Anh Tu Van1, Barbara Cervantes2, Hendrik Kooijman3, and Dimitrios C Karampinos2
1IMETUM, Technical University of Munich, Garching, Germany, 2Department of Diagnostic and Interventional Radiology, Technical University of Munich, Munich, Germany, 3Philips Healthcare, Hamburg, Germany
Synopsis
Diffusion-prepared
(dprep-TSE) TSE sequences are gaining attention for high-resolution distortion-free
body DWI. However, dprep-TSE suffers from phase errors induced by both motion and
eddy current effects. Motion compensation reduces motion effects, but eddy
currents remain a source of phase errors. The present study investigates the performance
of two alternative methods for compensating for eddy current effects in a
motion-compensated dprep-TSE sequence: the use of phase cycling and the use of
magnitude stabilizers.
Purpose
Motion-compensated
diffusion-prepared (dprep) sequences have been emerging as an alternative for
high resolution and low distortion diffusion imaging especially in body
applications1-4. In dprep sequences, phase errors induced by motion
and eddy currents during the diffusion encoding period affect not only the
magnitude but also the phase of the acquired signal5. With
motion-compensated diffusion preparation, the effect of motion-induced phase
errors is minimized but that of eddy-current-induced phase errors remains. In
the present study, we investigate the performance of the use of phase cycling
and the use of magnitude stabilizers in compensating for the eddy current effects
in a motion-compensated dprep-TSE sequence.Theory
Fig.
1a shows the sequence diagram for a flow-compensated dprep-TSE sequence. The
transverse magnetization at the tip-up pulse, $$$M_{xy}(90_{-x}-)$$$, in
the presence of a phase error $$$\phi_{voxel}$$$
induced
by the diffusion encoding period, becomes,
$$M_{xy}(90_{-x}-)
= M_{prep}e^{j\pi/2}e^{j\phi_{voxel}},\ (1)$$
where
$$$M_{prep}$$$
is
the magnitude of the diffusion-prepared magnetization. After the tip-up RF
pulse along the –x direction and the T1 relaxation during the time tm (Fig. 1), the longitudinal
magnetization right before the TSE readout excitation is
$$M_z(90_{+x}-)
= M_{prep}cos\phi_{voxel}e^{-tm/T1} + M_0(1 – e^{-tm/T1}). \ (2)$$
When
the tip-up RF pulse is along the –y direction, Equation (2) becomes
$$M_z(90_{+x}-)
= M_{prep}sin\phi_{voxel}e^{-tm/T1} + M_0(1-e^{-tm/T1}). \ (3)$$
Equations
(2) and (3) reveal a signal magnitude modulation dependent on the phase error.
When eddy currents are the major cause of $$$\phi_{voxel}$$$, it has been proposed
that the magnitude modulation can be eliminated by phase cycling of the tip-up
RF pulse between –x and –y (i.e., 90o out of phase) and taking the
sum-of-squares (SOS) of the resulted signals6. From Equations (2)
and (3), it can be seen that the phase cycling method only works if the T1
relaxation effect is negligible, which may not be true when $$$M_{prep}$$$ is small (high b-value
encoding, high diffusivity) or tm is
significant.
