A CAD system for early diagnosis of autism using different imaging modalities.

The term “autism spectrum disorder” (ASD) refers to a collection of neuro-developmental disorders that affect linguistic, behavioral, and social skills. Autism has many symptoms, most prominently, social impairment and repetitive behaviors. It is crucial to diagnose autism at an early stage for better assessment and investigation of this complex syndrome. There have been a lot of efforts to diagnose ASD using different techniques, such as imaging modalities, genetic techniques, and behavior reports. Imaging modalities have been extensively exploited for ASD diagnosis, and one of the most successful ones is Magnetic resonance imaging(MRI),where it has shown promise for the early diagnosis of the ASD related abnormalities in particular. Magnetic resonance imaging (MRI) modalities have emerged as powerful means that facilitate non-invasive clinical diagnostics of various diseases and abnormalities since their inception in the 1980s. After the advent in the nineteen eighties, MRI soon became one of the most promising non- invasive modalities for visualization and diagnostics of ASD-related abnormalities. Along with its main advantage of no exposure to radiation, high contrast, and spatial resolution, the recent advances to MRI modalities have notably increased diagnostic certainty. Multiple MRI modalities, such as different types of structural MRI (sMRI) that examines anatomical changes, and functional MRI (fMRI) that examines brain activity by monitoring blood flow changes,have been employed to investigate facets of ASD in order to better understand this complex syndrome. This work aims at developing a new computer-aided diagnostic (CAD) system for autism diagnosis using different imaging modalities. It mainly relies on making use of structural magnetic resonance images for extracting notable shape features from parts of the brainthat proved to correlate with ASD from previous neuropathological studies. Shape features from both the cerebral cortex (Cx) and cerebral white matter(CWM)are extracted. Fusion of features from these two structures is conducted based on the recent findings suggesting that Cx changes in autism are related to CWM abnormalities. Also, when fusing features from more than one structure, this would increase the robustness of the CAD system. Moreover, fMRI experiments are done and analyzed to find areas of activation in the brains of autistic and typically developing individuals that are related to a specific task. All sMRI findings are fused with those of fMRI to better understand ASD in terms of both anatomy and functionality,and thus better classify the two groups. This is one aspect of the novelty of this CAD system, where sMRI and fMRI studies are both applied on subjects from different ages to diagnose ASD. In order to build such a CAD system, three main blocks are required. First, 3D brain segmentation is applied using a novel hybrid model that combines shape, intensity, and spatial information. Second, shape features from both Cx and CWM are extracted and anf MRI reward experiment is conducted from which areas of activation that are related to the task of this experiment are identified. Those features were extracted from local areas of the brain to provide an accurate analysis of ASD and correlate it with certain anatomical areas. Third and last, fusion of all the extracted features is done using a deep-fusion classification network to perform classification and obtain the diagnosis report. Fusing features from all modalities achieved a classification accuracy of 94.7%, which emphasizes the significance of combining structures/modalities for ASD diagnosis. To conclude, this work could pave the pathway for better understanding of the autism spectrum by finding local areas that correlate to the disease. The idea of personalized medicine is emphasized in this work, where the proposed CAD system holds the promise to resolve autism endophenotypes and help clinicians deliver personalized treatment to individuals affected with this complex syndrome

Artificial Intelligence for Detection, Characterization, and Classification of Complex Visual Patterns in Medical Imaging; Applications in Pulmonary and Neuro-imaging

