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Automated segmentation of changes in FLAIR-hyperintense white matter lesions in multiple sclerosis on serial magnetic resonance imaging

机译:在连续磁共振成像中自动分割多发性硬化症中FLAIR-高强度白质病变的变化

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摘要

Longitudinal analysis of white matter lesion changes on serial MRI has become an important parameter to study diseases with white-matter lesions. Here, we build on earlier work on cross-sectional lesion segmentation; we present a fully automatic pipeline for serial analysis of FLAIR-hyperintense white matter lesions. Our algorithm requires three-dimensional gradient echo T1- and FLAIR- weighted images at 3 Tesla as well as available cross-sectional lesion segmentations of both time points. Preprocessing steps include lesion filling and intrasubject registration. For segmentation of lesion changes, initial lesion maps of different time points are fused; herein changes in intensity are analyzed at the voxel level. Significance of lesion change is estimated by comparison with the difference distribution of FLAIR intensities within normal appearing white matter. The method is validated on MRI data of two time points from 40 subjects with multiple sclerosis derived from two different scanners (20 subjects per scanner). Manual segmentation of lesion increases served as gold standard. Across all lesion increases, voxel-wise Dice coefficient (0.7) as well as lesion-wise detection rate (0.8) and false-discovery rate (0.2) indicate good overall performance. Analysis of scans from a repositioning experiment in a single patient with multiple sclerosis did not yield a single false positive lesion. We also introduce the lesion change plot as a descriptive tool for the lesion change of individual patients with regard to both number and volume. An open source implementation of the algorithm is available at .
机译:纵向MRI对白质病变变化的纵向分析已成为研究具有白质病变的疾病的重要参数。在此,我们以横截面病变分割的早期工作为基础;我们提供了用于FLAIR高敏性白质病变序列分析的全自动管线。我们的算法需要3特斯拉的三维梯度回波T1和FLAIR加权图像,以及两个时间点的可用横截面病变分割。预处理步骤包括病变填充和受试者体内配准。为了分割病变变化,融合了不同时间点的初始病变图。在本文中,在体素水平上分析强度的变化。通过与正常出现的白质内FLAIR强度的差异分布进行比较,可以估算出病变变化的重要性。该方法在来自两个不同扫描仪的40个患有多发性硬化症的受试者(每个扫描仪20个受试者)的两个时间点的MRI数据上得到了验证。病变的手动分割是金标准。在所有病变的增加中,体素方向的Dice系数(0.7)以及病变方向的检测率(0.8)和错误发现率(0.2)表明总体性能良好。对单发多发性硬化症患者进行重新定位实验的扫描结果分析未产生单个假阳性病变。我们还介绍了病变变化图,作为描述单个患者病变数量和体积的工具。该算法的开放源代码实现位于。

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