Katharina Tkotz1, Andrzej Liebert1, Jürgen Herrler2, Patrick Liebig3, Arnd Dörfler2, Michael Uder1, Moritz Zaiss2,4, and Armin M. Nagel1,5
1Institute of Radiology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany, 2Department of Neuroradiology, University Hospital Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany, 3Siemens Healthcare GmbH, Erlangen, Germany, 4Max Planck Institute for Biological Cybernetics, Tuebingen, Germany, 5Institute of Medical Physics, Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany
Synopsis
In Chemical Exchange Saturation Transfer MRI B1+-inhomogeneity
influences both saturation and acquisition of the signal. Typically only
a correction of the inhomogeneity of the CEST saturation is performed while the
inhomogeneity of the readout is neglected. The influence of the readout was
investigated in measurements using standard inhomogeneous 1Tx readout and a homogenized
readout with customized pTx pulses. Compared to the 1Tx readout the readout
with pTx pulses shows an increase of the homogeneity of the CEST contrast for
CEST agents with low SNR like the amides and in regions with low 1Tx flip angle like the cerebellum.
Introduction
The CEST contrast strongly depends on the B1+
field inhomogeneity, which becomes prominent at ultra-high (B0 ≥ 7
Tesla) magnetic field strengths. Therefore, several techniques for correction or
mitigation of the B1+ field inhomogeneity were developed1-4. However, most of these techniques concentrate
only on the inhomogeneity of the CEST saturation while the inhomogeneity of the
readout is neglected.
A spatial variation of the readout flip angle (FA) leads to
two effects in case of CEST acquisitions. On one hand it introduces a spatial
variation of the SNR of the images; on the other hand it directly influences
the measured CEST contrast. The latter effect is negligible if a saturation
steady state is achieved. However, to approach
clinically feasible scan times typically short recovery and saturation durations are chosen.
Therefore the magnetization at one frequency offset depends on the previous excitations.
This results in a change of the CEST spectra and contrasts with the FA.
In this
work, we investigate these influences of the readout inhomogeneity on the CEST
contrast and verify the advantages of a homogenized readout with parallel
transmission (pTx) over the single channel transmission readout (1Tx).Methods
Data Acquisition
For comparison of the 1Tx and the pTx readout, measurements
of a healthy volunteer were performed on a 7-Tesla whole-body MR system
(Magnetom Terra, Siemens Healthineers, Erlangen, Germany) with a 8Tx/32Rx head
coil (Nova Medical, Wilmington, USA). The CEST images were acquired with a
Snapshot-CEST sequence5 utilizing the
MIMOSA approach1 to achieve a more homogenous saturation. For
the pTx readout universal pulses with online customization based on a spiral
nonselective k-space trajectory were used6, 7. The pTx pulse customization was performed
based on pre-optimized trajectory, energy regularization, pulse shapes and
individually acquired B1+ and B0 maps.
For both readout types measurements with two different saturation
B1 values were performed to allow for further correction of the
saturation B1+ inhomogeneity. The CEST saturation
parameters were: τp = 46.08 ms, τD = 30 ms,
n = 50, Trec = 1 s, B1,Nominal = 0.72 µT and
1.08 µT, Gaussian pulse shape. Image acquisition for the 1Tx and the pTx
approach was performed using a GRE readout with the following parameters: FA = 6°,
TR = 3.4 ms, TE = 1.43 ms, matrix
size = 92x92x72, FoV = 230x230x180 mm3,
GRAPPA 3x2.
B1+ maps for MIMOSA and the 1Tx mode
were acquired using a pre-saturated 2D turbo-flash sequence8.
Anatomical images were acquired using an in-house pTx-MPRAGE
sequence with similar readout as the CEST pTx readout.
Data Analysis
All acquisitions were co-registered onto the anatomical
acquisition. Segmentation into gray (GM) and white matter (WM) was performed on
the anatomical images. Both, co-registration and segmentation, were performed using
SPM 129. The influence of the
saturation inhomogeneity on the CEST spectra was
corrected with a two point B1+ correction approach2. The inverse magnetic transfer ratio metric (MTRRex) of the relayed
Nuclear Overhauser Effect (rNOE), amide proton transfer (APT) and magnetization
transfer (MT) were calculated utilizing a multi-Lorentzian fitting2. To investigate the dependency of the CEST
contrast onto the FA, the CEST data was binned into equal sized (0.3°) bins of
the 1Tx FA distribution and the mean and standard deviation of the data were
computed. The binning was performed separately for the GM and WM segments.Results and Discussion
Comparing the CEST spectra for different FAs reveals that
the signal intensity decreases with increasing FA (Fig. 1 A, E).
Accordingly, one expects a decrease of the CEST contrast with the FA that is
stronger for the 1Tx than for the pTx measurement (compare the FA distributions
Fig. 2). This is mainly visible for the APT contrast in GM. For the other
contrasts the effect appears to be small compared to other influences like spatial
anatomical variations. The overestimation of the APT contrast for small FAs is
linked to higher standard deviations probably caused by the lower SNR5.
The advantage of the pTx readout can be depicted more
clearly by analyzing the distributions of the CEST contrasts for GM and WM
(Fig. 3). The pTx readout yields a narrower distribution of the CEST contrasts
especially for the APT contrast. This indicates that B1+
readout influences were partially compensated.
Considering the spatial distribution of the CEST contrasts (Fig. 4)
one sees that the APT and rNOE contrasts in the cerebellum are overestimated
for the 1Tx readout as has been reported before10. The pTx readout
reduces this artefact.Conclusion
The effect of an inhomogeneous readout FA on the CEST
contrast is small compared to the effect of the saturation B1+.
The CEST contrast for already B1+ corrected data though
can be further improved by a homogenization of the readout by pTx. This is
especially relevant for CEST agents producing only small contrasts like the
amides and in regions with low 1Tx FA like the cerebellum.Acknowledgements
The financial
support of the FAU Emerging Fields Initiative (MIRACLE, support to K.T., A.L. and A.M.N.) is gratefully acknowledged.References
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