Medical imaging is widely used in current healthcare and research settings for various purposes such as diagnosis, treatment options, patient monitoring, longitudinal studies, etc. The two most commonly used imaging modalities in the United States are Computed Tomography (CT) and Magnetic Resonance Imaging (MRI). Raw images acquired via CT or MRI need to undergo a variety of processing steps prior to being used for the purposes explained above. These processing steps include quality control, noise reduction, anatomical segmentation, tissue classification, etc. However, since medical images often include millions of voxels (smallest 3D units in the image containing information) it is extremely challenging to process them manually by relying on visual inspection and the experience of trained clinicians. In light of this, the field of medical imaging is seeking ways to automate data processing. With the impressive performance of Artificial Intelligence (AI) in the field of Computer Vision, researchers in the medical imaging community have shown increasing interest in utilizing this powerful tool to automate the task of processing medical imaging data. Despite AI’s significant contributions to the medical imaging field, large cohorts of data still remain without optimized and robust AI-based tools to process images efficiently and accurately. This thesis focuses on exploiting large cohorts of CT and MRI data to design AI-based methods for processing medical images using weakly-supervised and supervised learning strategies, as well as mathematical (and/or statistical) modeling and signal processing methods. In particular, we address four image processing problems in this thesis. Namely: 1) We propose a weakly-supervised deep learning method to automate binary quality control of diffusion MRI scans into ‘poor’ and ‘good’ quality classes; 2) We design a weakly-supervised deep learning framework to learn and detect visual patterns related to a set of different artifact categories considered in this work, in order to identify major artifact types present in dMRI volumes; 3) We develop a supervised deep learning method to classify multiple lung texture patterns with association to Emphysema disease on human lung CT scans; 4) We investigate and characterize the properties of two types of negative BOLD response elicited in human brain fMRI scans during visual stimulation using mathematical modeling and signal processing tools. Our results demonstrate that through the use of artificial intelligence and signal processing algorithms: 1) dMRI scans can be automatically categorized into two quality groups (i.e., ‘poor’ vs ‘good’) with a high classification accuracy, enabling rapid sifting of large cohorts of dMRI scans to be utilized in research or clinical settings; 2) Type of the major artifact present in ‘poor’ quality dMRI volumes can be identified robustly and automatically with high precision enabling exclusion/correction of corrupt volumes according to the artifact type contaminating them; 3) Multiple lung texture patterns related to Emphysema disease can be automatically and robustly classified across various large cohorts of CT scans enabling investigation of the disease through longitudinal studies on multiple cohorts; 4) Negative BOLD responses of different categories can be fully characterized on fMRI data collected from visual stimulation of human brain enabling researchers to better understand the human brain functionality through studying cohorts of fMRI scans

Restauration d'images en IRM anatomique pour l'étude préclinique des marqueurs du vieillissement cérébral

