Gastao Cruz1, Kerstin Hammernik2,3, Thomas Kuestner1, Daniel Rueckert2,3, René M. Botnar1, and Claudia Prieto1
1School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom, 2Technical University of Munich, Munich, Germany, 3Department of Computing, Imperial College London, London, United Kingdom
Synopsis
Motion-resolved reconstructions are standard for cardiac
CINE imaging by splitting data into multiple cardiac phases across several
heartbeats. Consequently, the reconstruction of each phase is highly
ill-posed, since only a subset of the data are used to
reconstruct it. In this work a novel motion corrected framework is developed
for highly accelerated cardiac CINE imaging. Each cardiac phase is
reconstructed with a motion corrected reconstruction and jointly regularized
with every other motion corrected cardiac phase via a non-rigidly aligned
patch-based denoiser. This approach leads to a substantial improvement in image
quality, enabling highly accelerated CINE images from a single heartbeat.
INTRODUCTION:
Cardiac CINE imaging is commonly obtained via
retrospective cardiac gating, by binning the acquired k-space data into
different cardiac phases (i.e. bins). Motion resolved Compressed Sensing
reconstructions have enabled considerable acceleration factors for this
application primarily by exploiting the redundant information along time.1,2,3
Motion corrected reconstructions4,5,6,7 can make use of all the
acquired data when the motion is known, which has higher theoretical
performance. Here we extend the general motion correction formulation4
to include soft-weighting and propose a novel regularization term based on
non-rigidly aligned patch-based reconstruction (PROST).8 By
reconstructing each cardiac phase as a motion corrected image the effective
undersampling factor is substantially reduced, leading to improved image
quality and enabling single-slice CINE imaging from a single heartbeat. The
proposed single heartbeat Motion Corrected CINE (MC-CINE) reconstruction was
tested in five healthy subjects and compared to conventional iterative SENSE
(itSENSE)9 and motion resolved XD-GRASP reconstructions.1METHODS:
The proposed framework
can be divided in four steps: 1) ECG-binning; 2) auxiliary XD-GRASP
reconstruction; 3) motion estimation via image registration; and 4) motion
corrected reconstruction for each cardiac frame (Fig.1). A preliminary motion
resolved reconstruction using XD-GRASP (temporal total variation) is performed
to produce an initial CINE reconstruction; these images are used to estimate
the non-rigid cardiac motion between all cardiac phases via free-form
deformation image registration.10,11 Once the motion fields between
all cardiac phases are known the proposed MC-CINE is applied to reconstruct
motion corrected images for each cardiac phase:
$$ L(x)= argmin_{x} ||W_n(Σ_nA_nFCM_nx-k)||_2^2 + \lambda Σ_b ||T_b||_* , s.t. T_b=Q_b((M_n)^Hx)$$
where
$$$W_n$$$ are
soft-weights for cardiac phase n, $$$A_n$$$
is
the corresponding sampling trajectory, $$$F$$$ is the Fourier transform, $$$C$$$ are coil sensitivities, $$$M_n=[U_n^1,...,U_n^m]^T$$$
are the motion fields
from
each cardiac phase m towards every cardiac phase n, $$$x=[x^1,...,x^m]^T$$$
are
the motion corrected CINE images
for
each cardiac phase m, $$$k$$$
is
the acquired k-space data and $$$Q_b$$$
assembles
a 3D PROST tensor from non-rigidly aligned cardiac phases for a local patch around pixel b.EXPERIMENTS:
Five healthy subjects were scanned on a 1.5T scanner (Philips Ingenia). Imaging
parameters included field
of view (FOV) = 256x256 mm2; 8 mm slice thickness; resolution = 2x2
mm2; TE/TR = 1.16/2.3 ms; radial tiny golden angle; flip angle 60º; 8960
radial spokes acquired; nominal scan time ~20s; breath-hold acquisition. Data were
reconstructed to produce 20 cardiac phases using itSENSE, XD-GRASP and the
proposed MC-CINE (n=m=20) with three different retrospective
acceleration factors of 1x (8960 spokes), 10x (896 spokes) and 20x (448 spokes),
corresponding to effective acquisition times of ~20s, 2s and 1s, respectively. RESULTS:
Cardiac CINE frames from
two representative subjects are shown in Fig.2 and Fig.3 for itSENSE, XD-GRASP
and MC-CINE at multiple acceleration factors. Residual streaking and blurring
artefacts are observed with itSENSE, particularly with 896 and 448 spokes. These
artefacts are reduced with XD-GRASP, but some blurring and residual incoherent
aliasing can still be observed, particularly with 448 spokes. MC-CINE achieves
the sharpest images with minimal artefacts, such that images with 448 spokes
(1s acquisition) have comparable quality to XD-GRASP with 8960 spokes (20s
acquisition). In Fig.4 a CINE animation shows normal cardiac contraction for
all methods; however, considerably more artefacts are observed for itSENSE (column 1) and
XD-GRASP (column 2), particularly with increasing acceleration. Consistent image quality is obtained with MC-CINE (column 3) even with 1s worth of data (row 3). A 1D temporal profile for
a representative subject is shown in Fig.5 where all the dynamics of cardiac
motion are correctly captured by all methods, with higher blurring and residual
noise/incoherent aliasing observed for XD-GRASP and itSENSE. Again, MC-CINE
with 448 spokes (1s acquisition) presents comparable quality to itSENSE and
XD-GRASP with 8960 spokes (20s acquisition).CONCLUSION:
A novel approach based on Motion Corrected CINE (MC-CINE) reconstruction
regularized by a non-rigidly aligned patch-based denoiser is proposed and
compared with conventional itSENSE and motion resolved XD-GRASP. MC-CINE
reconstructions from 1s CINE data acquisition present comparable quality to
itSENSE and XD-GRASP reconstructions from 20s data acquisition. The proposed
approach could enable higher resolution for CINE, real-time exercise CINE (i.e.
cardiac and respiratory motion corrected) and/or whole-heart multi-slice coverage
from a single breath-hold which will be investigated in future work.Acknowledgements
ACKNOWLEGDMENTS: This
work was supported by EPSRC (EP/P001009, EP/P032311/1, EP/P007619/1) and
Wellcome EPSRC Centre for Medical Engineering (NS/ A000049/1).References
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