Magnitude
stabilizers are gradients (grey trapezoids in Fig. 1b) that are added to the
dprep-TSE sequence for minimizing magnitude modulation due to phase errors
without the need of phase cyling7. In the presence of the magnitude
stabilizers, the magnetization at the first echo in the TSE readout (first
yellow circle in Fig. 1b) can be expressed as
$${M_{xy}}^1=\frac{1}{2}M_{prep}e^{-tm/T1}e^{-TE1/T2}e^{j(\phi_{voxel}+\pi/2)},
\ (4)$$
which
has the magnitude independent of the phase error but at a cost of 50% signal
loss.Methods
Phantom
(water) and in-vivo experiments (human calf muscle) were performed to compare
the performance of the phase cycling method and the use of magnitude
stabilizers (Fig. 1) on a 3 T Philips system (Philips Ingenia, Best, the
Netherlands) using a tranamit/receive 16-channel knee coil. Ten diffusion
encoding directions were acquired at a b-value of 400 s/mm2 with
TE/TR=60/1700 ms, tm=11 ms, TSE
factor=60, voxel size=2.5x2.5x4 mm3 (phantom) and 1.5 x1.5x6 mm3
(in-vivo calf muscle). Fat suppression was performed with SPAIR. In the phase
cycling method (Fig. 1a), two repetitions with the tip-up RF pulse along –x and
–y were acquired.Results
The “tip-up -x” and “tip-up -y”
diffusion signal curves across directions exhibited the expected opposite
signal variation (Fig. 2a). The “SOS” curve still showed significant oscillation
across diffusion directions (Fig. 2b) and the instability of diffusion-weighted
magnitude led to a fluctuation in the estimated ADC per direction (Fig. 3a) and
an erroneously high FA (Fig. 3c). Magnitude stabilizers gave more stable signal
across diffusion directions (Fig. 2c) and resulted in lower variation in
estimated ADC per direction (Fig. 3b) and low FA values (<0.05). In vivo
calf diffusion-weighted images showed a spatial magnitude modulation in “tip-up
-x” and “tip-up -y” images (Fig. 4). The “SOS” image only showed partial magnitude
modulation reduction while the image acquired with magnitude stabilizers
exhibited no magnitude modulation. More reasonable mean ADC (ROI average of
1.6x10-3 mm2/s) and FA (ROI average of 0.3) values were
achieved with magnitude stabilizers where as the phase cycling method overestimated
mean ADC and FA maps.Discussion and conclusion
Phase cycling of the tip-up RF pulse and taking the SOS of the resulted signals shows insufficient performance in removing the signal magnitude modulation caused by eddy-current-induced phase errors. It is presently shown that the phase cycling method failed even in a water phantom with a long T1. The performance of the phase cycling method is expected to be worse in tissues/substances with shorter T1 value. Therefore, magnitud stabilizers should be the method of choice for compensating eddy-current-induced phase errors in motion-compensated dprep-TSE sequences even at the cost of 50% in signal. Acknowledgements
The present work was partially supported by Philips Healthcare.References
1. Cervantes B, Zhang
Q, van de Ven K, et al. High-resolution DTI of distal peripheral nerves using
flow-compensated diffusion-prepared 3D TSE. Proc Intl Soc Mag Reson Med
2016;24:4530.
2. Nguyen C, Fan Z,
Xie Y, et al. In vivo diffusion-tensor MRI of the human heart on a 3 tesla
clinical scanner: An optimized second order (M2) motion compensated
diffusion-preparation approach. Magn Reson Med 2016;76(5):1354-1363.
3. Xie Y, Yu W, Fan
Z, et al. High resolution 3D diffusion cardiovascular magnetic resonance of
carotid vessel wall to detect lipid core without contrast media. J Cardiovasc
Magn Reson 2014;16:67.
4. Zhang Q, Cervantes
B, Karampinos DC, et al. High resolution 3D diffusion imaging of carotid vessel
wall using stimulated echo based diffusion prepared turbo spin echo sequence.
Proc Intl Soc Mag Reson Med 2016;24:959.
5. Van AT, Cervantes
B, Kooijman H, et al. How to minimize motion-induced phase and magnitude
modulation in diffusion-prepared sequences? Proc Intl Soc Mag Reson Med
2016;24:4530.
6. Thomas DL, Pell
GS, Lythgoe MF, et al. A quantitative method for fast diffusion imaging using
magnetization-prepared TurboFLASH. Magn Reson Med 1998;39(6):950-960.
7. Alsop DC. Phase
insensitive preparation of single-shot RARE: application to diffusion imaging
in humans. Magn Reson Med 1997;38(4):527-533.