Seong-Eun Kim1, Ye Tian2, Matthew Alexander1, Dennis L Parker1, Gerald S Treiman 3,4, Adam de Havenon5, and J Scott McNally1
1UCAIR, Department of Radiology and Imaging Sciences, University of Utah, Salt Lake City, UT, United States, 2Department of Physics and Astronomy, University of Utah, Salt Lake City, UT, United States, 3Department of Surgery, University of Utah, Salt Lake City, UT, United States, 4VASLCHCS, Salt Lake City, UT, United States, 5Department of Neurology, University of Utah, Salt Lake City, UT, United States
Synopsis
Carotid plaque
inflammation can be measured with dynamic contrast enhanced (DCE) MRI and is a
marker for plaque instability. Increased vascularity, which is one sign of
plaque inflammation, can be detected from kinetic analysis of DCE images
However, the trade-off between spatial and temporal resolution limits assessment
to a small number of slices and ~15 seconds per time frame. To overcome this
limitation, we implemented a short-TR 3D T1w Stack of Stars (SoS) sequence to
enable retrospective image formation with arbitrary numbers of radial views by
using Golden-angle radial sparse parallel (GRASP) reconstruction.
PURPOSE
Atherosclerosis is one of the most
common causes of ischemic stroke1. In histologic studies, plaque
enhancement correlates with vasa vasorum neovascularization and macrophages, and
contrast leakage may result from endothelial dysfunction or be secondary to intraplaque
inflammation and adventitial neovessel rupture2. Increased
vascularity, which is one sign of plaque inflammation, can be detected from
kinetic analysis of dynamic contrast enhanced (DCE) FLASH images3. However,
the trade-off between spatial and temporal resolution limits assessment to a
small number of 2D or 3D slices and ~15 seconds per time frame3,4. These
methods that simultaneously measure the contrast concentration in the blood
pool and plaque either experience saturated blood signal or low plaque SNR. To
overcome this limitation, we implemented a short-TR 3D T1w Stack of Stars (SoS)
sequence to enable retrospective image formation with arbitrary numbers of undersample
radial views by using Golden-angle
radial sparse parallel (GRASP) MRI reconstruction. METHODS
We implemented a short-TR 3D T1w SoS
sequence with golden angle view order to enable retrospective image formation
with arbitrary numbers of views. Acquisition matrix was 192x304x24, resolution
0.8mmx0.8mmx1.5mm, TE/TR=2ms/5ms, 10 total measurements over 372s (32s per
measurement). All imaging was performed on Siemens 3T scanners with a 3D radial
SoS sequence and using a home built 8-channel carotid coil. After scout scans
to locate the vessel regions of interest, 3D DCE SoS scans were acquired continuously
for 5 minutes. One minute after the start of the scan, a Gdbased contrast agent
(Gadovist; 0.1 mmol/kg) was injected intravenously. For image reconstruction,
19 or 76 spoke per time frame was used, resulting in a temporal footprint of 16
and effective temporal resolution of 2.1 or 8.4s, respectively. Fourier
transform was applied on the partition dimension followed by slice-by-slice
GRAPPA operator gridding (GROG)5,6 to grid the k-space data on a Cartesian
grid. Then a temporally constrained reconstruction7 was employed to reconstruct the image, by
minimizing the following cost function:
$$m={arg min_{m}}\parallel Am-d\parallel_2^2+λ_t\parallel\sqrt{(∇_t m)^2+ϵ}\parallel_1$$
where d is the GROG interpolated Cartesian k-space, A=DFS is the sampling matrix with S being the sensitivity map,
the undersampling mask, and λt =0.03C . The
data reconstructed with 16 temporal footprint was used to measure arterial
input function(AIF). The data with lower temporal footprint (4 temporal frames
per measurement) was used to find the tissue contrast uptake curves and Ktrans
calculation.RESULTS
Fig 1 shows reconstructed dynamic DCE source images from a patient with a
visible carotid plaque on T1w black blood images. Fig 2 shows static
close-ups of atherosclerotic plaque of the same patient. High perfusion in the
plaque shown on the blue ROI is apparent from the contrast uptake. Corresponding
signal intensity-time curves for AIF and plaque ROIs are shown in Fig 3. The
blue line represent arterial input functions from the high temporal reconstruction(1.8 sec time resolution). The
orange line corresponds to the signal measured in the area indicated by a blue
ROI in.Fig 2. Fig 4 shows the corresponding Ktrans map. Mean Ktrans on the plaque
ROI was 0.16±0.08mm-1. Fig 5
demonstrates a Ktrans map of a patient with intraplaque hemorrhage. Mean Ktrans
on hemorrhage was 0.21±0.11mm-1.
DISCUSSION
3D SoS DCE acquisition provides the high temporal and spatial resolution
when combined with a golden angle view ordering. The proposed method can measure the dynamics
of contrast uptake in the plaque or possibly adventitia (high spatial
resolution, 0.8 mm isotropic voxel dimension) with simultaneous measurement of the AIF (high temporal resolution, 1.8 sec time resolution of 3D DEC)
by retrospective GRASP image
reconstruction. The high-density central k-space sampling by the SoS sequence
can be used to detect and correct motion corrupted measurements to attain
accurate, consistent measures of plaque components during DCE acquisition. To
improve the accuracy of DCE measurement, we will investigate retrospective data
consistency and constrained reconstruction methods to deal with swallowing and
other motion-induced artifacts when they occur. CONCLUSION
3D
SOS DCE acquisition with GRASP reconstruction may provide a measure of
the microvessel surface area and permeability and surrogate for inflammation,
which may be more predictive of plaque vulnerability and a better metric to
monitor treatment effects compared to visual inspection. Acknowledgements
Supported by R01 HL127582, RSNA
Research Scholar Grant RSCH1414, AHA Scientist Development Grant 17SDG33460420,
Siemens Medical Solutions, and the Clinical Merit Review Grant from the
Veterans Administration health Care System.
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