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 Selection of Kernel Size for Unwrapping of
High-Resolution Phase Images
Computer 17
Julien
Milles1, Matthijs J.P. van Osch1, Louise van der Weerd1,
Rob J.A. Nabuurs1, Wouter M. Teeuwisse1, Jeroen van der
Grond1, Mark A. van Buchem1, Johan H.C. Reiber1
1Leiden
University Medical Center, Leiden, Netherlands
The
aim of this work is to investigate the use of objective criteria to determine
the optimal filtering kernel size in order to perform phase unwrapping while
preserving local features on high-resolution phase images by means of a k-space
filtering-based algorithm. We propose two local information-based criteria that
depict the trade-off involved in phase unwrapping. We study the effect of
kernel size on those criteria and show that their analysis allows determining
an optimal filtering kernel size that realizes the trade-off between wraps
removal and local features preservation.
13:30
3106.
Dual Echo Susceptibility Weighted Imaging (SWI) : Reducing the Error in
Making Phase Mask
Computer 18
Yoshiyuki
Ishimori1, Masahiko Monma, Yutaka Kouno, Makito Iizuka, Seiichi
Sasaki
1Ibaraki
Prefectural University of Health Sciences, Ami-machi, Inashiki-gun, Japan
The
high pass filter process utilizing in susceptibility weighted imaging has the
possibility of insufficient removal of phase wrapping and another artifact on
the phase mask. We calculated the phase difference caused in TE interval by
dual echo technique and calculated the
time-invariant component of the phase. We used this time-invariant phase for
making a phase mask. With this technique, severe phase wrappings were removed
and edge enhancement effect around the positive phase portion was reduced.
14:00
3107.
Intelligent Image Repository for MRI Brain Clinical Trials
Computer 18
Gianlorenzo
Fagiolo1, Nick Fox2, Derek L. Hill2,3,
Adam D. Waldman4, Jo V. Hajnal1
1Imperial
College,, London, UK; 2UCL, London, UK; 3London
Bioscience Center, London, UK; 4Charing Cross Hospital, London, UK
Longitudinal
MRI in which the same subject is scanned on multiple occasions is increasingly
being used for clinical trials, and for diagnosis/monitoring of patients,
particularly in brain studies. Minor errors in patient information entered into
hospital information systems are common and occasionally gross errors occur.
The result can be that images to be compared are wrongly identified leading to
information loss in clinical trials. In this work, a MRI brain clinical trials
image repository with intelligent text recognition and Image-based Subject
Identification was developed. The identification proved robust both to scan
quality deterioration and to progressing brain atrophy.
14:30
3108.
Rapid Prototyping of a 3D Grid Phantom for MR Image Guided Therapy
Quality Assurance
Computer 18
Barbara
Holshouser1, David Kittle2, James M. Slater2,
Robert D. Pearlstein3
1Loma
Linda University Medical Center, Loma Linda, California , USA; 2Loma
Linda University, Loma Linda, California , USA; 3Duke University and
Medical Center, Durham, USA
We
have used rapid prototyping technology to directly fabricate a 3D grid phantom
from CAD drawings. The phantom was then used to measure spatial inaccuracies in
3D images acquired in a 12 channel receive only head coil in a 3T MR scanner.
The ultimate purpose is to characterize MR imaging related spatial inaccuracies
for image guided surgery and radiotherapy.
Computer 18
Hervé
Boisgontier1,2, Vincent Noblet1, Fabrice Heitz1,
Lucien Rumbach3, Jean-Paul Armspach2
1Laboratoire
des Sciences de l'Image, de l'Informatique et de la Télédétection, UMR CNRS-ULP
7005, Illkirch, France; 2Laboratoire d'Imagerie et de Neurosciences
Cognitives, UMR CNRS-ULP 7191, Strasbourg, France; 3CHU Minjo
Studies
have already highlighted diffusion property alterations induced by multiple
sclerosis. This paper proposes an automatic method for detecting changes
between two or more scalar images characterizing diffusion properties.
Validation of the proposed approach and comparison of the impact of the scalar
index used (mean diffusivity, fractional anisotropy and lattice index) have
been done using synthetic simulations. Results show that the performance of the
method depends on the index considered. This is mainly explained by the nature
of noise, which varies from one index to the other
Hall D Wednesday 13:30-15:30 Chairs: Anja C. Brau and Donglai Huo
13:30
3110.
Motion Artifact Correction with MOJITO: Practical Implications
Computer 19
Candice
Anne Bookwalter1, Mark A. Griswold1, Jeffrey L. Duerk1
1Case
Western Reserve University, Cleveland, Ohio, USA
It
is a well known property of Fourier Transform MRI that rigid body translational
motion in image space results in linear phase accumulation in k-space. This work describes practical simulations and
MR experiments using Multiple Overlapping k-space Junctions for Investigating
Translating Objects (MOJITO), a correction scheme based on phase differences at
trajectory intersections caused by 2D object shifts. The algorithm allows both detection and
correction of motion artifacts caused by 2D rigid body translational
motion. Here, MOJITO is demonstrated
using the continuous sampling BOWTIE trajectory.
14:00
3111.
Effect of Motion-Induced Altered Coil Sensitivity on Parallel Imaging
Performance
Computer 19
Murat
Aksoy1, Roland Bammer1
1Stanford
University, Stanford, California , USA
Correction
of involuntary patient motion related artifacts remains to be one of the most
important topics in MRI. In the specific case of rigid body motion, rotation
and translation changes the position of the anatomy under examination with
respect to the receiver coil, which, in turn, changes the coil sensitivity
“seen” by the anatomy. In this study, we investigated the effects of this
change in coil sensitivity with rigid body motion. Our results show that
especially at higher reduction factors and in the case of severe patient
motion, coil sensitivity profiles have to be modified accordingly to reflect
the correct coil sensitivity exposure in order to accomplish accurate parallel
image reconstruction.
14:30
3112.
SENSE Motion Correction
Computer 19
Julian
R. Maclaren1, Bing Wu1, Philip Bones1, Rick P.
Millane1, Richard Watts1
1University
of Canterbury, Christchurch, New Zealand
A
motion-correction technique using a multiple-shot fast spin echo (FSE) sequence
is presented. SENSE is used to reconstruct a complete, albeit noisy, image from
data collected in each individual shot. These images are then registered and
combined to produce a motion-corrected reconstruction. This technique has the
advantage that a regular reconstruction can also be obtained from the same
k-space data set. Hence, little is lost by applying this technique and an advantage
is gained over a standard FSE acquisition in the case of patient motion.
15:00
3113.
Motion Mitigation for Eye Imaging Using Cloverleaf Navigators
Computer 19
Andre
J. W. van der Kouwe1, Thomas Benner1, Ashok Kumar1,
Timo van Kerkoerle1, Graham Wiggins1, Giorgio Bonmassar1
1Massachusetts
General Hospital, Charlestown, Massachusetts, USA
High-resolution
imaging of the human eye in-vivo is exacerbated by involuntary motion. The eye
performs small saccadic movements at irregular intervals, and moves during
blinking. These movements are manifest in the MR image as blurring, and
smearing in the phase encoding direction.
We present a suggestion for dealing with this type of motion during
imaging by oversampling in k-space while simultaneously collecting embedded
motion-detecting navigators at every repetition time of the running scan. We
reconstruct the image off-line by averaging only those lines of k-space that
are not corrupted by motion.
13:30
3114.
Requirements on the Accuracy of Navigators for Prospective Motion
Correction in High Resolution MR Imaging
Computer 20
Maxim
Zaitsev1, Oliver Speck, Jürgen Hennig1
1University
Hospital Freiburg, Freiburg, Germany
Prospectively
navigated MR imaging is becoming increasingly popular to overcome present measurement
time and/or resolution limitations in various imaging applications. Navigated
imaging appears to be the only way to overcome the limitation for isotropic
resolution in length high-resolution scans, in which involuntarily movements of
the order of millimetres are unavoidable. Despite of the popularity of
navigators, to our knowledge no data on the required navigator accuracy are
available in literature. Here, formalism is developed to analyse statistically
the image artefacts introduced by the prospective motion correction based on
the imaged sample properties and desired resolution.
14:00
3115.
The Investigation of T2 PROPLLER Motion Estimation Efficiency
Computer 20
Shaorong
Chang1, Xiaoli Zhao1, Ajeetkumar Gaddipati1
1GE
Healthcare, Waukesha, Wisconsin, USA
T2
PROPELLER reconstructs clinically valuable images with little motion
artifacts. However, studies show that
the motion correction efficiency depends on protocol parameter settings. In this work, the efficiency of PROPELLER
motion correction with respect to field of view (FOV), views per blade and
k-space coverage is analyzed using invivo data.
Rotation and translation estimation accuracy were studied individually,
and the overall effects of motion correction were inspected. Based on this study, tight FOV, at least 24
views per blade and 1 cm-1 k-space coverage are recommended in a T2 PROPELLER
scan to obtain brain images with little motion artifacts.
14:30
3116.
Respiratory Motion-Compensated Radial DCE-MRI of Chest and Abdominal
Lesions
Computer 20
Wei
Lin1, Junyu Guo1, Mark A. Rosen1, Hee Kwon
Song1
1University
of Pennsylvania, Philadelphia, Pennsylvania, USA
Accurate
assessment of lesion perfusion with dynamic contrast-enhanced MRI (DCE-MRI) in
the chest and abdominal regions is difficult due to respiratory motion. In this
work, we utilize the self-gating properties of radial imaging with
reconstruction flexibility afforded by the golden-angle view order scheme to
effectively compensate for respiratory motion. In addition, residual motion within
each image is compensated with the autofocusing technique, and motion between
images corrected with image correlation. Finally, the resulting data is
processed to reduce streaks and enhance SNR, using either k-space weighted
image contrast (KWIC) filtering or principal component analysis (PCA). In vivo
results demonstrate the effectiveness of our strategy in achieving high quality
images of lesions located in the lung and the liver.
