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Task-based optimization of flip angle for fibrosis detection in T1-weighted MRI of liver

机译:基于任务的翻转角优化在肝脏T1加权MRI中检测纤维化

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摘要

Chronic liver disease is a worldwide health problem, and hepatic fibrosis (HF) is one of the hallmarks of the disease. The current reference standard for diagnosing HF is biopsy followed by pathologist examination; however, this is limited by sampling error and carries a risk of complications. Pathology diagnosis of HF is based on textural change in the liver as a lobular collagen network that develops within portal triads. The scale of collagen lobules is characteristically in the order of 1 to 5 mm, which approximates the resolution limit of in vivo gadolinium-enhanced magnetic resonance imaging in the delayed phase. We use MRI of formalin-fixed human ex vivo liver samples as phantoms that mimic the textural contrast of in vivo Gd-MRI. We have developed a local texture analysis that is applied to phantom images, and the results are used to train model observers to detect HF. The performance of the observer is assessed with the area-under-the-receiver-operator-characteristic curve (AUROC) as the figure-of-merit. To optimize the MRI pulse sequence, phantoms were scanned with multiple times at a range of flip angles. The flip angle that was associated with the highest AUROC was chosen as optimal for the task of detecting HF. (C) The Authors. Published by SPIE under a Creative Commons Attribution 3.0 Unported License. Distribution or reproduction of this work in whole or in part requires full attribution of the original publication, including its DOI.
机译:慢性肝病是全球性的健康问题,肝纤维化(HF)是该疾病的标志之一。目前诊断HF的参考标准是活检,然后进行病理检查。但是,这受到采样误差的限制,并有发生并发症的风险。 HF的病理诊断是基于肝脏的纹理变化,它是在门三联征中发展的小叶胶原网络。胶原小叶的大小通常在1-5毫米左右,这近似于体内phase在延迟相中增强磁共振成像的分辨率极限。我们使用福尔马林固定的人离体肝脏样本的MRI作为模拟体内Gd-MRI质构对比的体模。我们已经开发了适用于幻影图像的局部纹理分析,并将结果用于训练模型观察者以检测HF。观察者的表现以接收者-操作者特征曲线下的面积(AUROC)作为品质因数进行评估。为了优化MRI脉冲序列,在一定的翻转角度范围内多次扫描了体模。选择与最高AUROC相关的翻转角作为检测HF的最佳选择。 (C)作者。由SPIE根据Creative Commons Attribution 3.0 Unported License发布。分发或复制此作品的全部或部分,需要对原始出版物(包括其DOI)进行完全归因。

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