Echo Planar Imaging is an attractive rapid imaging readout that can image hyperpolarized compounds in vivo. By alternating the sign of the phase encoding gradient waveform, spatial offsets arising from uncertain frequency shifts can be determined. We show here that blip-reversed EPI can also be used to correct for susceptibility and $$$B_0$$$ inhomogeneity effects that would otherwise produce image-domain distortion in the heart, through the use of an estimated deformation field that is calculated from the acquired data.
Hyperpolarized [1-$$$^{13}$$$C]pyruvate forms a versatile metabolic probe that has been used extensively to quantify cardiac metabolism and pH in health and disease.[1-5] Many conditions where metabolic dysregulation is implicated are often spatially localized, such as myocardial ischaemia. Echo Planar Imaging (EPI) is an attractive fast imaging readout to use for hyperpolarized experiments, owing to simplicity,[6-8] speed, commonly availability on commercial scanners, and the fact that it produces artefacts that are analytically understood. Within the context of hyperpolarized imaging, there are three main sources of artefact that need to be overcome: (1) the Nyquist ghost; (2) image-domain distortions such as compressions, expansions, and tearings that arise from susceptibility changes and their associated $$$B_0$$$ effects; and (3) slight errors in the central transmitter frequency that lead to frequency shifts. Here we show with 3D-spectral spatial EPI that by acquiring alternate images with the sign of the phase encoding direction reversed, it is possible to estimate geometric distortions and off-resonance artefacts simultaneously, and hence reconstruct undistorted images.
$$$^{13}$$$C-images were acquired either from a phantom or the healthy fed rat heart after infusion of hyperpolarized [1-$$$^{13}$$$C]pyruvate via a 3D-spectral-spatial EPI sequence described previously.[9] The reconstruction algorithm was as follows:
This method is graphically illustrated in Fig. 1.
We found that the method proposed is able to correct for susceptibility artefacts arising in the rodent heart or phantoms, even in the low SNR environment of hyperpolarized imaging experiments (Fig. 2).
By plotting the through-time behaviour of a single voxel any compression/stretching artefacts present would be observed as alternating regions of high/low signal on alternate frames, as the object imaged 'moves' between acquisitions. Such a profile is shown pre- and post-correction in Fig. 3. The Jaccard self-similarity index between odd and even frames was significantly increased by use of the technique, which indicates that alternating compression/expansion artefacts on nearly identical bright regions have been ameliorated.
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