Deep symmetric three-dimensional convolutional neural networks for identifying acute ischemic stroke via diffusion-weighted images.

Abstract

Acute ischemic stroke (AIS) results in high morbidity, disability, and mortality. Early and automatic diagnosis of AIS can help clinicians administer the appropriate interventions. To develop a deep symmetric 3D convolutional neural network (DeepSym-3D-CNN) for automated AIS diagnosis via diffusion-weighted imaging (DWI) images. This study includes 190 study subjects (97 AIS and 93 Non-AIS) by collecting both DWI and Apparent Diffusion Coefficient (ADC) images. 3D DWI brain images are split into left and right hemispheres and input into two paths. A map with 125×253×14×12 features is extracted by each path of Inception Modules. After the features computed from two paths are subtracted through L-2 normalization, four multi-scale convolution layers produce the final predation. Three comparative models using DWI images including MedicalNet with transfer learning, Simple DeepSym-3D-CNN (each 3D Inception Module is replaced by a simple 3D-CNN layer), and L-1 DeepSym-3D-CNN (L-2 normalization is replaced by L-1 normalization) are constructed. Moreover, using ADC images and the combination of DWI and ADC images as inputs, the performance of DeepSym-3D-CNN is also investigated. Performance levels of all three models are evaluated by 5-fold cross-validation and the values of area under ROC curve (AUC) are compared by DeLong's test. DeepSym-3D-CNN achieves an accuracy of 0.850 and an AUC of 0.864. DeLong's test of AUC values demonstrates that DeepSym-3D-CNN significantly outperforms other comparative models (p < 0.05). The highlighted regions in the feature maps of DeepSym-3D-CNN spatially match with AIS lesions. Meanwhile, DeepSym-3D-CNN using DWI images presents the significant higher AUC than that either using ADC images or using DWI-ADC images based on DeLong's test (p < 0.05). DeepSym-3D-CNN is a potential method for automatically identifying AIS via DWI images and can be extended to other diseases with asymmetric lesions.