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一种使用 DSC-MRI 进行定量脑血流动力学分析的全自动方法。

A fully automated method for quantitative cerebral hemodynamic analysis using DSC-MRI.

机构信息

Department of Medical Physics, The Interventional Centre, Rikshospitalet, Oslo University Hospital, Oslo, Norway.

出版信息

J Cereb Blood Flow Metab. 2010 May;30(5):1066-78. doi: 10.1038/jcbfm.2010.4. Epub 2010 Jan 20.

Abstract

Dynamic susceptibility contrast (DSC)-based perfusion analysis from MR images has become an established method for analysis of cerebral blood volume (CBV) in glioma patients. To date, little emphasis has, however, been placed on quantitative perfusion analysis of these patients, mainly due to the associated increased technical complexity and lack of sufficient stability in a clinical setting. The aim of our study was to develop a fully automated analysis framework for quantitative DSC-based perfusion analysis. The method presented here generates quantitative hemodynamic maps without user interaction, combined with automatic segmentation of normal-appearing cerebral tissue. Validation of 101 patients with confirmed glioma after surgery gave mean values for CBF, CBV, and MTT, extracted automatically from normal-appearing whole-brain white and gray matter, in good agreement with literature values. The measured age- and gender-related variations in the same parameters were also in agreement with those in the literature. Several established analysis methods were compared and the resulting perfusion metrics depended significantly on method and parameter choice. In conclusion, we present an accurate, fast, and automatic quantitative perfusion analysis method where all analysis steps are based on raw DSC data only.

摘要

基于动态对比磁共振成像的灌注分析已成为分析脑肿瘤患者脑血容量(CBV)的一种成熟方法。然而,到目前为止,由于相关技术复杂性的增加和临床环境下缺乏足够的稳定性,这些患者的定量灌注分析尚未得到重视。我们的研究目的是开发一种用于定量基于 DSC 的灌注分析的全自动分析框架。该方法可在无需用户交互的情况下生成定量血流动力学图,并自动分割正常脑组织。对 101 例经手术后证实的脑肿瘤患者进行验证,结果表明,从正常全脑白质和灰质中自动提取的 CBF、CBV 和 MTT 的平均值与文献值吻合良好。同一参数的测量年龄和性别相关性变化也与文献中的变化一致。对几种已建立的分析方法进行了比较,结果表明,所得到的灌注指标与方法和参数选择密切相关。总之,我们提出了一种准确、快速、自动的定量灌注分析方法,所有分析步骤均仅基于原始 DSC 数据。

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