Teresa M Correia1, Torben Schneider2, and Amedeo Chiribiri1
1School of Biomedical Engineering and Imaging Sciences, King's College London, London, United Kingdom, 2Philips Healthcare, Guildford, United Kingdom
Synopsis
First-pass perfusion cardiac MR (FP-CMR) is one
of the methods of choice for evaluating myocardial ischemia. Moreover, quantitative
FP-CMR methods that provide pixel-wise quantitative myocardial perfusion maps are
increasingly being applied as an alternative to visual inspection. Recently, a
DIRect QuanTitative (DIREQT) FP-CMR model-based reconstruction has been
proposed to directly estimate myocardial perfusion maps and highly accelerate
FP-CMR scans. Here, DIREQT is combined with the idea of view-sharing and KEYhole
imaging (DIREQT-KEY) to improve DIREQT reconstructions, particularly from
extremely accelerated FP-CMR acquisitions. DIREQT-KEY directly generates high-quality
quantitative myocardial perfusion maps from less than 4 radial spokes per time
frame.
Introduction
First-pass perfusion
cardiac MR (FP-CMR) is an emerging non-invasive tool for evaluating coronary
heart disease (CHD). Recently, FP-CMR methods that provide pixel-wise
quantification of myocardial perfusion have gained increased interest as an
alternative to visual inspection.1-3 Typically, these methods indirectly
generate quantitative myocardial perfusion maps by first reconstructing
individual dynamic contrast-enhanced images, which are then converted to
contrast agent concentration and, finally, tracer-kinetic (TK) modeling is used
to generate quantitative maps. However, FP-CMR time frames must be acquired in
real-time to capture the rapid passage of a contrast agent bolus through the
heart, and hence, the spatial resolution and coverage of the heart is
compromised.4,5 Undersampled reconstruction methods have been proposed
to moderately accelerate FP-CMR acquisitions as a means to improve spatial
resolution.6-9 Recently, a DIRect QuanTitative (DIREQT) FP-CMR
reconstruction method has been proposed to directly estimate quantitative TK
maps from highly undersampled acquisitions, by exploiting the redundancy of
spatial information between time frames.10 However, some TK models only
use the key frames of contrast arrival for quantitative analysis. Nonetheless, high spatial frequencies from the k-space periphery of the
non-key frames (or additionally acquired frames) may contain useful information
that could be shared to improve DIREQT reconstructions from highly accelerated
FP-CMR data. In this
work, DIREQT is combined with the idea of view-sharing and KEYhole imaging11
(DIREQT-KEY) to improve the quality of the TK maps, particularly from extremely
accelerated FP-CMR acquisitions. The proposed method was tested in four
patients with suspected CHD.Methods
Acquisition Rest FP-CMR fully-sampled acquisitions were
performed in four patients with suspected CHD (ethically approved; informed written consent obtained) using a dual-bolus technique with
0.0075+0.075mmol/kg Gadobutrol (Gadovist; Bayer, Germany). Patients 1&2
were scanned on a 3T Philips Achieva scanner and patients 3&4 were scanned on
a 1.5T Philips Ingenia scanner (Philips Healthcare, Netherlands). A
saturation-recovery turbo field echo (TFE) sequence was used to acquire one
short-axis slice in free-breathing using the following parameters: FOV=320x320mm2,
resolution=2.8x2.8mm2, slice thickness=10mm, TS/TR/TE= 120/1.96/0.93ms,
flip angle=15deg, acquisition window=224-228ms, total acquisition time=1min20s,
dynamic frames=90-125, and
contrast agent relaxivity=5.0 L/mmol·s. The AIF was found using a region of
interest in the left ventricle. The fully-sampled dynamic images were used to
estimate the frame-to-frame translational motion. Then, translational motion
correction was performed directly in k-space to generate motion-corrected
datasets.
Reconstruction Radial (k-t)-space sampling was used to
generate 40x (3 spokes), 60x (2 spokes) and 120x (1 spoke) undersampled
datasets, which were reconstructed using DIREQT and DIREQT-KEY (Fig.1). The
DIREQT method directly estimates TK parameter maps from the measured multicoil
(k-t)-space FP-CMR data. This is achieved by solving the following optimization
problem: $$$\widehat{\textbf{M}}=\underset{\textbf{M}}{\arg\min}\parallel\textbf{d}-f(\textbf{M})\parallel_2^2$$$, where $$$\textbf{M}$$$ are the TK parameters maps (e.g. KTrans and vp of
the Patlak model), $$$\textbf{d}$$$ is the undersampled (k-t)-space data and $$$f$$$ is the forward model (indicated by the small red arrows in Fig. 1a). A
limited memory BFGS quasi-Newton method was used to solve this nonlinear
inverse problem. Three
different versions of DIREQT-KEY were tested (Fig. 1b): 1) a central “keyhole”
keeps the acquired (k-t)-space data and the peripheral data from the non-key frames are shared; 2) same as 1, but the central region also
shares the weighted down (k-t)-space data from the non-key frames; 3) same as 1, but exponentially weighted down data from adjacent times
frames is used in each “keyhole". In the latter, most weights will be closer to
zero, except for the 4 closest time frames. Results and Discussion
Figure
2 shows the DIREQT and DIREQT-KEY reconstructions obtained for patient 1. The structural
similarity index (SSIM) indicates that all three versions of DIREQT-KEY generate
TK maps with superior image quality compared to the DIREQT method. The highest
SSIM was achieved with DIREQT-KEY version 2, which indicates a better agreement
with the reference. Hence, the remaining analysis was done using DIREQT-KEY
version 2. Figure 3 shows the quantitative maps obtained for patients 2-4 using
the DIREQT and DIREQT-KEY methods. Patient 2 had myocardial infarction and
patient 4 hypertrophic cardiomyopathy. Patients 1 and 3 had no
abnormalities on CMR. The perfusion defect in Patient 2 was identified
in both DIREQT and DIREQT-KEY maps and corresponds to an area of myocardial scarring. DIREQT-KEY improvements are more
noticeable for Patient 1&4 since these had more extra frames. However,
additional time frames could be acquired to improve DIREQT-KEY maps (Fig. 4-5).
DIREQT and DIREQT-KEY
provide high-quality maps even at extremely high acceleration rates (Fig. 3-5).
However, DIREQT-KEY provides the highest (SSIM) quality TK maps (Fig. 5). Spatial
regularization could be used to reduce noise amplification at high
accelerations. Conclusion
The proposed
DIREQT-KEY, combines DIREQT, a model-based reconstruction approach, with view-sharing
and keyhole imaging. Similar to DIREQT, DIREQT-KEY allows extremely high FP-CMR
scan acceleration factors (< 4 radial spokes) and quantitative imaging.
However, DIREQT-KEY provides higher quality TK maps. Moreover, DIREQT-KEY works
with existing (k,t)-sampling, dual-bolus and dual-sequence acquisitions
strategies. These aspects enhance the clinical applicability of the method. In
future studies, the DIREQT-KEY method will be evaluated in a large cohort of
patients with suspected CHD using prospectively undersampled acquisitions. These
studies will also aim to achieve much higher spatial resolution and coverage, and
hence, greater diagnostic accuracy. Acknowledgements
This work was supported by the Wellcome/EPSRC Centre
for Medical Engineering [WT 203148/Z/16/Z].References
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