Department of Biomedical Informatics, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; Department of Radiology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Department of Radiology, Children's Hospital of Pittsburgh of UPMC, Pittsburgh, PA, USA.
Neuroimage. 2018 Sep;178:183-197. doi: 10.1016/j.neuroimage.2018.05.049. Epub 2018 May 21.
Deep neural networks are increasingly being used in both supervised learning for classification tasks and unsupervised learning to derive complex patterns from the input data. However, the successful implementation of deep neural networks using neuroimaging datasets requires adequate sample size for training and well-defined signal intensity based structural differentiation. There is a lack of effective automated diagnostic tools for the reliable detection of brain dysmaturation in the neonatal period, related to small sample size and complex undifferentiated brain structures, despite both translational research and clinical importance. Volumetric information alone is insufficient for diagnosis. In this study, we developed a computational framework for the automated classification of brain dysmaturation from neonatal MRI, by combining a specific deep neural network implementation with neonatal structural brain segmentation as a method for both clinical pattern recognition and data-driven inference into the underlying structural morphology. We implemented three-dimensional convolution neural networks (3D-CNNs) to specifically classify dysplastic cerebelli, a subset of surface-based subcortical brain dysmaturation, in term infants born with congenital heart disease. We obtained a 0.985 ± 0. 0241-classification accuracy of subtle cerebellar dysplasia in CHD using 10-fold cross-validation. Furthermore, the hidden layer activations and class activation maps depicted regional vulnerability of the superior surface of the cerebellum, (composed of mostly the posterior lobe and the midline vermis), in regards to differentiating the dysplastic process from normal tissue. The posterior lobe and the midline vermis provide regional differentiation that is relevant to not only to the clinical diagnosis of cerebellar dysplasia, but also genetic mechanisms and neurodevelopmental outcome correlates. These findings not only contribute to the detection and classification of a subset of neonatal brain dysmaturation, but also provide insight to the pathogenesis of cerebellar dysplasia in CHD. In addition, this is one of the first examples of the application of deep learning to a neuroimaging dataset, in which the hidden layer activation revealed diagnostically and biologically relevant features about the clinical pathogenesis. The code developed for this project is open source, published under the BSD License, and designed to be generalizable to applications both within and beyond neonatal brain imaging.
深度神经网络越来越多地被用于监督学习的分类任务和无监督学习,以从输入数据中推导出复杂的模式。然而,在神经影像学数据集中成功实现深度神经网络需要足够的训练样本量和基于定义明确的信号强度的结构差异。尽管有转化研究和临床重要性,但缺乏可靠的用于检测新生儿期大脑发育不良的有效自动化诊断工具,这是由于样本量小和复杂的未分化的大脑结构所致。仅体积信息不足以用于诊断。在这项研究中,我们开发了一种从新生儿 MRI 自动分类大脑发育不良的计算框架,通过将特定的深度神经网络实现与新生儿结构脑分割相结合,用于临床模式识别和数据驱动推理,从而推断潜在的结构形态。我们实现了三维卷积神经网络(3D-CNN),专门用于对先天性心脏病患儿足月出生的表面下皮质下脑发育不良亚组进行分类。我们通过 10 倍交叉验证,在 CHD 中获得了 0.985±0.0241 的细微小脑发育不良分类准确率。此外,隐藏层激活和类激活图描绘了小脑上表面的区域易损性(主要由后叶和中线蚓部组成),以便将发育不良过程与正常组织区分开来。后叶和中线蚓部提供了区域分化,不仅与小脑发育不良的临床诊断相关,而且与遗传机制和神经发育结果相关。这些发现不仅有助于检测和分类新生儿脑发育不良的一个子集,而且为 CHD 中的小脑发育不良的发病机制提供了深入的了解。此外,这是深度学习在神经影像学数据集中的首次应用之一,其隐藏层激活揭示了有关临床发病机制的诊断和生物学相关特征。为此项目开发的代码是开源的,根据 BSD 许可证发布,旨在推广到新生儿脑成像内外的应用。