Joseph W Plummer1,2, Abdullah S Bdaiwi1,2, Stephanie A Soderlund1, Matthew M Willmering1, Jason C Woods1,3,4,5, Zackary I Cleveland1,2,4,5, and Laura L Walkup1,2,4,5
1Center for Pulmonary Imaging Research, Department of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States, 2Department of Biomedical Engineering, University of Cincinnati, Cincinnati, OH, United States, 3Department of Physics, University of Cincinnati, Cincinnati, OH, United States, 4Department of Radiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States, 5Department of Pediatrics, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, United States
Synopsis
Keywords: Hyperpolarized MR (Gas), Image Reconstruction
Hyperpolarized
129Xe MRI is a powerful pulmonary imaging modality to assess regional ventilation,
gas exchange, and lung microstructure. However, non-equilibrium magnetization decay and
relatively long breath-hold durations remain major limitations to routine
clinical dissemination. While non-Cartesian sampling methods can improve
sampling efficiency, these methods are yet to be combined with non-linear
reconstruction methods like compressed sensing to further increase speed and
reduce image noise. Here, we implement compressed-sense reconstructions across
a range of non-Cartesian
129Xe MRI techniques and show that SNR and image quality can
all be improved while reducing scan time.
Introduction
Hyperpolarized
Xe MRI is a powerful pulmonary imaging modality used to assess gas distribution
(ventilation1), airspace
dynamics (diffusion-weighted2), and gas-transfer to the red-blood
cells (gas-exchange3). Typically, Xe MRI scans are performed
within a ≤16-second breath-hold, limiting the attainable SNR, resolution, and
dynamic information. Non-Cartesian methods, including 2D-spiral and 3D-FLORET,
have improved sampling efficiency4; however, they are yet to be combined
with non-linear reconstruction methods like compressed sensing (CS). Here, we
demonstrate CS reconstructions across a range of non-Cartesian Xe MRI
techniques, and show that SNR, imaging speed, and image quality are improved.Theory
Non-Cartesian
measurements can be reconstructed into an image, $$$x$$$, by solving the following forward
model problem:
$$b = Ax + ε, \tag{1}$$
where $$$b$$$ is the k-space data; $$$A$$$ is the measurement matrix; and $$$ε$$$ is the additive noise. (1) is
solved by matrix inversion of $$$A=DF$$$ with $$$b$$$, where $$$D$$$ is the density compensation used to
precondition $$$A$$$, and $$$F$$$ is the non-uniform fast Fourier transform5 (NUFFT). However, the inverse model
approach ($$$A^{-1}$$$) is not robust to under-sampled
measurements or ill-conditioned $$$A$$$—as is often the case for non-Cartesian
sampling—leading to noisy reconstructions.
Alternately,
(1) can be solved using iterative optimization methods by recasting to a regularized
least squares problem, like an iterative NUFFT6. Such methods enable the use of
regularizers to converge on solutions that have minimal energy in some transformed
domain. A common example is the multi-regularizer CS problem7:
$$x^\star=\underset{x}{\min}\frac{1}{2}|| Ax -b ||_2 + \lambda_1 ||W(x)||_1 + \lambda_2||G(x)||_2, \tag{2}$$
where
the reconstructed image, $$$x^\star$$$, is regularized ($$$\lambda_i$$$) for both wavelet-transform energy ($$$W(x)$$$; efficient for preserving edges/low contrast
information) and total variation ($$$G(x)$$$; efficient at suppressing noise/streaking). To
date, such methods have yet to be rigorously investigated in non-Cartesian Xe
MRI. Here, we compare reconstructions using $$$A^{-1}$$$ versus CS
in ventilation, diffusion-weighted, and gas-exchange imaging.Methods
Seventeen
healthy subjects (21-65 y.o.; 10M/7F) were imaged after obtaining informed
consent per a protocol approved by our local Institutional Review Board
(2014-5279 with FDA IND-123,577). 86%-enriched 129Xe was polarized
to 30-40% using a continuous-flow hyperpolarizer (Polarean 9820A, Durham, NC)8. Images were collected on a Philips 3T-Ingenia
scanner with a custom chest coil (Clinical MR solutions, Brookfield, WI). Simulated
point-spread functions/ventilation sequences included: 2D-radial, 2D-spiral, 3D-radial,
and 3D-FLORET4; diffusion-weighted: 2D-spiral2; gas-exchange: 3D-radial9. Technical parameters are included in figure
captions.
$$$A^{-1}$$$ images were reconstructed via density-compensated
inverse NUFFT5,10. CS images were
reconstructed using the alternating direction method of multipliers
algorithm11 in SigPy12. $$$\lambda_1$$$ and $$$\lambda_2$$$ ranged from 1x10-5 to 1x10-3. Statistical differences were assessed with Wilcoxon signed-rank tests.
