Department of Medical Radiation Physics, Lund University, Lund, Sweden.
J Magn Reson. 2010 Sep;206(1):59-67. doi: 10.1016/j.jmr.2010.06.002. Epub 2010 Jun 9.
Specific parameters of the neuronal tissue microstructure, such as axonal diameters, membrane permeability and intracellular water fractions are assessable using diffusion MRI. These parameters are commonly estimated using analytical models, which may introduce bias in the estimated parameters due to the approximations made when deriving the models. As an alternative to using analytical models, a database of signal curves generated by fast Monte Carlo simulations can be employed. Simulated diffusion MRI measurements were generated and evaluated using the two-compartment Kärger model as well as the simulation model based on a database containing signal curves from approximately 60000 simulations performed with different combinations of microstructural parameters. A protocol based on a pulsed gradient spin echo sequence with diffusion times of 30 and 60 ms and with gradient amplitudes obtainable with a clinical MRI scanner was employed for the investigations. When using the analytical model, a major negative bias (up to approximately 25%) in the estimated intracellular volume fraction was observed for short exchange times, while almost no bias was seen for the simulation model. In general, the simulation model improved the accuracy of the estimated parameters as compared to the analytical model, except for the exchange time parameter.
使用扩散 MRI 可以评估神经元组织微观结构的特定参数,如轴突直径、膜通透性和细胞内水分数。这些参数通常使用分析模型进行估计,但由于模型推导时的近似处理,可能会导致估计参数存在偏差。作为使用分析模型的替代方法,可以使用由快速蒙特卡罗模拟生成的信号曲线数据库。使用双室 Kärger 模型以及基于包含约 60000 次模拟的信号曲线的数据库的模拟模型生成和评估了模拟扩散 MRI 测量值,这些模拟是使用不同的微观结构参数组合进行的。研究中采用了基于脉冲梯度回波序列的方案,扩散时间为 30 和 60 ms,梯度幅度可通过临床 MRI 扫描仪获得。当使用分析模型时,对于短的交换时间,观察到估计的细胞内体积分数存在较大的负偏差(高达约 25%),而对于模拟模型则几乎没有偏差。一般来说,与分析模型相比,模拟模型提高了估计参数的准确性,除了交换时间参数之外。