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A comprehensive approach to the segmentation of multichannel three-dimensional MR brain images in multiple sclerosis

机译:用于多发性硬化症的多通道三维MR脑图像分割的综合方法

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摘要

Accurate classification and quantification of brain tissues is important for monitoring disease progression, measurement of atrophy, and correlating magnetic resonance (MR) measures with clinical disability. Classification of MR brain images in the presence of lesions, such as multiple sclerosis (MS), is particularly challenging. Images obtained with lower resolution often suffer from partial volume averaging leading to false classifications. While partial volume averaging can be reduced by acquiring volumetric images at high resolution, image segmentation and quantification can be technically challenging. In this study, we integrated the brain anatomical knowledge with non-parametric and parametric statistical classifiers for automatically classifying tissues and lesions on high resolution multichannel three-dimensional images acquired on 60 MS brains. The results of automatic lesion segmentation were reviewed by the expert. The agreement between results obtained by the automated analysis and the expert was excellent as assessed by the quantitative metrics, low absolute volume difference percent (36.18 ± 34.90), low average symmetric surface distance (1.64 mm ± 1.30 mm), high true positive rate (84.75 ± 12.69), and low false positive rate (34.10 ± 16.00). The segmented results were also in close agreement with the corrected results as assessed by Bland–Altman and regression analyses. Finally, our lesion segmentation was validated using the MS lesion segmentation grand challenge dataset (MICCAI 2008).
机译:脑组织的准确分类和定量对于监视疾病进展,萎缩的测量以及将磁共振(MR)量度与临床残疾相关联非常重要。存在病变(例如多发性硬化症(MS))的MR脑图像的分类特别具有挑战性。以较低分辨率获得的图像通常会受到部分体积平均的影响,从而导致分类错误。尽管可以通过以高分辨率获取体积图像来减少部分体积平均,但是图像分割和量化在技术上可能具有挑战性。在这项研究中,我们将大脑解剖学知识与非参数和参数统计分类器集成在一起,以自动对在60个MS大脑上获得的高分辨率多通道三维图像上的组织和病变进行分类。专家审查了自动病变分割的结果。通过定量指标评估,自动化分析获得的结果与专家之间的一致性非常好,绝对体积差百分比低(36.18±34.90),平均对称表面距离低(1.64 mm±1.30 mm),真实率高( 84.75±12.69)和较低的假阳性率(34.10±16.00)。细分结果也与通过Bland–Altman和回归分析评估的校正结果非常吻合。最后,我们使用MS病变分割大挑战数据集(MICCAI 2008)验证了我们的病变分割。

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