论文标题

基于相互信息的超极化$^{13} $ c-c-pruvate MRI的最佳实验设计

Mutual-Information Based Optimal Experimental Design for Hyperpolarized $^{13}$C-Pyruvate MRI

论文作者

Jha, Prashant K., Walker, Christopher, Mitchell, Drew, Oden, J. Tinsley, Schellingerhout, Dawid, Bankson, James A., Fuentes, David T.

论文摘要

从超极化(HP)MRI测量值中恢复的关键参数是明显的丙酮酸到乳酸汇率,用于测量肿瘤代谢,$ K_ {PL} $。该手稿介绍了一种基于信息理论的最佳实验设计(OED)方法,该方法可最大程度地减少从HP-MRI测量值中恢复的速率参数的不确定性,$ k_ {pl} $。相互信息(MI)用于测量HP测量的信息含量,相对于丙酮酸转化为乳酸的一阶交换动力学。相互信息优化了脉冲序列采集的翻转角度。此外,提出并将基于块 - 呼吸区方程的空间变化模型(高保真)作为对照。随时间变化角度方案导致更高的参数优化,可以进一步改善恒定翻转角度方案的互信息的定量值。但是,在考虑噪声浪费的数据推断时,恒定的翻转角度方案会导致最佳准确性和精度。对于此处检查的特定MRI数据,就准确性和参数恢复的精度而言,丙酮酸和乳酸翻转角度分别为35度和28度。此外,从高保真模型生成的数据中的速率参数$ k_ {pl} $的恢复突出了血管源的扩散和强度对恢复速率参数的影响。由于现有的HP-MRI药代动力学模型无法解释空间变化,因此在更一般的3D设置中,优化的设计参数可能并不是完全最佳的。

A key parameter of interest recovered from hyperpolarized (HP) MRI measurements is the apparent pyruvate-to-lactate exchange rate, $k_{PL}$, for measuring tumor metabolism. This manuscript presents an information-theory-based optimal experimental design (OED) approach that minimizes the uncertainty in the rate parameter, $k_{PL}$, recovered from HP-MRI measurements. Mutual information (MI) is employed to measure the information content of the HP measurements with respect to the first-order exchange kinetics of the pyruvate conversion to lactate. Flip angles of the pulse sequence acquisition are optimized with respect to the mutual information. Further, a spatially varying model (high-fidelity) based on the Block-Torrey equations is proposed and utilized as a control. A time-varying flip angle scheme leads to a higher parameter optimization that can further improve the quantitative value of mutual information over a constant flip angle scheme. However, the constant flip angle scheme leads to the best accuracy and precision when considering inference from noise-corrupted data. For the particular MRI data examined here, pyruvate and lactate flip angles of 35 and 28 degrees, respectively, were the best choice in terms of accuracy and precision of the parameter recovery. Moreover, the recovery of rate parameter $k_{PL}$ from the data generated from the high-fidelity model highlights the influence of diffusion and strength of vascular source on the recovered rate parameter. Since the existing pharmacokinetic models for HP-MRI do not account for spatial variation, the optimized design parameters may not be fully optimal in a more general 3D setting.

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