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A bootstrap method for a totally non-invasive input function and pharmacokinetic parameters estimation in 18F-FDG PET images of the human brain

机译:18F-FDG PET图像中完全非侵入式输入功能和药代动力学参数估计的引导方法

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The pharmacokinetics extracted from PET images in the brain is relied to the physiological mechanisms that describe the processing of the tracer by the brain structures. These processes can be described through a multi-compartments model detailing the different states of the tracer and the transfer rate between these states. Numerous work have been proposed for the estimation of the input function (IF) from the internal carotids in the brain, but these methods are not able to extract efficiently the individual parameters of the model [1]. Feng et al. [2] have proposed a method for the simultaneous estimation of the input function (IF) and of the pharmacokinetic parameters (PK). This method takes as input a set of N Time Activity Curves (TAC), each related with a distinct structure of interest. This method may be applied to other compounds than FDG [3], but since it is highly sensitive to the noise that affects the input TACs, it has to resort to venous blood sampling.
机译:从脑中的PET图像中提取的药代动力学依赖于描述脑结构处理示踪剂的生理机制。这些过程可以通过多隔室模型描述细节示踪剂的不同状态和这些状态之间的传输速率。已经提出了许多工作来估计来自大脑中的内部颈动脉的输入功能(IF),但这些方法无法有效地提取模型的各个参数[1]。冯等人。 [2]提出了一种用于同时估计输入功能(IF)和药代动力学参数(PK)的方法。该方法用作输入一组n时间活动曲线(TAC),每个曲线(TAC)都与兴趣的不同结构相关。该方法可以应用于除FDG [3]的其他化合物中,但由于它对影响输入TAC的噪声非常敏感,因此它必须诉诸静脉血液采样。

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