David Leitão1, Ozlem Ipek1, Avanya Prathapan1, Daniel West1, Jo Hajnal1,2, Tobias C Wood3, and Shaihan Malik1,2
1Biomedical Engineering & Imaging Sciences, King's College London, London, United Kingdom, 2Centre for the Developing Brain, King's College London, London, United Kingdom, 3Department of Neuroimaging, King's College London, London, United Kingdom
Synopsis
Keywords: New Signal Preparation Schemes, Low-Field MRI
Motivation: Inherently reduced SAR at low B0 fields opens the possibility for sequences employing high B1 to generate contrasts inaccessible on common systems.
Goal(s): Explore generation of magnetization transfer (MT) and inhomogeneous MT (ihMT) contrast using high B1 sequences on low-field MRI system.
Approach: A tuned resonator was used to enhance B1 fields locally within a 0.55T scanner. Rapid gradient-echo based MT/ihMT sequences were tested on ex-vivo lamb brain sample.
Results: Achieved ~9-fold increase in B1, boosting observed MTR/ihMTR. Unexpectedly, RF pulses failed to function at high B1 due to Bloch-Siegert and spin-locking; new pulse designs for this regime will form future work.
Impact: Using high B1 fields at low B0 enables contrasts that were previously off-limits due to safety constraints at high B0.
To exploit these with clinical hardware we demonstrate a passive
resonator that increases the B1 by a factor of 9.
Introduction
Lower field MRI has inherently reduced specific absorption rate
(SAR) due to the lower Larmor frequency. While beneficial for safety, this also
implies that applications requiring strong B1 fields become feasible, such as Magnetization
transfer (MT) and inhomogeneous MT (ihMT). Figure 1 demonstrates simulated
maximum MT and ihMT ratios (MTR/ihMTR) as a function of root-mean-square B1
(B1rms) using rapid gradient echo sequences at 0.55T. Typical maximum B1rms
values on clinical scanners are around $$$4\mu{}T$$$ – it is clear that both contrasts could be
substantially increased in proportion with B1rms.
Based on the simplistic assumption that the maximum B1rms scales
inversely with B0 squared, at 0.55T one might expect to safely achieve B1rms$$$\approx{}30\mu{}T$$$
. In practice, the maximum B1rms
achievable for the commercial scanner used here is considerably less at $$$\approx{}4\mu{}T$$$
and determined by hardware limits. In order to
reach the high B1 regime and resulting contrasts, we explore use of a passive
resonator to locally enhance transmit efficiency (1).Methods
MT and ihMT contrast can be efficiently generated within rapid
gradient echo sequences using non-selective multiband pulses to simultaneously
excite and saturate (2) as illustrated in Figure 2. These pulses can have 1-band (1B),
2-bands (2B) or 3-bands (3B), such that they always generate the same flip
angle whilst saturating the semisolid magnetization at different frequencies.
MTR and ihMTR maps were computed from images acquired with each type of pulse:
$$MTR(\%)=100\times{}\frac{s_{1B}-s_{3B}}{s_{1B}}$$
$$ihMTR(\%)=100\times{}\frac{s_{2B}-s_{3B}}{s_{1B}}$$
where $$$s_{\mathrm{x}B}$$$ is the signal acquired with a pulse with $$$\mathrm{x}$$$ bands. A second scheme in which saturation and
excitation sub-pulses are separated is illustrated in Figure 3.
All experiments used a 0.55T scanner (MAGNETOM Free.Max, Siemens
Healthineers, Erlangen, Germany). A square loop coil (11x11cm) tuned to
23.8MHz was positioned underneath the sample being imaged. Additional water
phantoms were placed on top and beneath the resonator to load it correctly, and
ex-vivo lamb brains inside containers filled with water were placed inside the
resonator (Figure 4A). We acquired GRE and SSFP sequences for several B1rms levels and measured B1 using an AFI sequence (3). Results & Discussion
Figure 4B,C illustrate B1 with and without the resonator; transmit
efficiency increased by a factor of $$$9.2\pm2.8$$$ and $$$9.3\pm1.8$$$ in the two experiments.
An initial experiment using multiband pulses (Fig
4D) with SSFP showed that MTR could be increased significantly with B1rms in
line with predictions. However, it was found that ihMTR images contained
significant artefacts, which can be seen to originate from the 2B images.
Bloch simulations (Figure 2 right side) showed as B1 increases
the 2B pulses cause spin-locking, perturbing the intended trajectory. There is also
a Bloch-Siegert (BS) shift generated by the off-resonance component which
further interferes with SSFP imaging. These effects are absent for the 3B
pulses. We hence switched to a separated pulse design (Figure 3) where the 2B
pulses achieve their target flip angle (no spin-locking) but still generate a
significant BS shift.
A second experiment used GRE to avoid complications from the BS
shift. Figure 5 illustrates strong MTR with the effect plateauing at $$$\approx{}20\mu{}T$$$. Around the maximum
B1rms of the body transmit coil (without the resonator) of
$$$\approx{}4\mu{}T$$$ the MTR is $$$\approx{}30\%$$$
, whereas with the
resonator at $$$20\mu{}T$$$ the MTR increases to $$$80\%$$$. We also observe a direct saturation
effect in the water, possibly exacerbated by a high gadolinium concentration
that led to $$$T_2^*\approx{}25ms$$$
in the water. Conclusions
The resonator boosted the transmit B1 field up to 9-fold, yielding
significantly enhanced MTR and ihMTR contrasts (boosted from 30% to 80% and 3%
to 9%, respectively). This is an effective way to generate novel contrasts on
low field MR systems. We aim to design a resonator that would be safe for in
vivo use at 0.55T.
At very high B1 levels the RF pulses designed for lower B1 are no longer
effective, and so alternative RF design strategies tailored to high B1 are the
subject of ongoing research.Acknowledgements
The research was supported by core funding from the Wellcome/EPSRC Centre for Medical Engineering [WT203148/Z/16/Z] and by the National Institute for Health Research (NIHR) Biomedical Research Centre based at Guy's and St Thomas' NHS Foundation Trust and King's College London and/or the NIHR Clinical Research Facility. The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care.References
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