Computer 20
Mark
J. White1, David Atkinson1, Liz Charles-Edwards2,
Catherine Coolens2, Maria Hawkins2, Keiko Miyazaki3,
David Collins3, Martin O. Leach3, David J. Hawkes1
1UCL,
London, UK; 2Royal Marsden NHS Foundation Trust, UK; 3Institute
of Cancer Research, UK
Respiratory
motion needs managing in most liver MRI protocols. Given deformation fields
associated with each part of acquired k-space, artefacts in free-breathing
liver MRI may be corrected using a general matrix reconstruction method. iDROPS builds a parameterized non-rigid
breathing model from a low-resolution training series, then finds a time-series
of parameter values for an imaging acquisition by comparing the parts of
k-space which overlap with the training data.
The resulting estimated deformation fields are accurate to 1.5mm near
the diaphragm (average of 10 studies), and are demonstrated correcting real
continuously-acquired free-breathing liver data.
Computer 21
Brice
Fernandez1,2, Maelene Lohezic1,2,
Pierre-Andre Vuissoz2, Jacques Felblinger2
1General
Electric Healthcare, Buc, France; 2IADI, Inserm ERI 13, Nancy
University, Nancy, France
In
most clinical applications, standard external sensors (ECG and respiratory
belts) are usually used for triggering. We propose a method in two steps that
use external sensors to estimate the position of an organ of interest. The
first step consists in the calibration of external sensors output, based on
fast imaging and a parametric motion estimation algorithm. The second step is a
multivariate linear regression, computed between motion parameters and external
sensors. This linear relation is then used to demonstrate the accuracy of the
proposed method for prospective correction.
14:00
3119.
Robust Abdominal Imaging with Motion Sensitive Sequences Using Cardiac
and Respiratory Double Gating
Computer 21
Ananth
J. Madhuranthakam1, Ken-Pin Hwang2, Reed F. Busse3,
Jean H. Brittain3, Neil M. Rofsky4,5, David C.
Alsop4,5
1GE
Healthcare, Boston, Massachusetts, USA; 2GE Healthcare, Houston,
Texas, USA; 3GE Healthcare, Madison, Wisconsin, USA; 4Beth
Israel Deaconess Medical Center, Boston, Massachusetts, USA; 5Harvard
Me
Abdominal
imaging with motion sensitive sequences is challenging due to signal loss and
artifacts associated with cardio-respiratory motion. Breath hold acquisitions using cardiac gating
tend to decrease the signal loss, however poor patient cooperation and multiple
breath holds required for large volume acquisitions can make such studies
inefficient. In this work, we present an algorithm to perform prospective
cardiac and respiratory double gating and demonstrate artifact free images
acquired during free breathing.
14:30
3120.
A Real Time Optical Motion Correction System Using a Single Camera and
2D Marker
Computer 21
Murat
Aksoy1, Rexford Newbould1, Matus Straka1,
Samantha Holdsworth1, Stefan Skare1, Juan Santos1,
Roland Bammer1
1Stanford
University, Stanford, California , USA
Correction
of motion related artifacts remains one of the most important topics in MRI. In
this study, we present a real-time prospective motion correction system that
uses a single camera and a 2D marker to detect and correct for rigid body
motion. With the camera placed inside the magnet bore and the marker mounted
rigidly on patient’s head, it is possible to perform motion correction for both
in-plane and through-plane motion using this system with high accuracy and
stability.
Computer 21
Kiran
Kumar Pandey1, Douglas Noll1
1University
of Michigan, Ann Arbor, Michigan, USA
Movement
during fMRI causes false activations and image registration introduces
interpolation errors. Motion reorients the air-tissue interface in the brain
and causes dynamically varying off-resonance patterns. These artifacts reduce
accuracy of image registration and increase variability in time-series. This
study characterized position dependent off-resonance artifacts in a
susceptibility phantom and investigated effectiveness of CP gridding and
Iterative image reconstruction methods with several fieldmap based
off-resonance correction. Dynamically
updated fieldmaps most accurately characterized and compensated for position
dependent off-resonance artifacts. The commonly used static fieldmap
off-resonance correction method was least accurate. This trend was also observed in quality of
motion correction in phantom data.
13:30
3122.
Examination of Cardiac-Related Motion in the Lower Thoracic and Lumbar
Spinal Cord
Computer 22
Daphne
Yau1,2, Chase R. Figley1, Celina Nahanni1,
Patrick W. Stroman1
1Queen's
University, Kingston, Canada
Spinal
cord motion is the dominant source of error in functional magnetic resonance
imaging and diffusion tensor imaging. Correcting for spinal cord motion induced
by the cardiac cycle improves the sensitivity and reliability of these
modalities. However, this motion has not been fully characterized in the lower
thoracic and lumbar spinal cord. In the present study, we show minimal
displacement of these spinal cord regions in association with the cardiac
cycle. In conjunction with previous research, these findings demonstrate a
model of spinal cord motion, in which maximal cervical motion progressively
diminishes to a minimal displacement in the lumbar region.
14:00
3123.
High Resolution Image Co-Registration via Phase Modulation in the Reciprocal (K) Spatial Domain
Computer 22
James
A. Goodman1, Charles S. Springer, Jr2
1Oregon
Health and Science University, Portland, Oregon, USA; 2Oregon Health
and Science University, Portland, USA
For
many applications, it is essential that images be co-registered to a higher
resolution than that intrinsic to the image. This is especially important for
traditionally low spatial resolution data such as functional or DCE images.
Pixel interpolation in the spatial domain can introduce artifacts and are often
computationally burdensome. In this study we demonstrate the simplicity and
precision of inter-image translation correction via post hoc reciprocal spatial domain (k-space) phase modulation.
The co-registration method described here requires no addition image
acquisition, field mapping, or pulse sequence modification.
14:30
3124.
Flow Compensation in Non-Balanced SSFP
Computer 22
Francesco
Santini1, Oliver Bieri1, Klaus Scheffler1
1University
of Basel/University Hospital, Basel, Switzerland
Flow
compensation is a critical issue in non-balanced SSFP imaging because high
first-order moments are achieved in the dephasing direction. Phase accumulation
leads to steady-state disruption and consequent blurring artifacts and signal
loss, especially in presence of long-T2 tissues. In this work, a theoretical
explanation of the artifacts is given, showing how phase fluctuations influence
the amplitude and the stability of the signal, and optimized flow compensated
SSFP-FID and SSFP-echo sequences are presented. Finally, In vivo application of
the sequence is demonstrated.
Computer 22
Xi
Chen1, Meijin Lin1, Tao Lin1, Zhong Chen1,
Jianhui Zhong2
1Xiamen
University, Xiamen, People's Republic of China; 2University of
Rochester, Xiamen, New York, USA
A
new iZQC pulse sequence with stroboscopic acquisition is designed to achieve
high-resolution magnetic resonance spectroscopy in inhomogeneous and unstable
fields. Primary results suggest potential applications for suppressions of
motion-caused t1 noises and inhomogeneous broadenings in in vivo studies.
13:30
3126.
Improvement of Magnetic Field Homogeneity for Cardiac MRI at 3 Tesla
Computer 23
Miriam
Rabea Kubach1, Axel Bornstedt1, Michael Schär2,
Gerd Ulrich Nienhaus1, Volker Rasche1
1University
Ulm, Ulm, Germany; 2The Johns Hopkins University School of Medicine,
Baltimore, USA
A
cardiac phase resolved B0-map was used to find the optimal shim settings
depending on the current motion state. An optimal cardiac phase point for the
assessment of the shim coefficients providing sufficient main field homogeneity
over the entire cycle was assessed. It was found, that the shim values
corresponding to mid diastole achieve the best results all over the cardiac
cycle.
14:00
3127.
Application of the Pseudo-Polar Fourier Transform for In-Plane Rotation
Correction of MR Images
Computer 23
Irtiza
Ali Gilani1, Nadim Jon Shah1,2
1Institute
of Neurosciences and Biophysics (Medicine), Research Centre Juelich, Juelich,
Germany; 2Institue of Physics, University of Dortmund, Dortmund,
Germany
A
technique is proposed for in-plane rotational motion correction using the
registration of the 2D low-resolution images, termed implicit navigators,
inherent to the acquired MR images. Most MR image registration strategies use
the iterative correlation approach. The correlation is usually performed in the
polar Fourier domain, whereby the interpolation errors in the polar Fourier
domain are problematic. In this work the registration is performed by applying
the pseudo-polar Fourier transform to the low-resolution images which neither
requires interpolation nor iteration. Rotational motion in EPI images obtained
at 3T field strength was corrected.
14:30
3128.
Image Based Compensation of Breathing Motion Artifacts in MRI with
Continuously Moving Table Acquisitions
Computer 23
Matthias
Honal1, Ute Ludwig1, Simon Bauer1, Jochen
Leupold1
1University
Hospital Freiburg, Freiburg, Germany
MRI
with continuously moving table is an efficient method to image arbitrary large
body regions within one measurement. However, breathing motion causes problems
since standard techniques to avoid breathing motion artifacts such as breath
holding, prospective or retrospective gating are often not applicable or very
inefficient. This work introduces a method which allows the reconstruction of
artifact free images from data acquired during free breathing. Snapshots of
arbitrary breathing states are acquired and consistently combined using image
registration techniques. Typical breathing motion induced artifacts such as
ghosting, blurring and signal cancellations are thus eliminated.
15:00
3129.
Physiological Motion Correction of ASL FMRI Measurement of Rhesus Monkey
Computer 23
Xiaodong
Zhang1, Tsukasa Nagaoka1, Robbie Champion1,
Timothy Q. Duong1
1Emory
University, Atlanta, Georgia, USA
The
Arterial Spin Labeling (ASL)-based CBF quantification is significantly
vulnerable to the physiological motion because of the pair-wise subtraction of
the control and labeling images. In this paper, a robust approach based on the
optimal reference phase map was introduced for the physiological motion
correction of the ASL functional MRI measurement. The resultant CBF temporal
response and CBF activation map were improved dramatically. The method was
demonstrated in the non-human primate (rhesus monkey) CBF measurement under the
hypercapnia (5% CO2) condition.
13:30
3130.
