16:00 |
0325.
|
Functional Quantitative
Susceptibility Mapping (fQSM)
David Z Balla1,2, Rosa M Sanchez-Panchuelo2,
Sam Wharton2, Gisela E Hagberg3,
Klaus Scheffler1,4, Sue T Francis2,
and Richard W Bowtell2
1High-Field MR Centre, Max Planck Institute
for Biological Cybernetics, Tuebingen, Germany, 2Sir
Peter Mansfield Magnetic Resonance Centre, University of
Nottingham, Nottingham, United Kingdom, 3Physiology
of Cognitive Processes, Max Planck Institute for
Biological Cybernetics, Tuebingen, Germany,4Department
of Neuroimaging and MR-Physics, University of Tuebingen,
Tuebingen, Germany
Quantitative susceptibility mapping (QSM) was performed
on fMRI time-series to reconstruct maps with activation
induced local susceptibility changes. A multi-step image
processing algorithm was developed for filtering out
unwanted temporal and spatial signal variations. The
method was validated on GE-EPI BOLD-fMRI datasets
acquired at 7T with 1mm isotropic resolution during the
application of visual, motor and somatosensory
activation paradigms. Series of high-quality phase and
susceptibility maps with minimal temporal noise were
reconstructed, which resulted in activation maps
corresponding to estimations from the modulus data.
Functional QSM (fQSM) allows for quantification of the
BOLD-effect for any time-series with phase information.
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16:12 |
0326. |
Functional MRI with SWIFT
Silvia Mangia1, Ryan Chamberlain1,
Federico De Martino1,2, Steen Moeller1,
Curt Corum1, Tae Kim3, Chaitanya
Kalavagunta1, Shalom Michaeli1,
Michael Garwood1, Seong-Gi Kim3,
and Kamil Ugurbil1
1CMRR - Dept. of Radiology, University of
Minnesota, Minneapolis, Minnesota, United States, 2Department
of Cognitive Neuroscience, University of Maastricht,
Maastricht, Netherlands, 3Department
of Radiology, University of Pittsburgh, Pittsburgh,
Pennsylvania, United States
We applied in fMRI sweep imaging with Fourier
transformation (SWIFT), which measures fast 3D brain
coverage without producing echoes. The SWIFT signal
increased in the human visual cortex by 3-5% during
visual stimulation at 4T. In vitro, no MRI contrast was
observed with SWIFT on 5-mm tubes containing arterial or
venous blood. However, the SWIFT signal decreased in the
rat cortex during respiratory challenges at 9.4T, in
spite of the local blood flow increase, thus likely
reflecting decreased blood oxygenation in vivo. Other
cellular events occurring during activation might
contribute to the SWIFT functional contrast in addition
to oxygenation changes.
|
16:24 |
0327.
|
Human functional imaging
at 9.4 T: Spin echo and gradient echo EPI
Juliane Budde1, G. Shajan1, Maxim
Zaitsev2, Klaus Scheffler1, and
Rolf Pohmann1
1Max Planck Institute for Biological
Cybernetics, Tübingen, Germany, 2Department
of Diagnostic Radiology, University Hospital Freiburg,
Freiburg, Germany
Functional images with a finger tapping task were
acquired using spin echo and gradient echo EPI sequences
at 9.4 T with isotropic resolution of 1 mm. Resulting
activation was registered onto high-resolution anatomic
images. A mask of veins was identified; activated voxels
were divided into ‘venous’ and ‘non-venous’, and
averaged over subjects, voxels, and blocks. Activation
levels were 6.1 ± 5.4 % in non-venous and 9.1 ± 5.7 % in
venous locations. Time courses for the spin echo EPI are
very similar and show an activation level of 3.9 ± 7.2 %
outside and 4.2 ± 7.0 % inside veins.
|
16:36 |
0328.
|
MR-Encephalography using a
Spherical Stack of Spirals Trajectory
Jakob Assländer1, Marco Reisert1,
Benjamin Zahneisen1, Thimo Hugger1,
and Jürgen Hennig1
1Dep. of Radiology, Medical Physics,
University Medical Center, Freiburg, Baden-Württemberg,
Germany
A spherical stack of spirals trajectory for fast single
shot 3D-imaging is presented. Contrary to a shell
trajectory, in a stack of spirals trajectory
off-resonance leads to distortions rather than blurring
and signal dropout. Latter one is hard or impossible to
correct for. It is shown, that the off-resonance
behavior strongly depends on the direction of the
acquisition. Furthermore the stack of spirals easily
allows a reduction of the FOV in z-direction to save
acquisition time. This can be used to increase the
resolution.
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16:48 |
0329.
|
Distortion-free
high-resolution fMRI at 9.4 T
Philipp Ehses1,2, Juliane Budde1,
G. Shajan1, and Klaus Scheffler1,2
1Max Planck Institute for Biological
Cybernetics, Tübingen, Germany, 2Dept.
for Neuroimaging, University Hospital Tübingen, Tübingen,
Germany
SNR benefits allow for significantly higher resolution
in BOLD fMRI at ultra-high fields. On the flip side,
faster T2* relaxation
leads to blurring and increased B0 field
inhomogeneities aggravate distortion artifacts in EPI
BOLD imaging at higher fields. In this work, a
single-echo gradient-echo sequence is presented, that is
optimized for high BOLD SNR by combining the concept of
echo-shifting with an interleaved slice order. The
method is demonstrated in finger tapping experiments on
a human 9.4T system. The result is a BOLD activation map
with 1mm isotropic resolution virtually free from
distortions.
