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3D Fast Spin Echo using Frequency-Modulated RF Pulses for MRI in Highly Inhomogeneous Magnetic Fields
Naoharu Kobayashi1 and Michael Garwood1
1CMRR, Department of Radiology, University of Minnesota, Minneapolis, MN, United States

Synopsis

Keywords: Data Acquisition, Pulse Sequence Design, Inhomogeneous field

3D Fast spin echo (FSE) with frequency-modulated (FM) pulses has been introduced for MRI in highly inhomogeneous fields. B1 dependent phase in FM pulse excitation and refocus was adjusted in the FM-FSE pulse sequence. Refocus flip angles in FM-FSE were determined with prospective extended phase graph (EPG). Proposed flip angle and phase in FM-FSE were validated in EPG simulation and experiments at 3T by introducing a linear inhomogeneous field. Finally, in vivo human brain imaging with T1- and T2-weighting was performed using the proposed 3D FM-FSE sequence.

Introduction

Frequency-modulated (FM) pulses can achieve broadband excitation with long pulse width, while amplitude-modulated pulses (e.g. hard, sinc and gaussian) require very short pulse width for broadband excitation. FM pulses have recently been implemented in 3D MP-SSFP for MRI in highly inhomogeneous fields to cover the broad frequencies distributed by the field inhomogeneity1. Spin echo (SE) is also a well-known sequence for its immunity to the field inhomogeneity. Adiabatic double spin echo, which is the most common SE based technique with FM pulses, requires a pair of adiabatic/FM pulses to rewind the quadratic phase2. Therefore, when FM pulses are used in fast spin echo (FSE), even and odd echoes show inconsistent phase so that only even or odd echoes can be used for imaging (or simultaneous 2 k-space acquisitions). In this study, we introduce 3D FM-FSE with consistent phase in even and odd echoes for MRI in highly inhomogeneous fields.

Methods

The commonly used clinical 3D FSE sequence (aka SPACE/CUBE) uses a short hard pulse for refocusing without slab selection to minimize echo spacing, τ. While a hard pulse is highly efficient to refocus the magnetization with a short pulse width, it entails a high RF peak power especially when requiring broadband refocusing. For example, a 12-kHz hard pulse (pulse width, pw = 100 µs) requires RF power (B1max) of 58.7 µT for 90° flip angle, which exceeds the limit of standard clinical MRI systems. A flattened hyperbolic secant pulse (HS2)3 yields a better excitation profile and only requires B1max = 18.1 µT, although at the expense of pw = 3.6 ms (Fig.1A). In the proposed FM-FSE, an HS2 pulse was used for excitation and refocusing to make even and odd echo phase consistent (Fig.1B). Since FM pulses introduce B1/flip angle dependent phase to the magnetization, the excitation and refocusing pulse phase was adjusted with the B1 dependent phase, φ(α) (Fig.1C).

Flip angles in 3D FM-FSE were determined with prospective extended phase graph (EPG)4 including diffusion effects5,6. First, optimal flip angles were calculated with a target of |Mxy/M0| = 0.08 and a limit of 60° for an agar gel phantom with known parameters (Fig.2A,B). Refocused echo signal intensities matched the target until the flip angle reached the 60° limit. EPG simulations were also performed for experimental validation. For brain imaging, optimal flip angles were separately calculated with the brain parameters at 3T7,8 (Fig.2C).

MRI studies were conducted with a Siemens Prisma 3T MRI using a 32ch head coil. The optimal flip angles and B1 dependent phases were first validated with the agar gel phantom. Then, in vivo human brain T1/T2-weighted imaging was performed with healthy volunteers under an IRB approved protocol. Sequence parameters were: τ = 11 ms, TEeff = 11/396 ms, TR = 900/1800 ms, HS2 excitation and refocus (pw = 3.6 ms and BWexc = 12 kHz), BWro = 40 kHz, echo train length = 40/72, 1.5 mm isotropic resolution and scan time = 4:30/5:00. A linear inhomogeneous field ΔB0 of 10, 15 or 20 mT/m was turned on during the entire scan with the z channel of the gradient coil set, which was a field inhomogeneity of 61, 92, or 123 kHz over the FOV. The linear inhomogeneous field was partly compensated during excitation and readout to achieve BWexc and BWro by modulating the z gradient amplitude.

Results

In EPG simulation, the frequency profiles of the refocused echoes attained the desired flatness with the B1 dependent phase adjustment (Mopt), whereas the profiles without the phase adjustment (i.e. φ(α) = 0, Mzero) showed a mild descending slope towards the low frequency edge (Fig.3A,B). Consistent quadratic phase was observed in all echoes for either Mopt or Mzero (Fig.3C,D). The magnitude profile for Mopt and Mzero was identical at echo 1, but the non-flat intensity profile was clearly seen at echo numbers >18 (Fig.3E). Phase profiles for Mopt matched well for all echoes, but those for Mzero showed minor fluctuation (Fig.3F).