3D Non-Linear Model-Driven Registration for Motion Corrupted DCE-MRI
Data
Computer 24
Angela
Caunce1, Giovanni A. Buonaccorsi1, Caleb Roberts1,
Geoff JM Parker1
1The
University of Manchester, Manchester, UK
Many
dynamic contrast enhanced MRI sequences have some form of motion corruption
which may jeopardise the estimation of microvascular parameters. We present a model-driven registration which
uses non-linear matrix transforms to bring the time series closer into
alignment. The success of the registration
is illustrated using a new alignment measure and by an independent motion
assessment.
14:00
3131.
A Fast Flow Compensation Technique for Self-Gated Sequences
Computer 24
Jessica
Schulz1,2, Arne Hengerer2, Wolfhard Semmler1,
Michael Bock1
1Deutsches
Krebsforschungszentrum (dkfz), Heidelberg, Germany; 2Siemens Medical
Solutions, Erlangen, Germany
Self-gating
utilizes an additional short data acquisition in the pulse sequence for cardiac
motion detection. Self-gating increases the TR of a pulse sequence, especially,
if additional flow compensation gradients are used. Here, we demonstrate a new
flow compensation scheme for self-gating with nearly no time penalty over
conventional self-gating sequences without flow compensation.
14:30
3132.
Efficient Motion Artifact Reduction Technique Based on Post-Processing
Computer 24
Sang-Young
Cho1, Eung-Yeop Kim1,12,2,
Dong-Hyun Kim,1,23
1;
2; 3Yonsei University, Seoul, Republic of Korea
Post-processing
motion correction techniques have previously been introduced to reduce motion
artifacts. These techniques, which do not need any a priori information, have
been shown to reduce translational motion artifacts effectively. One of the
main limitations of these techniques however is the long processing time
required to find the optimal image. Here, we propose a simple method to reduce
this total processing time for metric based motion correction techniques.
15:00
3133.
Relevance of Cardiac-Gating in Longitudenal Diffusion Weighted MRI
Studies
Computer 24
Josef
Habib1, Jaroslav Hlinka1, Stamatios Sotiropoulos1,
Christopher Tench1, Dorothee Auer1, Paul Simon Morgan1
1University
of Nottingham, Nottingham, UK
While
the presence of artifacts in ungated DW-images and the ability of gating to
remedy these have been widely reported, the evaluation of benefits for the
clinically important Diffusion-Tensor parameters has received less attention.
This study aims to assess the relevance of cardiac-gating in clinical
DWI-applications. To this end, the effects of cardiac-gating on precision and
accuracy of Fractional Anisotropy and Mean Diffusivity measurements were
analyzed, and subsequently put into context with alterations in FA of
MS-patients. The observed results suggest that gating produces little benefit
in group-studies but should be considered when precise individual acquisitions
are needed.
Hall D Thursday 13:30-15:30
13:30
3134.
Time-Optimal 3D Gradient Design for RF Shimming
Computer 15
Maryam
Etezadi-Amoli1, Adam B. Kerr1, John M. Pauly1
1Stanford
University, Stanford, California , USA
Spoke
trajectories that play slice-selective RF subpulses along kz are known to be
effective at RF shimming. In this work,
we use gradient time-optimization to achieve acceleration factors of greater
than 10% for such spoke trajectories. We
present simulated RF shimming performance using the time-optimal gradients and
assuming an eight coil parallel transmit system.
14:00
3135.
Magnitude-Constrained Spokes Design for B1+
Inhomogeneity Correction
Computer 15
Rolf
F. Schulte1, Mika W. Vogel1, Adam B. Kerr2,
Hans-Peter Fautz1, Patrick Gross1, Yudong Zhu3,
Florian Wiesinger1
1GE
Global Research, Munich, Germany; 2Stanford University, Stanford,
California , USA; 3GE Global Research, Niskayuna, New York, USA
Transmit
field (B1+) inhomogeneity is impairing image quality at
higher field strengths (B0≥ 3T). A common approach to improve homogeneity is to
excite with a multi-channel excitation system in combination with the spokes
trajectory, which is a 3D excitation sequence. A slice is excited by regular
sinc-Gaussian type of pulses. The in-plane homogeneity is improved by placing a
few spokes in-plane. Traditionally, the excitation was constrained in both
phase and magnitude,
hence
requiring a considerable amount of spokes and consequently a long overall pulse
duration. In this work, we introduce a design constraining only the magnitude,
hence considerably improving
B1+
homogeneity. The design is solved with a non-linear least squares optimisation,
including B0 inhomogeneity and constraining the B1
amplitudes. Validation is performed on 3T with a torso-phantom.
14:30
3136.
Optimal Phase-Relaxed Design of Small-Tip-Angle Parallel Transmission RF
Pulses
Computer 15
Dan
Xu1, Kevin F. King1, Graeme C. McKinnon1
1General
Electric Healthcare, Waukesha, Wisconsin, USA
The
existing phase-relaxed parallel transmission RF pulse design relaxes the flat
phase constraint in conventional small-tip-angle (STA) design by allowing a
predetermined, spatially varying target phase profile to improve the quality of
magnitude profile of the resulting transverse magnetization. In this work, the
pulse design is reformulated as an optimization problem with a non-quadratic
cost function where the phase constraint is completed removed. It is further
shown that the gradient vector of the cost function can be expressed as a
closed form and a nonlinear conjugate gradient algorithm can be applied to
efficiently solve the optimization problem. Bloch simulation results
demonstrate that the optimal phase-relaxed design can achieve significantly
better magnitude profile and/or lower RF power than the conventional STA
design.
15:00
3137.
Ultra-Short 2D RF Pulse for Reduced Field-Of-View SSFP Imaging
Computer 15
Jing
Yuan1, Chang-Sheng Mei1,2, Lawrence P. Panych1
1Department
of Radiology, Brigham and Women's Hospital, Harvard medical School, Boston,
Massachusetts, USA; 2Department of Physics, Boston College, Boston,
Massachusetts, USA
Balanced
SSFP is a fast imaging sequence providing high signal-to-noise ratio. 2D RF
pulse could be used for further shortening the scan time for SSFP by reducing
phase encoding number in reduced field-of-view (rFOV). However, the critical
requirement of short TE and TR make the use of 2D RF pulse in SSFP challenging.
Ultra-short 2D RF pulse is specifically designed for rFOV imaging for SSFP.
Sub-pulse duration is as short as 384us for 10mm slice thickness with max slew
rate of 150T/m/s. 2.5x acceleration factor has been successfully achieved on GE
Signa 1.5T and 3T scanners
13:30
3138.
Segmented 2D-Selective RF Excitations Based on a Weighted Blipped-Planar
Trajectory
Computer 16
Jürgen
Finsterbusch1,2
1University
Medical Center Hamburg-Eppendorf, Hamburg, Germany; 2Neuroimage
Nord, Hamburg-Kiel-Lübeck, Germany
2D-selective
RF excitations based on a segmented blipped-planar trajectory suffer from a
reduced signal amplitude due to the lower flip angles of segments covering
outer k-space lines. In applications that involve averaging, like single-voxel
spectroscopy, a weighted blipped-planar trajectory can be used that favours
larger flip angles over averaging. While segments with high k-space intensity
are averaged as usual, a larger flip angle is assigned to low intensity
segments so that effectively the same signal amplitude of the segment can be
achieved without averaging. This approach considerable improves the signal-to-noise
ratio efficiency without degrading the excitation profile.
14:00
3139.
2D-Selective RF Excitations Based on a Half-Fourier Blipped-Planar
Trajectory
Computer 16
Jürgen
Finsterbusch1,2
1University
Medical Center Hamburg-Eppendorf, Hamburg, Germany; 2Neuroimage
Nord, Hamburg-Kiel-Lübeck, Germany
2D-selective
RF excitations based on a blipped-planar trajectory are well-suited for
applications like reduced field-of-view imaging but suffer from the fact that
half of the trajectory’s duration needs to be considered in the echo
time. Thus, the usage of this trajectory for applications that require a short
echo time, like proton-density weighting or single-voxel spectroscopy, is
hampered. By applying the half-Fourier method known from slice-selective
excitations, this problem can be solved using trajectories that start in outer
k-space and end in the centre because only half of a single line of the
trajectory contributes to the echo time.
14:30
3140.
Constant Time VERSE for RF Amplitude Reduction in Spectral-Spatial
Pulses with Improved Timing Robustness
Computer 16
Peder
E. Z. Larson1, Adam B. Kerr2, John M. Pauly2,
Daniel B. Vigneron1
1University
of California - San Francisco, San Francisco, California , USA; 2Stanford
University, Stanford, California , USA
Spectral-spatial
RF pulses often must contend with limits on RF power and amplitude,
particularly for highly spatially selective pulses, high-field applications,
and hyperpolarized 13C. We
present a new method for reducing the peak amplitude in spectral-spatial RF
pulses without introducing significant gradient delay sensitivity. Our method is an adaptation of the VERSE
algorithm applicable to spatial subpulses because it maintains a constant pulse
duration. It also includes an additional
slew rate limit that reduces the allowable rate for larger RF amplitudes,
improving the pulse performance in the presence of gradient delays.
15:00
3141.
High Bandwidth Low Power Spatial Saturation Pulses for 7T
Computer 16
Douglas
Arthur Charles Kelley1
1GE
Healthcare, San Francisco, California , USA
An
extension to the Shinnar-Le Roux algorithm is presented allowing the design of
scalable quadratic phase RF pulses, achieving significantly higher bandwidths
with similar peak amplitudes and pulse widths. The algorithm is applied to the
design of spatial saturation pulses for 7T. The performance of the pulses is
verified in a high dielectric permittivity phantom.
13:30
3142.
Selective Adiabatic Refocusing Pulse Pair for 3D RARE
Computer 17
Ziqi
Sun1, Jay L. Zweier1
1The
Ohio State University, Columbus, USA
A
compact selective adiabatic full passage (AFP) pulse pair, consisted of two 90
degree hyperbolic secant (HS1_R20) pulses of alternate frequency sweep (AFS)
directions, was successfully applied for spin refocusing in a 3D RARE pulse
sequence. In comparison to an amplitude-modulated refocusing pulse and to a
single 180 degree HS1_R20 AFP refocusing pulse, the AFS-AFP pulse pair
substantially improved signal sensitivity and uniformity across the 3D volume, which
is attributed to the effective compensation of the nonlinear phase dispersion
and off-resonance effect associated with selective AFP pulses.
