Implementing single-shot quantitative CEST/T1ρ measurements using bSSFPX
Shu Zhang1, Robert E Lenkinski1,2, and Elena Vinogradov1,2

1Radiology, UT Southwestern Medical Center, Dallas, TX, United States, 2Advanced Imaging Research Center, UT Southwestern Medical Center, Dallas, TX, United States

Synopsis

Recently properties of bSSFP were explored to detect exchange processes (bSSFPX), similar to CEST or off-resonance T experiments. We expand the study and implement a transient bSSFPX experiment that acquires bSSFP spectra continuously as the effective saturation time increases, allowing observation of the approach of magnetization to the steady state in a single shot. The magnetization dynamic is governed by the effective field and relaxation times parallel or perpendicular to it. Work is in progress to derive an exact quantification model. The method leads to fast acquisition of time-dependent data and may speed up QUEST-like quantification of the exchange processes.

Introduction

Chemical exchange saturation transfer (CEST) and the closely related off-resonance T methods are gaining popularity. However, quantitative CEST/T imaging can be time consuming since the experimental repetition with different saturation lengths/powers is needed. Recently, a new way to acquire CEST/T data was proposed1 based on the exchange-sensitive properties of balanced steady state free precession sequence (bSSFPX).

The bSSFP (or TrueFISP) is a versatile sequence2-4. The bSSFP sequence can be viewed as generating an effective off-resonance field analogous to CW and possessing similar spin-lock and saturation properties1,5. In the previous study, the effective field approach was derived and proof-of-concept was demonstrated in steady-state conditions. Here, we implement the transient bSSFPX. The sequence has features similar to Look-Locker6 and IR-TrueFISP7. However, the current sequence does not require any additional preparation pulses and specifically focuses on saturation and off-resonance effects. The motivation is to acquire the transient information in a single shot, thus paving the way to fast, quantitative CEST/T imaging.

Methods

All of the experiments were performed on a 3T MRI scanner (Ingenia, Philips Healthcare) using a 15-channel head-spine coil at room temperature. The pulse program was modified to acquire images continuously during the preparation echoes in a standard bSSFP sequence as shown in Fig.1. Thus the sequence acquires all, transient and steady-state images. Note that the bSSPFX acquires an XY-spectrum and not a Z-spectrum. The transient bSSFPX sequence was tested in two phantoms (i) 2% agar with 0.14 mM gadolinium and (ii) 10, 50 and 100 mM choline water solutions. The imaging parameters were TR/TE=2.0/1.0 ms, voxel size=3*3*8 mm, FA=40o, half alpha startup echoes. 51 points in the XY-spectrum1 were acquired at the frequency range ±500 Hz. 20 images (corresponding to different saturation times) were acquired at each off-resonance frequency. Since the number of phase encoding lines was 73 and the linear ordering was used, the effective saturation time for the ith image tsat=[37+(i-1)*73]*TR. Images were processed on a pixel-by-pixel basis using custom Matlab routines. The B0 inhomogeneities and drifts were corrected using a procedure similar to the one described in Ref.11. MTRasym was calculated and normalized to the upfield side of the XY-spectrum.

Results and Discussions

The evolution of the transient signal is governed by the relaxation times T and T, parallel and perpendicular to the effective field, respectively8 and by the precession frequency around the effective field1. Similar to the CW case, both relaxation times depend on the off-resonance value as well as on the flip angle1,8,9 and contain exchange contributions.

Fig.2a shows the evolution of agar XY-spectra from the transient state (lighter) into the steady state (darker) as the effective saturation time increases. In Fig.2b, the signals at +1.2 and -1.2 ppm are plotted against tsat. The signals decay exponentially with T as they approach the steady-state. Agar has no exchanging moieties, hence its steady-state bSSFP profile is symmetric around water and the steady-state signals are similar for both frequencies. Moreover, the measured T at +1.2 and -1.2 ppm are similar (360±30 and 420±20 ms, respectively). Since the intrinsic T2 in agar is short, the signal is largely governed by the T decay and no transient oscillations were observed.

Fig.3 shows the 10 and 100 mM choline XY-spectra against effective saturation time. The T1 and T2 of the aqueous solutions are very long and prominent transient oscillations and spurious effects are observed, especially at the earlier time points. However, as the saturation time increases the profiles approach steady-state values. The steady-state profiles are asymmetric around water due to chemical exchange at ~1 ppm downfield (Fig.3b, arrow). The MTRasym (1 ppm) also approaches its steady state values of ~2%, 10% and 16% for 10, 50 and 100 mM respectively (Fig.4). After initial transient oscillations (asterisks in Fig.4) the MTRasym ­demonstrates exponential growth similar to QUEST curves10. Some residual oscillations due to transient effects or experimental imperfections are still observed. As shown in Fig.1, the acquisition is effectively performed during the saturation; hence one “shot” of the transient bSSFPX sequence acquires sufficient data for T and/or exchange rate quantification, which may largely speed up the quantification process. The T and, potentially, the exchange rate could be then obtained by fitting the curves (Fig.2b or Fig.4).

Conclusion

We have presented experimental implementation of transient bSSFPX measurements, aimed at the single-shot quantitative CEST/T measurements. The sequence has a potential to quickly acquire quantitative information. Work is in progress setting up an analytical model for the signal evolution and extracting quantitative information (i.e. exchange rate) from the profiles.

Acknowledgements

No acknowledgement found.

References

[1] Zhang S, et al. Proc ISMRM 2015; 23:0785. [2] Bieri O, et al. MRM 2007; 58:511-518. [3] Hargreaves BA, et al. MRI 2006; 24:113-122. [4] Deoni SCL, et al. JMRI 2008; 27:1421-1429. [5] Mehring M. Principles of High Resolution NMR in Solids, 1983. [6] Henderson E, et al. MRI 1999; 17:1163-1171. [7] Scheffler K, et al. MRM 2001; 45:720-723. [8] Ganter C. MRM 2004; 52:368-375. [9] Trott O, et al. JMR 2002; 154:157-160. [10] McMahon MT, et al. MRM 2006; 55:836-847. [11] Miller K. MRM 2010; 63:385-395.

Figures

Figure 1. Sequence schematic for transient bSSFPX. M images are acquired at the nth saturation frequency. Thus, each nm image corresponds to off-resonance frequency n and saturation time point m.

Figure 2. Agar XY-spectra acquired using transient bSSFPX (a). Signals at ±1.2ppm of a representative agar pixel against effective saturation time (b).

Figure 3. XY-spectra (blue) and MTRasym (red) of 10 mM (a) and 100mM (b) choline solutions acquired using transient bSSFPX as a function of the effective saturation time, tsat. All 20 tsat­ points are acquired in a single shot with only 5 profiles shown.

Figure 4. Single-shot MTRasym (1 ppm) vs saturation time (QUEST) curves for 10 mM (blue), 50mM (brown) and 100mM (yellow) concentrations of choline solution.



Proc. Intl. Soc. Mag. Reson. Med. 24 (2016)
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