Alan Chu1, Yulin Chang2, André J. W. van der Kouwe3, and M. Dylan Tisdall1
1Radiology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, United States, 2Siemens Medical Solutions USA, Inc., Malvern, PA, United States, 3Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, United States
Synopsis
We demonstrate the
feasibility and validity of field mapping using a dual-echo vNav based on a
fly-back EPI readout. A human subject was scanned using the proposed method and
a standard FLASH acquisition for comparison. The proposed method does not
require additional reconstruction or acquisition complexity and is easily
computed on typical MR scanners to support real-time motion and shim
correction.
Introduction
The use of navigators in
MRI is one method of motion tracking that does not require the use of
additional hardware. In particular, volumetric navigators (vNavs) have been
shown to enable accurate prospective and retrospective motion correction with negligible
change in contrast and intensity of the parent sequence in neuroimaging.1, 2, 3, 4 To account for the significant changes in off-resonance that occur with
motion,5 multiple navigator echoes can be used to generate field maps.1 Previous
dual-echo approaches, while effective, require too much time to fit reasonably
in standard MPRAGE protocols.1 We propose to accelerate the dual-echo vNav strategy
by acquiring a highly undersampled second “fly-back” echo within each EPI
partition train. We demonstrate this method’s validity by comparing it to field
maps from a standard multi-echo FLASH scan.Methods
The first navigator echo was
acquired as in existing vNav sequences, using 3D-encoded EPI with a matrix size
of 32x32x32.2 A second vNav echo was implemented by acquiring an additional
8 lines after a flyback past the ky=0-axis, as illustrated in Figure 1 for one
partition. This ensured that the directionality of the second echo matched the
first for similar eddy current effects and matched distortion. The TEs of the
first and second echoes were 6.685 ms and 12.545 ms, respectively, giving a
difference of 5.86 ms, which enables off-resonance measurement up to +/- 85 Hz
without wrapping. vNavs are normally acquired with an additional partition
prepended to collect phase-correction and frequency drift information.6 In
our novel navigator, this first partition acquired 32 reference lines for the
first echo and 8 additional reference lines for the second echo by using the
same trajectory as in Figure 1, except with phase encode blipping turned off. EPI
ghost correction was performed by estimating even/odd line phase modulation
using Wiener filters based on the temporal noise variance in the vNav data.
Field maps were generated by dividing the phase difference between the echoes
by the TE difference.
Our dual-echo vNavs were
embedded in a custom multi-echo MPRAGE (MEMPRAGE) sequence, and evaluated in a
single human subject, who provided prior informed consent, in a 3 T scanner
(MAGNETOM Prisma, Siemens Healthcare, Erlangen, Germany) using the vendor’s
64-channel head and neck coil. Our protocol included both the proposed dual-echo
vNav MEMPRAGE sequence, and a multi-echo FLASH scan for comparison. The FLASH
scan had a TR of 25 ms and TEs of 4.92, 9.84, 14.76, and 19.68 ms, and the
first and third echoes were used to generate a field map comparison. The FLASH
echo spacing was chosen to keep fat and water at the same resonance offset for
a 3 T field strength. The vNavs, by contrast, used a water-selective excitation
and so should have less effect from fat phase differences between echoes. Two
runs were performed: the first with the subject's head held in a fixed neutral
position, and the second with the subject's head held in a fixed upward-extended
position. Sagittal views of these two runs are shown in Figure 2 for the
higher-resolution FLASH scan as well as for both the first and second vNav
echoes.Results
Magnitude images of the
second vNav echo in Figure 2 show expected blurring in the anterior-posterior
phase encode direction due to the lower traversal of k-space using only 8 phase
encode lines. However, we are interested only in whether this lower resolution is
sufficient for the global off-resonance and first order shim correction that
standard MR scanners typically allow dynamically during scanning.
Figures 3 (sagittal) and 4
(axial) show the field maps computed from the proposed dual-echo vNav sequence
as well as from the FLASH scan, for each of the first and second runs. The
FLASH field maps were downsampled by a factor of 4 to match the resolution of
the vNavs for easier comparison. In the FLASH field map, the second run clearly
shows a change between runs with the posterior aspect of the brain going from
around 0 Hz in the first run to 30-40 Hz in the second run. The vNav field maps
match this behavior closely both in a quantitative and qualitative sense, with
a similar increase of 30-40 Hz between runs in that region and a similar change
in overall shape of the field map between runs.Discussion and Conclusion
We have demonstrated the
feasibility and validity of field mapping using a dual-echo vNav for
off-resonance and first order shim correction by the acquisition of 8
additional phase encode lines in a 32x32x32 3D EPI sequence. Unlike
parallel-accelerated strategies for shortening dual-echo acquisitions, the
proposed method does not require additional reconstruction or acquisition
complexity and is easily computed on typical MR scanners for real-time motion
and shim correction. In addition, the proposed method enables global off-resonance
measurement based on a desired region of interest, unlike standard
non-selective methods currently in use.7 Future work will explore the
additional technical challenges of real-time parallel reconstruction. Our goal
will be to further accelerate the first and second vNav echos, reducing both the
delay between TE1 and TE2 in the navigator, and our overall navigator duration,
making it comparable to current single-echo vNavs.Acknowledgements
The project described was
supported by RSNA Research & Education Foundation through grant number RR2014
and by NIH award R34DA050297. The content is solely the responsibility of the
authors and does not necessarily represent the official views of the RSNA
R&E Foundation.References
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