Stroke. 2006;37:2162-2164
Published online before print June 29, 2006,
doi: 10.1161/01.STR.0000231648.74198.f7
(Stroke. 2006;37:2162.)
© 2006 American Heart Association, Inc.
An Integrated Automated Analysis Method for Quantifying Vessel Stenosis and Plaque Burden From Carotid MRI Images
Combined Postprocessing of MRA and Vessel Wall MR
Isabel M. Adame, MSc;
Patrick J.H. de Koning, MSc;
Boudewijn P.F. Lelieveldt, PhD;
Bruce A. Wasserman, MD;
Johan H.C. Reiber, PhD
Rob J. van der Geest, MSc
From the Division of Image Processing (I.M.A., P.J.H.d.K., B.P.F.L., J.H.C.R., R.J.v.d.G), Department of Radiology, Leiden University Medical Center, Leiden, the Netherlands, and the Russell H. Morgan Department of Radiology and Radiological Sciences (B.A.W.), Johns Hopkins Hospital, Baltimore, Md.
Correspondence to Isabel Maria Adame, Division of Image Processing (LKEB), Department of Radiology, Leiden University Medical Center (LUMC), Albinusdreef 2, PO Box 9600, 2300 RC Leiden, The Netherlands. E-mail I.M.Adame{at}lumc.nl
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Abstract
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Background and Purpose We report the evaluation of a
semiautomated method for in vivo assessment of the severity
of carotid atherosclerosis with minimal user interaction that
combines 3-dimensional contrast-enhanced magnetic resonance
angiography (CE-MRA) and vessel wall magnetic resonance imaging
(MRI).
Methods Lumen and outer-wall contours were automatically detected, and stenosis and plaque burden were estimated. The method was tested on 22 subjects (352 postcontrast, T1-weighted cross sections and 3-dimensional CE-MRA).
Results We observed good correlation with expert contours: lumen and outer-wall area (r=0.96) and the degree of stenosis (r=0.97).
Conclusions The fusion of MRA and MRI reduces user interaction and improves contour detection, providing reproducible parameters to assess the severity of atherosclerosis.
Key Words: atherosclerosis carotid artery magnetic resonance angiography magnetic resonance imaging
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Introduction
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Contrast-enhanced magnetic resonance angiography (CE-MRA) determines
the location and severity of stenotic lesions,
1 whereas vessel
wall magnetic resonance imaging (MRI) can depict outward remodeling
and distinguish among plaque components.
The purpose of this work was to develop an automated method for quantitative assessment of atherosclerosis from the combined data of CE-MRA and postcontrast T1-weighted MRI images (PC-T1W MRI) of the vessel wall. Automated detection of luminal contours is performed in both datasets (2 initialization points are needed), followed by automated detection of the outer-wall contours on the PC-T1W MRI images. The degree of stenosis is derived from the luminal dimensions, whereas plaque burden is quantified from wall thickness and area measurements on the PC-T1W MRI images.
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Subjects and Methods
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Data for this analysis was part of the Atherosclerosis Risk
in Communities study. The study was approved by the institutional
review board. Twenty-two participants (aged 55 to 74 years)
were randomly selected for this study. Three-dimensional (3D)
CE-MRA (pixel size, 0.94 mm) and 16 axial PC-T1W MRI slices
per subject (pixel size, 0.54 mm) of the carotid arteries were
acquired on a 1.5-T whole-body scanner (EXCITE, GE Medical Systems)
equipped with a 4-element phased-array carotid coil. Gadodiamide
was administered intravenously (0.1 mmol/kg) at a rate of 2
mL/s.
Description of the Algorithm
MRA Segmentation
The user needs to place 2 points to define the vessel segment of interest. A 3D pathline is then automatically detected connecting these points and follows the center line of the vessel. The threshold-based vessel segmentation is based on the detected pathline. The threshold is derived from the maximum intensity at a particular cross section with a full-width 30% maximum criterion.
Lumen and Outer-Wall Contour Detection
The algorithm works on 2-dimensional (2D) images on a slice-by-slice basis. After automated registration, a minimum-cost approach (dynamic programming2) is performed on the vessel wall image to refine the lumen contour,3 which was obtained from MRA. A geometrical model (ellipse) is used to automatically trace the outer boundary of the vessel, as previously described.3 This contour is also refined by using dynamic programming.2 To assess accuracy, all automatically detected contours were compared with manual contours drawn by radiologists blinded to the results of the algorithm.
