Nuno André da Silva1, Desmond H. Y. Tse2, Benedikt A Poser2, and N Jon Shah1,3,4
1Institute of Neuroscience and Medicine - 4, Forschungszentrum Jülich, Jülich, Germany, 2Faculty of Psychology and Neuroscience, Maastricht University, Maastricht, Netherlands, 3Department of Neurology, Faculty of Medicine, RWTH Aachen University, JARA, Aachen, Germany, 4Department of Electrical and Computer Systems Engineering, and Monash Biomedical Imaging, School of Psychological Sciences, Monash University, Melbourne, Australia
Synopsis
To demonstrate the benefits from the increased spectral
bandwidth at ultra-high field (UHF) by using parallel transmission (pTx) to
mitigate flip-angle inhomogeneity in chemical exchange saturation transfer
(CEST) imaging. A pTx basis pulse is
homogenised by magnitude least-squares (MLS) optimisation and expanded to form
a frequency-selective saturation pulse for CEST. The pTx saturation pulse was
validated by both Bloch-McConnell simulation and in vivo imaging at 7T.
Improved homogeneity in contrasts and relaxation-compensated CEST metrics were
observed in our in vivo data when the
pTx saturation pulse was used instead of the standard CP-mode Gaussian pulse.
Purpose
To demonstrate the benefits
from the increased spectral bandwidth at ultra-high field (UHF) by using parallel
transmission (pTx) to mitigate flip-angle inhomogeneity in chemical exchange
saturation transfer (CEST) imaging.Methods
Flip-angle
homogenised pTx basis pulse designed by magnitude least-squares (MLS)
optimisation1,2,3 was expanded to form a frequency-selective pulse for CEST
in a two-step process (Fig. 1). The saturation pulse was simulated with a
three-pool Bloch-McConnell equation to evaluate its CEST contrast properties4.
Experiments were performed on a 7T whole-body MR scanner (MAGNETOM, Siemens Healthineers,
Erlangen, Germany) with an 8-channel transmit/32-channel receive head coil
(Nova Medical, Wilmington, MA, USA). B0 and B1+
maps for pulse optimisation were obtained from a dual-echo 3D GRE and a transmit
phase-encoded5, T2 and T2* compensated
version of DREAM6, respectively. PreSat-TFL7 was used to map the flip-angle
of the designed pulses8. In vivo
CEST imaging performance of the pTx saturation pulse (pTxCEST) and the standard
Gaussian saturation in CP-mode were compared. 2-spokes pTx homogeneous
excitation was used to ensure fair comparison of the two saturation pulses9.
A 2D GRE (single-shot centric-acquisition, TE=4.39ms, TR=9.2ms, matrix size =
80×80, flip-angle=10˚, slice-thickness=6.5mm) with a train of 120 saturation
pulses (50% duty-cycle) was used as the CEST imaging sequence. Z-spectra were sampled
from -300 to 300ppm at 69 unevenly distributed points using an effective power
of 0.6µT 10. Magnetisation transfer ratio and inverse Z-spectrum analyses
were used as metrics in evaluating the data from three healthy volunteers11.Results
The results of Bloch
simulations of the two saturation pulses, CP-mode CEST and pTxCEST, as well as
the pTx basis pulse are presented in Fig. 2(a-d). Small side bands at ± 20 ppm
can be seen in the pTxCEST saturation. The inserts in Fig. 2 (c) and (d) are the
spatial distribution of the normalised flip-angle integrated over the central
peak (± 0.5 ppm), which show a more spatially homogeneous saturation provided
by the pTxCEST (NRMSE 0.042) in comparison to the CP-mode CEST pulse (NRMSE
0.122). Bloch-McConnell simulations (Fig. 2e-f) showed that side bands of the
pTx saturation pulse at ± 20 ppm did not affect any CEST contrast. The B0
off-resonance maps, the PreSat-TFL flip-angle maps of the CP-mode and 2-spokes
excitations, as well as the CP-mode CEST and pTxCEST saturations at the
position of the CEST imaging slice from three healthy volunteers are presented
in Fig. 3. The average excitation NRMSE across the three volunteers reduced
from 0.11 (CP-mode) to 0.05 (2-spokes). The CP-mode CEST saturation pulse only
reached the desired 0.6 μT effective B1+ power in the
central brightening spot, while the pTxCEST pulse managed to homogeneously
deliver the desired saturation power across the entire brain region within the
imaging slice. Fig. 4 shows the Z-spectra from both CP-mode CEST and pTxCEST
saturations from two different locations in white matter. The spectra from
CP-mode CEST saturation display noticeable differences, caused by the B1+
inhomogeneity. CEST parametric maps are presented in Fig. 5. Undesired contrast
variations, e.g. due to B1+ inhomogeneity rather than
tissue difference, can be observed in the maps acquired with the CP-mode CEST
saturation, but not in those with the pTxCEST saturation.Discussion
This work presents a
method to design a parallel-transmit saturation pulse for CEST to mitigate
undesired contrast variations caused by the B1+
inhomogeneity at UHF. The homogeneous pTxCEST saturation pulse was evaluated by
simulations as well as in vivo human
brain imaging at 7T. The pTxCEST saturation was designed in two steps which
combine the benefits of the spatially homogenised flip from the pTx basis pulse
with the frequency selectivity of a Gaussian pulse, a typical choice for
saturation in CEST experiments. While the pTx saturation preserves the
bandwidth of the Gaussian envelope, it creates side bands as shown in Figs. 1-2.
This leaves a usable range of ± 10 ppm, which exceeds the typical saturation
range in CEST experiments using MTRasym and hence poses no practical
constraints. Furthermore, no influence in CEST contrasts was found in the
Bloch-McConnell simulations (Fig. 2). Both Bloch simulations (Fig. 2) and in vivo mapping (Fig. 3) show that
pTxCEST provided spatially more homogeneous saturation than CP-mode, which
translated into more reliable CEST contrast. This is indicated by the reduced
variability in the white matter Z-spectra between ± 5 ppm (Fig. 4) when pTxCEST
saturation was used. Also, the same improvements can be seen in the CEST
parametric maps (Fig. 5).Conclusion
A pTx-based pulsed
CEST pre-saturation scheme is proposed and validated by simulations and 7T in vivo imaging.Acknowledgements
We thank Christopher
Wiggins for the helps on various technical issues at the scanner. Scan hours
were funded under Scannexus/Brains Unlimited development project dev_b0_b1 and
intramural MBIC funding projects (F8000C09 and F8015). NJS is funded in part by
the Helmholtz Alliance ICEMED - Imaging and Curing Environmental Metabolic
Diseases, through the Initiative and Network Fund of the Helmholtz Association.
Further, NJS is supported in part by TRIMAGE, an EU FP7 project (grant
agreement n° 602621)References
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