Richard Thompson1, Christopher Keen1, Hefin Jones2, Richard Coulden2, Peter Seres1, and Justin Grenier1
1Biomedical Engineering, University of Alberta, Edmonton, AB, Canada, 2Radiology & Diagnostic Imaging, University of Alberta, Edmonton, AB, Canada
Synopsis
Keywords: Pulse Sequence Design, Lung, UTE, Heart Failure, Cartesian
The Cartesian UTE (CUTE) sequence
provides high quality three-dimensional imaging of the lung parenchyma (TE =
140 us) without the requirement for k-space gridding in a short breath-hold. Phantom
validation and comparison to an existing UTE sequence (Spiral VIBE) is provided
in 64 healthy subjects and in clinical examples.
INTRODUCTION
Quantitative imaging of
the lung parenchyma requires ultrashort echo time (UTE) acquisitions, typically
with TE ≤ 150 µs to avoid excessive signal decay (T2* ~2ms at 1.5T and ~0.7ms
at 3.0T)1, which necessitates
non-Cartesian center-out k-space trajectories.
The required Cartesian gridding of k-space prior to image reconstruction
is computationally demanding and sensitive to gradient imperfections and timing
errors that can give rise to artifacts and signal non-uniformity that may limit
or preclude quantitative applications, in particular, quantitative imaging of
lung water density.2 As an alternative, we
propose a three-dimensional (3D) gradient-echo Cartesian UTE (CUTE) acquisition approach that
combines two separate half-k-space readouts to enable UTE with k-space sampling
directly on a Cartesian grid. The CUTE approach was compared to the available Spiral
VIBE UTE3 method in phantoms, in
a large cohort of healthy subjects and clinical examples.METHODS
Figure 1 displays the
proposed pulse sequence for the 3D gradient-echo CUTE approach. A non-selective rectangular radiofrequency
(RF) excitation pulse enabled full-torso spatial excitation and minimal
excitation duration. Each ky and kz phase-encoding step
was acquired separately with both a positive (kx+) and a
negative readout gradient, kx- (Fig. 1A). The readout gradient pre-phaser enabled 50%+ΔKx coverage
of kx-space for both readout directions for sampling of the middle
of k-space over a range ±ΔKx for both readouts
(Fig. 1B). The minimum achievable TE was
used for each k-space point, TE (ky,kz), with the
shortest times at the middle of k-space. The repetition time (TR) was held constant. CUTE
was compared to Spiral VIBE UTE1 approach for phantom and in-vivo
acquisitions.
MRI
Acquisition: CUTE - 400x500x300
mm FOV (read-encoding superior-inferior), TE=140μs
(260μs at edge of k-space),
TR=1.7ms, 1595 Hz/pixel, GRAPPA=2, 128x160x64 matrix (3.125x3.125x5mm,
reconstructed to 2.08mm isotropic), 2° flip angle, 13 seconds
acquisition (breath-hold). 3T PRISMA and
1.5T AERA scanners (Siemens, Erlangen, Germany) using 18 chest/32 back coil array
for reception. Spiral VIBE - 550x550x336mm
FOV, TE=50 ms, TR=2.46 ms, 945
Hz/pixel, 192x192x96 (2.86x2.86x3.5mm reconstructed to 1.43x1.43x3.5mm) 10 seconds
acquisition (only available at 3T).
Phantom
Experiments: CUTE
and Spiral VIBE acquisitions were performed on a composite water and fat
phantom with repeated studies using a 0Hz and 200Hz off-resonance field shift
to evaluate off-resonance performance (3T).
In-Vivo
Experiments: CUTE
and Spiral VIBE acquisitions were performed on 65 healthy subjects (end-expiration
breath-hold) (3T). One healthy subject
was imaged with the CUTE method at 1.5T and 3.0T with additional illustrative
clinical cases also at 1.5T.
In-Vivo Image
Processing: A
previously reported processing pipeline was used to perform image normalization
to units of relative lung water density (rLWD)
and segmentation of the lung parenchyma to provide lung water density quantification.2 In addition to average rLWD, total lung parenchyma water volume was calculated as rLWV = ΣrLWD·voxel_volume. Finally, segmented rLWD images for all 64 subjects were
resampled on a grid (32(RL)x32(HF)x10(CB) pixels) to generate average regional rLWD maps. Airway signal intensities in the trachea,
ideally a noise region, were measured to assess the artifact level, in the same
units of rLWD.
RESULTS
Phantom studies illustrate the
superior performance of CUTE as compared to Spiral VIBE in terms of reduced
sensitivity to blurring from off-resonance effects from global field shifts and
fat (Fig. 2). Mean whole-lung values of rLWD and rLWV and total lung volume were similar for CUTE and Spiral VIBE
(p>0.05) but with significantly higher artifact level (mean airway signal)
for VIBE, p<0.05 (Fig. 3). Spiral
VIBE had some cases of artifacts and consistent patterns of spatial heterogeneity in rLWD as compared to
CUTE that were consistent in all 64 subjects (Fig. 3). Repeated CUTE scans in one volunteer at 1.5T
and 3.0T showed consistent appearance and similar rLWD and rLWV values
measured over the whole lung volume (Fig. 4). Clinical examples illustrated the
measurement of increased water density, globally in a case of chronic heart
failure, and regionally in cases of pulmonary hypertension and dilated
cardiomyopathy (CUTE, 1.5T) (Fig. 4). Average values for lung water content and
volumes were similar between CUTE and Spiral VIBE (Fig. 5). All CUTE image
reconstruction was performed online (~25 seconds using the Siemens FIRE
application).DISCUSSION
The Cartesian UTE (CUTE) sequence
was shown to provide high quality three-dimensional imaging of the lung
parenchyma without the requirement for k-space gridding in a short breath-hold
(140μs echo time). In comparison to the
available Spiral VIBE UTE sequence, CUTE was shown to have more uniform lung
water density values over space and significantly less dependence on
off-resonance frequencies. Acquisition
of k-space on a Cartesian grid enabled fast on-scanner reconstruction and
eliminated the signal non-uniformities observed with the non-Cartesian Spiral
VIBE sequence. Image quality and quantitative lung water densities were
illustrated to be similar at 1.5T and 3.0T (i.e. field-strength and
gradient-performance independent) and clinical cases at 1.5T showed globally
and regionally elevated lung water content.
CONCLUSION
The Cartesian UTE (CUTE) sequence
provides high quality quantitative three-dimensional imaging of the lung parenchyma without
the requirement for k-space gridding in a short breath-hold acquisition.Acknowledgements
No acknowledgement found.References
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