14:00
3143.
Selective Adiabatic Pulses for T1-Weighted Contrast Enhancement at 0.38
T
Computer 17
Ziqi
Sun1, Sergey Petryakov1, Wael Alzawahra1, Jay
L. Zweier1
1The
Ohio State University, Columbus, USA
T1-weighted
contrast enhancement was achieved in a MnCl2 doped phantom and an isolated rat
heart perfused with free radical (TAM) doped St. Thomas solution using selective
adiabatic full passage (AFP) inversion and excitation pulses (HS1_R15) in a 3D
inversion-recovery (IR) GRE pulse sequence. In comparison to an amplitude
modulated selective inversion pulse, the selective adiabatic inversion pulse
substantially increased signal sensitivity and image contrast, which is
ascribed to the mutual cacellation of the nonlinear phase dispersion between
the inversion AFP pulse and the excitation AFP pulse in the IR-GRE3D sequence.
14:30
3144.
The Steady State Properties of Actual Flip Angle Imaging (AFI)
Computer 17
Kay
Nehrke1
1Philips
Research Europe, Hamburg, Germany
The
RF and gradient spoil scheme of the Actual Flip Angle Imaging (AFI) sequence
has been studied. It is shown that conventional RF spoiling using a linearly increasing
spoil phase shift between successive RF pulses may interfere with the formation
of a proper steady state for this specific sequence. Instead, an adapted RF
spoil regime is derived, which essentially preserves the quadratic increase of
the spoil phase over time. In addition, the spoiler gradient arrangement is
adjusted to improve the off-resonance sensitivity of the sequence. Phantom
experiments show a significantly improved image quality compared to the
original spoiling regime.
15:00
3145.
Regularized B1+ Map Estimation with Slice Selection Effects
Computer 17
Amanda
Kay Funai1, Jeffrey A. Fessler1, William Grissom1,
Douglas C. Noll1
1University
of Michigan, Ann Arbor, Michigan, USA
Spatially
varying contrast and signal at high fields make a B1+ map a requirement in
parallel transmit excitation. The
standard method for estimating the magnitude, using the double angle formula,
ignores noise and neglects effects from slice selection. This new regularized method incorporates
multiple coils and multiple tip angles to estimate the magnitude and phase of
the field map and accounts for slice selection effects based on the achieved
slice profile. Phantom and experimental
results show a smoother estimate and increased accuracy with the proposed
method. The phase estimate can be used
to design pulse sequences in parallel excitation.
Hall D Thursday 13:30-15:30
13:30
3146.
Accelerated HYPR Reconstruction
Computer 18
Andres
Carrillo1, Reed F. Busse2, Jean H. Brittain2,
Oliver Wieben3, Yan Wu3, Charles A. Mistretta3,
Frank R. Korosec3
1GE
Healthcare, Evanston, Illinois, USA; 2GE Healthcare, Madison,
Wisconsin, USA; 3University of Wisconsin, Madison, Wisconsin, USA
The
use of HYPR in time resolved contrast-enhanced angiography can produce temporal
resolutions up to 100 times greater than traditional unaccelerated methods.
However, the increase in computational requirements and data throughput can
result in long reconstruction times, hampering the use of the technique. We
propose an optimized, distributed reconstruction algorithm capable of reducing
reconstruction times from several hours to several minutes, enabling the
clinical use of the HYPR CE-MRA.
14:00
3147.
L-Map: Exploiting Spatial-Temporal Correlation of Phase in MRI
Computer 18
Kang
Wang1, Steven Kecskemeti1, Rafael O'Halloran1,
Sean Fain1, Kevin Johnson1, Oliver Wieben1,
Jiang Du2, Charles Mistretta1
1University
of Wisconsin-Madison, Madison, Wisconsin, USA; 2University of
California, San Diego, San Diego, California , USA
Several
image reconstruction techniques that are aimed to exploit the spatial-temporal
correlation of MR magnitude images, such as Highly Constrained backPRojection
(HYPR) and HYPR with Local Reconstruction (HYPR-LR) have been developed
recently. These techniques have been developed for magnitude processing and
cannot be directly applied to phase sensitive datasets due to phase wrapping
and potential signal cancellations in the composite image. Here we propose a
novel approach, the “L-map” concept, to overcome these limitations and evaluate
the algorithm in simulations.
14:30
3148.
MR Spectroscopic Imaging of Short T2 Tissue Using Complex Division (CD)
HYPR-LR Reconstruction
Computer 18
Kang
Wang1, Rafael O'Halloran1, Sean Fain1, Steven
Kecskemeti1, Oliver Wieben1, Kevin Johnson1,
Charles Mistretta1, Jiang Du2
1University
of Wisconsin-Madison, Madison, Wisconsin, USA; 2University of
California, San Diego, San Diego, California , USA
Highly
Constrained Back-Projection (HYPR) and HYPR with Local Reconstruction (HYPR-LR)
techniques have been developed to exploit the spatial-temporal correlation for
time-resolved MR using magnitude data. Here we propose a complex-valued HYPR-LR
method which can be applied to other MR applications where complex images are
needed, such as MR spectroscopy. We demonstrate that the Complex Division
HYPR-LR, combined with ultrashort echo time (UTE) technique, can provide
quantitative spectroscopic information of short T2 tissues, such as cortical
bone.
15:00
3149.
Image Reconstruction of Variable Density Undersampled EPI Images
Computer 18
Annie
M. Tang1, Man Cheuk Ng1, Edmund Y. Lam1
1The
University of Hong Kong, Pokfulam, Hong Kong
We
applied a mathematical theory, Compressive Sensing (CS), for image
reconstruction to EPI images. With the use of CS, it is possible to undersample
the k-space data while preserving image quality. Thus, it allows a more extend
coverage of the imaged object per unit time. EPI image qualities resulted from
the CS reconstruction and its feasibility of application in functional MRI are
discussed. Results indicated that CS outperforms traditional time reduction
techniques. The statistical mapping in a typical fMRI experiment is comparable
to the fully sampled EPI data.
13:30
3150.
Prediction of HYPR and HYPR LR Performance Based on Image Sparsity and
Temporal Correlation
Computer 19
Julia
V. Velikina1, Yan Wu1, Charles A. Mistretta1
1University
of Wisconsin - Madison, Madison, Wisconsin, USA
We
derive analytical formulae for the estimation of the reconstruction error using
HYPR and HYPR LR algorithms. We conclude that the performance of these
algorithms for each potential clinical application can be accurately predicted
based on the a priori knowledge of image sparsity and expected temporal
behavior of the image time series.
14:00
3151.
Compressed Sensing MRI with Random B1 Field
Computer 19
Florian
M. Sebert1, Yi Ming Zou1, Bo Liu1, Leslie Ying1
1University
of Wisconsin - Milwaukee, Milwaukee, Wisconsin, USA
Considerable
attention has been focused on the design of practical sampling schemes to apply
compressed sensing (CS) to MR. In this abstract, we revisit the sufficient
conditions for CS matrices, and show that if the coil sensitivities or the RF
excitation profiles can be designed to be spatially random, then the image can
be recovered from uniformly undersampled k-space data. Our finding provides an
alternative to the random sampling design for reducing the acquisition time
using CS. In addition, it has the advantage that the number of samples needed
is less than what is needed in the random sampling scheme.
14:30
3152.
Randomly Perturbed Radial
Trajectories for Compressed Sensing MRI
Computer 19
Ali
Bilgin1,2, Ted P. Trouard1, Arthur F. Gmitro1,
Maria I. Altbach1
1University
of Arizona, Tucson, Arizona , USA
The
recently introduced Compressed Sensing (CS) theory has the potential to
significantly accelerate data acquisition in MRI. Recent results in CS theory
indicate that introducing randomization into regularly structured trajectories
can be beneficial. We introduce randomly perturbed radial trajectories for CS
MRI and illustrate their potential benefits with examples.
15:00
3153.
Data Reordering for Improved Constrained Reconstruction from
Undersampled K-Space Data
Computer 19
Ganesh
Adluru1, Edward VR DiBella1
1University
of Utah, Salt Lake City, USA
Here
we propose a new data reordering method to improve the constrained
reconstruction techniques from undersampled k-space data in MRI. In the data reordering technique the
undersampled data are reordered in the signal space according to an a priori
determined ordering and then appropriate constraints are applied within an
iterative reconstruction. The method is
widely applicable to reconstructions in which the data do not perfectly match
the constraints being used and it can be used in the contexts which are based
on regularization techniques. The method
can be used to accelerate 2D and multi-image data acquisition cases in MRI.
13:30
3154.
SparseSENSE: Randomly-Sampled Parallel Imaging Using Compressed Sensing
Computer 20
Bo
Liu1, Florian M. Sebert1, Yi Ming Zou1, Leslie
Ying1
1University
of Wisconsin - Milwaukee, Milwaukee, Wisconsin, USA
Recent
work has applied compressed sensing (CS) to reduce scanning time in
conventional Fourier imaging and demonstrated impressive results. In this
abstract, we investigate the structure of the sensitivity encoding matrix in
parallel imaging, and apply CS to parallel imaging to achieve an even higher
reduction in scanning time than what can be achieved by each individual method
alone. Our experiments show that the proposed method, named SparseSENSE, can
achieve a reduction factor higher than the number of channels.
14:00
3155.
Homotopic L0-Minimization for Highly-Undersampled MRI
Reconstruction
Computer 20
Joshua
D. Trzasko1, Armando Manduca1
1Mayo
Clinic, Rochester, Minnesota, USA
Compressive
Sensing and related L1-minimization techniques have recently been demonstrated
to accurately and efficiently reconstruct sparse or compressible MR images even
at sampling rates far below the Nyquist limit.
