Gastao Cruz1, Jesse Hamilton1,2, Evan Cummings1,2, Vikas Gulani1, and Nicole Seiberlich1,2
1Radiology, University of Michigan, Ann Arbor, MI, United States, 2Biomedical Engineering, University of Michigan, Ann Arbor, MI, United States
Synopsis
Keywords: Motion Correction, Low-Field MRI, Real-time
Motivation: Real-time cardiac MR could provide new insights into function of the myocardium while avoiding artefacts arising from cardiac and/or respiratory motion.
Goal(s): High temporal resolution real-time cardiac MR is particularly challenging at low field (0.55T) due reduced SNR and coil elements available on commercial systems.
Approach: Here, we leverage motion compensated reconstructions and Hermitian symmetry to enable the highly undersampled reconstructions required for real-time cardiac MR at low field.
Results: Experiments at 0.55T show that the proposed approach enables imaging with a temporal resolution of 6 ms (R~48x) with minimal aliasing, outperforming conventional compressed sensing (considerable aliasing) and parallel imaging (aliasing dominated).
Impact: TR-resolved (6ms
temporal resolution) real-time cardiac is demonstrated at 0.55T where SNR is
limited. Such highly accelerated imaging may reveal finer details in myocardial
function. Additionally, the high acceleration factors achieved here could also
be leveraged for 3D real-time imaging.
INTRODUCTION:
MR
cardiac cine is the gold-standard to evaluate ejection fraction, a key evaluation
of cardiac function, and a predictor/assessor of heart failure. Conventional
cine images are acquired during a breath-hold to avoid respiratory motion
artefacts, but residual artefacts may arise from respiratory drift, arrhythmia
or bulk motion. Real-time imaging is an approach in which images are collected
with a high temporal resolution such that these limitations can be bypassed. However,
high acceleration factors are required for real-time imaging, potentially resulting
in aliasing and noise amplification. While parallel imaging1,2,3 and
compressed sensing4,5,6,7 have been successfully deployed for this application
at 1.5T and above, these methods may be insufficient at lower fields due to
reduced SNR and reduced/sub-optimal number of coils available. Here, we develop
a novel Hermitian Motion Corrected (MCH) reconstruction that
incorporates knowledge of real-time motion and Hermitian symmetry into the
forward model, allowing the MCH approach to tackle high acceleration
factors in low SNR applications. We deploy MCH for 2D real-time
cardiac MR at 0.55T, demonstrating its ability to achieve a temporal resolution
of 6 ms (same as the TR) with a spatial resolution of 2.2x2.2 mm2. The proposed
approach was evaluated in five healthy subjects and compared with iterative
SENSE and Total Variation (TV) reconstructions.METHODS:
The proposed MCH incorporates motion
into the reconstruction8,9 in combination with the Virtual Coil
Concept (VCC)10, further leveraging Hermitian symmetry. MCH
employs the following optimization:
$$\widehat{x}=argmin_{x}\left\|SF\binom{P}{P^{*}}\binom{C}{C^{*}}Mx-\binom{s}{s'}\right\|_{2}^{2}$$
where x is the real-time image series; S is
the sampling trajectory; F is the Fourier transform; P is the image phase; C are coil sensitivities; s are the acquired k-space data; $$$s'(k)=s^{*}(-k)$$$ (where k denotes the k-space coordinate); and M are
the deformation fields capturing the real-time motion. A single phase map is estimated from a reconstruction of the complete
acquired data. Preliminary spatial and temporal
TV (as employed by XD-GRASP11) reconstruction is performed using
data over 10 TRs (60 ms temporal resolution). Elastic motion is estimated via local
cross-correlation based image registration12,13 of this preliminary
image series. The estimated motion fields (assumed to be smooth over time) are
interpolated to a 6 ms (single-TR) temporal resolution. Finally, the 6 ms
temporal resolution motion fields are incorporated into the proposed MCH
reconstruction (Fig.1).EXPERIMENTS:
Numerical simulations based on MRXCAT14 were performed, with
realistic (respiratory and cardiac) motion, noise, spiral undersampling, phase
inhomogeneities and coil sensitivities. Five subjects were imaged at 0.55T with
FOV=280x280mm2;
8mm slice thickness; resolution=2.2x2.2mm2; TE/TR=1.8/6.3 ms; flip
angle=105º; bSSFP readout; golden angle spiral trajectory (48 arms for full
sampling). Data were reconstructed with iterative SENSE, TV and the proposed MCH
with an acceleration factor of R~48 (6 ms temporal resolution). Iterative SENSE
and MCH were solved with (linear) conjugate gradient; TV was solved
with the non-linear conjugate gradient.RESULTS:
In simulations,
aliasing artefacts dominate the SENSE reconstruction (RMSE=16.3E-2);
considerable aliasing remains in TV (RMSE=7.0E-2); and only minor residual aliasing
remains in MCH (RMSE=2.6E-2)
(Fig.2). Different simulated respiratory and cardiac motion states are
correctly resolved using both MCH and TV, albeit with more
artefacts in the latter; significant aliasing is present with iterative SENSE
(Fig.3). Corresponding performance is observed in vivo, with major,
considerable and minor residual aliasing observed for SENSE, TV and MCH, respectively (Fig.4). Similar
performance can be observed in a second in-vivo case in Fig.5. In both in-vivo
cases, 1D temporal profiles indicate that MCH captures real-time
motion at high temporal resolution with only minimal aliasing, unlike TV and iterative
SENSE. CONCLUSION:
A novel approach
combining Hermitian symmetry (via VCC) with motion corrected reconstructions is
proposed to enable TR-resolved real-time cardiac MR at 0.55T, outperforming
conventional compressed sensing. The high temporal resolution achieved could
reveal finer details of cardiac motion in challenging applications such as
valve imaging or exercise stress imaging, and may be particularly useful for
higher coverage applications (e.g. 3D cine). Continued work will evaluate the
performance of MCH
in a larger cohort and evaluate beat-to-beat ejection fractions to complement
existing functional analysis.Acknowledgements
This work was
supported by the NIH (R01 HL153034, R01HL163991, R01HL163030) and
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