Haining Wei1, Mingzhu Fu1, Hanyu Wei1, Zhongsen Li1, and Rui Li1
1Center for Biomedical Imaging Research, Department of Biomedical Engineering, Tsinghua University, Beijing, China
Synopsis
Keywords: Software Tools, Software Tools, Aneurysm Wall Enhancement
Motivation: Aneurysm wall enhancement visualized on high-resolution magnetic resonance imaging is considered as an indicator of inflammation.
Goal(s): Recently, there has been increased attention on 3D AWE mapping, which is seen as an objective tool for examining rupture risk of aneurysms.However, the roughly estimated vessel wall location and thickness result in some measurement errors.
Approach: In this study, we propose a fast measurement method that can automatically access wall thickness and generate the 3D spatial distribution of wall enhancement ratio.
Results: The automatic method simplifies and accelerates the workflow of aneurysm wall identification and analysis.
Impact: We propose a fast measurement method that can automatically access wall thickness and generate the 3D spatial distribution of wall enhancement ratio. The automatic method simplifies and accelerates the
workflow of aneurysm wall identification and analysis.
INTRODUCTION
The prevalence of intracranial aneurysms
(IA) is estimated to be 3%-5% worldwide[1]. The rupture of IAs can be a catastrophic
event and leading to intracranial subarachnoid hemorrhage, which has a
mortality rate of up to 50%[2].
Increasing histopathological evidence suggested that the inflammation processes
on vessel wall may mediate the growth and rupture of IA[3]. Aneurysm wall enhancement (AWE)
visualized on high-resolution magnetic resonance imaging (HR-MRI) is considered
as an indicator of inflammation[4]. Recently,
there has been increased attention on 3D AWE mapping[5, 6, 7], which is seen
as an objective tool for examining rupture risk of aneurysms. However, the roughly
estimated vessel wall location and thickness result in some measurement errors.
Meanwhile, more accurate measurement of the vessel wall requires too much
manual operation. In this study, we propose a fast measurement method that can automatically
access wall thickness and generate the 3D spatial distribution of wall enhancement
ratio. METHODS
MRI
acquisition
MRI
sequences including 3D black-blood T1-weighted volumetric isotropic turbo spin
echo acquisition (T1) and TOF were performed on a 3.0T Philips Achieva scanner. The parameters
for T1 and CE-T1 were as follows: TR/TE=800/21ms, FOV=200x180x40mm3,
voxel size = 0.6x0.6x0.6mm3. The parameters for TOF were TR/TE =
25/3.5ms, FOV = 160×160×60mm3, voxel size = 0.8×0.8×0.8mm3. CE-T1 was
performed about 6 min after an injection of GdDTPA.
3D
AWE assessment
The workflow for 3D AWE assessment is shown
in Fig.1. T1 and CE-T1 are registered to TOF images to
obtain the corresponding signal intensity distribution. After choosing ROI, 3D
model of aneurysm was generated by threshold segmentation of TOF images. The
original threshold is calculated by triangle method and can be manually
adjusted. For each vertex in the aneurysm surface model, we create the spokes
along normal direction and sample the T1 and CE-T1 signal. As shown in Fig.2(A), a spoke is
projected from inner to the outer boundary of the aneurysm and colored with T1 signal
intensity at the corresponding location. The calculation algorithm for aneurysm
wall thickness based on T1 images is shown in Fig.2(B). For each signal intensity profile after
linear interpolation, there exist three key indexes[8]. In general, the vertex on the aneurysm
surface model are located between index1 and index2. After access the derivative
of signal intensity profile, Index1 is defined as: from vertex to the inner, the
closest point to the vertex cross zero. Index2: from vertex to the outer, the
closest point to the vertex cross zero. Index3: from Index2 to the outer, the
point cross zero. The distance between two half peaks points is defined as aneurysm wall of this spoke. Specific
spoke has same Index2 and Index3 when the outer wall of the aneurysm could not
be differentiated from the adjacent brain tissue. T1 AWE mapping is calculated
by the average signal intensity of the aneurysm wall. CE-T1 AWE mapping is calculated
within the same indexes. The final wall enhancement ratio is obtained by
following formula:
$$AWE-ratio=\frac{Intensity_{T1}-Intensity_{CE-T1}}{Intensity_{T1}}$$
Statistical
analysis
AWE was categorized
into three grades as follow: grade 0 (no enhancement), grade 1 (enhancement less
than that of the pituitary infundibulum and higher than normal vessel wall),
and grade 2 (enhancement equal to or greater than that of the pituitary infundibulum)[9]. We calculated the value
distribution of AWE ratio in the three groups. Skewness, kurtosis, average and variance
are used to describe its characteristics.RESULTS
12
patients harbored with 13 aneurysms were recruited in this study. Fig.3 shows the histograms
of AWE and corresponding AWE ratio in three grades. The characteristics of histogram are different
for aneurysms with different degree of enhancement. As the range and extent of
enhancement increase, we can intuitively see a higher density of high signal
regions on the AWE histograms of T1 and CE-T1. Table I calculated the statistic results of AWE
ratio for each group. Grade 2 aneurysms have the highest average AWE ratio. The average skewness value increases with the increasing of enhancement
degree. DISCUSSION and CONCLUSION
In this study, we investigated the 3D
spatial distribution of AWE by combination of T1 and TOF
images. The automatic method simplifies and accelerates the workflow of aneurysm
wall identification and analysis. 3D-Heatmaps and histograms were generated to
better visualize enhancement topography for different enhancement degrees. Different from previous studies that wall intensity
is determined by the maximum value on the spoke, our algorithm automatically
and accurately measured the wall signal through the key indexes on signal
intensity profile. The future work included a larger group of aneurysm patients
will be performed to validate the validity and reliability of this tool.
Acknowledgements
No acknowledgement found.References
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