通过PET/CT图像估计疾病量化的正常代谢活动。

Jieyu Li, Jayaram K Udupa, Yubing Tong, Drew A Torigian
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引用次数: 0

摘要

在本文中,我们提出了一种新的管道,用于在解剖学上预先定义的物体上进行正电子发射断层扫描/计算机断层扫描(PET/CT)图像的疾病量化。该管道由标准化摄取值(SUV)标准化、目标分割和疾病量化(DQ)组成。DQ是对由CT图像导出的非线性标准化的PET图像和目标物体的掩模进行处理。总病变负荷(TLB)是通过估计对象的正常代谢活动(TMAn)并从对象的总代谢活动(TMA)中减去该实体来量化的,从而测量感兴趣区域的总体疾病数量,而无需明确分割单个病变。使用特定目标的SUV分布模型计算TMAn。在建模阶段,从一组正常受试者获得的PET/CT图像中构建SUV模型,并手动勾画目标物体的掩模。探索了两种SUV建模方法,在硬策略中利用建模样本均值的均值作为一致的正态性值,在模糊策略中根据每个SUV值的SUV分布(直方图)确定代表正常组织的似然。评估实验是在一个单独的正常受试者临床数据集和一个带有病变的幻影数据集上进行的。以绝对TLB与TMA之比作为度量,减轻了体积大小和摄取水平的个体差异。结果表明,正常物体的比值接近于0,病变组织的比值接近于1,表明正常组织对TLB的贡献最小,主要来自病变组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estimating normal metabolic activity for disease quantification via PET/CT images.

In this paper, we propose a novel pipeline for conducting disease quantification in positron emission tomography/computed tomography (PET/CT) images on anatomically pre-defined objects. The pipeline is composed of standardized uptake value (SUV) standardization, object segmentation, and disease quantification (DQ). DQ is conducted on non-linearly standardized PET images and masks of target objects derived from CT images. Total lesion burden (TLB) is quantified by estimating normal metabolic activity (TMAn) in the object and subtracting this entity from total metabolic activity (TMA) of the object, thereby measuring the overall disease quantity of the region of interest without the necessity of explicitly segmenting individual lesions. TMAn is calculated with object-specific SUV distribution models. In the modeling stage, SUV models are constructed from a set of PET/CT images obtained from normal subjects with manually delineated masks of target objects. Two ways of SUV modeling are explored, where the mean of mean values of the modeling samples is utilized as a consistent normality value in the hard strategy, and the likelihood representing normal tissue is determined from the SUV distribution (histogram) for each SUV value in the fuzzy strategy. The evaluation experiments are conducted on a separate clinical dataset of normal subjects and a phantom dataset with lesions. The ratio of absolute TLB to TMA is taken as the metric, alleviating the individual difference of volume sizes and uptake levels. The results show that the ratios in normal objects are close to 0 and the ratios for lesions approach 1, demonstrating that contributions on TLB are minimal from the normal tissue and mainly from the lesion tissue.

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