Division of Radiation Physics, Department of Radiation Sciences, Umeå University, Umeå, Sweden.
Magn Reson Med. 2013 Apr;69(4):992-1002. doi: 10.1002/mrm.24328. Epub 2012 Jun 19.
Using dynamic contrast-enhanced MRI (DCE-MRI), it is possible to estimate pharmacokinetic (PK) parameters that convey information about physiological properties, e.g., in tumors. In DCE-MRI, errors propagate in a nontrivial way to the PK parameters. We propose a method based on multivariate linear error propagation to calculate uncertainty maps for the PK parameters. Uncertainties in the PK parameters were investigated for the modified Kety model. The method was evaluated with Monte Carlo simulations and exemplified with in vivo brain tumor data. PK parameter uncertainties due to noise in dynamic data were accurately estimated. Noise with standard deviation up to 15% in the baseline signal and the baseline T1 map gave estimated uncertainties in good agreement with the Monte Carlo simulations. Good agreement was also found for up to 15% errors in the arterial input function amplitude. The method was less accurate for errors in the bolus arrival time with disagreements of 23%, 32%, and 29% for K(trans) , ve , and vp , respectively, when the standard deviation of the bolus arrival time error was 5.3 s. In conclusion, the proposed method provides efficient means for calculation of uncertainty maps, and it was applicable to a wide range of sources of uncertainty.
使用动态对比增强磁共振成像(DCE-MRI),可以估计药代动力学(PK)参数,这些参数提供有关生理特性的信息,例如肿瘤中的信息。在 DCE-MRI 中,误差以非平凡的方式传播到 PK 参数中。我们提出了一种基于多元线性误差传播的方法,用于计算 PK 参数的不确定性图。我们研究了修正后的 Kety 模型中 PK 参数的不确定性。该方法通过蒙特卡罗模拟进行了评估,并通过体内脑肿瘤数据进行了示例。准确估计了由于动态数据噪声引起的 PK 参数不确定性。在基线信号和基线 T1 图中的噪声标准偏差高达 15%的情况下,估计的不确定性与蒙特卡罗模拟非常吻合。动脉输入函数幅度的误差高达 15%时,也得到了很好的一致性。对于到达时间的误差,方法的准确性较差,当到达时间误差的标准偏差为 5.3 秒时,K(trans)、ve 和 vp 的偏差分别为 23%、32%和 29%。总之,所提出的方法为计算不确定性图提供了有效的手段,并且适用于广泛的不确定性源。