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Diffusion-weighted imaging-based probabilistic segmentation of high- and low-proliferative areas in high-grade gliomas

机译:基于扩散加权成像的高级别胶质瘤高和低增生区域的概率分割

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摘要

The apparent diffusion coefficient (ADC) derived from diffusion-weighted imaging (DWI) correlates inversely with tumor proliferation rates. High-grade gliomas are typically heterogeneous and the delineation of areas of high and low proliferation is impeded by partial volume effects and blurred borders. Commonly used manual delineation is further impeded by potential overlap with cerebrospinal fluid and necrosis. Here we present an algorithm to reproducibly delineate and probabilistically quantify the ADC in areas of high and low proliferation in heterogeneous gliomas, resulting in a reproducible quantification in regions of tissue inhomogeneity. We used an expectation maximization (EM) clustering algorithm, applied on a Gaussian mixture model, consisting of pure superpositions of Gaussian distributions. Soundness and reproducibility of this approach were evaluated in 10 patients with glioma. High- and low-proliferating areas found using the clustering correspond well with conservative regions of interest drawn using all available imaging data. Systematic placement of model initialization seeds shows good reproducibility of the method. Moreover, we illustrate an automatic initialization approach that completely removes user-induced variability. In conclusion, we present a rapid, reproducible and automatic method to separate and quantify heterogeneous regions in gliomas.
机译:从扩散加权成像(DWI)得出的表观扩散系数(ADC)与肿瘤增殖率成反比。高级别神经胶质瘤通常是异质性的,部分体积效应和边界模糊阻碍了高和低增殖区域的描绘。与脑脊液的潜在重叠和坏死进一步阻碍了常用的手动描绘。在这里,我们提出了一种算法,可重现地描述和概率量化异质性神经胶质瘤中高和低增殖区域中的ADC,从而导致组织不均匀性区域中的可重现量化。我们使用了期望最大化(EM)聚类算法,该算法应用于高斯混合模型,该模型由高斯分布的纯叠加组成。在10例神经胶质瘤患者中评估了这种方法的可靠性和可重复性。使用聚类发现的高和低扩散区域与使用所有可用成像数据绘制的感兴趣的保守区域非常吻合。模型初始化种子的系统放置显示了该方法的良好重现性。此外,我们说明了一种自动初始化方法,该方法完全消除了用户引起的可变性。总之,我们提出了一种快速,可重现和自动的方法来分离和量化神经胶质瘤中的异质区域。

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