In this work, we propose an alternative minimization framework based on
homotopic approximation of the L0-recovery problem and show that accurate MRI reconstructions are possible at
sampling rates even lower than are achievable using L1-based methods.
14:30
3156.
Matrix Formulation and Tikhonov Regularization of HYPR Reconstruction
Computer 20
Maximilian
Haeberlin1,2, Stefan Skare1, Rexford D.
Newbould1, Klaas Paul Pruessmann2, Roland Bammer1
1Stanford
University, Stanford, California , USA; 2ETH Zurich, Zurich,
Switzerland
A
matrix formulation for HYPR reconstruction is presented, allowing to
incorporate arbitrary regularization methods in iterative variants of HYPR. It
is shown that Tikhonov regularization stabilizes recently proposed CG-HYPR
without compromising speed or image quality.
15:00
3157.
Redundant Spatial Harmonic Information in Zeugmatography with Linear
Encoding (R-SHIZLE) Theoretically Encodes Intra-Acquisition Decay
Computer 20
Andrew
S. Nencka1, Andrew D. Hahn1, Daniel B. Rowe1
1Medical
College of Wisconsin, Milwaukee, Wisconsin, USA
Redundant
spatial harmonic information is acquired in MRI because of the real-valued
nature of the object being imaged. The redundancy is manifested as conjugate
symmetry about the k-space origin. This symmetry is broken by both magnetic
field inhomogeneity, intra-acquisition T2 decay and noise. In this abstract we
simulate the generated k-space signal, including a non-negligible magnetic
field inhomogeneity and a spatially varying T2 profile. We then correct the
magnetic field inhomogeneity and recover the original T2 profile, with minor
error, based upon the broken symmetry of the simulated k-space data. This
offers the potential for quantitative T2 or T2* time series instead of usual T2
or T2* weighted image time series.
Hall D Thursday 13:30-15:30
13:30
3158.
Spherical Harmonic Representation Based Haptic Rendering for Medical
Image Perception
Computer 21
Zhengyi
Yang1, Quang Tieng1, Viktor Vegh1, Deming Wang1
1University
of Queensland, Brisbane, Australia
Haptics
is referred as the technologies of generating artificial sense of touch in the
interaction with the objects in virtual space. The use of visual interpretation
in conjunction with a haptic device can provide a higher level of perception of
medical images towards diagnosis and treatment planning. Spherical harmonics
were found to be a feasible representation for haptic rendering with very good
feedback characteristics. Spherical harmonics are a compact representation and
can be efficiently used for both graphic and haptic representations.Haptic
feedback provides another channel for the information flow in medical image
perception. Multimodality images can be displayed simultaneously with less
confusion by using visual and haptic feedback separately, which is envisioned
as a better way for image fusion interaction. Haptically guided medical image
exploration can aid the user in various tasks, such as finding and measuring
anatomical and pathological features or investigating the spatial relationship
between them. Force feedback can improve user performance in image manipulation
tasks, such as interactive landmark selection, organ delineation and image
registration.
14:00
3159.
Structure-Specific White Matter Analysis of Amyotrophic Lateral
Sclerosis
Computer 21
Hui
Zhang1, Paul A. Yushkevich1, John H. Woo1,
Sumei Wang1, Elias R. Melhem1, James C. Gee1
1University
of Pennsylvania, Philadelphia, Pennsylvania, USA
In
this study, we evaluated the use of a structure-specific WM analysis (SSWMA)
framework to detect the location and magnitude of FA changes in patients with
ALS. The SSWMA framework allows us to
focus our analysis on the corticospinal tracts.
The significant FA reductions were identified, which demonstrates the
efficacy of the SSWMA framework.
14:30
3160.
Automatic Segmentation of Intra-Abdominal and Subcutaneous Adipose
Tissue in 3D Whole Mouse MRI
Computer 21
Petter
Ranefall1, Abdel W. Bidar1, David J. Svensson1,
Paul David Hockings1
1AstraZeneca,
Mölndal, Sweden
We
developed fully automatic segmentation of intra-abdominal (IAT) and
subcutaneous (SAT) adipose tissue in mice. The novel algorithm outlines the
body, extracts fat, and segments IAT and SAT of in vivo high resolution whole
mouse 3D images. It uses the Narrowest Passage Transform which codes each pixel
with the radius of the narrowest passage on the widest possible 3D path to the
body outline, and competitive region growing such that competing classes meet
at narrow passages. The new method was tested on 32 fat fed mice independent to
those used for algorithm development and shows good correlation to manual
segmentation.
15:00
3161.
Accurate Assessment of Muscle/fat Distribution on MR Images of the Thigh
Computer 21
Vincenzo
Positano1, Tore Christiansen2, Maria Filomena Santarelli1,
Amalia Gastaldelli1, Steffen Ringgaard2, Luigi Landini3
1Institute
of Clinical Physiology, Pisa, Italy; 2Aarhus University Hospital,
Aarhus, Denmark; 3University of Pisa, Pisa, Italy
13:30
3162.
Structure-Specific Statistical Mapping of White Matter Tracts
Computer 22
Paul
A. Yushkevich1, Hui Zhang1, Tony Simon2, James
C. Gee1
1University
of Pennsylvania, Philadelphia, Pennsylvania, USA; 2M.I.N.D.
Institute, University of California, Davis, California , USA
We
present a novel technique for analyzing diffusion imaging data in white matter
studies. Data associated with six major white matter tracts is analyzed with
the help of a geometrical model that exploits the sheet-like structure of these
tracts.
Computer 22
Ke
Nie1, Siwa Chan2, Ivy Chau2, Tiffany Tseng1,
Jeon-Hor Chen1, Orhan Nalcioglu1, Min-Ying Su1
1University
of California, Irvine, Irvine, California , USA; 2China Medical
University Hospital, Taichung 404, Taiwan
A
reliable method using computer-assisted segmentation for the breast and the
fibroglandular tissue on breast MRI was developed. Breast segmentation was
achieved based on individual womanˇŻs body landmarks for initial estimation,
then with a combination of fuzzy C-means, b-spline fitting, and dynamic
searching algorithms. 12 cases were selected for reproducibility test. The
inter- and intra-operator consistency was evaluated, and the correlation was
found to be higher than 0.97. This method may be applied to monitor the density
change over time to evaluate the benefits or risks for each individual woman
when considering chemoprevention or hormonal replacement therapy.
14:30
3164.
Robust Segmentation and Classification of Heterogeneous Myocardial
Infarct Zones
Computer 22
Jay
S. Detsky1, Alexander J. Dick1, Graham A. Wright1
1Sunnybrook
Health Sciences Centre, Toronto, Canada
Myocardial
infarcts can be comprised of heterogeneous "gray zones" that may lead
to ventricular arrhythmias. Image
analysis and clustering tools have been developed and applied to
inversion-recovery SSFP images to segment and classify the infarct core, gray
zone, healthy myocardium, and blood.
Pixel-by-pixel parameter maps are derived from the images and a
modification of the fuzzy C-means algorithm is then applied. This method has been shown to be more robust
than the conventional methods for the delineation of infarct gray zones.
15:00
3165.
Segmentation of MR Brain Images with Intensity Correction and Partial
Volume Averaging
Computer 22
Sushmita
Datta1, Balasrinivasa R. Sajja1, Renjie He1,
Joseph M. Dieber1, Ponnada A. Narayana1
1Medical
School, University of Texas Health Science Center at Houston, Houston, USA
The
classification of brain tissues is important factor to follow changes in tissue
volumes. However, the intensity non-uniformity and partial volume averaging
(PVA) within voxels compromise accurate volumetric measurements. An iterative
segmentation procedure that explicitly considers PVA effect along with bias
field correction is proposed. Significant improvement in segmentation was
observed with this method.
13:30
3166.
Atlas-Based Segmentation for Quantitative Analysis of Brain Structures
in the Rhesus Monkey
Computer 23
Louis
Collins1, Alexandre Coimbra2, Marie Holahan2,
Richard Hargreaves2, Jacquelynn Cook2, Donald S. Williams2,
Stephen Frey1
1McGill
University, Montreal, Canada; 2Merck Research Laboratories, West
Point, Pennsylvania, USA
Animal
models are often used in pre-clinical studies of potential pharmaceuticals to
study physiological mechanisms or evaluate efficacy or toxicity. We have
designed and implemented an automated atlas-based segmentation (ABS) procedure
for the analysis of rhesus macaque brain MRI data. This study briefly describes
the image processing pipeline and presents initial results from the analysis of
a group of rhesus macaques. This study shows feasibility of automatic regional
segmentation of brain MRI data from rhesus monkeys.
14:00
3167.
Knowledge-Based Left Ventricle Segmentation and Partial Volume
Calculation in Cardiac Cine MRI
Computer 23
Hae-Yeoun
Lee1, Yi Wang1
1Cornell
University, New York, USA
In
this study, we propose a knowledge-based left ventricle segmentation and
partial volume calculation algorithm to segment short-axis cine cardiac MRI.
Coil sensitivity of magnitude image is corrected. The intensity statistics of
left ventricle and myocardium are estimated by edge classification. Graph searching
and expansion are applied to detect the myocardium. We segment the left
ventricle using a region-growing scheme and then calculated partial volume
effects by a weighting function from statistics of the left ventricle and
myocardium. Using 38 subjects, we measure blood volume, ejection fraction, and
myocardium mass and compare with manual contour tracing.
Computer 23
Chu-Fang
Lin1, Christopher M. Collins2, George Kesidis1,
David J. Miller1
1The
Pennsylvania State University, University Park, Pennsylvania, USA; 2Penn
State College of Medicine, Hershey, Pennsylvania, USA
We
developed a method to identify the location of specific tissues and organs
using patient-specific 3D images and with reference to a labeled 3D template of
a single “reference” body. Our segmentation approach employs an active contours
algorithm and a Markov random field segmentation algorithm (MRF), with optimization
based on mean-field annealing (MFA). We have derived satisfactory results when
the body shape in patient-specific scans is similar to the labeled template. To
obtain robust tissue/organ segmentation for diverse body shapes, we are working
on deriving optimal local 3D matching that accounts for changes in tissue
location, orientation, and volume.
