Liwen Wan1, Na Zhang1, Lei Zhang1, Shi Su1, Cheng Wang1, Baochang Zhang1, Hao Peng1, Haoxiang Li1, Dong Liang1, Xin Liu1, and Hairong Zheng1
1Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, China
Synopsis
Intracranial and extracranial
atherosclerotic disease are major causes of ischemic stroke. Manual analyses of
intracranial and extracranial artery vessel wall are time consuming and
experience dependent. The purpose of this study was to develop an automated
method to analyze 3D intra- and extracranial arterial vessel wall images,
including vessel centerline tracking, vessel straightened reformation, vessel
wall segmentation based on CNN, and morphological quantification. In
conclusion, the proposed method facilitates the large-scale quantitative
analysis of vessel wall, and is promising in promoting the clinical
applications of MR vessel wall imaging.
Introduction
Atherosclerotic
plaque rupture of intracranial and extracranial arteries is major cause of
ischemic stroke [1, 2]. In recent years, several high-resolution isotropic 3D black-blood
sequences, particularly 3D turbo spin-echo (TSE) with variable refocusing flip
angles, have been introduced to image either intracranial [3-5] or carotid [6, 7]
arterial vessel walls and has proven to be reproducible for arterial vessel
wall and plaque morphological measurements [8]. However, existing arterial vessel
wall analysis is based on two-dimensional (2D) cross-sectional images reconstructed
from the isotropic 3D images by neuroradiologist, which is time consuming and
experience dependent. Therefore, it is expected that an automated analysis method
based directly on 3D black-blood MR images will be easier to operate and more
accurate. In this study, we aim to develop an automated method to analyze 3D
intra- and extracranial arterial vessel wall images, including vessel
centerline tracking, vessel straightened reformation, vessel wall segmentation,
and morphological quantification. Methods
The automated analysis framework of
arterial vessel wall morphology is built based on intra- and extracranial
arterial vessel wall images acquired by recently developed T1-weighted
DANTE-SPACE sequence [9] and TOF MRA images. TOF MRA is used to facilitate the
tracking task at the location of small arterial segments, which is commonly challenging
with only vessel wall images. The integrated workflow of image analysis is
shown in Fig.1, along with example images at each stage. To begin with,
comprehensive pattern recognition model is applied to vessel segmentation of
TOF MRA. Next, the vessel centerline is extracted from the segmented TOF MRA
using fast marching algorithm, and then co-registered to 3D vessel wall MR using
coordinate transformation. After that, 3D curved multi-planar reformation (MPR)
is employed to straighten the vessel of interest, and cross-sectional 2D slices
of the vessel segment are obtained through resampling. Finally, the proposed
U-net-like fully convolutional neural network (CNN) is applied to vessel wall
segmentation (Fig.2), and then calculate the maximum wall thickness, wall and
lumen areas, as well as normalized wall index (NWI). Dice coefficient was used
to evaluate the overlapping ratio between the automated segmentation and manual
ground truth. Also, two-tailed paired student’s t-tests were used for the
comparison of quantification metrics derived from proposed method and manually reformatted.Results
A total of 47 subjects completed the MR
examinations and the proposed framework was used for image processing. Large-range
anterior circulation (from internal carotid artery to M2 of the middle cerebral
artery) and posterior circulation (from the vertebral artery to P1 of the
posterior cerebral arteries) vasculatures were traced and straightened, 13680 2D
slices of the interested vessel segments were generated. Representative processed
images of a subject were presented in Fig. 3. Vessel wall can be clearly seen
in both the longitudinal and transverse views, which largely facilitates the
diagnosis of vessel wall diseases. The U-net-like network was trained and
validated on 12960 slices and tested on 720 slices. The proposed segmentation
method demonstrated satisfactory agreement with manual segmentation, as shown
in Fig.4, the Dice coefficient of intracranial arteries was 0.93 for lumen and
0.80 for vessel wall while 0.94 for lumen and 0.87 for vessel wall of extracranial
arteries. Moreover, our method was able to locate the vessel region and provide
reasonable segmentation, even when the boundaries in neighboring tissues were
essentially invisible to naked eyes. Tab.1 summarized the vessel wall
morphological measurements of intra- and extracranial arteries from automated
and manual methods, respectively on 20 random subjects. Although the maximum
wall thickness and NWI of the proposed method were larger than the manual
results for both intra- and extracranial arteries results, the differences are small
and cannot be considered to be statistically significant (p > 0.05).Discussion and Conclusion
In this work, a framework to automatically
segment the intra- and extracranial arterial vessel wall was developed,
including functions of vessel path tracking, 3D MPR, vessel wall segmentation,
and measurement calculation. The proposed method achieved good agreements with
manual segmentation. The Dice coefficient of extracranial arteries, especially
for the wall, was higher than that of intracranial arteries. This may be due to
the possible leak at low-contrast outer wall boundary of smaller intracranial
arteries. The Dice coefficient was slightly higher than previous studies [10],
which benefited from the residual information added to preserve the original
image features, and the spatial pyramid pooling used to extract multi-scale
features of the proposed network. In conclusion, this automated analysis method
makes large-scale quantitative vessel wall analysis easier and more accurate, which
could potentially promote the adoption of Vessel Wall MRI in clinical
application.Acknowledgements
This work was supported in part by National
Natural Science Foundation of China (81830056, 81801691).References
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