Stenosis Estimation
The North American Symptomatic Carotid Endarterectomy Trial (NASCET) and the European Carotid Surgery Trial (ECST) criteria were used to measure the degree of stenosis.4,5
Plaque Burden Estimation
Plaque index (percentage of wall volume relative to the volume of the whole vessel lumen and vessel wall inclusively) and vessel wall thickness were measured on the PC-T1W images. Wall volume was estimated in the segment covered by the PC-T1W slices by multiplying the average wall area by the slice thickness.
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Results
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Lumen and Outer-Wall Contour Detection
The descriptive statistics yielded by the automated method were
36.53±22.58 mm
2 for lumen area and 75.71±31.24
mm
2 for outer-wall area. Those measurements derived from manually
traced contours were 40.90±23.45 mm
2 for lumen area and
73.57±31.09 mm
2 for outer-wall area. Those expert contours
were used as a standard to assess the accuracy of the automated
detection method.
A high correlation between automated and manual area measurements was observed for both the lumen and outer wall (r=0.96). The average paired difference between the automatic-manual measurement pairs was 4.35±5.59 mm2 (11.74±15.08%; P=0.0002) for lumen area and 2.13±10.62 mm2 (2.97±14.80%; P=0.0001) for outer-wall area. The automated vessel wall contour detection (both on CE-MRA and PC-T1W-MRI) takes less than 20 seconds per subject.
Stenosis and Plaque Burden Measurements
Table 1 presents estimates of the severity of stenosis. The average paired difference between the ECST/NASCET combination measurement pairs was 7.42±8.71% (P=NS) and between the ECST/NASCET MRA, it was 7.58±11.14% (P=NS). Table 1 also shows values for plaque index and vessel wall thickness. In 6 cases (I-II, American Heart Association classification6) where CE-MRA found almost no stenosis, analysis of the PC-T1W MRI images showed that there was an abnormal vessel wall, corresponding to the early stages of atherosclerosis: low plaque burden and marginal luminal reduction (Figure, B). The rest of the subjects, who had higher degrees of stenosis (c, d; III-VI), had a high plaque index and increased vessel wall thickness. Table 2 presents statistics for interobserver and intraobserver reproducibility. The measurements from different analyses were also compared with Students 2-sided paired t test and showed no statistically significant difference (P>0.05).

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Automatically detected contours superimposed over the maximum-intensity projection (MIP). A, Severely stenotic vessel. B, Nonstenotic vessel with outward remodeling. CCA indicates common carotid artery; ICA, internal carotid artery.
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Discussion
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Only a few studies have been reported that combine different
MRI sequences to characterize plaque composition.
7,8 In the
present study, CE-MRA and PC-T1W MRI are combined to delineate
the contours of the vessel wall. Reproducibility was higher
for the combined approach (
Table 2), which demonstrates that
the combination of CE-MRA and vessel wall PC-T1W images reduces
subjectivity from the process of stenosis estimation.
Table 1 demonstrates that with the combined approach, the effect of
outward remodeling can be observed, as different subjects showed
a low stenosis percentage by CE-MRA (type c in
Table 1 and panel
B of the
Figure), despite a large amount of plaque detected
by PC-T1W MRI.
Although the average paired difference between automatic/manual measurement pairs was statistically significant (P<0.05), this is not assumed to be clinically relevant, as the differences are very small (lumen,
2 mm2; outer-wall,
4 mm2) in comparison with the average values (lumen,
37 mm2; outer-wall,
76 mm2).
In conclusion, the fusion of MRA and MRI reduces user interaction and improves contour detection, providing reproducible parameters to assess the severity of atherosclerosis. Nevertheless, further work needs to be done including more patients (multicenter study) and comparing the reported algorithm with ultrasound data.
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Acknowledgments
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Source of Funding
This work was supported by the Dutch Science Foundation under innovational research incentive grant No. 016.026.017.
Disclosures
None.
Received March 17, 2006;
accepted May 11, 2006.
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