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A Generative Model for Automatic Detection of Resolving Multiple Sclerosis Lesions

机译:用于多发性硬化症病变自动检测的生成模型

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The appearance of new Multiple Sclerosis (MS) lesions on MRI is usually followed by subsequent partial resolution, where portions of the newly formed lesion return to isointensity. This resolution is thought to be due mostly to reabsorption of edema, but may also reflect other reparatory processes such as remyelination. Automatic identification of resolving portions of new lesions can provide a marker of repair, allow for automated analysis of MS lesion dynamics, and, when coupled with a method for detection of new MS lesions, provide a tool for precisely measuring lesion change in serial MRI. We present a method for automatic detection of resolving MS lesion voxels in serial MRI using a Bayesian framework that incorporates models for MRI intensities, MRI intensity differences across scans, lesion size, relative position of voxels within a lesion, and time since lesion onset. We couple our method with an existing method for automatic detection of new MS lesions to provide an automated framework for measuring lesion change across serial scans of the same subject. We validate our framework by comparing to lesion volume change measurements derived from expert semi-manual lesion segmentations on clinical trial data consisting of 292 scans from 73 (54 treated, 19 untreated) subjects. Our automated framework shows a) a large improvement in segmentation consistency over time and b) an increased effect size as calculated from measured change in lesion volume for treated and untreated subjects.
机译:在MRI上出现新的多发性硬化症(MS)病变后,通常会出现随后的部分消退,其中新形成的病变部分会恢复到等强度。认为该分辨率主要归因于水肿的重吸收,但也可能反映了其他修复过程,例如髓鞘再生。自动识别新病变的可解决部分可以提供修复标记,允许对MS病变动态进行自动分析,并且当与检测新MS病变的方法结合使用时,可以提供一种在串行MRI中精确测量病变变化的工具。我们提出了一种使用贝叶斯框架自动检测串联MRI中MS病变体素的方法,该方法结合了MRI强度,跨扫描的MRI强度差,病变大小,病变内体素的相对位置以及病变开始时间的模型。我们将我们的方法与用于自动检测新的MS病变的现有方法相结合,以提供一个自动框架来测量同一受试者的连续扫描中的病变变化。我们通过与来自专家半手动病灶分割的病灶体积变化测量结果进行比较来验证我们的框架,该临床试验数据包括来自73位(54位经治疗,19位未经治疗)受试者的292次扫描。我们的自动化框架显示a)随时间变化的分割一致性有了很大的改善,并且b)从治疗和未治疗的受试者的病变体积的测量变化计算得出的效应大小增加了。

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