Nadine Luedicke Dispenza1, Sebastian Littin2, Maxim Zaitsev2, R. Todd Constable3,4, and Gigi Galiana3
1Department of Biomedical Engineering, Yale University, New Haven, CT, United States, 2Department of Diagnostic Radiology, Medical Physics, University Medical Center Freiburg, Freiburg, Germany, 3Department of Radiology and Biomedical Imaging, Yale University, New Haven, CT, United States, 4Department of Neurosurgery, Yale University, New Haven, CT, United States
Synopsis
Despite potential for
more flexible and efficient encoding that better complements receiver geometry,
the past decade of work with nonlinear gradients (NLGs) has shown relatively
modest improvements on accelerated image quality. In this work we present the
first experimental evidence that the previously introduced ROtary Nonlinear Spatial
ACquisition (FRONSAC) can notably improve accelerated image quality, both in
vitro and in humans. Furthermore, this work introduces and demonstrates a
number of robust and flexible attributes of this method, which are crucial to
reducing scan times in a clinical setting.
Introduction
In
this work we demonstrate in vivo and in vitro that the application of sinusoidal
NLGs improve undersampled Cartesian encoding (Figure 1a). Linear gradients sample k-space one point at
a time, and receiver arrays sample a static distribution of k-space. In contrast, NLGs dynamically vary the size
and shape of the sampling functions in k-space (Figure 1c), which provides more
degrees of freedom to design an efficient trajectory to measure k-space. The
encoding efficiency is increased when an undersampled linear acquisition is
enhanced with FRONSAC encoding as measured with a previously introduced k-space
metric (Figure 1d) (1).
Previous
work showed that FRONSAC reduces undersampling artifacts in accelerated imaging
for a variety of linear gradient sequences (2). In the current work
presented here, we show the first experimental Cartesian FRONSAC results,
confirming the theoretical reduction of under sampling artifacts and we investigate
features of FRONSAC critical to clinical imaging. In addition to providing
experimental confirmation of the reduced undersampling artifact, we demonstrate
that FRONSAC yields more benefit from the new generation reconstruction algorithms,
now becoming commercially available (3-5). We also show that Cartesian FRONSAC yields benign
artifacts in the presence of experimental imperfections or when the gradient fields
deviate from the perfect spherical harmonics used in the original paper, thereby
providing robust performance in a clinical setting. A single FRONSAC gradient is
also shown to enhance undersampled image quality for nearly any imaging
prescription, despite changes in the linear gradients associated with different
image dimensions, slice orientation or spatial resolution. As such, the method does not require extensive
field mapping. It is applicable to a number of different sequence types and is
demonstrated here using both gradient echo and fast spin echo sequences. Methods
In
vivo and phantom experiments on a 3T MRI scanner (MAGNETOM Trio Tim, Siemens
Healthcare, Erlangen, Germany) with an 8 channel RF head coil (Siemens) were
performed at Yale University using a NLG insert (Tesla Engineering Ltd,
Storrington, UK) (Figure 1b) that generates 3 spherical harmonic gradient
fields: GC3 (X3-3XY2), GS3 (3YX2-Y3),
and GZ2 (X2+Y2) with maximum strengths of
3254.8 mT/m3, 3155.4 mT/m3 and 475.08 mT/m2.
Phantom experiments performed at the University Medical Center Freiburg used an
84 channel matrix gradient coil (6). A non-optimized cluster
of elements approximated a C3 field with maximum strength of 452 mT/m3.
Transverse slices at isocenter with a FOV of 250 mm were acquired with 1024 readouts
with 128 excitations.
GRE
imaging parameters at Yale University were: TR=1000 ms/TR=600 ms; TE=18 ms;
bandwidth=50 Hz/pixel; flip angle=30°/15°; slice thickness=3 mm, maximum
C3/S3/Z3 strength=325.3 mT/m3, 316.7 mT/m3 and 41.6 mT/m2
with oscillation frequency of ω0/2pi=3.2 kHz.
TSE imaging at Yale University parameters
were: TR=3000 ms; turbo factor=8; echo spacing=24 ms; bandwidth=100 Hz/pixel;
slice thickness=5 mm, maximum C3/S3/Z2 strength=390.7 mT/m3, 380.1
mT/m3 and 50.0 mT/m2 with oscillation frequency of ω0/2pi=4.8 kHz.
University
of Freiburg Medical Center parameters were: TR=700 ms; TE=11.2 ms; bandwidth=78.125
Hz/pixel; flip angle=20°; slice thickness=5 mm, maximum C3 strength=293.9 mT/m3
with oscillation frequency of ω0/2pi=5 kHz.
Undersampling
in the phase encoding direction was performed after acquisition during the
image reconstruction by discarding echoes. All calculations were performed in
MATLAB (MathWorks Inc, Natick, Massachusetts, USA). All reconstructions were
performed via a conjugate gradient algorithm with 10 iterations using the GPU. Results
Figure 2a shows improving
image quality as function of increasing NLG waveforms added to a Cartesian
trajectory. The FRONSAC encoding reduces the undersampling artifact, particularly
in the presence of 2 or more waveforms, which provide more degrees of freedom
to manipulate the sampling function. Figure
2b shows the addition of NLGs in FRONSAC2 better condition the data for a
compressed sensing approach, while no benefit is seen in under sampled
Cartesian data.
FRONSAC is resilient to experimental
imperfections including timing errors (Figure 3a) and off-resonance spins
(Figure 3b), and the resulting artifacts are indistinguishable from well-known
and generally benign Cartesian artifacts. Field purity is also not required
with this approach since the reduction in undersampling artifacts using an
approximate C3 shape is similar to comparable pure C3 FRONSAC1 (Figure 3c).
Figure
4 shows that once a FRONSAC NLG waveform has been well characterized by spatial
and temporal mapping, it can be applied to a variety of different Cartesian
scan prescriptions and still produce profound improvements in accelerated image
quality.
Figure 5 demonstrates
that FRONSAC is synergistic with other acceleration strategies such as turbo
spin echo (TSE) imaging and FRONSAC gradients do not interfere with the standard
contrast. Conclusion
FRONSAC
represents highly effective general tool for increased spatial encoding
efficiency that can lead to significant further reductions in scan times. Acknowledgements
This
works was funded by the National Institutes of Health under 5R01EB012289-04,
4R01 EB016978-04, K01EB168977 and R01EB022030. We would like to thank Andrew Dewdney, Keith
Heberlein, and Rodney Mick from Siemens for hardware support. We would like to
thank Stefan Kroboth for his help imaging with the Freiburg nonlinear gradient
setup and Dr. Ying-Hua (Eva) Chu for providing the field camera and for support
with the corresponding measurements. We would also like to thank Terry Nixon
and Scott McIntyre for support with the Yale nonlinear gradient hardware. References
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