|
17:00 |
0330. |
SE fMRI in human bilateral
auditory cortex using B1 shimming
Federico De Martino1,2, Sebastian Schmitter1,
Kamil Ugurbil1, Elia Formisano2,
Essa Yacoub1, and Pierre-Francois van de
Moortele1
1Radiology, Center for Magnetic Resonance
Research, Minneapolis, Minnesota, United States, 2Cognitive
Neuroscience, Maastricht University, Maastricht,
Netherlands
We aim at using SE-fMRI to push further the
investigation of functional organization in the human
auditory cortex. To do so we investigate the use of an
RF coil that includes 8 Transceivers (8TCx), allowing
for the use of B1 shimming over right and left auditory
cortices, as well as 24 Receive only channels (24Rx),
providing higher SNR. We demonstrate successful SE-fMRI
in bilateral auditory cortex at 7T highlighting
significant differences between responses to voice vs.
non-voice stimuli in anterior areas of the superior
temporal sulcus and gyrus.
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17:12 |
0331. |
Slab-Selective,
BOLD-Corrected VASO (SS-VASO) in Human Brain at 7T
Laurentius Huber1, Dimo Ivanov1,
Markus Streicher1, and Robert Turner1
1Neurophysics, Max Planck Institute for Human
Cognitive and Brain Sciences, Leipzig, Germany
To understand human brain neural activity it is helpful
to study direct physiological variables, such as
cerebral blood volume (CBV). Vascular space occupancy (VASO)
is a non-invasive fMRI method that measures change in
CBV. VASO at 7 T is limited by low signal and BOLD
contamination. Here we present a slab-selective,
BOLD-corrected SS-VASO variant that avoids these
problems, and provides reliable CBV changes in vivo with
high sensitivity. Temporal and spatial properties of
BOLD and VASO signal are directly compared.
|
17:24 |
0332.
|
A quantitative spatial
comparison of high-density diffuse optical tomography and
fMRI mapping of visual cortex
Adam T Eggebrecht1, Brian R White1,
Silvina L Ferradal1,2, Chunxiao Chen3,
Yuxuan Zhan4, Abraham Z Snyder5,6,
Hamid Dehghani7, and Joe P Culver8,9
1Radiology, Washington University School of
Medicine, St Louis, MO, United States, 2Biomedical
Engineering, Washington University in St. Louis, St
Louis, MO, United States, 3Department
of Biomedical Engineering, Nanjing University of
Aeronautics and Astronautics, Nanjing, Jiangsu, China, 4School
of Computer Science, University of Birmingham, 5Radiology,
Washington University School of Medicine, 6Neurology,
Washington University School of Medicine, St Louis, MO,
United States, 7School
of Computer Science, University of Birmingham, United
Kingdom, 8Radiology,
Washington University School of Medicine, Saint Louis,
MO, United States, 9Biomedical
Engineering, Washington University in St. Louis, Saint
Louis, MO, United States
fMRI has commanded a dominant role in current
neuroscience research, yet its use in neuro-scientific
or bedside clinical studies has been limited because the
current tools lack the combination of being portable
while maintaining moderate resolution and localization
accuracy. Optical neuroimaging overcomes these
obstacles, but, until recent advancements in
high-density diffuse optical tomography (HD-DOT), has
been hampered by limited resolution. We evaluate the
image-quality of HD-DOT against fMRI using functional
maps of the visual cortex as a benchmark and quantify
localization error with center-of-mass and phase
metrics. This work provides support for adoption of
HD-DOT as a surrogate for fMRI.
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17:36 |
0333.
|
Simultaneous small animal
PET/MR in activated and resting state reveals multiple brain
networks
Hans F Wehrl1, Konrad Lankes1,2,
Mosaddek Hossain1, Ilja Bezrukov1,3,
Chih-Chieh Liu1, Petros Martirosian4,
Gerald Reischl1, Fritz Schick4,
and Bernd J Pichler1
1Department for Preclinical Imaging and
Radiopharmacy, University of Tuebingen, Tuebingen,
Germany, 2Bruker
BioSpin MRI, Ettlingen, Germany, 3Max
Planck Institute for Intelligent Systems, Tuebingen,
Germany, 4Section
on Experimental Radiology, University of Tuebingen,
Tuebingen, Germany
Simultaneous small animal PET/MR allows the study of
functional processes on multiple levels. Here we present
a comparison between simultaneous activation as well as
resting state fMRI and PET in rats. Additional activated
components of brain networks are found in PET, not
present in fMRI. The data show complementarities of both
techniques in respect to activation as well as default
mode network imaging in the brain.
|
17:48 |
0334.
|
Enhanced fMRI Sensitivity
using CBV based Contrast with the Blood Pool USPIO Agent
Ferumoxytol in Humans
Deqiang Qiu1, Greg Zaharchuk1,
Thomas Christen1, Wendy W Ni1, and
Michael E Moseley1
1Radiology, Stanford University, Stanford,
CA, United States
In this paper, we present the first human study of the
use of ultrasmall superparamagnetic iron particle (USPIO)
for contrast agent based blood Volume functional MRI (fBVI).
The temporal response function of fBVI was
characterized, and was found to include both a slow and
a fast component. The contrast to noise ratio (CNR) of
fBVI was found to be of up to a factor of 2.9 than the
commonly used BOLD (Blood oxygenation level dependent)
technique. The significant CNR gain with fBVI opens the
possibility of high-resolution fMRI, including mapping
of ocular orientation column in human.
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