Deep learning has a great potential for estimating biomarkers in diffusion weighted magnetic resonance imaging (dMRI). Atlases, on the other hand, are a unique tool for modeling the spatio-temporal variability of biomarkers. In this paper, we propose the first framework to exploit both deep learning and atlases for biomarker estimation in dMRI. Our framework relies on non-linear diffusion tensor registration to compute biomarker atlases and to estimate atlas reliability maps. We also use nonlinear tensor registration to align the atlas to a subject and to estimate the error of this alignment. We use the biomarker atlas, atlas reliability map, and alignment error map, in addition to the dMRI signal, as inputs to a deep learning model for biomarker estimation. We use our framework to estimate fractional anisotropy and neurite orientation dispersion from down-sampled dMRI data on a test cohort of 70 newborn subjects. Results show that our method significantly outperforms standard estimation methods as well as recent deep learning techniques. Our method is also more robust to stronger measurement down-sampling factors. Our study shows that the advantages of deep learning and atlases can be synergistically combined to achieve unprecedented accuracy in biomarker estimation from dMRI data.
翻译:深层学习极有可能估计扩散加权磁共振成像(dMRI)的生物标志。另一方面,阿特拉斯是一个独特的工具,用于模拟生物标志的spatio-时空变异性。在本文中,我们提出了第一个框架,用于在dMRI中利用深层学习和地图集进行生物标志估计。我们的框架依靠非线性扩散粒子登记来计算生物标记图集和估算地图集的可靠性。我们还使用非线性阵列登记使地图集与一个对象相匹配,并估计这一对齐的错误。我们除了使用DMRI信号外,还使用生物标志图集的图集、图集可靠性图集和校准错误图,作为生物标志估计深度学习模型的投入。我们使用我们的框架来估算70个新生儿试验组的分数性亚索罗比和中子方向分散。结果显示,我们的方法大大优于标准估计方法,以及最近的深层学习技术。我们的方法还可以更强有力地显示,从我们生物标志学的精确度研究中可以取得更坚实的数据。