Hongwei Li1, Peng Wu2, Weibo Chen2, He Wang1,3, and Zhensen Chen1,3
1Institute of Science and Technology for Brain-inspired Intelligence, Fudan University, Shanghai, China, 2Philips Healthcare, Shanghai, China, 3Key Laboratory of Computational Neuroscience and Brain-Inspired Intelligence (Fudan University), Ministry of Education, Shanghai, China
Synopsis
Keywords: Data Processing, Perfusion, ASL
Motivation: VE-DASL is promising in achieving fast vascular territory mapping by using short labeling duration and post-labeling delay, but the accuracy is limited, especially in the border zones.
Goal(s): To achieve a robust vascular territories separation using VE-DASL.
Approach: We adopted optimal encoding scheme and simulated the signal for each territory. The voxels that best matched the simulated signal were identified and their signal was used as the reference. The vascular territories were obtained using matrix inversion or correlation analysis.
Results: The proposed method achieved results comparable to VEASL and demonstrated the capability to differentiate the four vascular territories.
Impact: We improved VE-DASL by using OES and the proposed vessel-decoding method.
This approach enabled us to achieve results comparable to VEASL while offering
the potential for extension to more complex vascular scenarios.
Introduction
Distinguishing arterial blood supply to specific brain regions is crucial
in the assessment of collateral flow in steno-occlusive cerebrovascular
diseases. Super-selective ASL and vessel-encoded arterial spin labeling (VEASL)
are currently the two primary non-invasive techniques for vascular territory
mapping1,2. However, they both suffer from long scan
time. The previously proposed vessel-encoded dynamic ASL (VE-DASL) is promising
in achieving very fast cerebral territory mapping due to the use of short
labeling duration (LD) and post-labeling delay (PLD)3. However, the accuracy of VE-DASL is limited,
especially in the border zones. This study proposed to improve VE-DASL by using
optimal encoding scheme (OES)4 and a novel vessel-decoding method. This
approach enabled us to achieve results comparable to VEASL while offering the
potential for extension to more complex vascular scenarios.Materials and methods
Sequence design
The IRB-approved experiment was performed on a 3T Philips Ingenia CX
scanner. As shown in Figure 1, leveraging Philips' Pride tool, we developed an interaction interface to
select the 4 vessels of interest (i.e. two ICAs and two VAs) on a 2D image at
the labeling plane on the console. The OES algorithm was implemented for
automated encoding pattern calculation, which included the angles of the
in-plane gradient, encoding spacing, and encoding offset to determine the label
conditions. Several non-selective cycles were added to the beginning and end of
the sequence in order to enhance the robustness of vessel-decoding.
Image acquisition
Traditional VEASL, 2D VE-DASL and 3D VE-DASL with OES labeling patterns
were scanned on one healthy volunteer. The imaging parameters were as follows.
Traditional VEASL: 2D EPI readout, 20 slices, LD 1650 ms, PLD 1575 ms, voxel
size 2.75×2.75×5 mm3. VE-DASL: LD 800 ms, flip angle 25°, PLD 70 ms
for 3D TFEPI readout, 10 ms for 2D multislice EPI readout, OES labeling
pattern, each pattern repeated ten times, and the whole labeling scheme was
repeated twice (see Figure 1), resulting in a total of 160 volumes.
Vessel-decoding methods
A two-compartment model was used to simulate the signal evolution in a
particular territory as the initial reference3, where the labeling efficiency was directly obtained through the OES. As
shown in Figure 2, the signal preprocessing steps included spatial denoising, temporal
smoothing, and detrending. Then, we first identified the high-confidence voxels
that best matched the simulated signal using matrix inversion. In the second
step, we replaced the simulated signal with the mean signal of these
high-confidence voxels, which served as the new reference, and further
classified the signal for each voxel. In the preprocessing, the impact of
detrending was assessed on the final vessel-decoding. In the second step of
processing, we compared the matrix inversion approach and maximum-correlation approach
for vessel-decoding. The proposed novel vessel-decoding approach was also
compared to the direct k-means clustering algorithm and simple matrix
inversion, while using identical preprocessing procedures.Results
The proposed approach showed a significant
improvement compared to traditional clustering or matrix inversion methods,
particularly in the posterior circulation territory, achieving a Dice
coefficient of approximately 80% with the VEASL used as gold standard, as shown
in Figure 3A and 3B. As shown in Figure 3C and 3D, detrending could improve the Dice coefficient by about 10%.
Additionally, the maximum-correlation approach was slightly better than the
matrix inversion approach in all vascular territories. The resulting territory
maps are shown in Figure 4. The proposed method achieves results comparable to VEASL and
demonstrates the capability to differentiate between the four vascular
territories.Discussion and conclusions
Among the evaluated approaches, the use of detrending in preprocessing,
followed by maximum-correlation analysis using the high-confidence voxels’
signals as reference, seems to result in the best vessel-decoding for VE-DASL.
The large discrepancy between the high-confidence voxels’ signals and the
simulated signals is likely due to the presence of partial labeling in the OES
design. In real scan, factors such as B1 inhomogeneity and head motion may
contribute to this discrepancy. In future work, efforts will be made to
optimize the OES design and ASL scan parameters, aiming to bring each labeling
arteries as close as possible to the label and control states. On the flip
side, our proposed method to some extent can mitigate the impact of partial
labeling, resulting in a more robust territory mapping, although further
validation is needed.Acknowledgements
This work was supported by Natural Science Foundation of Shanghai
(22ZR1403900).References
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Webb, A.G. & van Osch, M.J.P. Fast cerebral flow territory mapping using
vessel encoded dynamic arterial spin labeling (VE-DASL). Magnetic Resonance in Medicine 75,
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