Haikun Qi1, Huiyu Qiao1, Shuo Chen1, Zechen Zhou2, Xinlei Pan1, Yishi Wang1, Chun Yuan1,3, and Huijun Chen1
1Center for Biomedical Imaging Research, School of Medicine, Tsinghua University, Beijing, People's Republic of China, 2Philips Research China, Shanghai, People's Republic of China, 3Department of Radiology, University of Washington School of Medicine, Seattle, WA, United States
Synopsis
Intra-plaque hemorrhage (IPH) is a dynamic
process and change of the IPH MR signal was found to be correlated with plaque
developments. So quantitative T1 mapping of plaque is essential to monitor
plaque progression. In this study, we proposed an IR prepared 3D golden angle
radial sampling sequence, enabling multiple T1 contrasts acquisition in a
single scan (MASS) with application to carotid artery T1 mapping. The accuracy and
feasibility of MASS was demonstrated in phantom studies and in vivo imaging experiments
on healthy volunteers and carotid atherosclerosis patients. MASS may be a
one-stop solution to carotid atherosclerotic plaque imaging.
Purpose
Carotid atherosclerosis has become the
major cause of ischemic cerebrovascular event (1).
Intra-plaque hemorrhage (IPH) is considered a characterization of vulnerable plaque,
and can be detected by T1 weighted (T1W) MR sequences, such as MPRAGE (2),
or SNAP (3).
Recently, studies found that the T1 signal of IPH is changing across time (4),
indicating IPH is a dynamic process. Moreover, the signal change of IPH on T1W MR
images was found to be associated with plaque developments (5).
Therefore, quantitative T1 mapping of plaque is important to better assess
atherosclerotic plaque. In this study, we have developed a sequence enabling Multiple
T1 contrasts Acquisition in a Single Scan (MASS) for 3D T1 mapping of carotid vessel
wall.Methods
Sequence Design: The proposed
sequence consists of an IR preparation pulse and a 3D radial sampling
acquisition (Fig. 1). Spokes of the same Inversion Time (TI) in different IRTRs
conform to the golden angle distribution (6), to achieve a uniformly distributed
k-space at certain TI for reconstruction. Water excitation pulse was used to
suppress fat signal. MR Imaging: All scans were performed on a 3T
Philips Scanner. For phantom studies, 9 tubes containing diluted Gd-DTPA with different
concentrations were designed. T1 mapping of phantoms were performed using both
MASS and a standard 2D IR-SE sequence (7). For in vivo experiments, after institutional
review board approval, 6 healthy volunteers and 5 patients with carotid
atherosclerotic plaques were imaged using a custom-designed 36-channel
neurovascular coil (8). The scan included the T1W QIR-TSE
black-blood sequence (9), SNAP (3), and a 5 min MASS scan with imaging
parameters shown in Table 1. Image Reconstruction: Sliding window and narrow-KWIC
filter with CG-SENSE (10) were used together to generate image
series along the inversion recovery curve. For coil sensitivities estimation, MASS
image at TI=1300ms was reconstructed with temporal window width (TW)=35 and
KWIC filter (11). Because image contrast is dominated by
the central parts of k-space, the reconstructed image intensity is determined
by averaging the signal at spoke number of n to n+TW-1, where n is the start
spoke index, ranging from 1 to N-TW+1 with an interval of TW, and N is the TFE
factor. By setting TW=19, 8 frames of images were reconstructed. The last frame
was used to remove the background phase in phase-sensitive reconstruction. Then,
T1 mapping was performed by fitting the signal curve from the reconstructed
image series to the theoretically calculated signal equation (3) voxel-by-voxel. Image Analysis: MASS
images were reformatted to 2mm axial slices with the same geometry to QIR-TSE,
and matched to QIR-TSE based on carotid bifurcation. Then, for healthy arteries,
5 axial slices were selected from CCA. For atherosclerotic arteries, 5 axial
slices centered at the carotid bifurcation were selected. The lumen, outer wall
and adjacent muscle contours were drawn on QIR-TSE images of the selected
slices. Then the mean T1 of the carotid vessel wall or plaque, and muscle
region were calculated for each slice. The slice-averaged T1 values for healthy
vessel wall and muscle were reported. For each atherosclerotic artery, the mean
T1 of the slices with plaque were averaged to generate the overall T1 of the plaque.
Moreover, the corresponding SNAP images were reviewed to identify IPH. Results
The
T1 mapping results of phantom are shown in Fig. 2. The T1 values from MASS were
in good agreement with 2D IR-SE with measurement bias of 4.3%±2.5%. For in vivo
imaging, 7 carotid arteries were detected with plaque in the 5 patients, among
which 3 arteries were identified to have IPH on SNAP images. An example of MASS
images at multiple TIs and the generated T1 map of an artery with IPH are shown
in Fig. 3. Strong hyperintensities were seen in the plaque on the SNAP image,
and the IPH regions showed strongly reduced values on the T1 map (IPH1: 412ms;
IPH2: 353ms). The T1 measurements were summarized in Table 2. The plaque with
IPH has lower T1 value than healthy vessel wall and the plaque without IPH. Discussion and Conclusions
In
this study, we have developed a 3D technique that can acquire co-registered
images with multiple T1 contrasts in a single scan in short scan time (5min).
The feasibility of MASS in quantitative T1 mapping of carotid artery has been
demonstrated in healthy volunteers and atherosclerotic patients. In conclusion,
MASS may be a useful tool to detect T1 changes of atherosclerotic plaque, and thus monitor
its progression.Acknowledgements
No acknowledgement found.References
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