4D flow MRI is time consuming, since it requires the acquisition of time-resolved images with three-directional velocity encoding. Undersampled reconstruction techniques have been proposed to accelerate 4D flow carotid imaging, however scan time remains lengthily for high-resolution acquisitions. In this work, we propose to further accelerate 4D flow carotid MR imaging by exploiting patch-based similarities in local, non-local and multi-contrast dimensions with high-dimensional patch-based undersampled reconstruction (HD-PROST). The results show similar velocities for both k-t SENSE and the proposed HD-PROST, however higher precision was obtained with HD-PROST.
HD-PROST has been recently introduced [3] to jointly reconstruct multi-contrast MR images by exploiting the high redundancy in information, on local (similar patches within a neighborhood) and non-local (between patches) scales, and the strong correlation shared between the multiple contrast images. For 4D flow carotid imaging all the cardiac phases for the different velocity encodings (VE) can be considered as different contrasts, and thus correlation in that direction can be exploited for joint reconstruction. This joint multi-contrast undersampled reconstruction can be formulated as the following joint optimization problem:
$$\mathcal{L}(X,\mathcal{T}):=\underset{X,\mathcal{T}}{\arg\min} \frac{1}{2}||EX-Y ||^2_F + \sum_{p} \lambda_p ||\mathcal{T}_p||_* \quad s.t.\mathcal{T}_p = R_p(X) $$
Where $$$Y$$$ denotes the acquired undersampled data, $$$E$$$ is the encoding operator (including coil sensitivities, Fourier operator, and sampling), and $$$X$$$ denotes the multi-contrast MR images to reconstruct.
The operator $$$R_p(.)$$$ constructs a third order tensor of similar 3D patches from the patch $$$p$$$ centered at pixel $$$p$$$ (see optimization 2). The nuclear norm is used to enforce multi-dimensional low-rank on a multi-contrast patch scale and $$$\lambda_p > 0$$$ controls the strength of sparsity. This optimization problem can be solved via alternating direction method of multipliers (ADMM) by iteratively solving the two following sub-problems:
Optimization 1: A regularized multi-contrast MR reconstruction (optimization on $$$X$$$) is performed using the multi-contrast denoised volume ($$$\mathcal{T}$$$) obtained from optimization 2 as prior knowledge. This optimization is solved using the conjugate gradient (CG) algorithm.
Optimization 2: A high-order denoising on a patch level (optimization on $$$\mathcal{T}_p$$$) is performed by building a 3D tensor from similar 3D+L patches (L being the concatenation of velocity encodings and cardiac phases) and applying a high-order singular value thresholding. The denoised images are then obtained by patch aggregation and used as prior in optimization 1 (Fig.2).
Experiments:
4D flow MRI acquisition was performed free-running (with retrospective ECG synchronization) in three healthy subjects. Acquisitions were performed on a 1.5T scanner (Siemens Magnetom Aera). VE with minimal TE was applied to obtain a reference image and encoding in three directions (x,y,z) [4]. A free-running variable density Cartesian sampling with spiral-like ordering and golden angle step was employed (Fig.1) [3,5]. Acquisitions were performed with a 3D gradient echo sequence using undersampling factors of 2 (17:43 min), 4 (8:52 min), and 8 (4:35 min). Acquisition parameters included: FOV = 200 × 214 × 45 mm3; resolution 0.9 × 0.9 ×1.5 mm3; TR/TE =9.1/4.55ms; FA=15º, and maximum VE = 100cm/s.
Two frameworks were compared to reconstruct 10 cardiac phases: iterative kt-SENSE with TV constraint in the time direction [6], and the proposed HD-PROST. In the first approach each of the three VE and reference are reconstructed separately, while HD-PROST takes advantage of the redundant information across cardiac phases and VE contrasts to reconstruct them simultaneously.
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[3] Bustin A, Ginami G, Cruz G, et al. Five-minute whole-heart coronary MRA with sub-millimeter isotropic resolution, 100% respiratory scan efficiency, and 3D-PROST reconstruction. Magn Reson Med. 2018;00:1–14.
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