Les maladies neurovasculaires et neurodégénératives liées à l'âge sont en forte augmentation. Alors que ces changements pathologiques montrent des effets sur le cerveau avant l'apparition de symptômes cliniques, une meilleure compréhension du processus de vieillissement normal du cerveau aidera à distinguer l'impact des pathologies connues sur la structure régionale du cerveau. En outre, la connaissance des schémas de rétrécissement du cerveau dans le vieillissement normal pourrait conduire à une meilleure compréhension de ses causes et peut-être à des interventions réduisant la perte de fonctions cérébrales associée à l'atrophie cérébrale. Par conséquent, ce projet de thèse vise à détecter les biomarqueurs du vieillissement normal et pathologique du cerveau dans un modèle de primate non humain, le singe marmouset (Callithrix Jacchus), qui possède des caractéristiques anatomiques plus proches de celles des humains que de celles des rongeurs. Cependant, les changements structurels (par exemple, de volumes, d'épaisseur corticale) qui peuvent se produire au cours de leur vie adulte peuvent être minimes à l'échelle de l'observation. Dans ce contexte, il est essentiel de disposer de techniques d'observation offrant un contraste et une résolution spatiale suffisamment élevés et permettant des évaluations détaillées des changements morphométriques du cerveau associé au vieillissement. Cependant, l'imagerie de petits cerveaux dans une plateforme IRM 3T dédiée à l'homme est une tâche difficile car la résolution spatiale et le contraste obtenus sont insuffisants par rapport à la taille des structures anatomiques observées et à l'échelle des modifications attendues. Cette thèse vise à développer des méthodes de restauration d'image pour les images IRM précliniques qui amélioreront la robustesse des algorithmes de segmentation. L'amélioration de la résolution spatiale des images à un rapport signal/bruit constant limitera les effets de volume partiel dans les voxels situés à la frontière entre deux structures et permettra une meilleure segmentation tout en augmentant la reproductibilité des résultats. Cette étape d'imagerie computationnelle est cruciale pour une analyse morphométrique longitudinale fiable basée sur les voxels et l'identification de marqueurs anatomiques du vieillissement cérébral en suivant les changements de volume dans la matière grise, la matière blanche et le liquide cérébral.Age-related neurovascular and neurodegenerative diseases are increasing significantly. While such pathological changes show effects on the brain before clinical symptoms appear, a better understanding of the normal aging brain process will help distinguish known pathologies' impact on regional brain structure. Furthermore, knowledge of the patterns of brain shrinkage in normal aging could lead to a better understanding of its causes and perhaps to interventions reducing the loss of brain functions. Therefore, this thesis project aims to detect normal and pathological brain aging biomarkers in a non-human primate model, the marmoset monkey (Callithrix Jacchus) which possesses anatomical characteristics more similar to humans than rodents. However, structural changes (e.g., volumes, cortical thickness) that may occur during their adult life may be minimal with respect to the scale of observation. In this context, it is essential to have observation techniques that offer sufficiently high contrast and spatial resolution and allow detailed assessments of the morphometric brain changes associated with aging. However, imaging small brains in a 3T MRI platform dedicated to humans is a challenging task because the spatial resolution and the contrast obtained are insufficient compared to the size of the anatomical structures observed and the scale of the xpected changes with age. This thesis aims to develop image restoration methods for preclinical MR images that will improve the robustness of the segmentation algorithms. Improving the resolution of the images at a constant signal-to-noise ratio will limit the effects of partial volume in voxels located at the border between two structures and allow a better segmentation while increasing the results' reproducibility. This computational imaging step is crucial for a reliable longitudinal voxel-based morphometric analysis and for the identification of anatomical markers of brain aging by following the volume changes in gray matter, white matter and cerebrospinal fluid

Analysis of Sub-Cortical Morphology in Benign Epilepsy with Centrotemporal Spikes