15:00
3169.
SNR Performance of Automated Geodesic Active Contour Based Liver
Segmentation
Computer 23
Dattesh
D. Shanbhag1, Ajay Narayanan1, Kajoli Krishnan1,
Patrice Hervo2, Rakesh Mullick1
1GE
Global Research, Bangalore, India; 2GE Healthcare, Buc, France
SNR
performance of geodesic active contour based automated segmentation algorithm
is evaluated for 3D MRI of liver. Segmentation was performed on contrast-enhanced,
T1-weighted liver volumes obtained from five patients, consequently degraded to
lower SNR. The automated segmented liver volumes were compared with manually
segmented liver volumes and kappa statistic (&[kappa]) calculated.
Degrading the SNR from original ~294 to 12 changed &[kappa] by less than
5%. The results suggest that the algorithm will perform robustly (&[kappa]
> 0.8) for SNR ~= 9, translating into faster scans and shorter breath hold
times for obtaining 3D MRI liver data for liver volumetry.
13:30
3170.
MR Travel to Scan Image Processing for Real-Time Liver Identification
Computer 24
Sebastian
Peter Michael Dries1, Daniel Bystrov1, Vladimir Pekar2,
Harald S. Heese1, Peter Koken1, Jochen Keupp1,
Peter Börnert1
1Philips
Research Europe, Hamburg, Germany; 2Philips Research North America,
Markham, Canada
A
method to detect the liver region on-the-fly in continuously moving bed
magnetic resonance imaging was developed and tested on 3-D image data from ten
volunteer survey examinations. The proposed method is based on first detecting
the superior and inferior margin of the liver and next adapting a deformable
liver model to the data. While the superior margin of the liver was detected
with an accuracy of less than one voxel, the detection of the inferior margin
was less precise with an accuracy of 4±3 voxels. For the envisioned application
of diagnostic scan geometry definition, this detection accuracy was deemed
acceptable, taking into account that the shape was captured well and the volume
was not underestimated.
14:00
3171.
Robust Anatomy Recognition Approach for Automated Scan Planning of Spine
MRI Examinations
Computer 24
Harald
Sepp Heese1, Daniel Bystrov1, Vladimir Pekar2,
Sebastian P. M Dries1, Rüdiger Grewer1, Chiel J. den
Harder3, Rene Bergmans3, Arjan W. Simonetti3,
Arianne M. van Muiswinkel3
1Philips
Research Europe, Hamburg, Germany; 2Philips Research North America,
Markham, Canada; 3Philips Medical Systems, Best, Netherlands
Robust,
unattended and fast anatomy recognition is the key pre-requisite for automated
MRI scan planning. With its segmental, repetitive anatomy, spine adds the
difficulty of level identification to previously existing approaches. The
proposed method uses a combination of filtering techniques, prior knowledge on geometric
properties of adjacent intervertebral discs as well as a statistical model of
the lumbosacral transition to identify and label the spine column in presence
of anatomic variability due to posture or disease. Recognition rate and
processing speed from an evaluation on 90 cases prove clinical feasibility of
the method.
14:30
3172.
Real-Time Myocardial Segmentation in MRI
Computer 24
Qi
Duan1, Andrew Francis Laine1, Vinay M. Pai2
1Columbia
University, New York, New York, USA; 2SUNY Upstate Medical University,
Syracuse, New York, USA
In
order to quantitatively evaluate cardiac functional images, segmentation of
endocardial and epicardial boundaries of the myocardium is essential. Recent
advances of high speed imaging, such as Phase Train Imaging (PTI), can provide
large image data sets with very high temporal resolution that can be very
valuable for diagnosing and detecting systolic dyssynchrony. An automated
real-time segmentation was developed. The proposed method was tested on 414
frames of PTI data. The performance of myocardial segmentation was visually and
quantitatively validated. Implemented in Matlab©, current method took less
than 1.2 ms per cardiac phase, allowing realization of true real-time online
segmentation.
15:00
3173.
Automated Liver Volume Assessment from Contrast Scans: Impact of
Pathology
Computer 24
Ajay
Narayanan1, Kajoli Banerjee Krishnan1, Rakesh Mullick1,
Uday Patil1, Patrice Hervo2
1GE
Global Research, Bangalore, India; 2GE Healthcare, Buc, France
Liver
volume assessment for transplant, pathologic and metabolic changes using MR has
primarily been via semi-automated methods. We have developed an automated
method based on statistically driven data adaptive geodesic active contours to
extract the liver from fast 3D high resolution T1-weighted, LAVA scans. This
study is aimed at evaluating the sensitivity of our method to a range of
patient pathologies against expert manual segmentation. The algorithm provides
consistent assessment of liver volume compared to the expert manual segmentation
(k=0.88) for embedded and focused liver pathology. The relative performance
tends to degrade in the presence of peripheral liver pathology.
Spectroscopy Localization, Quantitation, & Methodology
Hall D Monday 14:00-16:00
Computer 25
Cristina
Cudalbu1, Vladimir Mlynárik, Lijing Xin, Rolf Gruetter,2
1
Ecole Polytechnique Federale de Lausanne, Lausanne, Switzerland; 2Departments
of Radiology, Universities of Lausanne and Geneva, Switzerland
The
aim of the present study was to assess two approaches based on using LCModel
which take the macromolecule contributions into account in the quantification
step of in vivo rat brain spectra at 14.1 T: 1) the spectrum of macromolecules
measured in vivo; and 2) the built-in LCModel spline baseline. Even if the
fitted splines reproduce the in vivo macromolecules very well, the measured
macromolecular “baseline” represents an additional prior knowledge and lead to
a more accurate and reliable quantification at higher field strengths, which
was attributed to an effectively increased spectral resolution of the
macromolecule components.
14:30
3175.
Comparison of Spectral Fitting Methods for Overlapping J-Coupled
Metabolite Resonances
Computer 25
Ati
Gonenc1, Varanasi Govindaraju1, Andrew A. Maudsley1
1University
of Miami, Miami, Florida, USA
The
results of an automated spectral analysis package capable of performing two
dimensional prior-knowledge fitting of multi-TE spectra, one dimensional
fitting of TE-averaged spectra, and one dimensional fitting of conventional
(single-TE) PRESS spectra, are presented for single-voxel data acquired at 3T.
Improved performance and accuracy has been observed for the spectral fitting
using the full 2D model in comparison to the TE-averaged and conventional PRESS
fit for both in vivo and in vitro data.
Computer 25
Anthony
Khuu1, Jimin Ren1, James Murdoch2, Ivan
Dimitrov2, Donald Woessner1, A. Dean Sherry1,
Craig Malloy1,3
1University
of Texas Southwestern Medical Center, Dallas, Texas, USA; 2Philips
Medical Systems, Cleveland, USA; 3VA North Texas Healthcare System,
Dallas, USA
Accurate
determination of intramyocellular lipid content (IMCLs) by single-voxel proton
spectroscopy or chemical shift imaging is important in clinical research
projects. However, there is often significant
overlap with extramyocellular lipids (EMCLs) due in part to angular dispersion
of the strands of extracellular fat.
Simulations of proton spectra generated from known fiber orientations
and dispersion, analyzed using conventional symmetric lineshapes, resulted in
overestimation of IMCL content. A new fitting algorithm assuming a Gaussian
distribution of EMCLs centered from 0 to 90 degrees was developed and used for
analysis of spectra acquired from calf muscle of healthy humans at 7T.
15:30
3177.
A Note on the Accurate Model-Based Spectral Fitting of Proton MRS in the
Frequency Domain
Computer 25
Zhengchao
Dong1,2, Zhishun Wang1,2, Bradley
Peterson1,2
1Columbia
University, New York, New York, USA; 2New York State Psychiatric
Institute, New York, New York, USA
Model
based spectral fitting is widely used in quantitative in vivo MRS. However,
there is a discrepancy between the discrete Fourier transform (DFT)
reconstructed MR spectrum and continuous Fourier transform (CFT) deduced
spectral models, which will introduce systematic errors in the spectral
quantification, especially when the quantification is based on ratios of
spectral peaks. Although this discrepancy can be easily eliminated, they are
often overlooked in the long TE MRS spectral fitting. We show here by computer
simulation and in vivo MRS data that eliminating the difference between DFT and
CFT spectra allows accurate spectral fitting in the frequency domain.
14:00
3178.
Interleaved Dual-Angle Measurements for the Correction of Partial Saturation
in 31P MR Spectroscopy
Computer 26
Orlando
Lopez1, Damian J. Tyler2, Mark A. Cole2,
Carolyn A. Carr2, Daniel J. Stuckey2, Edward Lakatta1,
Kieran Clarke2, Richard G. Spencer1
1NIH
/ National Institute on Aging, Baltimore, Maryland, USA; 2University
of Oxford, Oxford, UK
Use
of short repetition times (TR), relative to metabolite T1's, is common in NMR
spectroscopy of biological samples.
However, accurate quantification of metabolite concentrations from
spectral resonances acquired with short TR values requires proper correction
for saturation effects. The goal of this
work was to determine whether accurate metabolite measurements could be
performed by continuous dual-angle data collection using partially saturated
spectra in the setting of chemical exchange.
Simulations appropriate to a hypoxic intervention experiment in the
heart were performed. Results
demonstrated the feasibility of using continuous dual-angle acquisition to
correct for partial saturation of metabolite resonances in bioenergetic
experiments.
14:30
3179.
Reproducibility of 31P Cardiac Magnetic Resonance Spectroscopy at 3T
Computer 26
Lowri
E. Cochlin1, Damian J. Tyler1, Yaso Emmanuel1,2,
Lucy Hudsmith3, Cameron J. Holloway1,2, Stefan
Neubauer3, Kieran Clarke1, Matthew Robson3
1University
of Oxford, Department of Physiology, Anatomy and Genetics, UK; 2Department
of Cardiovascular Medicine, UK; 3University of Oxford, Department of
Cardiovascular Medicine, UK
The
purpose of this work was to investigate the application, reproducibility and
reliability of cardiac 31P MRS at 3 Tesla, with a view to taking advantage of
the increased signal available at 3T by improving spatial resolution and
increasing myocardial specificity. We present a technique that routinely
provides high quality spectra along with a robust analysis method which is free
from potential bias through spectral information or quality. The presented
technique is suitable for widespread application both across research groups
and across disease models.
