3D imaging sequences such as GRASE or RARE-SoSP are the preferable choice for acquiring ASL images. However, a tradeoff between the number of segments and blurring in the images due to the T2 decay has to be chosen. In this study we propose a reconstruction algorithm based on total generalized variation for reducing the number of segments and therefore the acquisition time of one image. We incorporate the averaging procedure in the reconstruction process instead of reconstructing each image individually. This allows exploiting temporal redundancy and spatial similarity for improving the reconstruction quality of ASL images.
Four healthy volunteers were scanned at a 3T MR system (Prisma, Siemens Healthcare, Germany) using pseudo-continuous ASL labeling with a 3D GRASE readout.9 The following imaging parameters were used: matrix = 64x64x46, 46 slices with 10% slice oversampling, 3mm isotropic resolution, TR/TE=4000/16 ms, EPI-factor=21, TF=17, PLD=1800ms, 9 segments, 4 C/L-pairs resulting in an acquisition time of 4min 48s for the whole k-space. K-space data were retrospectively under sampled as illustrated in Figure 1, using 21 phase encodings in ky which corresponds to an EPI factor of 21. In slice direction every second line is acquired yielding two segments and a third additional segment covering the center of k-space is used for each average (21 central lines of the 17 central slices). For baseline evaluations a synthetic CBF-map was generated.10 Zero mean complex Gaussian noise was added to the C/L-raw-data. For the synthetic dataset 3D coil sensitivity profiles were simulated using Biot-Savart’s law. For in-vivo datasets coil sensitivity profiles were estimated using the method proposed by Walsh.11 The image reconstruction is done solving the following minimization problem using primal dual algorithm12:
$$\min_{u_c, u_l} \frac{\lambda_c}{2}\left\|(MFC\mathbf{1}u_c - U_c^{\delta})\right\|_2^2 + \frac{\lambda_l}{2}\left\|(MFC\mathbf{1}u_l - U_l^{\delta})\right\|_2^2 + \gamma_1(s)TGV_{\alpha1,\alpha0}(u_l) + \gamma_2(s)TGV_{\alpha1,\alpha0}(u_c - u_l)$$
where $$$u_c\,$$$and$$$\,u_l$$$ are the 3D reconstructions, $$$\lambda_c$$$ is the regularization parameter for the control data and set to 11, $$$\lambda_l$$$ is the regularization parameter for the label data and set to 15. The parameter s controls the weighting between the two TGV terms and is calculated as described in13, $$$ U_c^{\delta}\,$$$and$$$\,U_l^{\delta}$$$ are the acquired 4D C/L-images, $$$\alpha1\,$$$and$$$\,\alpha0\ $$$ are fixed model parameters.8 The $$$\mathbf{1}$$$-operator generates a number of identical copies of $$$u_c\,$$$and$$$\,u_l$$$ over the temporal dimension. $$$C$$$ are the coil sensitivity maps, $$$M$$$ is a mask containing the undersampling pattern and $$$F$$$ is the Fourier operator.
This work was funded by the Austrian Science Fund "SFB 3209-18".
NVIDIA Corporation Hardware grant support.
1. Guenther M, Oshio K, Feinberg DA. Single-shot 3D imaging techniques improve arterial spin labeling perfusion measurements. Magn. Reson. Med. 2005:54:491–498.
2. Vidorreta M, Wang Z, Rodríguez I, et al. Comparison of 2D and 3D single-shot ASL perfusion fMRI sequences. NeuroImage. 2013;0:662-671.
3. Alsop DC., Detre JA., Golay X, et al. Recommended implementation of arterial spin-labeled perfusion MRI for clinical applications: A consensus of the ISMRM perfusion study group and the European consortium for ASL in dementia. Magn. Reson. Med. 2015:73:102–116.
4. Shao X and Wang D JJ. Single shot high resolution 3D arterial spin labeling using 2D CAIPI and ESPIRiT reconstruction. Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
5. Ivanov D, Pfeuffer J, Gardumi A, et al. 2D CAIPIRINHA improves accelerated 3D GRASE ASL. Proc. Intl. Soc. Mag. Reson. Med. 25 (2017)
6. Chang YV, Vidorreta M, Wang Z, et al. 3D-accelerated, stack-of-spirals acquisitions and reconstruction of arterial spin labeling MRI. Magn Reson Med. 2017;78(4):1405-1419
7. Breuer FA, Blaimer M, Heidemann RM, et al. Controlled aliasing in parallel imaging results in higher acceleration (CAIPIRINHA) for multi-slice imaging. Magn Reson Med. 2005;53(3):684-91
8. Bredies K, Kunisch K, Pock T. Total Generalized Variation. SIAM J Imaging Sci. 2010;3(3):492-526.
9. Wang D JJ, Alger JR, Qiao JX, et al. The Value of Arterial Spin-Labeled Perfusion Imaging in Acute Ischemic Stroke – Comparison with Dynamic Susceptibility Contrast Enhanced MRI. Stroke; a Journal of Cerebral Circulation. 2012;43(4):1018-1024.
10. Bibic A, Knutsson L, Ståhlberg F, et al. Denoising of arterial spin labeling data: wavelet-domain filtering compared with Gaussian smoothing. MAGMA. 2010;23(3):125-137.
11. Walsh DO, Gmitro AF, Marcellin MW. Adaptive reconstruction of phased array MR imagery. Magn Reson Med. 2000 May;43(5):682-90
12. Chambolle A, Pock T. A First-Order Primal-Dual Algorithm for Convex Problems with Applications to Imaging. J. Math. Imaging Vis. 2010;40:120–145.
13. Spann SM, Kazimierski KS, Aigner CS, et al. Spatio-temporal TGV denoising for ASL perfusion imaging. Neuroimage. 2017;157:81-96.