13:30 |
0449.
![](MAGNA25.jpg) |
3D MRI Microscopy of the
Lens, Vitreous, and Anterior Chamber Volumes in Normal Mouse
Eyes and Eyes with Retinal Degeneration ![](play.gif)
Eric R. Muir1 and
Timothy O. Duong2
1Research Imaging Institute, University of
Texas Health Science Center, San Antonio, TX, United
States, 2Research
Imaging Institute, UT Health Science Center at San
Antonio, San Antonio, TX, United States
Retinitis pigmentosa (RP), which causes photoreceptor
death and blindness and affects 1.5 million people
worldwide, is characterized by progressive loss of the
retina. While the retinal degeneration is well
characterized, it is unclear how other structures of the
eye in RP are affected. The goal of this study was to
develop a 3D MRI approach to image the whole mouse eye
in vivo at 47x78x79 µm with high contrast and
sensitivity using balanced steady state free precession.
We applied this approach to quantify volumes of the
lens, vitreous, and anterior chamber in a mouse model of
RP.
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13:42 |
0450.
![](SUMMA25.jpg) |
Anatomical and ASL Imaging
of the Retina at 7 T ![](play.gif)
Daniel James Lee1, Ehsan Vaghefi2,
Kevin F. Webb3, Alexander J E Foss4,
Richard W. Bowtell1, and Susan T. Francis1
1SPMMRC, University of Nottingham,
Nottingham, Nottinghamshire, United Kingdom, 2University
of Auckland, Auckland, New Zealand, 3University
of Nottingham, Nottingham, Nottinghamshire, United
Kingdom, 4Queen's
Medical Centre, Nottingham, Nottinghamshire, United
Kingdom
Using a dedicated receive coil and the high
signal-to-noise of a 7 T system, high resolution
anatomical images of the human eye have been obtained in
vivo. Perfusion images showing retinal blood flow were
acquired using a FAIR ASL scheme with a TurboFLASH
readout across a range of post-label delay times (TI) ,
showing largest perfusion signals at the longest TI used
here (1550 ms), with average baseline perfusion of 104 ±
41 ml/100 mL/min . Perfusion changes in response to 8 Hz
visual stimulation were measured and a 61 % increase in
retinal perfusion is detected.
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13:54 |
0451.
![](SUMMA25.jpg) |
A Fingerprinting Approach
to Compute Blood Volume, Vessel Diameter and Blood
Oxygenation Maps in the Human Brain ![](play.gif)
Thomas Christen1, Nicolas Pannetier2,3,
Wendy W. Ni1, Deqiang Qiu1,
Norbert Schuff2,3, Michael E. Moseley1,
and Greg Zaharchuk1
1Radiology, Stanford University, Stanford,
California, United States, 2Radiology,
University of California San Francisco, San Francisco,
California, United States, 3Center
for Imaging of Neurodegenerative diseases, Veterans
Affairs Medical Centre, San Francisco, California,
United States
In this work, we acquired the MR signal time evolution
(FID and spin echo) pre and post injection of an
intravascular contrast agent in volunteers. We then
compared the ratio of the signals to a dictionary of
curves obtained using advanced numerical simulations. We
show that it is possible with this approach to extract
quantitative information about the microvascular
network.
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14:06 |
0452.
![](SUMMA25.jpg) |
Multi-Spectral T1 Weighted
Imaging and T1 Quantification Using 3D Radial K-Space
Trajectory ![](play.gif)
Steven Kecskemeti1, Nagesh Adluru1,
Samuel A. Hurley2, and Andrew L. Alexander1
1University of Wisconsin, Madison, Wisconsin,
United States, 2University
of Wisconsin-Madison, Madison, Wisconsin, United States
In this study, 3D radial k-space sampling with inversion
recovery is used to image more than 100 points along the
magnetization recovery curve in a single exam of
duration similar to a standard 3D Cartesian IR-fGRE
image. The effective inversion times may be
reconstructed as finely as a single TR, enabling the
user to retrospectively select the images with the
optimal contrast, thereby eliminating the need to select
a single, specific inversion time prior to data
acquisition. T1 maps are created by fitting the image
signals from the different inversion times to a
theoretical signal model.
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14:18 |
0453. |
MRI Measurements of ICP in
Simulated Acute Mountain Sickness (AMS) ![](play.gif)
Justin Stevan Lawley1, Noam Alperin2,
Sang H. Lee2, Paul Gerald Mark Mullins3,
Samuel James Oliver1, and Jamie Hugo
Macdonald1
1Health and Exercise Sciences, Bangor
University, Bangor, Gwynedd, United Kingdom, 2University
of Miami, Miami, FL, United States, 3Bangor
Imaging Center, Bangor University, Bangor, Gwynedd,
United Kingdom
Prolonged exposure to high altitude is often followed by
Acute Mountain Sickness, which presents as a number of
symptoms including headache, nausea and vomiting. The
prevalence of AMS increases with rate of ascent, total
altitude gain and irrespective of altitude, a striking
individual susceptibility, thought to be the result of a
predisposition to intracranial hypertension. Despite the
elegance and longevity of this hypothesis, evidence for
elevated intracranial pressure (ICP) in concert with AMS
is rare due, in part, to the challenging measurement of
ICP in healthy individuals. MR estimates of ICP were
employed to further elucidate the pathophysiology of AMS.