15:00 3180.
31P 3D K-Space
Weighted MRSI with Adiabatic Excitation: 3D Absolute Quantification of
Phosphorus Metabolites in Human Liver
Computer 26
Marek
Chmelik1,2, Albrecht Ingo Schmid1,2,
Stephan Gruber2, Julia Szendroedi3, Martin Krssak2,
Siegfried Trattnig2, Ewald Moser2, Michael Roden,13
1Karl-Landsteiner
Institute for Endocrinology and Metabolism, Vienna, Austria; 2Medical
University of Vienna, Vienna, Austria; 3Hanusch Hospital, Vienna,
Austria
A
protocol for measuring absolute concentrations of hepatic phosphorus metabolites
by using a 3D k-space-weighted SI sequence with B1 homogeneity
insensitive adiabatic pulses was designed and tested. Compared to excitation
pulses used in previous studies adiabatic pulses used here do not need exact
pulse calibration. In addition k-space weighted acquisition and 3T B0
field lead to relative high spatial resolved spectra (3.65ml) in reasonable
time (34 min). The processing tool allows user friendly data processing and
quantifying of hundreds of spectra per patient and producing absolute metabolic
maps of 31P metabolite concentration distribution in the liver.
15:30
3181.
Automatic 31P MRS Quantification in the Human Brain Based on OASIS-HSVD
Algorithm
Computer 26
Xin
Wang1, Jing-Huei Lee1
1University
of Cincinnati, Cincinnati, USA
A
new algorithm termed Optimal Adaptive Separation of Interference Signal Hankel
Singular Value Decomposition (OASIS-HSVD) is proposed as an automatic time
domain method to adaptively separate distorted baselines and to quantify the
target peaks from interested chemical compounds of human 31P MRS data at 4
T. This algorithm was tested on both
simulation and in vivo data. The simulation used the Monte Carlo method for
testing the robustness and accuracy of this algorithm. In vivo data was
obtained from a 3D 31P MRS from human brain. Both studies demonstrate that the
OASIS-HSVD is a promising algorithm for automatic 31P MRS quantification.
14:00
3182.
Lactate Imaging with Hadamard Encoded Slice Selective SelMQC-CSI
Computer 27
Stephen
Pickup1, Seung Cheol Lee1, Jerry D. Glickson1
1University
of Pennsylvania, Philadelphia, Pennsylvania, USA
WeˇŻve
presented here lactate imaging of tumor. Previously published lactate editing
technique, the SelMQC sequence, is a doubly frequency selective, double quantum
filtering method that is highly selective for lactate and filters out lipid
signals that fall in the same chemical shift range as lactate. To enable slice
selection, we added Hadamard-encoding inversion pulses in front of the SelMQC
sequence with slice gradients. It achieved slice selection without conflict
with lactate editing capability. We applied the sequence to a subcutaneously
implanted tumor bearing mouse. Multi-slice lactate maps with 1x1x2 mm3 spatial
resolution were obtained from the tumor within an hour at 9.4 T.
14:30
3183.
Multi-Volume GABA-Edited Spectroscopy of the Human Brain
Computer 27
Laura
Sacolick1, Douglas L. Rothman1, Robin A. de Graaf1
1Yale
University, New Haven, Connecticut, USA
The
acquisition of multiple, independent volumes within a single repetition time is
often desirable, but is typically limited by the inability to provide adequate
magnetic field homogeneity across the volumes. Here we present multi-volume
GABA-edited MRS in combination with dynamic shim updating to obtain high-quality
MR spectra at 4.0 T from three volumes located in the occipital cortex, corpus
callosum, and baso-frontal cortex. The three volumes were segmented into gray
matter, white matter and CSF, and GABA concentrations were calculated for gray
and white matter to be 1.26±0.32 and 0.54±0.15. These and other metabolite
concentrations were found to be within the ranges reported in the literature.
15:00
3184.
Elevated Phosphocholine as a Marker of Carcinogenesis in the Woodchuck
Model of Hepatocellular Carcinoma
Computer 27
Eilean
J. McKenzie1,2, Marco L.H. Gruwel1
1National
Research Council - Institute for Biodiagnostics, Winnipeg, Canada; 2University
of Manitoba, Winnipeg, Canada
Woodchucks
are the only animal model of chronic viral hepatitis and underwent repeated
31P-MRS to follow tumor growth in vivo. It was discovered that phosphomonoester
resonances are elevated in tumors compared to controls. Ex vivo analysis by
31P-NMR confirmed elevations to phosphocholine contribute to PME elevation in
vivo.
15:30
3185.
Strategies for Reliable Quantification of Intracerebral GABA by 1H-MRS
Computer 27
Wolfgang
Bogner1, Stephan Gruber1, Andreas Stadlbauer2,
Marc Doelken2, Siegfried Trattnig1, Arnd Doerfler2,
Hermann Stefan2, Thilo Hammen2
1MR
Center of Excellence, MUW, Vienna, Austria; 2Uniklinik
Erlangen-Nuremberg, Erlangen, Germany
Gamma-aminobutyric
acid (GABA) is an important inhibitatory neurotransmitter in human brain with
anticonvulsive character. Because of an increased interest in GABA metabolism
we tested the reliability of a special single-voxel spectroscopy (SVS) editing
sequence which allows non-invasive intracerebral measurements of this
neurotransmitter in 9 healthy adults on a 3 Tesla Scanner (Siemens TimTrio).
Intra- and inter-subject reproducibility was assessed. Reliability of GABA/Cr
and GABA/H2O ratios was compared in occipital lobe. Different quantification
algorithms were compared (time-domain-line fitting and integration of signals).
Computer 28
Zhong
Chen1, Congbo Cai1, Yanqin Lin1, Shuhui Cai1,
Jianhui Zhong2
1Xiamen
University, Xiamen, People's Republic of China; 2University of
Rochester, Rochester, New York, USA
Coherence
selection gradient has been thought to be essential for high resolution NMR
spectra in inhomogeneous field based on intermolecular multiple quantum
coherences (iMQC). However, our experimental results show that it can be
omitted if correct phase cycling is applied. This means that the measured
line-width of high resolution spectral peaks is not determined by the dipolar
correlation distance caused by coherence selection gradient, but only affected
by the effects of diffusion and T2 relaxation. This result prompts us to
reconsider the iMQC high resolution mechanism.
14:30
3187.
Detection of Low Levels of Brain Galactitol in Galactosemia Using 1H 2D Double-Quantum Spectroscopy
Computer 28
Zhiyue
Jerry Wang1,2, Fernando Scaglia1,2,
Vernon Reid Sutton1,2, Kerri M. Lamance2, Jill
V. Hunter1,2
1Baylor
College of Medicine, Houston, USA; 2Texas Children's Hospital,
Houston, USA
Galactosemia
is an autosomal recessive hereditary disease of galactose metabolism. Patients
have elevated urine galactitol even under the dietary restriction of galactose,
due to endogenous production of galactose. With conventional proton MRS a low
level galactitol (below 0.5 mM) cannot be resolved from other brain
metabolites. We demonstrate a two-dimensional double-quantum 1H
spectroscopy technique at 3T for detecting low levels of galactitol in the
brain of galactosemics under dietary restrictions. This work opens the
possibility for further investigations of the role of residual brain galactitol
in the well-being of galactosemia patients.
Computer 28
Xi
Chen1, Meijin Lin1, Jincan Chen1, Tao Lin1,
Zhong Chen1
1Xiamen
University, Xiamen, People's Republic of China
A
series of intermolecular double-quantum filtered (iDQF) sequence with efficient
solvent suppression and different scaling factors of J-coupling constants,
named iDQF-HOMOGENIZED II (abbreviated as iDH2), are designed to achieve fast
acquisition of high-resolution spectra in inhomogeneous fields. Experiments on
swine brain tissues were performed to test the feasibility of the new method.
The results suggest potential applications for in vivo spectroscopy.
15:30
3189.
A Flexible IMQC Method for Accurate Determination of J-Coupling
Constants in Inhomogeneous Fields
Computer 28
Yanqin
Lin1, Shuhui Cai1, Yuqing Huang1, Zhong Chen1,
Jianhui Zhong2
1Xiamen
University, Xiamen, People's Republic of China; 2University of Rochester,
Rochester, New York, USA
An
improved pulse sequence was developed to scale apparent J coupling constants by
a scaling factor ranging theoretically from zero (completely decoupled) to
infinity under inhomogeneous fields via intermolecular multiple-quantum
coherences. Scaling up the apparent J coupling constants allows more accurate
measurement of small J coupling constants, and a completely decoupled
homonuclear spectrum can be of considerable help for improving signal
separation and thus peak assignment in MRS. The resulting spectrum retains
conventional high-resolution NMR spectral information.
Hyperpolarized 13C & Other Nuclei
Hall D Monday 14:00-16:00
14:00
3190.
Reduction of the Myocardial Intracellular Matrix as Measured by
Hyperpolarized 13C NMR
Computer 29
Matthew
E. Merritt1,2, Crystal Harrison2, Rajesh
Pidikiti1, Charles Storey1, Shawn C. Burgess1,
Craig R. Malloy1, A. Dean Sherry1,2
1UTSW
Medical Center, Dallas, Texas, USA; 2UT Dallas, Richardson, Texas,
USA
Infusion
of a combination of octanoate and pyruvate is shown to inhibit pyruvate
dehydrogenase (PDH) flux as measured using hyperpolarized [1-13C]-pyruvate
and 13C NMR in a perfused rat heart. Octanoate,a medium chain fatty
acid that freely diffuses into the cell, provides extra reducing equivalents to
the mitochondria, ultimately shifting the REDOX state of the heart and
increasing the production of lactate as well as blocking the appearance of 13CO8
and H13CO3-.
