Precise and fast prediction methods for ischemic areas comprised of dead tissue, core, and salvageable tissue, penumbra, in acute ischemic stroke (AIS) patients are of significant clinical interest. They play an essential role in improving diagnosis and treatment planning. Computed Tomography (CT) scan is one of the primary modalities for early assessment in patients with suspected AIS. CT Perfusion (CTP) is often used as a primary assessment to determine stroke location, severity, and volume of ischemic lesions. Current automatic segmentation methods for CTP mostly use already processed 3D parametric maps conventionally used for clinical interpretation by radiologists as input. Alternatively, the raw CTP data is used on a slice-by-slice basis as 2D+time input, where the spatial information over the volume is ignored. In addition, these methods are only interested in segmenting core regions, while predicting penumbra can be essential for treatment planning. This paper investigates different methods to utilize the entire 4D CTP as input to fully exploit the spatio-temporal information, leading us to propose a novel 4D convolution layer. Our comprehensive experiments on a local dataset of 152 patients divided into three groups show that our proposed models generate more precise results than other methods explored. Adopting the proposed 4D mJ-Net, a Dice Coefficient of 0.53 and 0.23 is achieved for segmenting penumbra and core areas, respectively. The code is available on https://github.com/Biomedical-Data-Analysis-Laboratory/4D-mJ-Net.git.

Precise identification of mouse brain microscopy images is a crucial first step when anatomical structures in the mouse brain are to be registered to a reference atlas. Practitioners usually rely on manual comparison of images or tools that assume the presence of complete images. This work explores Siamese Networks as the method for finding corresponding 2D reference atlas plates for given partial 2D mouse brain images. Siamese networks are a class of convolutional neural networks (CNNs) that use weight-shared paths to obtain low dimensional embeddings of pairs of input images. The correspondence between the partial mouse brain image and reference atlas plate is determined based on the distance between low dimensional embeddings of brain slices and atlas plates that are obtained from Siamese networks using contrastive learning. Experiments showed that Siamese CNNs can precisely identify brain slices using the Allen mouse brain atlas when training and testing images come from the same source. They achieved TOP-1 and TOP-5 accuracy of 25% and 100%, respectively, taking only 7.2 seconds to identify 29 images.

In this study, we propose a model which may assist in diagnosis of Alzheimer’s disease (AD) using T1 weighted MRI brain images. The proposed model involves construction of statistical features from multiple trans-axial slices from hippocampus and amygdala regions, which play a significant role in AD diagnosis. Features from multiple slices are then averaged, which resulted into a smaller set of relevant features. The reduced set of features enhances the performance of decision learning system, and takes less memory and computation time. Effectiveness of the proposed model is compared with recent voxel-based-morphometry work in terms of sensitivity, specificity and accuracy. Experimental results on a publicly available MRI dataset showed that the proposed method outperforms the recent voxel-based-morphometry model.