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14:30 |
0454. |
Spatial Distribution of
Sevoflurane in the Human Brain Revealed by in-vivo 19F
Imaging at Clinical-Relevant Concentrations: Preliminary
Results ![](play.gif)
Maolin Qiu1, Ramachandran Ramani2,
and Robert Todd Constable3
1Diagnostic Radiology, Yale University School
of Medicine, New Haven, CT, United States, 2Anesthesiology,
Yale University School of Medicine, New Haven, CT,
United States, 3Diagnostic
Radiology, Yale University, New Haven, CT, United States
This study aims to examine the sensitivity of 19F
imaging in detecting cerebral Sevoflurane concentrations
in humans during 0.5MAC anesthesia and to investigate
the spatial distribution during Sevoflurane anesthesia.
We have successfully conducted the first 19F imaging
study in humans to assess the cortical distribution of
the inhalational anesthetic agent – Sevoflurane at
clinically-relevant concentrations and demonstrated the
possibility of directly mapping the regional Sevoflurane
concentration in the brain using 19F imaging with a
1H/19F dual-tuned CP head coil even though the cortical
concentration is extremely low. Preliminary results
demonstrate the non-uniformity of Sevoflurane
distribution in the human brain and provide new insights
by directly measuring cortical concentrations during
anesthesia.
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14:42 |
0455. |
Brain Sodium Accumulation
Correlates with Electrical Abnormalities in Drug-Resistant
Epilepsy: A 23Na MRI and Intracranial EEG Recording Study ![](play.gif)
Wafaa Zaaraoui1, Caroline Rey1,
Fabrice Bartolomei2,3, Patrick Chauvel2,3,
Elisabeth Soulier1, Sylviane Confort-Gouny1,
Patrick J. Cozzone4, Lothar R. Schad5,
Jean-Philippe Ranjeva1, and Maxime Guye1,6
1CRMBM, UMR 7339, CNRS, Aix-Marseille
Université, Marseille, France, 2Pôle
de Neurosciences Cliniques, APHM, Marseille, France, 3Laboratoire
de Neurophysiologie et Neuropsychologie, U751, INSERM,
Aix-Marseille Université, Marseille, France, 4Aix-Marseille
Université, Marseille, France, 5Computer
Assisted Clinical Medicine, Heidelberg University,
Mannheim, Germany, 6Pôle
d’Imagerie Médicale, APHM, Marseille, France
Patients suffering from pharmacoresistant partial
epilepsy are potential candidates for epilepsy surgery
consisting of removal of the epileptogenic zone (EZ).
Localization of the EZ during presurgical assessment is
a crucial issue and requires invasive intracranial EEG
recordings. Therefore, developments of new non-invasive
localizing methods are of particular interest. We
demonstrated for the first time that abnormal
accumulation of sodium concentrations succeeded to
lateralize epilepsy and that sodium concentrations in
the grey matter of patients are correlated with the
interictal electrical abnormalities in regions of the
epileptogenic zone. Brain sodium MRI appears as a
promising non-invasive presurgical tool in
drug-resistant epilepsy.
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14:54 |
0456. |
Quiet T1-Weighted Head
Scanning Using PETRA ![](play.gif)
David Manuel Grodzki1 and
Bjoern Heismann1,2
1Siemens AG, Erlangen, Germany, 2Friedrich-Alexander-University
Erlangen-Nuremberg, Erlangen, Germany
Silent T1-weighted head scanning using the PETRA
sequence is investigated in this work. Inversion pulses
are used to enhance the T1 contrast. Optimization of the
settings for the inversion and waiting times are
performed by simulation and volunteer scans. The in-vivo
results show that the PETRA sequence generates image
quality, SNR and CNR between grey and white brain matter
comparable to the MPRAGE sequence. Without the need of
hardware changes, PETRA might be a silent substitute for
the MPRAGE sequence in many applications.
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15:06 |
0457.
![](MAGNA25.jpg) |
7T MRSI in Temporal Lobe
Epilepsy
-permission withheld
David Bonekamp1, He Zhu1, Gregory
Bergey2, and Peter B. Barker1
1The Russell H. Morgan Department of
Radiology and Radiological Science, Johns Hopkins
University, Baltimore, Maryland, United States, 2Department
of Neurology, Johns Hopkins University, Baltimore,
Maryland, United States
In this study, control subjects and a cohort of epilepsy
patients with a clinical diagnosis of unilateral
epilepsy underwent MRSI at 7T. Similar to prior studies
at lower fields, 7T MRSI of the hippocampi showed
bilateral mid-hippocampal tNAA decreases, accentuated at
the side of clinical and MRI abnormality. Lateralization
of the clinical focus was not possible, due to
significant contralateral tNAA decrease. Future
comparative studies are needed to compare the relative
value of 7T vs. 3T MRSI, as well as the relative value
of 7T MRSI to other MRI sequences, in patients with
temporal lobe epilepsy.
|
15:18 |
0458. |
Imaging of Focal Cortical
Dysplasia at 7 Tesla ![](play.gif)
Mathijs Buijs1, Albert Colon1,2,
Matthias van Osch1, Jeroen van der Grond1,
Paul A. Boon2,3, Paul A.M. Hofman2,4,
and Mark A. van Buchem1
1Leiden University Medical Center, Leiden,
Zuid-Holland, Netherlands, 2Epilepsy
Centre Kempenhaeghe, Heeze, Noord-Brabant, Netherlands, 3Ghent
University Hospital, Ghent, Oost-Vlaanderen, Belgium, 4Maastricht
University Medical Center, Maastricht, Limburg,
Netherlands
Focal cortical dysplasia (FCD) is thought to be a major
cause of cryptogenic localization-related epilepsy, in
which conventional MRI is unable to detect a lesion.
Scanning at higher field strenghts is likely to increase
sensitivity to small lesions, improving the chances of a
better surgical outcome. In this pilot study we scanned
10 patients who were diagnosed at 3 Tesla with FCD type
II with a 7 Tesla MRI scanner. Features of FCD at 7T
were described and compared to the findings at 3T.
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