RÉSUMÉ Au Canada, l’épilepsie affecte environ 5 à 8 enfants par 3222 âgés de 2 à 37 ans dans la population globale. Quinze à 47 % de ces enfants ont une épilepsie bénigne avec des pointes centrotemporelles (BECTS), ce qui fait de BECTS le syndrome épileptique focal de l’enfant bénin le plus fréquent. Initialement, BECTS était considéré comme bénin parmi les autres épilepsies car il était généralement rapporté que les capacités cognitives ont été préservées ou ramenées à la normale pendant la rémission. Cependant, certaines études ont trouvé des déficits cognitifs et comportementaux, qui peuvent bien persister même après la rémission. Compte tenu des différences neurocognitives chez les enfants atteints de BECTS et de témoins normaux, la question est de savoir si des variations morphométriques subtiles dans les structures cérébrales sont également présentes chez ces patients et si elles expliquent des variations dans les performence cognitifs. En fait, malgré les preuves accumulées d’une étiologie neurodéveloppementale dans le BECTS, peu est connu sur les altérations structurelles sous-jacentes. À cet égard, la proposition de méthodes avancées en neuroimagerie permettrait d’évaluer quantitativement les variations de la morphologie cérébrale associées à ce trouble neurologique. En outre, l’étude du développement morphologique du cerveau et sa relation avec la cognition peut aider à élucider la base neuroanatomique des déficits cognitifs. Le but de cette thèse est donc de fournir un ensemble d’outils pour analyser les variations morphologiques sous-corticales subtiles provoquées par différentes maladies, telles que l’épilepsie bénigne avec des pointes centrotemporelles. La méthodologie adoptée dans cette thèse a conduit à trois objectifs de recherche spécifiques. La première étape vise à développer un nouveau cadre automatisé pour segmenter les structures sous-corticales sur les images à resonance magnètique (IRM). La deuxième étape vise à concevoir une nouvelle approche basée sur la correspondance spectrale pour capturer précisément la variabilité de forme chez les sujets épileptiques. La troisième étape conduit à une analyse de la relation entre les changements morphologiques du cerveau et les indices cognitifs. La première contribution vise plus spécifiquement la segmentation automatique des structures sous-corticales dans un processus de co-recalage et de co-segmentation multi-atlas. Contrairement aux approches standards de segmentation multi-atlas, la méthode proposée obtient la segmentation finale en utilisant un recalage en fonction de la population, tandis que les connaissances à prior basés sur les réseaux neuronaux par convolution (CNNs) sont incorporées dans la formulation d’énergie en tant que représentation d’image discriminative. Ainsi, cette méthode exploite des représentations apprises plus sophistiquées pour conduire le processus de co-recalage. De plus, étant donné un ensemble de volumes cibles, la méthode proposée calcule les probabilités de segmentation individuellement, puis segmente tous les volumes simultanément. Par conséquent, le fardeau de fournir un sous-ensemble de vérité connue approprié pour effectuer la segmentation multi-atlas est évité. Des résultats prometteurs démontrent le potentiel de notre méthode sur deux ensembles de données, contenant des annotations de structures sous-corticales. L’importance des estimations fiables des annotations est également mise en évidence, ce qui motive l’utilisation de réseaux neuronaux profonds pour remplacer les annotations de vérité connue en co-recalage avec une perte de performance minimale. La deuxième contribution vise à saisir la variabilité de forme entre deux populations de surfaces en utilisant une analyse morphologique multijoints. La méthode proposée exploite la représentation spectrale pour établir des correspondances de surface, puisque l’appariement est plus simple dans le domaine spectral plutôt que dans l’espace euclidien conventionnel. Le cadre proposé intègre la concordance spectrale à courbure moyenne dans un plateforme d’analyse de formes sous-corticales multijoints. L’analyse expérimentale sur des données cliniques a montré que les différences de groupe extraites étaient similaires avec les résultats dans d’autres études cliniques, tandis que les sorties d’analyse de forme ont été créées d’une manière à réduire le temps de calcul. Enfin, la troisième contribution établit l’association entre les altérations morphologiques souscorticales chez les enfants atteints d’épilepsie bénigne et les indices cognitifs. Cette étude permet de détecter les changements du putamen et du noyau caudé chez les enfants atteints de BECTS gauche, droit ou bilatéral. De plus, l ’association des différences volumétriques structurelles et des différences de forme avec la cognition a été étudiée. Les résultats confirment les altérations de la forme du putamen et du noyau caudé chez les enfants atteints de BECTS. De plus, nos résultats suggèrent que la variation de la forme sous-corticale affecte les fonctions cognitives. Cette étude démontre que les altérations de la forme et leur relation avec la cognition dépendent du côté de la focalisation de l’épilepsie. Ce projet nous a permis d’étudier si de nouvelles méthodes permettraient de traiter automatiquement les informations de neuro-imagerie chez les enfants atteints de BECTS et de détecter des variations morphologiques subtiles dans leurs structures sous-corticales. De plus, les résultats obtenus dans le cadre de cette thèse nous ont permis de conclure qu’il existe une association entre les variations morphologiques et la cognition par rapport au côté de la focalisation de la crise épileptique.