Yasuhiro Fujiwara1 and Yoshiyuki Muranaka2
1Department of Medical Imaging, Faculty of Life Sciences, Kumamoto University, Kumamoto, Japan, 2Radiological Center, Fukui Prefectural Hospital, Fukui, Japan
Synopsis
We evaluated the uniformity of
the intracranial vascular signal using a Silent MR angiography (MRA).
Experiments with phantoms and healthy subjects revealed that this sequence
improved the uniformity of the vascular signal under the condition of complex
flow. Silent MRA improved contrast, coefficient of variation, and accuracy for
intracranial blood vessels with turbulent flow compared with time-of-flight
MRA. The signal intensities obtained by Silent MRA were independent of flow
conditions. Although it has limited spatial resolution and requires additional
imaging time, this sequence may have the potential to improve the image quality
of intracranial blood vessels.
INTRODUCTION
Three-dimensional (3D)
time-of-flight MR angiography (TOF MRA) has been widely used. In TOF MRA, complex
or turbulent flow, such as carotid artery bifurcation, causes phase dephasing
artifacts that lead to an intraluminal signal decrease or a loss of signal. Silent
MRA is an imaging technique using arterial spin labeling that make it possible
to zero echo time (TE) by applying 3D radial acquisition and ultra-fast
switching of the magnetic gradient [1]. A previous report has shown Silent MRA
was able to visualize flow in an intracranial stent more effectively than TOF
MRA [2]. Silent MRA is expected to decrease the effect of intra-voxel dephasing
for turbulent flow and allow for accurate assessment of flow in blood vessels. This
study quantified the accuracy of Silent MRA for visualizing turbulent flow in
flow-phantom and
in vivo studies.
MATERIALS AND METHODS
The MRA studies were
performed on a 3.0T Discovery 750w MRI system with a 12 channel phased array
coil (GE Healthcare, Waukesha, Wisconsin).
Phantom study
Flow phantoms were 5.0
mm inner diameter polyvinyl tubes with and without stenosis that were submerged
in polyvinyl alcohol gel (T1 = 1447 ms). The flow phantoms were connected to a pump
with polyvinyl tubing. A blood analog (30% glycerin and 70% distilled water, T1
= 1400 ms) mimicking the viscosity and T1 relaxation time of blood was circulated
with steady flow at a velocity of 20 and 40 cm/s, respectively, through the
phantoms (Fig. 1).
MRA images were obtained
using TOF and Silent MRA with and without stenosis at both flow velocities. The
imaging parameters were: field of view (FOV) = 200 mm, repetition time (TR)/TE =
20/2.7 ms, Flip angle (FA)[A2] = 20°, matrix size = 416 x
192, slice thickness = 1.2 mm, bandwidth (BW) ± 42 kHz.
Silent MRA uses a continuous
arterial spin labeling technique as a preparation pulse, and a 3D radial
acquisition [1]. Silent MRA in the sagittal plane was acquired with control
images and labeling images, and they were subtracted for the MRA image. The imaging
parameters were: FOV = 180 mm, TR/TE = 1114/0.016 ms, FA = 5°, spokes per segment =
512, resolution = 1.2 mm, BW ± 20 kHz.
Signal intensity was
measured in the tube for a normal model and in the distal region that passed
through the stenosis for the stenosis model. Then, the image contrast between the
signal intensity of the tube and peripheral region were measured at flow
velocities of 20 and 40 cm/s, with and without stenosis. The coefficient of
variation (CV) in the tube was measured using the same conditions with the previous
settings.
In vivo experiments
Seven healthy subjects
(mean age 38.7 years) were enrolled under an Internal Review Board-approved protocol.
TOF and Silent MRA images were obtained with the same imaging parameters as
used in the phantom study. Next, signal intensities were measured for each MRA
image at the level of the S1, S3, S4, and S5 segment of the internal carotid
artery and at the S4 level of the segment basilar artery.
The contrast between each
vessel and the peripheral brain parenchyma were measured in TOF and Silent MRA.
Moreover, signal intensity profiles were measured along directions
perpendicular to vessels at the level of the S3 and S5 segment. Finally, to
assess signal changes in the blood vessel, an accuracy that was defined as the
ratio normalized maximum signal for minimum signal was measured.
RESULTS
In the phantom study, although
the contrast of TOF MRA decreased with high flow velocity or distal to the stenosis
region, that of Silent MRA was not changed by these conditions (Fig. 2a). Moreover,
the mean CV of TOF MRA was higher than that of Silent MRA in the stenosis
condition (Fig. 2b). These results are consistent with a previous report [3]. In
the
in vivo study, the mean contrast of
Silent MRA was statistically significantly higher than that of TOF MRA in all segments
(Fig. 3). Representative MRA images and the signal intensity profile of TOF and
Silent MRA are shown in Figure 4. Moreover, the accuracy of Silent MRA was
statistically significantly higher than that of TOF MRA in the S3 and S5
segments (P < 0.05) (Fig. 5).
DISCUSSION AND CONCLUSION
Silent MRA improved contrast,
CV, and accuracy for intracranial blood vessels with turbulent flow. Signal
intensities obtained by Silent MRA were independent of flow conditions. Although
it was limited in spatial resolution and required additional imaging time, it may
have the potential to improve uniformity of signal intensity of intracranial
vessels.
Acknowledgements
No acknowledgement found.References
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