between
therapy-induced inflammation and residual disease becomes amenable. Since,
tumor volumes are preserved during the transformation, mis-interpretation of
results can be avoided.
14:30
3096.
Image Registration of Mouse Brains Containing Varying Amounts of Extra
Cortical CSF
Computer 15
Matthijs
C. van Eede1, Jason P. Lerch1, John G. Sled1
1Toronto
Centre for Phenogenomics, Toronto, Canada
In
recent studies we encountered brains containing varying amounts of extra
cortical CSF. Using our groupwise registration method for analysis of the
brains, we found this resulted in incorrect alignment. That would lead to
incorrect findings. We have developed a modulation strategy to deal with this
extra cortical CSF, alleviating the registration problem.
15:00
3097.
Non-Rigid Registration of Diffusion Weighted MRI Using Progressive
Principal Component Registration (PPCR)
Computer 15
Andrew
Melbourne1, David Hawkes1, David Atkinson1
1University
College London, London, UK
Artefacts
as a result of patient motion & eddy current distortions often corrupt
Diffusion Weighted MR images, reducing the success of subsequent analysis.
Registration of images that contain different contrast from each gradient
direction may produce inaccurate results. The PPCR scheme allows diffusion
direction images to be registered into a common coordinate frame by combining
overlapping diffusion contrast using principal components analysis. PPCR registration
is compared to data registered using an affine registration of each diffusion
direction to the corresponding B0 volume. The use of the PPCR method allows
enhanced feature demarcation by removing geometric distortion artefacts.
Computer 16
Ruparani
Chittineni1, SeungHoon Ha1, Werner Roeck1,
Min-Ying Su1, Orhan Nalcioglu1
1University
of California, Irvine, Irvine, USA
Restoring
form of compressed or deformed images is of utmost significance. Automatic
non-rigid registration techniques have been applied extensively to address
non-linear deformations. However, it is interesting to note that such
algorithms may fail or be biased towards dominant intensity regions in the
images and hence have minimal local registration. We demonstrate and compare
the applicability of automatic and landmark based methods for the particular
case of addressing deformation in the presence of constriction or applied
compression. The near future application of the developed method is for
co-registration of breast images acquired using MRI (uncompressed) and
scintimammography (under light compression).
14:00
3099.
Registration of 3D MR Images of the Mouse Embryos
Computer 16
Mojdeh
Zamyadi1,2, R Mark Henkelman1,2,
Shoumo Bhattacharya3, Jurgen E. Schneider3, John G. Sled1,2
1University
of Toronto, Toronto, Canada; 2Mouse Imaging Centre, Hospital for
Sick Children, Toronto, Canada; 3University of Oxford, Wellcome
Trust Centre for Human Genetic, Oxford, UK
We
are developing an image registration technique to detect subtle anatomical
shape differences between 3D MR images of mouse embryos. In order to assess
feasibility, we have used non-linear registration to align a group of
genetically identical embryos. We tested the assumption that embryo anatomy is
highly conserved among specimens by registering six 3D embryos together. The
result of the registration process is shown in form of a final average image
consisting of data from the 6 individuals, and the root mean squared (RMS)
displacement image which is a representation of the
anatomical
variation among the genetically identical embryos. These initial findings
suggest that embryo anatomy is highly conserved among specimens and that image
registration of 3D MRI data is a feasible approach for subsequently detecting
abnormal phenotypes.
14:30
3100.
Quality Control in a Longitudinal Multi Center Alzheimer's Disease Study
Computer 16
Eric
Westman1, Andy Simmons2, Sebastian Muehlboeck3,
Tony Segerdahl4, Johan Bengtsson4, Lars-Olof Wahlund1,
Simon Lovestone2, Christian Spenger4
1Department
of Neurobiology, Health Care Sciences and Society, Karolinska Institutet,
Stockholm, Sweden; 2MRC Centre forNeurodegeneration Research,
Institute of Psychiatry King's College, London, UK; 3McConnell Brain
Imagi
Within
the InnoMed/AddNeuroMed research project funded by the European Union, sixth
frame work program, data has been successfully collected for a multi site MRI
study. Quality control and quality assurance are performed on routine basis at
data collection centers and at the data coordination centre. The feature-set of
the database system covers the entire process from image acquisition, storage,
quality control to data querying for analysis. Quality control statistics show
that the performance of the participating sites is very high; 97 % of all T1
images passed QC.
15:00
3101.
Validation of User Independent Planning Tool for Consistent Data Acquisition
in Multi-Center Trials
Computer 16
Esben
Thade Petersen1,2, Ivan Zimine1,3,
Xavier Golay,14, The QUASAR Reproducibility study
1National
Neuroscience Institute, Singapore, Singapore; 2Aarhus University
Hospital, Aarhus, Denmark; 3Philips Medical Systems, Tokyo, Japan; 4Singapore
Bioimaging Consortium, Singapore, Singapore
In
this work, we evaluated the accuracy of automatic slice positioning which
recently has become available on standard MRI systems. The success of MRI
studies often depends on the consistency of the image acquisition and is
especially important in longitudinal and multi-center trials. Differences in
slice angulations and positioning can easily affect the “subjective” reading by
radiologists but also the quantification in DTI, perfusion or
volumetric-imaging. Three automatically planned images were acquired in 170
subjects and minor rotation and translation between scans were observed after
co-registration of the images, resulting in high consistency for future trials
using these tools.
Computer 17
Karen
J. Mullinger1, Gerda B. Geirsdottir1, Matthew J. Brookes1,
Peter F. Liddle1, Richard W. Bowtell1
1University
of Nottingham, Nottingham, UK
The
correlation of preceding alpha power and driven power with the BOLD response to
a visual stimulus has been investigated using simultaneous EEG/fMRI experiments
at 3 T. Despite good characterisation of the BOLD and electrical responses no
correlation was found between the fluctuations in the alpha power preceding the
stimulus or in the driven power and the BOLD response in data from individual
subjects. A positive trend was however found when comparing the fractional
difference in BOLD response and preceding alpha power in trials falling in the
top and bottom quartiles binned according to the preceding alpha power across
subjects.
14:00
3103.
Hemispherical Constrained Surface Controller for 3D Navigation
Computer 17
Martin
John Graves1, David John Lomas1
1University
of Cambridge and Addenbrooke's Hospital, Cambridge, UK
Although
there has been significant development of volumetric image acquisition
methodologies there has been little development of methods for subsequent
reformatting of data beyond standard linear tools. This work describes the
development of a 3D constrained surface controller for interrogating volumetric
data. The controller allows for intuitive navigation by following an ultrasound-style
motion paradigm in which data reformatting is performed over a virtual
hemispherical surface around the organ of interest. Constraining the motion to
an anatomically consistent surface reduces the possibility of the operator
becoming spatially disorientated. The controller was evaluated in comparison to
conventional reformatting software.
Computer 17
Jan
Sedlacik1,2, Jürgen R. Reichenbach1
1University
Clinics of the Friedrich Schiller University, Jena, Germany
Blood
oxygenation level and volume fraction are essential input parameters of
theoretic models of spin dephasing in a vascular network. It is possible to
estimate these parameters by fitting the simulated signal to measured
signal-time curves. However, if the blood oxygenation level and volume fraction
are unknown, they can not be reliably estimated by simply fitting theoretical
signal curves to the measured signal decay. The purpose of this work was to
unravel this difficulty of a simultaneous estimation of blood oxygenation level
and volume fraction.
15:00 3105. Local Feature-Preserving Sele