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Computer-aided Detection of Ischemic Lesions Related to Subcortical Vascular Dementia on Magnetic Resonance Images

Rationale and Objectives

The purpose of this study was to develop an automated method for detection of the hyperintense ischemic lesions related to subcortical vascular dementia based on conventional magnetic resonance images (T1-weighted, T2-weighted, and fluid-attenuated inversion-recovery images [FLAIR]).

Materials and Methods

Our proposed method was based on subtraction between the T1-weighted image and the FLAIR image. First, a brain region was extracted by an automated thresholding technique based on a linear discriminant analysis for a pixel value histogram. Next, for enhancement of ischemic lesions, the T1-weighted image was subtracted from the fluid-attenuated inversion-recovery image. Ischemic lesion candidates were identified using a multiple gray-level thresholding technique and a feature-based region-growing technique on the subtraction image. Finally, an artificial neural network trained with 15 image features of the ischemic candidates was used to remove false-positives. We applied our method to nine patients with vascular dementia (age range, 64−94 years, mean age, 69.4 years; four males and five females), who were scanned on a 1.5-T magnetic resonance unit.

Results

Our method achieved a sensitivity of 90% with 4.0 false-positives per slice in detection of ischemic lesions. The overlap measure between ischemic lesion areas obtained by our method and a neuroradiologist was 60.7% on average. The ratio of ischemic lesion area to the whole brain area obtained by our method correlated with that determined by a neuroradiologist with a correlation coefficient of 0.911.

Conclusion

Our preliminary results suggest that the proposed method may have feasibility for evaluation of the ischemic lesion area ratio.

Subcortical vascular dementia (VaD) is the second most common type of dementia in Japan. The prevalence of dementia disorders in Japanese population older than 70 years is 51% to 58% for Alzheimer’s disease (AD), which is the most common dementia disorder; 24% to 26% for VaD, 2% for mixed dementia (AD/VaD), and 14% to 23% for other types of dementia ( ). Ischemic lesions related to subcortical VaD are shown as hyperintense regions in the cerebral white matter on fluid-attenuated inversion-recovery (FLAIR) or T2-weighted images at magnetic resonance (MR) imaging. Several studies reported that the degree of the VaD correlated with a ratio of ischemic lesion area to the whole brain (ischemic lesion area ratio) ( ), which could provide the diagnostic information for VaD. Thus, it is very important to estimate the ischemic lesion area ratio to evaluate the degree of VaD. However, it would be difficult and very time consuming in routine clinical practice for neuroradiologists to evaluate the ischemic lesion area manually. A number of researchers attempted to develop methods for identifying and segmenting the ischemic lesions of the stroke ( ). Mohamed et al. ( ) developed a method for segmenting white matter lesions including the ischemic lesions in patients with VaD based on a modified k-nearest-neighbor method, using multispectral three-dimensional (3D) tissue MR images (i.e., T1-weighted, T2-weighted, and proton-density images). They showed that the 3D tissue segmentation technique could characterize white matter lesions with similar intensities on T2-weighted images. However, there is a need for a study that focuses on the ischemic lesions of VaD, because white matter lesions are similar in terms of intensity but their characteristics (eg, shape and location) differ. Therefore, the purpose of this study was to develop an automated method for detection of the hyperintense ischemic lesions related to subcortical VaD based on three types of MR images—T1-weighted, T2-weighted images, and FLAIR images.

Materials and methods

Subjects and MR Imaging

Nine clinical cases used in this study were imaged on a 1.5-T MR unit (Excelart; Toshiba, Tochigi, Japan) under the protocol approved by the institutional review board of Kyorin University Hospital after the nature of the procedure had been fully explained. The nine patients with clinically diagnosed VaD (age range, 64−94 years; mean age, 69.4 years; four males and five females) were scanned, using a slice thickness of 5 mm and a slice gap of 1.5 mm with T1-weighted (TR [repetition time]/TE [echo time]: 496/12 ms), T2-weighted (TR/TE 4280/105 ms), and FLAIR (TR/TE/TI [inversion time] 8000/105/2300 ms) sequences. Each MR image consisted of 320 × 320 to 512 × 512 pixels with a pixel size of 0.43 mm, and the number of gray levels was 10 bits. An experienced neuroradiologist and an experienced medical physicist selected a slice with the most hyperintense ischemic lesions (9.4 lesions on average) from each case, considering size, shape, and contrast. The total number of the ischemic lesions was 85, and the mean area was 147 ± 256 mm 2 . Figure 1 shows the area histogram of all ischemic lesions used for this study. The ischemic lesions with an area smaller than 100 mm 2 are 65% of 85 “truth” lesions determined visually by an experienced neuroradiologist.

Figure 1, Area histogram of all ischemic lesions used for this study.

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Detection of Hyperintense Regions in MR Images

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R=1XY∑X−1X=0∑Y−1Y=0(T(x,y)−T¯¯¯)(F(x,y)−F¯¯¯)tf R

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Figure 2, Overall algorithm for detection of ischemic lesions based on magnetic resonance image. ANN, artificial neural network; FP, false-positive.

Figure 3, ( a ) Original T1-weighted image. ( b ) Segmented brain image. ( c ) Original fluid-attenuated inversion-recovery (FLAIR) image with hyperintense regions. ( d ) Subtraction image between the FLAIR image and T1-weighted image.

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where a is the anteroposterior length of a brain as shown in Figure 4 ; b is the longest distance from a centroid of a head to an ischemic region; c is the shortest distance from a centroid of a head to an ischemic region; and D is the distance from a centroid to each ischemic region. The parameter a was automatically calculated for each case from a binalized brain image. The parameters c and b in Equation 2 shown in Figure 4 were empirically determined and fixed for all cases in this study so that all ischemic lesions in the white matter regions related to the VaD could be detected.

Figure 4, Distance for identification of initial candidates. ( a ) Anteroposterior length of a brain. ( b ) Longest distance from a centroid of a head to an ischemic region. ( c ) Shortest distance from a centroid of a head to an ischemic region. ( d ) Distance from a centroid to each ischemic region.

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Reduction of False-Positives by Using an Artificial Neural Network

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Evaluation of Performance

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OverlapMeasure=n(T∩M)n(T∪M)×100 O

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T is the “truth” regions determined visually by an experienced neuroradiologist, M is the candidate regions obtained by our method, and n is the number of pixels. This overlap measure indicates the degree of consistency between the “truth” regions and candidate regions. The FROC curve was produced by changing a threshold value for the ANN output, which was considered as the possibility of the ischemic lesion.

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Results

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Figure 5, Relationship between maximum pixel value of candidate region in T2-weighted image (normalized) and the angle of a candidate to the x -axis from the centroid of the segmented brain region. Hyperintense and false-positive regions are indicated by solid circles and triangles , respectively.

Figure 6, Free-response receiver-operating characteristic curve for overall performance of our method in detection of ischemic lesions. FP, false-positive.

Figure 7, Bar graph of overlap measure, which indicates the degree of consistency with the truth, for all patients (1 through 9).

Figure 8, Relationship in the ischemic lesion area ratios obtained by our method and by the neuroradiologist.

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Discussion

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Figure 9, Case 7, with the highest measure of 79.0%. ( a ) Hyperintense “truth” regions. ( b ) Candidate regions indicated by white lines .

Figure 10, Case 9, with the lowest measure of 28.9%. ( a ) Hyperintense “truth” regions. ( b ) Candidate regions indicated by white lines .

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Conclusion

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Acknowledgments

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References

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