10:00 |
0409. |
Blipped-CAIPI Spiral for
Simultaneous Multi-Slice BOLD FMRI
Benjamin Zahneisen1, Benedikt A. Poser1,
Thomas Ernst2, and Victor Andrew Stenger1
1Department of Medicine, John A. Burns School
of Medicine, University of Hawaii, Honolulu, Hawaii,
United States, 2Department
of Medicine, John A. Burns School of Medicine,
University of Hawaii at Manoa, Honolulu, Hawaii, United
States
Sub-second whole brain fMRI is advantageous since it
resolves physiological signal fluctuations, virtually
freezes head motion, has greater statistical power, and
allows the detection of subtle HRF shifts or delays.
Recently, the “blipped-CAIPI” EPI method was introduced
as a means to reduce the g-factor penalty in
simultaneous multi-slice (SMS) imaging. However, the
approach is limited to Cartesian trajectories with their
unique fold-over artifact. Here, we present a new
framework for SMS imaging based on 3D Fourier encoding
of simultaneously excited slices. We show that the
blipped-CAIPI approach can be generalized to
non-Cartesian trajectories and SENSE-like
reconstructions including a new design for blipped-CAIPI
spiral trajectories. Spiral has a more efficient
gradient utilization and shorter readouts are possible.
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10:12 |
0410. |
Characterization of
Artifactual Correlation in Highly-Accelerated Simultaneous
Multi-Slice (SMS) fMRI Acquisitions
Kawin Setsompop1,2, Jonathan R. Polimeni1,2,
Himanshu Bhat3, and Lawrence L. Wald1,2
1A.A. Martinos Center for Biomedical Imaging,
MGH, Charlestown, MA, United States, 2Harvard
Medical School, Boston, MA, United States, 3Siemens
Medical Solutions, Charlestown, MA, United States
Simultaneous Multi-Slice (SMS) acquisition with blipped-CAIPI
scheme has enabled dramatic reduction in imaging time
for fMRI acquisitions, enabling high-resolution
whole-brain acquisitions with short repetition times.
The characterization of SMS acquisition performance is
crucial to wide adoption of the technique. In this work,
we examine an important source of artifact: spurious
thermal noise correlation between aliased imaging voxels.
This artifactual correlation can create undesirable bias
in fMRI resting-state functional connectivity analysis.
Here we provide a simple method for characterizing this
artifactual correlation, which should aid in guiding the
selection of appropriate slice- and inplane-acceleration
factors for SMS acquisitions during protocol design.
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10:24 |
0411. |
An Approach to
3-Dimensional Multi-Band Acquisition
Bruno Riemenschneider1, Jakob Assländer1,
and Jürgen Hennig1
1Dept. of Radiology, Medical Physics,
University Medical Center Freiburg, Freiburg, Germany
Multi-band excitation in conjunction with a
3-dimensional read-out helps to overcome the limitation
in number of slices that can be resolved with parallel
imaging techniques. Other than slab-wise excitation, it
leads to exploitation of the coil sensitivities in all
three dimensions and inhomogeneities at the interface
between adjacent slabs are avoided. The feasibility of
the approach is demonstrated by a sample measurement
with a 32-channel headcoil. The field of view of (0.192
m)³ with voxel size 3mm was measured in 400 ms.
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10:36 |
0412.
|
Simultaneous SE-BOLD and
T2* Measurement by Functional MRS of Water Signal
Peng Cao1,2, Jevin W. Zhang1,2,
Victor B. Xie1,2, Iris Y. Zhou1,2,
and Ed X. Wu1,2
1The University of Hong Kong, Hong Kong, Hong
Kong SAR, China, 2Department
of Electrical and Electronic Engineering, Hong Kong,
Hong Kong SAR, China
Blood-oxygen-level-dependent (BOLD) contrast is known to
be modulated by vascular origins such as intravascular,
extravascular, venular and capillary. The relative
contributions of these factors to BOLD signal are
dependent of magnetic field strength and whether spin
echo or gradient echo detection is used. MRS voxel
selective excitation method (e.g. PRESS) can measure the
SE-BOLD (i.e., amplitude of SE BOLD signal) and T2*
(i.e., the FID decay rate) directly simultaneously. With
this approach, we simultaneously acquired SE-BOLD
signals and T2* and quantitatively compared their
characteristics.
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10:48 |
0413.
|
T2- Prepared
Blood-Oxygenation-Level-Dependent (BOLD) fMRI Using
Single-Shot 3D Fast Gradient Echo (GRE) Sequence with Whole
Brain Coverage at 7T
Jun Hua1,2, Craig K. Jones1,2, Qin
Qin1,2, and Peter C.M. van Zijl1,2
1Neurosection, Div. of MRI Research, Dept. of
Radiology, Johns Hopkins University School of Medicine,
Baltimore, Maryland, United States, 2F.M.
Kirby Research Center for Functional Brain Imaging,
Kennedy Krieger Institute, Baltimore, Maryland, United
States
We introduce a new acquisition scheme for T2-weighted
BOLD fMRI. It employs a T2-preparation module to
generate the BOLD contrast, followed by a single-shot 3D
fast gradient echo readout. We implemented it on 7T
human scanners with whole brain coverage (2.5mm voxel,
55 slices). In fMRI experiments of simultaneous visual
and sensory stimulation, this sequence showed comparable
sensitivity as the conventional 2D SE-EPI, and
advantages of minimal geometric distortion and signal
dropouts, lower power deposition, and greater spatial
coverage. This approach would be particularly useful for
fMRI studies that require whole brain coverage, or focus
on regions near air cavities.
