用于连续采样弥散核磁共振成像信号重建的几何深度学习(DISCUS)

Christian Ewert, David Kügler, R. Stirnberg, A. Koch, A. Yendiki, Martin Reuter
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摘要

摘要 扩散加权磁共振成像(dMRI)可对神经解剖学微观结构进行详细的体内分析,对临床和人群研究非常有价值。然而,要准确推断不同成像体素内的潜在组织微观结构,必须使用不同的扩散编码方向和可能的 b 值进行多次测量。有两个挑战尤其限制了 dMRI 的实用性:较长的采集时间限制了只能进行少量方向测量的可行扫描,而不同研究中采集方案的异质性使得合并数据集变得十分困难。以往基于学习的方法只接受与训练所用特定采集方案一致的 dMRI 数据,但却无法解决这些问题,因此需要一种能接受和预测任意扩散编码信号的方法。为了应对这些挑战,我们介绍了第一种几何深度学习方法,用于对输入和输出的任意扩散采样方案进行连续的 dMRI 信号重建。我们的方法结合了以往基于学习方法的重建精度和鲁棒性,以及基于模型方法(如球谐波或 SHORE)的灵活性。我们证明了我们的方法优于基于模型的方法,并且在单壳、多壳和基于网格的弥散 MRI 数据集上的表现与基于离散学习的方法相当。在 dMRI 衍生分析方面,我们的研究表明,与其他重建方法相比,我们的重建方法能对常用的微结构模型进行更高质量的估算,甚至能对很短的 dMRI 采集数据进行高质量的分析。
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Geometric deep learning for diffusion MRI signal reconstruction with continuous samplings (DISCUS)
Abstract Diffusion-weighted magnetic resonance imaging (dMRI) permits a detailed in-vivo analysis of neuroanatomical microstructure, invaluable for clinical and population studies. However, many measurements with different diffusion-encoding directions and possibly b-values are necessary to infer the underlying tissue microstructure within different imaging voxels accurately. Two challenges particularly limit the utility of dMRI: long acquisition times limit feasible scans to only a few directional measurements, and the heterogeneity of acquisition schemes across studies makes it difficult to combine datasets. Left unaddressed by previous learning-based methods that only accept dMRI data adhering to the specific acquisition scheme used for training, there is a need for methods that accept and predict signals for arbitrary diffusion encodings. Addressing these challenges, we describe the first geometric deep learning method for continuous dMRI signal reconstruction for arbitrary diffusion sampling schemes for both the input and output. Our method combines the reconstruction accuracy and robustness of previous learning-based methods with the flexibility of model-based methods, for example, spherical harmonics or SHORE. We demonstrate that our method outperforms model-based methods and performs on par with discrete learning-based methods on single-, multi-shell, and grid-based diffusion MRI datasets. Relevant for dMRI-derived analyses, we show that our reconstruction translates to higher-quality estimates of frequently used microstructure models compared to other reconstruction methods, enabling high-quality analyses even from very short dMRI acquisitions.
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