Simultaneous estimation of a model-derived input function for quantifying cerebral glucose metabolism with [18F]FDG PET.

IF 3 2区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Lucas Narciso, Graham Deller, Praveen Dassanayake, Linshan Liu, Samara Pinto, Udunna Anazodo, Andrea Soddu, Keith St Lawrence
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引用次数: 0

Abstract

Background: Quantification of the cerebral metabolic rate of glucose (CMRGlu) by dynamic [18F]FDG PET requires invasive arterial sampling. Alternatives to using an arterial input function (AIF) include the simultaneous estimation (SIME) approach, which models the image-derived input function (IDIF) by a series of exponentials with coefficients obtained by fitting time activity curves (TACs) from multiple volumes-of-interest. A limitation of SIME is the assumption that the input function can be modelled accurately by a series of exponentials. Alternatively, we propose a SIME approach based on the two-tissue compartment model to extract a high signal-to-noise ratio (SNR) model-derived input function (MDIF) from the whole-brain TAC. The purpose of this study is to present the MDIF approach and its implementation in the analysis of animal and human data.

Methods: Simulations were performed to assess the accuracy of the MDIF approach. Animal experiments were conducted to compare derived MDIFs to measured AIFs (n = 5). Using dynamic [18F]FDG PET data from neurologically healthy volunteers (n = 18), the MDIF method was compared to the original SIME-IDIF. Lastly, the feasibility of extracting parametric images was investigated by implementing a variational Bayesian parameter estimation approach.

Results: Simulations demonstrated that the MDIF can be accurately extracted from a whole-brain TAC. Good agreement between MDIFs and measured AIFs was found in the animal experiments. Similarly, the MDIF-to-IDIF area-under-the-curve ratio from the human data was 1.02 ± 0.08, resulting in good agreement in grey matter CMRGlu: 24.5 ± 3.6 and 23.9 ± 3.2 mL/100 g/min for MDIF and IDIF, respectively. The MDIF method proved superior in characterizing the first pass of [18F]FDG. Groupwise parametric images obtained with the MDIF showed the expected spatial patterns.

Conclusions: A model-driven SIME method was proposed to derive high SNR input functions. Its potential was demonstrated by the good agreement between MDIFs and AIFs in animal experiments. In addition, CMRGlu estimates obtained in the human study agreed to literature values. The MDIF approach requires fewer fitting parameters than the original SIME method and has the advantage that it can model the shape of any input function. In turn, the high SNR of the MDIFs has the potential to facilitate the extraction of voxelwise parameters when combined with robust parameter estimation methods such as the variational Bayesian approach.

利用[18F]FDG PET 同步估算用于量化脑葡萄糖代谢的模型输入函数。
背景:用动态[18F]FDG PET 定量脑葡萄糖代谢率(CMRGlu)需要侵入性动脉采样。使用动脉输入函数(AIF)的替代方法包括同步估计(SIME)方法,该方法通过一系列指数对图像衍生输入函数(IDIF)进行建模,这些指数的系数是通过拟合多个感兴趣容积的时间活动曲线(TAC)获得的。SIME 的局限性在于假设输入函数可以通过一系列指数精确建模。作为替代方案,我们提出了一种基于双组织区室模型的 SIME 方法,从全脑 TAC 中提取高信噪比(SNR)的模型衍生输入函数(MDIF)。本研究旨在介绍 MDIF 方法及其在动物和人体数据分析中的应用:方法:进行模拟以评估 MDIF 方法的准确性。进行了动物实验,将得出的 MDIF 与测得的 AIF 进行比较(n = 5)。使用神经健康志愿者(n = 18)的动态 [18F]FDG PET 数据,将 MDIF 方法与原始 SIME-IDIF 方法进行比较。最后,通过实施变异贝叶斯参数估计方法,研究了提取参数图像的可行性:模拟结果表明,MDIF 可以从全脑 TAC 中准确提取。在动物实验中发现,MDIF 与测量的 AIF 之间存在良好的一致性。同样,从人类数据中得出的 MDIF 与 IDIF 曲线下面积比为 1.02 ± 0.08,这使得灰质 CMRGlu 与 MDIF 有很好的一致性:MDIF 和 IDIF 分别为 24.5 ± 3.6 和 23.9 ± 3.2 mL/100 g/min。事实证明,MDIF 方法在表征[18F]FDG 的首次通过方面更胜一筹。使用 MDIF 获得的分组参数图像显示了预期的空间模式:结论:本文提出了一种模型驱动的 SIME 方法来推导高信噪比输入函数。在动物实验中,MDIF 与 AIF 之间的良好一致性证明了该方法的潜力。此外,人体研究中获得的 CMRGlu 估计值与文献值一致。与原始的 SIME 方法相比,MDIF 方法所需的拟合参数更少,其优点是可以对任何输入函数的形状进行建模。反过来,MDIF 的高信噪比在与稳健的参数估计方法(如变异贝叶斯方法)相结合时,有可能促进体素参数的提取。
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来源期刊
EJNMMI Physics
EJNMMI Physics Physics and Astronomy-Radiation
CiteScore
6.70
自引率
10.00%
发文量
78
审稿时长
13 weeks
期刊介绍: EJNMMI Physics is an international platform for scientists, users and adopters of nuclear medicine with a particular interest in physics matters. As a companion journal to the European Journal of Nuclear Medicine and Molecular Imaging, this journal has a multi-disciplinary approach and welcomes original materials and studies with a focus on applied physics and mathematics as well as imaging systems engineering and prototyping in nuclear medicine. This includes physics-driven approaches or algorithms supported by physics that foster early clinical adoption of nuclear medicine imaging and therapy.
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