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An SPM12 extension for multiple sclerosis lesion segmentation

机译:SPM12扩展,用于多发性硬化病灶分割

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Purpose: Magnetic resonance imaging is nowadays the hallmark to diagnose multiple sclerosis (MS), characterized by white matter lesions. Several approaches have been recently presented to tackle the lesion segmentation problem, but none of them have been accepted as a standard tool in the daily clinical practice. In this work we present yet another tool able to automatically segment white matter lesions outperforming the current-state-of-the-art approaches. Methods: This work is an extension of Roura et al. [1], where external and platform dependent pre-processing libraries (brain extraction, noise reduction and intensity normalization) were required to achieve an optimal performance. Here we have updated and included all these required pre-processing steps into a single framework (SPM software). Therefore, there is no need of external tools to achieve the desired segmentation results. Besides, we have changed the working space from Tlw to FLAIR, reducing interpolation errors produced in the registration process from FLAIR to T1w space. Finally a post-processing constraint based on shape and location has been added to reduce false positive detections. Results: The evaluation of the tool has been done on 24 MS patients. Qualitative and quantitative results are shown with both approaches in terms of lesion detection and segmentation. Conclusion: We have simplified both installation and implementation of the approach, providing a multiplatform tool~1 integrated into the SPM software, which relies only on using Tlw and FLAIR images. We have reduced with this new version the computation time of the previous approach while maintaining the performance.
机译:目的:如今,磁共振成像已成为诊断以白质病变为特征的多发性硬化症(MS)的标志。最近提出了几种方法来解决病变分割问题,但是没有一种方法被接受为日常临床实践中的标准工具。在这项工作中,我们提供了另一个工具,该工具能够自动对白质病变进行分割,其性能优于当前的最新方法。方法:这项工作是Roura等人的扩展。 [1],需要外部和平台相关的预处理库(大脑提取,降噪和强度归一化)以实现最佳性能。在这里,我们已将所有这些必需的预处理步骤更新并包含在一个框架(SPM软件)中。因此,不需要外部工具即可获得所需的分割结果。此外,我们将工作空间从Tlw更改为FLAIR,减少了在注册过程中从FLAIR转换为T1w所产生的插值错误。最后,添加了基于形状和位置的后处理约束,以减少误报检测。结果:该工具已对24名MS患者进行了评估。两种方法在病变检测和分割方面均显示了定性和定量结果。结论:我们简化了该方法的安装和实现,提供了一个多平台工具〜1集成到SPM软件中,该工具仅依赖于使用Tlw和FLAIR映像。我们使用此新版本减少了以前方法的计算时间,同时保持了性能。

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