There are ongoing researches for the automatic diagnosis of Alzheirer’s disease(AD) based on traditional machine learning techniques. And deep learning-based approaches are becoming popular choice for AD diagnosis. The state-of-the-art techniques that consider multimodal diagnosis have been shown to have accuracy better than manual diagnosis. However, collecting data from different modalities is time consuming and expensive, and some modalities may have radioactive side effects. Our study is confined to structural magnetic resonance imaging (sMRI). The objectives of our attempt are as follows: 1) to increase the accuracy level that is comparable to the state-of-the-art methods; 2) to overcome the overfitting problem; and 3) to analyze proven landmarks of the brain that provide discernible features for AD diagnosis. Here, we focused specifically on both the left and right hippocampus areas. To achieve the objectives, at first, we incorporate ensembles of simple convolutional neural networks (CNNs) as feature extractors and softmax cross-entropy as the classifier. Then, considering the scarcity of data, we deployed a patch-based approach. We have performed our experiment on the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database. We verified the models on the dataset provided by the National Research Center for Dementia (NRCD), Gwangju, South Korea. We manually localized the left and right hippocampus and fed three view patches (TVPs) to the CNN after the preprocessing steps. We achieve 85.55% accuracy on the ADNI dataset and 90.05% accuracy on the NRCD test dataset. Our result is comparable to other state-of-the-art methods.
Alzheimer's disease (AD) is a progressive neurodegenerative disorder that is mostly prevalent in people older than 65 years. The hippocampus is a widely studied region of interest (ROI) for a number of reasons, such as memory function analysis, stress development observation and neurological disorder investigation. Moreover, hippocampal volume atrophy is known to be linked with Alzheimer's disease. On the other hand, several biomarkers, such as amyloid beta (aß 42 ) protein, tau, phosphorylated tau and hippocampal volume atrophy, are being used to diagnose AD. In this research work, we have proposed a method to diagnose AD based on slice-wise volumetric features extracted from the left and right hippocampi of structural magnetic resonance imaging (sMRI) data. The proposed method is an aggregation of a convolutional neural network (CNN) model with a deep neural network (DNN) model. The left and right hippocampi have been localized automatically using a two-stage ensemble Hough-CNN. The localized hippocampal positions are used to extract (80 × 80x80 voxels) 3-D patches. The 2-D slices are then separated from the 3-D patches along axial, sagittal, and coronal views. The pre-processed 2-D patches are used to extract volumetric features from each slice by using a discrete volume estimation convolutional neural network (DVE-CNN) model. The extracted volumetric features have been used to train and test the classification network. The proposed approach has achieved average weighted classification accuracies of 94.82% and 94.02% based on the extracted volumetric features attributed to the left and right hippocampi, respectively. In addition, it has achieved area under the curve (AUC) values of 92.54% and 90.62% for the left and right hippocampi, respectively. Our method has outperformed the other methods by a certain margin in the same dataset.
FIFor The Alzheimer’s Disease Neuroimaging Initiative
For The Alzheimer’s Disease Neuroimaging Initiative
Patches from three orthogonal views of selected cerebral regions can be utilized to learn convolutional neural network (CNN) models for staging the Alzheimer disease (AD) spectrum including preclinical AD, mild cognitive impairment due to AD, and dementia due to AD and normal controls. Hippocampi, amygdalae and insulae were selected from the volumetric analysis of structured magnetic resonance images (MRIs). Three-view patches (TVPs) from these regions were fed to the CNN for training. MRIs were classified with the SoftMax-normalized scores of individual model predictions on TVPs. The significance of each region of interest (ROI) for staging the AD spectrum was evaluated and reported. The results of the ensemble classifier are compared with state-of-the-art methods using the same evaluation metrics. Patch-based ROI ensembles provide comparable diagnostic performance for AD staging. In this work, TVP-based ROI analysis using a CNN provides informative landmarks in cerebral MRIs and may have significance in clinical studies and computer-aided diagnosis system design.
Fingerprints are known to be easily synthesized to trick identification systems. In this paper, we propose a new method that incorporates template fingerprints stored for identification in the liveness detection system. The fingerprint identification platform must have a list of template fingerprints stored for matching with new probe fingerprints trying to access the system. Thus, instead of simply detecting the liveness of the probe fingerprints, the proposed approach uses the matching template fingerprints along with probe fingerprints through convolutional neural networks to make the liveness decision, which comprises two sequential convolutional neural networks for classification. The proposed method can be built on the top of existing liveness detection methods to increase accuracy without a significant increase in computation time. The evaluation over the LivDet dataset shows that the proposed fingerprint liveness detection method is able to obtain state-of-the-art accuracy.
The minimally invasive transcatheter aortic valve implantation (TAVI) is the most prevalent method to treat aortic valve stenosis. For pre-operative surgical planning, contrast-enhanced coronary CT angiography (CCTA) is used as the imaging technique to acquire 3-D measurements of the valve. Accurate localization of the eight aortic valve landmarks in CT images plays a vital role in the TAVI workflow because a small error risks blocking the coronary circulation. In order to examine the valve and mark the landmarks, physicians prefer a view parallel to the hinge plane, instead of using the conventional axial, coronal or sagittal view. However, customizing the view is a difficult and time-consuming task because of unclear aorta pose and different artifacts of CCTA. Therefore, automatic localization of landmarks can serve as a useful guide to the physicians customizing the viewpoint. In this paper, we present an automatic method to localize the aortic valve landmarks using colonial walk, a regression tree-based machine-learning algorithm. For efficient learning from the training set, we propose a two-phase optimized search space learning model in which a representative point inside the valvular area is first learned from the whole CT volume. All eight landmarks are then learned from a smaller area around that point. Experiment with preprocedural CCTA images of TAVI undergoing patients showed that our method is robust under high stenotic variation and notably efficient, as it requires only 12 milliseconds to localize all eight landmarks, as tested on a 3.60 GHz single-core CPU.
Generating fingerprint images for biometric purposes is both necessary and challenging. In this study, we presented a fingerprint generation approach based on generative adversarial network [1]. To ensure GAN training stability, we have introduced conditional loss doping that allows a continuous flow of gradients. Our study utilizes a careful combination of a residual network and spectral normalization [21] to generate fingerprints. The proposed average residual connection shows more immunity against vanishing gradients than a simple residual connection. Spectral normalization allows our network to enjoy reduced variance in weight generation, which further stabilizes the training [21]. Proposed scheme uses spectral bounding only in the input and the fully connected layers. Our network synthesized fingerprints up to 256 by 256 in size. We used the multi-scale structural similarity (MS-SSIM) metric [2] for measuring the diversity of the generated samples. Our model has achieved 0.23 MS-SSIM scores for the generated fingerprints. The MS-SSIM score indicates that the proposed scheme is more likely to produce more diverse images and less likely to face mode collapse.