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11:00 |
0414.
|
T2-Weighted BOLD
fMRI at 9.4 T Using a S2-SSFP-EPI Sequence
Philipp Ehses1,2, Juliane Budde1,
Gunamony Shajan1, and Klaus Scheffler1,2
1High-Field MR Center, Max Planck Institute
for Biological Cybernetics, Tübingen, Germany, 2Dept.
of Biomedical Magnetic Resonance, University of Tübingen,
Tübingen, Germany
It has been hypothesized that T2-weighted
BOLD fMRI at ultra-high field shows higher spatial
specificity than T2*-weighted BOLD, since the
main signal contribution is expected to come from the
extravascular spins of the microvasculature.
Unfortunately, the number of slices that can be acquired
in multi-slice SE-EPI is limited at ultra-high field due
to SAR constraints. T2-weighted steady-state
sequences, such as S2-SSFP, have been
previously used as an alternative to spin-echo based
BOLD fMRI. In this work, we present a 3D S2-SSFP
sequence that is accelerated using an EPI readout and
show first results from finger tapping experiments at
9.4 T.
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11:12 |
0415. |
Simultaneous Spin Echo and
Gradient Echo for fMRI Using the USPIO Agent Ferumoxytol in
Humans: Enhanced Sensitivity and Potentials for High
Resolution Mapping
Deqiang Qiu1, Thomas Christen1,
Wendy W. Ni1, Heiko Schmiedeskamp1,
Greg Zaharchuk1, and Michael E. Moseley1
1Radiology, Stanford University, Stanford,
CA, United States
In this paper, we present the study of the use of
ultrasmall superparamagnetic iron particle (USPIO) for
fMRI (termed ICE-BVI) using both gradient and spin echo
methods. The contrast to noise ratio (CNR) of ICE-BVI
was found to be of up to a factor of 3.8 higher than
BOLD for gradient echo based method, and the gain is
about a factor of 2 for spin echo based method. ICE-BVI
has the potential of increasing robustness and accuracy
for presurgical mapping and enhanced sensitivity in
studying cognitive neuroscience.
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11:24 |
0416. |
Diffusion fMRI Can Detect
Neural Activation When the BOLD fMRI Response Is Abolished
by Nitroprussiate
Tomokazu Tsurugizawa1, Boucif Djemai1,
Luisa Ciobanu1, and Denis Le Bihan1
1Neurospin/CEA, Gif-sur-Yvette, Essonne,
France
Diffusion-weighted functional MRI (DfMRI) has been shown
to be sensitive to neural activation, however, its
vascular or non-vascular origin has been a subject of
controversy. We have compared the DfMRI and BOLD
responses at 7T in the rat brain during forepaw
electrical stimulation with and without nitroprussiate,
a neurovascular coupling inhibitor, and compared these
responses with recorded neural activity. Under the
nitroprussiate infusion, while the BOLD signal was
completely suppressed, the neuronal activation and DfMRI
signal were conserved, demonstrating that DfMRI includes
a genuine diffusion component which directly reflects
neuronal activation.
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11:36 |
0417.
|
Diffusion fMRI Detects
White-Matter Dysfunction in Mice with Acute Optic Neuritis
Tsen-Hsuan Lin1, William M. Spees2,3,
Robert Mikesell4, Anne H. Cross3,5,
and Sheng-Kwei Song2,3
1Physics, Washington University, St. Louis,
MO, United States, 2Radiology,
Washington University School of Medicine, St. Louis, MO,
United States, 3The
Hope Center for Neurological Disorders, Washington
University School of Medicine, St. Louis, MO, United
States, 4Neurology,
Washington University School of Medicine, St. Louis, MO,
United States, 5Neurology,
Washington University in St. Louis, St. Louis, MO,
United States
Our previous investigation in healthy mice has shown
that visual stimulation caused a significant (~27%) drop
in the apparent diffusion coefficient for water
perpendicular to the axonal fibers (ADCƒÎ) in optic
nerve. In the current study, we have extended these
diffusion fMRI measurements in a mouse experimental
autoimmune encephalomyelitis (EAE) model at the onset of
optic neuritis to investigate the functional integrity
of white matter. Our results show that visual
stimulation produced a significant 25% decrease in ADCƒÎ
in EAE sham optic nerves, while only a 5% decrease in
ADCƒÎ was seen in EAE mice. Histological results of
SMI31, MBP, and SMI32 staining show axonal swelling and
injury distorted myelin sheaths in EAE optic nerves.
This suggests that diffusion fMRI could be used as a
non-invasive approach to localizing axons with impaired
functional integrity.
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11:48 |
0418. |
Magnetic Resonance Imaging
of Neuronal Currents in an in Vitro Turtle Cerebellum
Padmavathi Sundaram1, William Wells2,
Darren B. Orbach1, Daniel Orringer3,
Mukund Balasubramanian1, Robert Mulkern1,
and Yoshio Okada4
1Radiology, Children's Hospital Boston,
Harvard Medical School, Boston, MA, United States, 2Radiology,
Brigham and Women's Hospital, Harvard Medical School,
Boston, MA, United States,3Neurosurgery,
University of Michigan, Ann Arbor, MI, United States, 4Neurology,
Children's Hospital Boston, Harvard Medical School,
Boston, MA, United States
This work investigates the relationship between neuronal
currents and MR signals in an in vitro bloodless turtle
cerebellum (Cb). While prior work has demonstrated
sensitivity of MR signals to currents, the
spatiotemporal relationship between MR phase and
neuronal currents remains to be characterized in brain
tissue. We use the turtle Cb because: (1) there are no
signal contributions from blood, respiration or motion,
(2) the cellular circuit is intact, (3) the preparation
can withstand anoxia and is physiologically functional
for several hours, and (4) it is a flat tissue with the
principal neurons oriented parallel to each other.
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