----------ABSTRACT In Canada, epilepsy affects approximately 5 to 8 children per 3222 aged from 2 to 37 years in the overall population. Fifteen to 47% of these children have benign epilepsy with centrotemporal spikes (BECTS), making BECTS the most common benign childhood focal epileptic syndrome. Initially, BECTS was considered as benign among other epilepsies since it was generally reported that cognitive abilities were preserved or brought back to normal during remission. However, some studies have found cognitive and behavioral deficits, which may well persist even after remission. Given neurocognitive differences among children with BECTS and normal controls, the question is whether subtle morphometric variations in brain structures are also present in these patients, and whether they explain variations in cognitive indices. In fact, despite the accumulating evidence of a neurodevelopmental etiology in BECTS, little is known about underlying structural alterations. In this respect, proposing advanced neuroimaging methods will allow for quantitative assessment of variations in brain morphology associated with this neurological disorder. In addition, studying the brain morphological development and its relationship with cognition may help elucidate the neuroanatomical basis of cognitive deficits. Therefore, the focus of this thesis is to provide a set of tools for analyzing the subtle sub-cortical morphological alterations in different diseases, such as benign epilepsy with centrotemporal spikes. The methodology adopted in this thesis led to addressing three specific research objectives. The first step develops a new automated framework for segmenting subcortical structures on MR images. The second step designs a new approach based on spectral correspondence to precisely capture shape variability in epileptic individuals. The third step finds the association between brain morphological changes and cognitive indices. The first contribution aims more specifically at automatic segmentation of sub-cortical structures in a groupwise multi-atlas coregistration and cosegmentation process. Contrary to the standard multi-atlas segmentation approaches, the proposed method obtains the final segmentation using a population-wise registration, while Convolutional Neural Network (CNN)- based priors are incorporated in the energy formulation as a discriminative image representation. Thus, this method exploits more sophisticated learned representations to drive the coregistration process. Furthermore, given a set of target volumes the developed method computes the segmentation probabilities individually, and then segments all the volumes simultaneously. Therefore, the burden of providing an appropriate ground truth subset to perform multi-atlas segmentation is removed. Promising results demonstrate the potential of our method on two different datasets, containing annotations of sub-cortical structures. The importance of reliable label estimations is also highlighted, motivating the use of deep neural nets to replace ground truth annotations in coregistration with minimal loss in performance. The second contribution intends to capture shape variability between two population of surfaces using groupwise morphological analysis. The proposed method exploits spectral representation for establishing surface correspondences, since matching is simpler in the spectral domain rather than in the conventional Euclidean space. The designed framework integrates mean curvature-based spectral matching in to a groupwise subcortical shape analysis pipeline. Experimental analysis on real clinical dataset showed that the extracted group differences were in parallel with the findings in other clinical studies, while the shape analysis outputs were created in a computational efficient manner. Finally, the third contribution establishes the association between sub-cortical morphological alterations in children with benign epilepsy and cognitive indices. This study detects putamen and caudate changes in children with left, right, or bilateral BECTS to age and gender matched healthy individuals. In addition, the association of structural volumetric and shape differences with cognition is investigated. The findings confirm putamen and caudate shape alterations in children with BECTS. Also, our results suggest that variation in sub-cortical shape affects cognitive functions. More importantly, this study demonstrates that shape alterations and their relation with cognition depend on the side of epilepsy focus. This project enabled us to investigate whether new methods would allow to automatically process neuroimaging information from children afflicted with BECTS and detect subtle morphological variations in their sub-cortical structures. In addition, the results obtained in this thesis allowed us to conclude the existence of the association between morphological variations and cognition with respect to the side of seizure focus

Advanced Biometrics with Deep Learning

Biometrics, such as fingerprint, iris, face, hand print, hand vein, speech and gait recognition, etc., as a means of identity management have become commonplace nowadays for various applications. Biometric systems follow a typical pipeline, that is composed of separate preprocessing, feature extraction and classification. Deep learning as a data-driven representation learning approach has been shown to be a promising alternative to conventional data-agnostic and handcrafted pre-processing and feature extraction for biometric systems. Furthermore, deep learning offers an end-to-end learning paradigm to unify preprocessing, feature extraction, and recognition, based solely on biometric data. This Special Issue has collected 12 high-quality, state-of-the-art research papers that deal with challenging issues in advanced biometric systems based on deep learning. The 12 papers can be divided into 4 categories according to biometric modality; namely, face biometrics, medical electronic signals (EEG and ECG), voice print, and others