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Ranking diffusion-MRI models with in-vivo human brain data

机译:具有体内人脑数据的排名扩散-MRI模型

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Diffusion MRI microstructure imaging provides a unique non-invasive probe into the microstructure of biological tissue. Its analysis relies on mathematical models relating microscopic tissue features to the MR signal. This work aims to determine which compartment models of diffusion MRI are best at describing the signal from in-vivo brain white matter. Recent work shows that three compartment models, including restricted intra-axonal, glial compartments and hindered extra-cellular diffusion, explain best multi b-value data sets from fixed rat brain tissue. Here, we perform a similar experiment using in-vivo human data. We compare one, two and three compartment models, ranking them with standard model selection criteria. Results show that, as with fixed tissue, three compartment models explain the data best, although simpler models emerge for the in-vivo data. We also find that splitting the scanning into shorter sessions has little effect on the models fitting and that the results are reproducible. The full ranking assists the choice of model and imaging protocol for future microstructure imaging applications in the brain.
机译:扩散MRI微结构成像提供了一种独特的非侵入性探针进入生物组织的微观结构。其分析依赖于将微观组织特征与MR信号相关的数学模型。这项工作旨在确定扩散MRI的哪个隔室模型最佳地描述来自体内脑白质的信号。最近的工作表明,三个隔间模型,包括限制的内部轴突,胶质隔层和阻碍的额外细胞扩散,解释了来自固定大鼠脑组织的最佳B值数据集。在这里,我们使用体内人体数据进行类似的实验。我们比较一个,两个和三个隔间模型,用标准模型选择标准排列它们。结果表明,与固定组织一样,三个隔间模型最佳解释数据,尽管较简单的模型出现了体内数据。我们发现将扫描拆分为更短的会话对模型拟合的影响几乎没有影响,结果是可重复的。全排名有助于选择模型和成像协议,以便在大脑中进行未来的微结构成像应用。

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