Large FOV Zero Echo-Time (ZTE) has been challenging due to chemical shift artifacts, caused primarily by fat water dephasing, for low readout band-widths (rBW). To correct for this Perfect In-Phase ZTE (pipZTE) is proposed where the chemical shift artifact is removed by acquiring data from multiple rBWs, and then separating the signal into an in-phase and off-resonance compartment in the reconstruction. In this work we explore the performance and properties of the pipZTE approach when scanning large FOV and demanding subjects.
In radiotherapy (RT) planning and PET/MR attenuation correction proton density (PD) weighted Zero Echo-Time (ZTE) acquisition strategies have received a prominent role over the last years (1). This is primarily due to its ability of detection MR bone signals and differentiating them from surrounding soft-tissue and air. For common post-processing procedures such as bone enhancement (2) and pseudo-CT generation (1) a high soft-tissue uniformity is crucial. Despite a nominal echo time of TE = 0, ZTE images can still contain significant chemical shift induced out-phase effects and thereby significantly degrade soft-tissue appearance, especially at fat-water tissue interfaces. This is because the ZTE readout is of finite duration and distant k-space points are sampled at effective echo times which can approach fat-water out-phase echo time (TEout-phase~1.15ms at 3T) (cf. Fig. 1).
$$data(\mathbf{k}_{n})= \\ \int_{}^{}d^{3}r\begin{bmatrix}image_{in-phase}(\mathbf{r})\frac{e^{i\omega_{water}} {TE}_{n}+e^{i\omega_{fat}} {TE}_{n}}{2}+image_{out-phase}(\mathbf{r})\frac{e^{i\omega_{water}} {TE}_{n}-e^{i\omega_{fat}} {TE}_{n}}{2}\end{bmatrix}e^{i\mathbf{k}_{n}\mathbf{r}}\\= image_{in-phase}(\mathbf{k}_{n})\frac{e^{i\omega_{water}} {TE}_{n}+e^{i\omega_{fat}} {TE}_{n}}{2}+image_{out-phase}({\mathbf{k}_{n}})\frac{e^{i\omega_{water}} {TE}_{n}-e^{i\omega_{fat}} {TE}_{n}}{2}$$
In this work we present a novel method, called perfect in-phase ZTE (pipZTE), which produces ZTE images clean of out-phase disturbances via a k-space based in-phase/out-phase chemical shift decomposition. The pipZTE method is investigated in terms of spatial resolution and SNR characteristics and demonstrated for musculoskeletal imaging and whole-body bone imaging.
ZTE imaging was performed based on a modified Rotating Ultra-Fast Imaging Sequence (RUFIS) (5). In order to allow magnetization preparation (such as IR preparation, and T2 preparation) the ZTE readout is divided into segments, with each segment containing a certain number of spokes per segment. In pipZTE each segmented gets repeated with the readout gradient being scaled providing k-space samples (i.e. data(kn)) acquired at different effective echo times (TEn=n*Δt, where Δt ithe sampling time).
Assuming a fat-water shift of 3.4ppm each k-space sample can then be reconstructed into two compartments (in-phase and off-resonance) (Eq. 1), using either regularized pseudo-inversion or truncated single value decomposition (SVD). With the first k-space samples acquired at TE ~0 the off-resonance effects become increasingly destructive approaching ~1.15ms at 3.0T. Data reconstruction was performed on the scanner using ORCHESTRA (ORCHESTRA, GE Healthcare, Chicago, IL) and DICOM images were automatically inserted into the scanner database. Healthy volunteers were scanned on a 3.0T clinical MRI system (SIGNA Premier, GE Healthcare, Chicago, IL) using a 60ch AIR technology receive coil (AIR AA+PA, GE Healthcare, Chicago, IL) with relevant scan parameters being FOV 320mm, resolution 1.5x1.5x1.5mm3, rBW ±62.5/50.0kHz, NEX 1, flip angle 0.8°, and a total scan time of 3:42min. Scan time and resolution matched ZTE data was acquired in addition for comparison.