In experiments, echo signal intensities for Mopt showed a good match with the echo signal intensities from EPG simulation (Fig.4A). In profile validation, the echo profiles acquired in experiments for Mopt and Mzero showed similar profile at echo 1, but a consistent intensity drop towards the low frequency edge was observed in Mzero/Mopt at echo 18 and after (Fig.4B), which is consistent to the EPG simulation (Fig.3E). In in vivo brain imaging, SAR was 50-70% of the limit with the vendor provided SAR monitor depending on subjects. 3D FM-FSE provided good T1/T2-weighted images by using centric-out and sequential k-space filling (Fig.5).

Discussion

In this study, 1.5-mm isotropic brain imaging was demonstrated with acceptable scan time of 5 min. The proposed 3D FM-FSE can readily be accelerated by introducing partial Fourier reconstruction, parallel imaging and/or compressed sensing reconstruction.

SAR is a serious limitation for 3D FM-FSE in highly inhomogeneous fields. However, most inhomogeneous field MRI systems (e.g. portable MRIs) target lower field strengths (typically <1.5T) than 3T herein. Therefore, this SAR limitation is highly mitigated in actual highly inhomogeneous MRI systems.

Conclusion

3D FSE with frequency-modulated pulse has been introduced for MRI in highly inhomogeneous fields.

Acknowledgements

Supporting grants: NIH U01EB025153 and P41EB027061

References

1. Kobayashi N, Parkinson B, Idiyatullin D, Adriany G, Theilenberg S, Juchem C, et al. Development and validation of 3D MP-SSFP to enable MRI in inhomogeneous magnetic fields. Magnetic resonance in medicine. 2021;85(2):831-44. Epub 2020/09/07. doi: 10.1002/mrm.28469. PubMed PMID: 32892400; PubMed Central PMCID: PMC8132587.

2. Conolly S, Glover G, Nishimura D, Macovski A. A reduced power selective adiabatic spin-echo pulse sequence. Magnetic resonance in medicine. 1991;18(1):28-38. Epub 1991/03/01. doi: 10.1002/mrm.1910180105. PubMed PMID: 2062239.

3. Garwood M, DelaBarre L. The return of the frequency sweep: designing adiabatic pulses for contemporary NMR. J Magn Reson. 2001;153(2):155-77. Epub 2001/12/13. doi: 10.1006/jmre.2001.2340. PubMed PMID: 11740891.

4. Busse RF, Hariharan H, Vu A, Brittain JH. Fast spin echo sequences with very long echo trains: design of variable refocusing flip angle schedules and generation of clinical T2 contrast. Magnetic resonance in medicine. 2006;55(5):1030-7. Epub 2006/04/07. doi: 10.1002/mrm.20863. PubMed PMID: 16598719.

5. Weigel M. Extended phase graphs: dephasing, RF pulses, and echoes - pure and simple. Journal of magnetic resonance imaging : JMRI. 2015;41(2):266-95. Epub 2014/04/17. doi: 10.1002/jmri.24619. PubMed PMID: 24737382.

6. Kiselev VG. Calculation of diffusion effect for arbitrary pulse sequences. J Magn Reson. 2003;164(2):205-11. Epub 2003/09/27. PubMed PMID: 14511588.

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Figures

Figure 1. (A) 12-kHz 90° excitation profile of hard (pulse width, pw, = 100 ms) and HS2 (pw = 3.6 ms) pulses. The hard pulse requires B1max = 58.7 μT, whereas the HS2 requires 18.1 μT. (B) Sequence diagram of 3D fast spin echo (FSE) with HS2 excitation and refocusing pulses. (C) B1/flip angle dependent RF phase for the HS2 pulse.

Figure 2. Prospective extended phase graph (EPG) to determine refocus flip angles. Echo signal intensities matched the target signal intensity (0.08, A) until the flip angle reached the maximum flip angle of 60° for an agar gel phantom with known T1/T2 (=1110/115 ms) and ADC (= 2.35x10-3 mm2/s) (B). (C) For in vivo brain imaging, flip angles were determined with T1/T2 = 1000/100 ms and ADC = 1.0x10-3 mm2/s.

Figure 3. EPG simulation for 3D FM-FSE. The magnitude profiles were nearly flat with the phase adjustment (Mopt) for all echoes (A), but not without the phase adjustment (Mzero, B). The phase profiles showed consistent quadratic phase in all echoes either with or without the phase adjustment (C,D). Comparison of the magnitude (E) and phase (F) profiles between with and without the phase adjustment for selected echoes (echoes 1, 18, 36, 54, 72).

Figure 4. Experimental validation. (A) Echo signal intensities of an agar gel phantom with known T1/T2 and ADC matched the simulation results. A ROI was set in a region where the local B1+ value matched the nominal B1. (B) The signal intensities with the phase adjustment (Mopt) matched those without the phase adjustment (Mzero) at echo 1, but at echo 18 and after, a consistent signal intensity change was observed along the slab-selective dimension. Ratio (Mzero/Mopt) was computed to remove B1- effects.

Figure 5. In vivo brain T2- (A-C) and T1-weighted (D-F) 3D FM-FSE images with three linear background field inhomogeneity along the z dimension (ΔB0 = 10, 15, 20 mT/m from top to bottom). T1/T2 image contrasts did not show clear differences as the background field increased.

Proc. Intl. Soc. Mag. Reson. Med. 31 (2023)
0538
DOI: https://doi.org/10.58530/2023/0538