A self-navigated radial 4D-PC sequence is presented for accelerated ECG-free 4D flow measurements in the murine aortic arch. Self-navigation signals were extracted from the radial DC signal and used for retrospective motion synchronization. 3D-Cines with 30 frames were reconstructed with a spatial resolution of 100 µm. The volume flow was determined at 4 2D slices extracted from the 3D dataset and the 3D flow was visualized with streamlines. The results are in good accordance with results reported for ECG-triggered measurements. The new method yields high potential for preclinical studies of hemodynamics and can also be transferred to applications in humans.
MR measurements
All measurements are carried out on a 17.6T small animal MRI scanner with a 1 T/m gradient system and a 24 mm birdcage coil. Mice were anesthetized with isoflurane (1.5-2% in oxygen) and kept on a constant body temperature of 37°C. For the 3-dimensional flow encoding a radial 4D-PC-MRI sequence with a balanced 4-point encoding sequence1 was used. The acquisition parameters were: VENC=125 cm/s, TR/TE=3.0/1.1 ms, echo asymmetry: 10%, 160000 spokes, FOV: 25x25x4 mm3. For slice excitation a sinc-shaped pulse with a flip angle of 15° was used. The 4D flow measurements were conducted without triggering during free breathing and required a total scan time of 32 minutes.
Reconstruction
Cardiac and respiratory motion signals were extracted from the radial DC signal. High frequency noise was suppressed with a matched filter2 and a baseline correction was applied. The processed self-gating signals were afterwards used for breath gating and for the assessment of trigger time stamps and the relative positions in the heart cycle, as described recently3,4. The information about the cardiac phases was used for the subsequent sliding window (window width: 1/30 of the cardiac period) selection of the radial projections needed for the 4D-Cine reconstruction. For each velocity encoding step 3D images with an isotropic spatial resolution of 100x100x100 µm3 were reconstructed with convolution gridding5 at 30 different cardiac phases. All reconstructions were done with Matlab (The Mathworks, Inc., Natick, USA) and the velocity information was visualized with Ensight (CEI Software, USA).
Discussion and Conclusion
In this abstract we demonstrate the feasibility of accelerated self-navigated 4D flow measurements in the mouse with very high temporal (30 frames / cardiac cycle) and spatial resolutions (100 µm). Since flow measurements in the aortic arch are achievable in 32 minutes the coverage of the complete aorta is possible in about 1 hour. The proposed method does not require ECG signals for motion synchronization and should hence lead to higher robustness and an increased animal handling. The retrospective approach allows a very flexible data analysis that can be optimized to increase either temporal or spatial resolution. Possible applications of this new method are studies of the hemodynamics in atherosclerotic mouse models, 3D measurements of the aortic pulse-wave-velocity and of the endothelial shear stress. This method can also be transferred to applications in humans.[1] Pelc et al., Jour Magn Reson Med, [1991]; 405-413
[2] Herold et al., Proc. ISMRM 2016; 0466
[3] Winter et al., JCMR, [2013], 15:88-98
[4] Winter et al., Magn Reson Med, [2016]; DOI: 10.1002/mrm.26068
[5] Fessler JA; IEEE Trans Signal Process 2003;51(2):560–574.
[6] Janizcek et al., Magn Reson Med, [2011]; 66:1382-1390