Dynamic Contrast-Enhanced imaging is an important tool in diagnosing hepatic diseases. Improving spatiotemporal resolution is of great significance for clinical purpose. In this work we introduce the partial separability constraint to the reconstruction of stack-of-stars golden angle radial data. Both in-vivo and stimulated liver experiment were conducted and the proposed method (PS+S) showed better reconstruction quality compared to the existing methods without partial separability constraint.
The aim of proposed method is to minimize the following cost function.
$$\tilde{U_{s}}=arg min\left\{\parallel F\cdot S\cdot U_{s} \cdot V_{t}-m\parallel_2^2+\gamma_{t}\phi_{t}(U_{s}\cdot V_{t})+\gamma_{s}\phi_{s}(U_{s}\cdot V_{t})\right\}$$ where m is the sampled k-t-space signal arranged in Casorati matrix form, S represents the SENSE encoding map and F is the non-uniform Fourier transform. $$$\phi_{t}$$$ is the temporal sparsity constraint, and $$$\phi_{s}$$$ is the spatial penalty. To extract temporal projection more efficiently, the redundancy of sampling in the center of k-space is exploited. $$$V_{t}$$$ is estimated a priori by applying principal component analysis on the temporal dimension of image-series, which is reconstructed by zero-padded central k-space signal. The selection of $$$V_{t}$$$’s rank is a trade-off between preserving structural and dynamic information, which will be discussed in the latter section. The initial value of $$$V_{t}$$$ is obtained by multiplying the pseudo-inverse of $$$V_{t}$$$ with $$$d\prime$$$, which is the NUFFT solution to the inverse problem, to minimize the number of iterations. In all experiments, the number of conjugated gradient iterations are same for both methods.
Experiments: The test was conducted on two sets of data. In the simulated experiment, we generated the simulated series of images from an in-vivo acquired T1-weighted hepatic imaging. Aorta, portal vein, and liver tissue were selected as ROIs. From a pre-fitted equation described in [4, 5, 6], the AIF (arterial input function) curve, PIF (portal venous input function) curve and liver tissue curve were generated. In the in-vivo experiment, we scanned a healthy volunteer on a 3.0T Phillips scanner (Achieva, Philips Healthcare, Best, Netherlands) with 36-channel cardiac coils. The parameters are following: FOV=320×320×200$$$mm^{3}$$$, Flip Angle=20°, TR/TE= 3.60/1.44ms, in-plane resolution=1.25×1.25$$$mm^{2}$$$. 1280 radial projections were acquired with 256 readout points in each line. Gd-DTPA with concentration of 0.1mmol/kg was injected at 2 ml/s, and the acquisition started simultaneously.
Analysis Methods: Each frame was reconstructed by 21 spokes in both scenarios. Non-linear conjugated gradient method was used for the optimization. In simulation, the concentration curve were calculated and the parameter was fitted to the curve, in order to measure the fidelity. In in-vivo experiment, standard deviation of a small blank region without streaking artifacts was assumed to be background noise level and was used to calculate the SNR.
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Table 1 RMSE comparison
for reference, GRASP and PS+S results.
Table 2 The signal-to-noise ratio of in-vivo data. Standard deviation of a small blank region without obvious streaking artifacts is assumed to be background noise level.