14:30
3191.
Strategies to Prolong the T1 Times in Hyperpolarized 13C
and 15N Biomolecules
Computer 29
Jan-Bernd
Hövener1
1HMRI,
Pasadena, California , USA
The
advantage of hyperpolarization, with signal enhancement approaching 100.000
fold, is limited by the intrinsic lifetime T1. Biomedical applications which
can be achieved within a timeframe of 5 T1 (~100s) are limited. A major hurdle
is therefore to retain the high polarization over time.
Here,
we describe a simple measure which significantly prolongs T1. After deuteration
of 4 PASADENA molecules (13C, 15N), or by dissolution in D2O, the T1 was
increased 6.5 fold max., ~two-fold in average. This widens the range for
applications of long-lived, hyperpolarized biomolecules in-vivo, including
oncology, vulnerable plaque, cancer biomarkers and oncogene tracking.
15:00
3192.
In Vivo Hyperpolarized 13C MRS/MRSI Using 13C-Lactate
as the Pre-Polarized Substrate
Computer 29
Albert
P. Chen1, John Kurhanewicz1, Robert Bok1, Duan
Xu1, David Joun1, Vickie Zhang1, Sarah J.
Nelson1, Ralph E. Hurd2, Daniel B. Vigneron1
1UCSF,
San Francisco, California , USA; 2GE Healthcare, Menlo Park,
California , USA
Prior
studies have shown the ability to detect the metabolic conversion of the
hyperpolarized 13C-pyruvate into 13C-lactate, 13C-alanine
and 13C-bicarbonate in animal models. In this study, a
hyperpolarized MR probe based on 13C1-lactate as the
substrate for in vivo 13C MRS/MRSI studies was developed. After injection of hyperpolarized 13C1-lactate,
metabolic products 13C1-pyruvate and 13C1-alanine
were observed in normal rats and in transgenic mouse prostate cancer
models. This study demonstrated the
feasibility of using pre-polarized 13C1-lactate to study
lactate metabolism as well as tumor lactate uptake in vivo.
15:30
3193.
Establishment of Hyperpolarized 13C MR in the Isolated Perfused Heart
Computer 29
Marie
Allen Schroeder1, Lisa C. Heather1, Mark A. Cole1,
Kieran Clarke1, George K. Radda1, Damian J. Tyler1
1University
of Oxford, Oxford, UK
This
metabolic information available from hyperpolarized 13C MR could provide the
basis for kinetic modelling of cellular uptake and enzymatic activity; however,
understanding of the physiological interactions between the hyperpolarized
substrate and tissue is necessary. The isolated perfused heart provides the
ideal model system to gain this understanding, as many parameters can be easily
controlled. This study demonstrated the methodology we have developed to inject
hyperpolarized 1-13C-pyruvate into the perfused heart without affecting heart
function, and to monitor pyruvate uptake and metabolism. Further, we have
directly compared our perfused heart spectra with analogous in vivo results.
14:00
3194.
The Effect of Hyperpolarized Tracer Concentration on Myocardial Uptake
and Metabolism
Computer 30
Damian
J. Tyler1, Marie A. Schroeder1, Lowri E. Cochlin1,
Kieran Clarke1, George K. Radda1
1University
of Oxford, Oxford, UK
Hyperpolarization
of 13C-labelled metabolic substrates provides the MR signal
necessary to visualize in vivo
substrate uptake and metabolism in real time. This dynamic information could
provide the basis for the kinetic modeling of cellular uptake and enzymatic
activity. However, to achieve this end, an understanding of the physiological
interactions between the hyperpolarized substrate and tissue is necessary. In
this study, the relationship between initial pyruvate tracer concentration and
the MR signal of pyruvate and its metabolic products was examined in the heart
of living rats.
14:30
3195.
In Vivo Detection of Hyperpolarized 15N Choline in the Rat
Computer 30
Cristina
Cudalbu1, Arnaud Comment2, Kai Uffmann, Ruud B. van
Heeswijk, Chiara Perazzolo, Fiodar Kurdzesau2,3, Sami
Jannin2, Vladimir Denisov4, Deniz Kirik4,
Jacques J. vna der Klink2, Rolf Gruetter,5
1
Ecole Polytechnique Federale de Lausanne, Lausanne, Switzerland; 2Laboratory
for Physics of Nanostructured Materials, Ecole Polytechnique Fédérale de
Lausanne, Lausanne, Switzerland; 3Paul Scherrer Institute, Villigen,
,
The
aim of the present study was to demonstrate the feasibility of detecting
hyperpolarized 15N labeled Choline in vivo in the rat.
All
the 15N MRS data were acquired on a 9.4T system. 15N choline was polarized at
3.35T and 1.2K. The long T1 combined with the potential to observe
hyperpolarized 15N Cho in vivo makes this compound useful for early detection of
tumors and also for a potential utilization in the assessment of blood flow. To
our knowledge the in vivo detection of hyperpolarized 15N has not been
demonstrated to date. We conclude that it is feasible to detect hyperpolarized
15N in live animals.
15:00
3196.
Localized Detection of Hyperpolarized [1-13C]Pyruvate and Its
Metabolic Products in Rat Brain
Computer 30
Dinesh
K. Deelchand1, Isabelle Iltis1, Malgorzata Marjanska1,
Chris Nelson1, Kamil Ugurbil1, Pierre-Gilles Henry1
1University
of Minnesota, Minneapolis, Minnesota, USA
This
work examines the feasibility of measuring 13C signals from
hyperpolarized 13C metabolic products in the rat brain in vivo following i.v. injection of
hyperpolarized [1-13C]pyruvate. Enhanced 13C resonances
from pyruvate, pyruvate hydrate, lactate and alanine were observed. Comparison
of unlocalized 13C spectra with 13C-localized LASER
spectra suggests that a significant fraction of [1-13C]lactate
signal arises from brain tissue.
15:30
3197.
Detecting the Invisible: DNP-Enhanced Detection of 13C in
Carboxyl Resonances of Rat Brain Extracts
Computer 30
Chiara
Perazzolo1, Arnaud Comment1, Kai Uffmann1,
Ruud B. van Heeswijk1, Fiodar Kurdzesau1,2,
Sami Jannin1, Jacques J. van der Klink1, Rolf Gruetter1,3
1Ecole
Polytechnique Fédérale de Lausanne, Lausanne, Switzerland; 2Paul
Scherrer Institute, Villigen, Switzerland; 3Universities of Lausanne
and Geneva,, Switzerland
13C
spectra are largely used in MRS to investigate brain metabolism in vivo;
hyperpolarization has been used to enhance the signal of a specific 13C tracer
with the aim to observe metabolism. Brain extracts may yield important
additional insight into the measurement of metabolic rates. The aim of the
current study was to establish hyperpolarization of 13C in brain extract for
the detection of low concentration 13C with intrinsically low sensitivity. To
the best of our knowledge, for the first time a brain extract solution has been
successfully hyperpolarized.
14:00
3198.
Hyperpolarized 13C Acetate Detection in the Rat Brain in Vivo
Computer 31
Kai
Uffmann1, Arnaud Comment1, Ruud B. van Heeswijk1,
Chiara Perazolla1, Sami Jannin1, Fiodar Kurdzesau1,2,
J. A. Konter2, Patrick Hautle2, Ben van der Brandt2,
Jacques J. van der Klink1, Rolf Gruetter1,3
1Ecole
Polytechnique Fédéral de Lausanne (EPFL), Lausanne, Switzerland; 2Paul
Scherrer Institute, Villigen, Switzerland; 3Universities of Lausanne
and Geneva, Switzerland
Hyperpolarized
1-13C-acetate was infused into three rats, followed by collection of
20 spectra (TR=3s). The decay of the enhanced signal of the tracer could be
sampled. In an additional experiment performing spectroscopic imaging the
localization of the acetate signal was proven to be in the brain. A T1
relaxation time of 20.7s of the labeled compound was derived by fitting the
decay using a biexponential curve. Furthermore a resonance peak at 174.1ppm was
observed, which followed the similar decay as the acetate signal. The origin of
this peak remains to be investigated.
14:30
3199.
Can Hyperpolarized 89Y Be Used as a Molecular Imaging Agent?
Computer 31
Matthew
E. Merritt1,2, Crystal Harrison1,2,
Zoltan Kovacs1, Craig R. Malloy1, A Dean Sherry1,2
1UTSW
Medical Center, Dallas, Texas, USA; 2UT Dallas, Richardson, Texas,
USA
Yttrium-89
is an NMR active nucleus with exceptionally long T1's but low
sensitivity compared to protons. It is shown that dynamic nuclear polarization
can be used to enhance 89Y sensitivity 250 to 1500-fold. Yttrium has
similar coordination chemistry to gadolinium, and could potentially be used as
a molecular imaging agent if bound to the appropriate ligand.
15:00
3200.
Direct Optical Hyperpolarization of Liquids
Computer 31
Daniel
Robert Elgort1, Remus Albu1
1Philips
Research North America, Briarcliff Manor, New York, USA
This
novel hyperpolarization method uses light with orbital angular momentum (OAM)
to enable the direct hyperpolarization of liquids. The feasibility of this
technique was verified experimentally by performing NMR spectroscopy on liquid
sample (index matching oil, refractive index of 1.516) at 0.18T. A proton NMR signal was generated with an
SNR of 5.3 (sample size = 30µL, polarization time = 70ms, FID measurement time
= 8ms, 200ksamples, 20 averages). The
resulting NMR spectra corresponded well with a standard MR spectroscopy
measurement performed on a commercial 1.0T Philips Panorama scanner (PRESS
sequence, FOV=1cm3, FA=90&[deg], TE/TR=50/2500ms, NSA=24, BW=8000Hz,
NP=16384).
15:30
3201.
Methyl Group Tunnelling and Dynamic Nuclear Polarization
Computer 31
Martyn
Paley1
1University
of Sheffield, Sheffield, UK
A
tunnel magnetic resonance switched field experiment on zinc acetate shows
generation of dynamic nuclear polarization without the use of microwave
irradiation based on tunnelling methyl groups interacting with a free electron.