Sören Johst1, Karsten H Wrede1,2, Harald H Quick1,3, and Mark E Ladd1,4
1Erwin L. Hahn Institute for Magnetic Resonance Imaging, University Duisburg-Essen, Essen, Germany, 2Department of Neurosurgery, University Hospital Essen, Essen, Germany, 3High Field and Hybrid MR Imaging, University Hospital Essen, Essen, Germany, 4Medical Physics in Radiology, German Cancer Research Center (dkfz), Heidelberg, Germany
Synopsis
Imaging of intracranial plaques and
thrombi is important, as they play a role e.g. in rupture risk of cerebral
aneurysms. 7T provides the potential to increase spatial resolution due to
increased SNR. A time-of-flight MR angiography (TOF MRA) sequence was extended
to a hybrid of opposite-contrast MRA sequence providing two contrasts, bright
and black blood. Inverting and subtracting both contrasts makes thrombi/plaques
visible. Sufficient flow dephasing moments for black-blood contrast were
determined for three resolutions, image post-processing was implemented, and
contrast evaluated. This approach potentially enables patient studies with
higher resolution than previously achievable while maintaining reasonable acquisition
times.Purpose
Imaging of
intracranial plaques and thrombi is important, as they play a role in e.g. formation,
development and rupture risk of cerebral aneurysms.1 7T MRI provides
the potential to increase spatial resolution due to its increased SNR.
Hybrid of
opposite-contrast MR angiography (HOP-MRA)1 was developed to
increase the visibility of small vessels in MRA. However, it was recently also applied
for vessel wall imaging at 3T.2 An advantage, compared to recently
published TSE-based vessel wall imaging at 7T,3 is that no contrast
agent is necessary. The principle of HOP-MRA is a gradient-echo-based time-of-flight
(TOF) MRA with a 2nd echo providing black-blood (BB) contrast by
preceding flow dephasing gradients (FDG). Plaques/thrombi appear hypointense in
both echoes. As the blood lumen is bright in both images, TOF
and inverted BB contrast, only the signal of the plaques remains bright after subtraction.
Methods
A second echo was
implemented in a custom TOF MRA sequence4 that is routinely used in various
7T MRA studies.5 Similar to 1, a bipolar gradient pair
was introduced right before the 2nd echo to dephase the spins of the
flowing blood (Fig. 1), while stationary spins are rephased after both
gradients.
In an initial
volunteer, the FDG were successively increased, 14.3/20.8/33.8/46.8/59.8/114.4/140.4
ms*mT/m (=moment of one single FDG), for three different image resolutions (Fig.
2) until sufficient vessel suppression was reached. TE1 was kept constant while
TE2 and TR increased accordingly with gradient area (Fig. 2). In all protocols,
the shortest possible TR and echo times were used. For lower resolutions, shorter
2nd echo times can be chosen, as lower readout gradients are needed
and thus the acquisition bandwidth can be increased. To confirm the
observations, protocols with sufficient FDG were applied in two additional
volunteers.
Imaging was
performed on a 7T whole-body MRI system (MAGNETOM 7T; Siemens). The sequences
used asymmetric tilt-optimized non-saturated excitation (TONE) RF pulses and
asymmetric echoes. A venous saturation pulse with 35° flip angle was used to
suppress the veins in the TOF contrast.4 To ameliorate SAR
restrictions, the variable-rate selective excitation (VERSE) algorithm was used
for both excitation and saturation RF pulses.4 Protocol parameters
are given in Fig. 2.
In post-processing, a
N3 Bias Field Correction was applied to correct for B1 field inhomogeneities,
then the TOF images were subtracted from the inverted BB images (FMRIB Software
Library; FSL version 5.0.1; Jenkinson et al., 2012).
Vessel-background contrast was measured in TOF, BB, subtraction, and
summation images with circular ROIs placed in the middle cerebral artery (MCA) and
adjacent brain tissue (2mm/5mm diameter, respectively).
Results
Gradient stimulation thresholds were almost at
the limits for these protocols (87% - 98%). Highest SAR was 76% and decreased
with increasing dephasing gradients (respectively TR). There is a trade-off
between FDG area and TE2 in this sequence, as higher FDG increases T2*
weighting in the BB
contrast. A FDG moment of 114.4 ms*mT/m (diffusion b-value = 0.1 s/mm2)
provided sufficient suppression of blood signals (Fig. 3) for all resolutions, corresponding
to TE2 of 16.49/14.66/13.59 ms and measurement times of 9:29/6:06/3:38 min:s
(Fig. 4). Smaller vessels were in general more difficult to suppress; direction
of flow (through-plane or in-plane) also influenced the effect of the FDG.
In Figure 5, TOF, BB,
and subtraction images are shown. Summation of the contrasts (Fig. 5d) showed fewer
flow artifacts, as no flow artifacts were visible in the 2nd echo. However,
contrast is reduced.
In the volunteer
shown in Fig. 4 and 5, a Michelson contrast for TOF of 0.62/0.63/0.49 (±0.1; highest
to lowest resolution), BB 0.19/0.3/0.61, subtracted 0.44/0.54/0.82, and summed
images 0.49/0.50/0.31 was determined. No measureable difference in vessel diameter was found comparing
TOF and subtraction images.
Discussion
The subtracted
images lead to sufficient contrast (better contrast than BB images alone).
Due to gradient
system/nerve stimulation limitations, there is not much potential to further reduce
TE2 while maintaining sufficient FDG moment. Masking (part of) the artery of
interest should relieve effects (background signal difference/veins) introduced
in the 2nd echo by the relatively high TE2 values.
Expanding a given TOF
protocol4,5 facilitates integration into current MRA patient
studies. Also, no additional BB sequence and no contrast agent are necessary
while saving measurement time, decreasing SAR, and minimizing misregistrations.
Based on these results, a patient study is now planned to evaluate imaging of intracranial
plaques/thrombi.
Conclusion
Patient studies evaluating
imaging of plaques/thrombi are now feasible with a HOP-MRA double contrast sequence
using the tested protocol parameters. Spatial resolution could be increased in
this 7T UHF application compared to recent methods (0.93x0.93x1/0.8x0.8x0.8mm
3)
2,3
while maintaining reasonable scan times.
Acknowledgements
The research leading
to these results has received funding from the European Research Council under
the European Union's Seventh Framework Programme (FP/2007-2013) / ERC Grant
Agreement n. 291903 MRexcite.References
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