Results
Figure
1 contains simulated point-spread functions to examine noise incoherence using 100% and 50%
of projections for 2D-radial/spiral and 3D-radial/FLORET
acquisitions. The same settings are
demonstrated in ventilation imaging (Figure 2). In all cases, CS increased SNR/image
quality, even with 50% sub-sampling.
$$$A^{-1}$$$ and CS reconstructions
are shown for diffusion-weighted imaging (single subject: Figure 3A/B; all
subjects: Figure 3C/D). CS significantly increased SNR across all b-values (P<0.01),
preserved the mean apparent diffusion coefficient (ADC) (P=0.63), and
decreased ADC variation (P<0.01).
Gas-exchange
reconstructions are shown in Figure 4A/B. CS reduced streaking artifacts, increased
SNR, and preserved phase. Additionally, CS preserved the median signal
intensity, μ, and reduced variation, σ, and skewness, ν (Figure
4C/D).
Finally, 50%
sub-sampled gas-exchange reconstructions were performed with CS in a healthy
cohort (Figure 5). Mean SNR increased significantly (P<0.01) using CS
in 100% and 50% sampling relative to $$$A^{-1}$$$. μ was preserved, while σ decreased
(dissolved) and ν increased
(gas/dissolved) significantly (P<0.05).
Discussion
CS most
benefits under-sampled acquisitions that produce incoherent noise/aliasing. Point-spread
functions for sub-sampled radial projections demonstrate this, as 50% and 100% sub-sampled
reconstructions varied only by an incoherent noise floor (Figure 1A/B). Point-spread
functions for sub-sampled spirals showed similar patterns inside the
field-of-view, with coherent aliasing only appearing on the edges (Figure 1C/D).
Consequently, when applied to ventilation (Figure 2), CS suppressed noise and increased
SNR for all sequences. Notably, improvements in 3D-radial/FLORET (even with 50%
sub-sampling) suggest that significant reductions to scan duration are possible
(i.e., decreasing required breath-hold from 16- to 8-seconds).
CS also
improved diffusion-weighted imaging, increasing SNR for each b-value image by
>50% (Figure 3C), thereby reducing ADC measurement uncertainty13 (Figure 3D). Consequently, CS reduced the
variation in ADC, while preserving the mean.
Gas-exchange
MRI is prospectively under-sampled to fit within a 16-second breath-hold (~19%-Nyquist)
and suffers from low Xe solubility in pulmonary tissues (<14%)14, ultimately
limiting gas/dissolved-phase signal. However, in Figures 4/5, CS increased SNR
~two-fold in both gas and dissolved-phases. Across the healthy cohort, CS
preserved μ while decreasing σ, consistent with noise suppression. CS
increased ν, consistent with underlying bias-field
effects or gravitational-induced physiology (especially in the dissolved-phase)
being uncovered. Gas-exchange images exhibited largely incoherent noise when using
50%-total projections, which CS effectively suppresses. The mean SNR increased
for 50% sub-sampled CS compared to 100% sampled $$$A^{-1}$$$ reconstructions, while μ/σ were preserved/reduced (Figure 5C-F).
Practically, a CS-reconstructed, 50% sub-sampled 3D-radial gas-exchange
sequence reduces a breath-hold by two-fold, becoming more feasible for young
children and advanced lung disease patients.Conclusion
This work
demonstrates that combining non-Cartesian sampling with CS reconstruction improves
SNR/image quality while reducing scan duration in Xe ventilation,
diffusion-weighted, and gas-exchange MRI.Acknowledgements
The authors would also like to thank hyperpolarized
gas research assistant: Carter McMaster; MRI technologists: Kaley Bridgewater,
Kelsey Murphy, Sarah Miozzi, and Matthew Lanier; clinical
research coordinators: Priyanka Desirazu, Megan Schmitt, and Alex Rizkallah; and the research nurses at Cincinnati Children’s Hospital.References
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