Simon Lévy1, Jürgen Herrler2, Andrzej Liebert1, Katharina Tkotz1, Moritz S. Fabian2, Christian Eisen1, Michael Uder1, David Grodzki3, Moritz Zaiss2, and Armin M. Nagel1,4
1Institute of Radiology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany, 2Department of Neuroradiology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU), Erlangen, Germany, 3MR Application Predevelopment, Siemens Healthcare, Erlangen, Germany, 4Division of Medical Physics in Radiology, German Cancer Research Center (DKFZ), Heidelberg, Germany
Synopsis
Fat signal can cause strong artifacts in MR images and/or bias measurements such as in Chemical Exchange Saturation Transfer (CEST) where metabolites peaks are reduced. At 7T, the signal-to-noise ratio and the peak separation are increased but the Specific Absorption Rate (SAR) constraints too, limiting the use of fat suppression pulses. Parallel transmit dynamic pulses for fat saturation (using kT-points) and water-selection (using a Spiral Non-Selective trajectory) were implemented for a whole-brain CEST protocol and optimized to reduce SAR compared to the standard circularly-polarized approach. Results showed high improvements in flip angle homogeneity and fat suppression efficiency, with reduced SAR.
Introduction
Chemical Exchange Saturation Transfer (CEST) can
provide whole-brain metabolic maps, with potentially-high clinical value, especially since the
clinical approval of 7T systems. Indeed, at ultra-high field, it benefits from
an increased signal-to-noise ratio and a wider spectral peak separation, which facilitate
the measurement of metabolites generally indistinguishable at standard field
strengths.
However, CEST at 7T comes with higher Specific
Absorption Rate (SAR) constraints, limiting the use of fat suppression pulses. Due
to the chemical shift with water, lipids can cause artifacts in MR images and/or bias the
measurement of metabolites (e.g., Nuclear Overhauser Enhancement, NOE)1. The fat signal is generally detrimental to CEST
measurements as it reduces the z-spectrum amplitude2.
Parallel transmission (pTx) of channel-specific pulse
shapes increases the degrees of freedom (DOFs) to manipulate the spatial transmit-field (B1+) distribution3. Dynamic pulses (temporally varying pulse shapes with
simultaneously applied B0
gradients) additionally increase these DOFs to improve the flip angle (FA)
homogeneity while reducing SAR.
This study aimed to
evaluate the potential of dynamic pTx pulse design for fat suppression in whole-brain
CEST MRI at 7T.Materials & Methods
Pulse design.The initial CEST
protocol4 consisted of a saturation module with two interleaved
complimentary sets of phase difference between adjacent channels5 and a spiral-centric-reordered-square readout6 with
online-customized pTx pulses based on a “universal” Spiral Non-Selective
(SPINS) transmit trajectory7. This whole-brain protocol demonstrated an improved
reproducibility4 (parameters in Fig.1).
Two widely used fat suppression approaches were considered:
(1) Fat saturation
pulse before the
readout,
(2) Water-selective
pulses in the readout.
For approach (1), the standard approach was a circularly-polarized
(CP) Gaussian pulse (FA=110°, duration=6120µs, frequency=-3.3ppm). It was compared to a dynamic pTx
pulse based on a “universal”8 kT-points9 trajectory with a 25% shorter duration (4550µs) to reduce B0
sensitivity. The kT-points coordinates and sub-pulse durations were
determined through a global search10 (Matlab 2017b, Mathworks, USA) minimizing the Root-Mean-Squared-Error
(RMSE) on the resulting FA in a healthy population (10 women, 10 men, same as for the SPINS trajectory).
Then, the pulse amplitude and phase were optimized at the acquisition based on the subject’s B0
and B1+ data with the determined kT-points (Fig.2-A). For this
optimization, the maximum local Specific Energy Dose (SED, energy absorbed per mass of
tissue, proportional to SAR) was limited to 75% of the Gaussian pulse
SED and the FA RMSE in the brain was minimized with a target of 110° at -3.3ppm
(main fat frequency) and 0° at 0ppm (water frequency).
For approach (2), the readout pulses were replaced by
water-selective pulses with the same “universal” SPINS trajectory (Fig.2-B). The water-selectivity was achieved during the subject-specific
optimization, with a target of 5° at 0ppm and 0° at -3.3ppm. The SED limit for
this optimization was set so that the maximum local SED of the readout remained
below 90% of the value for a readout with the CP fat saturation and the original non-water-selective pulses.
Acquisition.The experiments
were performed on a 7T whole-body system (Terra, Siemens Healthcare, Erlangen,
Germany) with an 8Tx/32Rx brain coil (Nova Medical). The protocol (Fig.1) was applied in 6 healthy
volunteers (aged 40.3±8.3 y.o., 3 women) with the 4 strategies:
no fat suppression, Gaussian fat saturation (CP mode), fat saturation with kT-points
trajectory (pTx), water-selective
pulses with SPINS trajectory (pTx). The subject-specific pTx optimizations did
not add time to the protocol since they could be performed during the anatomic
image acquisition.
Analysis.The Amide Proton
Transfer (APT), NOE, Magnetization-Transfer (MT) and Amine contrasts were
calculated voxel-wise for each fat suppression strategy after temporal motion
correction, B0 and B1+ correction11,12, denoising and 5-pool Lorentzian fitting12. These maps were
registered to the MNI template and structural atlas13,14 using ANTs15 with an affine
registration to the anatomic image before a non-linear registration of the
anatomic image to the template. The differences in CEST contrasts with respect
to the acquisition without fat suppression were quantified for each fat
suppression strategy in different brain regions.Results & Discussion
A successful design of water-selective pulses with
reduced SED compared to the non-selective pulses was achieved (Fig.3), although performances were
decreased in the lower brain at the water frequency (averaged normalized RMSE
across subjects=22.6%, versus 10.1% for non-water-selective pulses). The fat saturation homogeneity was highly
improved with pTx, compared to the CP mode. Additionally, the two pTx
fat suppression approaches reduced the sequence energy deposition. Longer
pulse duration might improve the spectral selectivity but might be sub-optimal
for fast CEST imaging.
No large difference between strategies were observed in
the CEST maps (Fig.4), except for
APT where ringing artifacts at the top of the brain (potentially due to the
scalp fat) seemed removed with the pTx fat suppressions.
Regarding CEST contrasts
values (e.g., MT), the improved homogeneity of the pTx fat saturation reflected
in the cerebellum where the same trend as in other regions was retrieved (Fig.5). Given the reported
repeatability of the protocol4, these differences are
unlikely due to test-retest variability.Conclusion & Perspectives
Homogeneous
fat suppression with reduced energy deposition was obtained with individually
optimized dynamic pTx pulses, in particular for fat saturation, compared to the standard CP approach.
Future work will aim to implement those pulses for CEST MRI in other body
regions (e.g., knee), where fat is more problematic.Acknowledgements
This work was supported by the emerging field
initiative (project 4 Med 05 “MIRACLE”) of the Friedrich-Alexander University
(FAU) Erlangen-Nürnberg.References
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