论文标题

从扩散-MRI:可渗透细胞组织中的分隔模型的微观结构估计

Microstructure estimation from diffusion-MRI: Compartmentalized models in permeable cellular tissue

论文作者

Gardier, Rémy, Haro, Juan Luis Villarreal, Canales-Rodrıguez, Erick J, Jelescu, Ileana O., Girard, Gabriel, Rafael-Patino, Jonathan, Thiran, Jean-Philippe

论文摘要

扩散加权磁共振成像(DW-MRI)用于表征使用组织特异性生物物理模型的脑组织微观结构。但是,当前的局限性是,大多数提出的模型基于假设在细胞内和细胞外室之间可以忽略不计的水交换,这在各种脑组织中可能无效,包括无髓鞘的轴突,灰质和肿瘤。这项工作的目的是量化膜通透性对忽略交换的两个流行模型的估计的估计的影响,并将其性能与包括交换的模型进行比较。为此,在具有蒙特卡洛模拟的受控环境中进行了DW-MRI实验。 DW-MRI信号是在模仿带有球形细胞制成的生物组织的数值底物中产生的,该组织具有渗透性的膜,如癌组织或脑灰质。从这些信号中,使用SANDI和判决(两个基于隔间的模型忽略Exchange)和CEXI(包括交换的新模型)估算了底物属性。我们的结果表明,在细胞渗透的组织中,具有交换模型的模型优于模型,而无需在组织性质估算中进行更稳定的估计,对细胞大小,细胞内体积分数和细胞外扩散系数的估计。此外,具有交换的模型准确地估计了用于细胞组织的渗透率范围内的交换时间。最后,在这项工作中进行的模拟表明,细胞内和细胞外空间之间的交换不能用常规的PGSE序列在可渗透组织中忽略,以获得准确的估计。因此,现有的不可渗透组织的分隔模型不能用于细胞渗透组织的微观结构估计。

Diffusion-weighted magnetic resonance imaging (DW-MRI) is used to characterize brain tissue microstructure employing tissue-specific biophysical models. A current limitation, however, is that most of the proposed models are based on the assumption of negligible water exchange between the intra- and extracellular compartments, which might not be valid in various brain tissues, including unmyelinated axons, gray matter, and tumors. The purpose of this work is to quantify the effect of membrane permeability on the estimates of two popular models neglecting exchange, and compare their performance with a model including exchange. To this aim, DW-MRI experiments were performed in controlled environments with Monte-Carlo simulations. The DW-MRI signals were generated in numerical substrates mimicking biological tissue made of spherical cells with permeable membranes like cancerous tissue or the brain gray matter. From these signals, the substrates properties were estimated using SANDI and VERDICT, the two compartment-based models neglecting exchange, and CEXI, a new model which includes exchange. Our results show that, in cellular permeable tissue, the model with exchange outperformed models without exchange in the estimation of the tissue properties by providing more stable estimates of cell size, intracellular volume fraction and extracellular diffusion coefficient. Moreover, the model with exchange estimated accurately the exchange time in the range of permeability reported for cellular tissue. Finally, the simulations performed in this work showed that the exchange between the intracellular and the extracellular space cannot be neglected in permeable tissue with a conventional PGSE sequence, to obtain accurate estimates. Consequently, existing compartmentalized models of impermeable tissue cannot be used for microstructure estimation of cellular permeable tissue.

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