Multimodality carotid plaque tissue characterization and classification in the artificial intelligence paradigm: a narrative review for stroke application

Cardiovascular disease (CVD) is one of the leading causes of morbidity and mortality in the United States of America and globally. Carotid arterial plaque, a cause and also a marker of such CVD, can be detected by various non-invasive imaging modalities such as magnetic resonance imaging (MRI), computer tomography (CT), and ultrasound (US). Characterization and classification of carotid plaque-type in these imaging modalities, especially into symptomatic and asymptomatic plaque, helps in the planning of carotid endarterectomy or stenting. It can be challenging to characterize plaque components due to (I) partial volume effect in magnetic resonance imaging (MRI) or (II) varying Hausdorff values in plaque regions in CT, and (III) attenuation of echoes reflected by the plaque during US causing acoustic shadowing. Artificial intelligence (AI) methods have become an indispensable part of healthcare and their applications to the non-invasive imaging technologies such as MRI, CT, and the US. In this narrative review, three main types of AI models (machine learning, deep learning, and transfer learning) are analyzed when applied to MRI, CT, and the US. A link between carotid plaque characteristics and the risk of coronary artery disease is presented. With regard to characterization, we review tools and techniques that use AI models to distinguish carotid plaque types based on signal processing and feature strengths. We conclude that AI-based solutions offer an accurate and robust path for tissue characterization and classification for carotid artery plaque imaging in all three imaging modalities. Due to cost, user-friendliness, and clinical effectiveness, AI in the US has dominated the most

The matter of white and gray matter in cognitive impairment

Cognitive impairment spans from minor subjective cognitive impairment to disabling dementia. Many biomarkers have been developed to monitor different aspects of cognitive impairment. Magnetic resonance imaging is the most used neuroimaging biomarker in research and can measure gray matter (GM) and white matter (WM) changes. Although there is a consensus that atrophy in GM is a marker for neuronal loss, there is little evidence assessing the role of WM changes. The aim of this thesis is to first develop a tool to reliably measure the changes in WM in the form of white matter hyperintensities (WMH) and second to evaluate the role of WM and GM changes in the early stages of cognitive decline. In Study I and Study II, a fully automated method for segmentation of WMH has been developed and validated. Validation results indicated that the WMH segmentation was performed with high similarity to manual delineation and with superb reproducibility. In Study III, coronary heart disease (CHD) and hypertension, which are known to contribute to WM damage, were examined and their effect on GM and WM changes was investigated on a group of 69 individuals with 30-year follow-up. We showed that CHD and hypertension indeed affect the GM volume and thickness and the effect of CHD is partially independent of hypertension. However, the results indicate no significant effect on WMH, which we believe is due to the fact that WMH were measured as a crude total volume. In Study IV, a pipeline was developed to isolate the WM tract connecting each GM region to the rest of the brain and to measure the burden of WMH on each tract, hereinafter tractbased WMH. We used a cohort of 257 cognitively normal (CTL), 87 subjective cognitive impairment (SCI) and 124 mild cognitive impairment (MCI) subjects and examined their GM volume, tract-based WMH and cognitive performance. Our results indicated that the fraction of variance in GM volume that can be explained by tract-based WMH in SCI subjects is significantly higher than in both CTL and MCI subjects. The results also showed that in subjects with high and low cognitive performance, tract-based WMH can barely explain any GM volume change. However, in subjects with slight cognitive impairment tract-based WMH can explain the changes in GM volume. In summary, we investigated different ways of measuring the damage of WMH and showed that the role of WMH is more pronounced when measuring them in relation to the WM tract they affect. The effect of WMH on GM has been shown to be mainly in the earlier stages of cognitive impairment

Automated image segmentation and registration of vessel wall MRI for quantitative assessment of carotid artery vessel wall dimensions and plaque composition

The main goal of this thesis was to develop methods for automated segmentation, registration and classification of the carotid artery vessel wall and plaque components using multi-sequence MR vessel wall images to assess atherosclerosis. First, a general introduction into atherosclerosis and different stages of the disease were described including the importance to differentiate between stable and vulnerable plaques. Several non-invasive imaging techniques were discussed and the advantages of multi-sequence MRI were highlighted. Different novel automated image segmentation and registration techniques for analysis of the MRI images have been developed. A 3D vessel model to automatically segment the vessel wall was presented. Automated image registration was applied to correct for patient movement during the acquisition of an MRI scan and between MRI scans. The last topic is the automatic classification of the different plaque components which can be present inside the vessel wall. All techniques were developed and validated using relevant patient data and reference standards. The work presented is an important contribution to the automated analysis of multi-sequence MR vessel wall imaging of the carotid artery. These techniques can speed up the current manual analysis and are potentially more accurate and more reproducible.ASCI research school. Bontius Stichting inz. Doelfonds beeldverwerking. Library of the University of Leiden. Medis medical imaging systems bv, Leiden. Pie Medical Imaging BV, MaastrichtUBL - phd migration 201

Analysis of contrast-enhanced medical images.

Early detection of human organ diseases is of great importance for the accurate diagnosis and institution of appropriate therapies. This can potentially prevent progression to end-stage disease by detecting precursors that evaluate organ functionality. In addition, it also assists the clinicians for therapy evaluation, tracking diseases progression, and surgery operations. Advances in functional and contrast-enhanced (CE) medical images enabled accurate noninvasive evaluation of organ functionality due to their ability to provide superior anatomical and functional information about the tissue-of-interest. The main objective of this dissertation is to develop a computer-aided diagnostic (CAD) system for analyzing complex data from CE magnetic resonance imaging (MRI). The developed CAD system has been tested in three case studies: (i) early detection of acute renal transplant rejection, (ii) evaluation of myocardial perfusion in patients with ischemic heart disease after heart attack; and (iii), early detection of prostate cancer. However, developing a noninvasive CAD system for the analysis of CE medical images is subject to multiple challenges, including, but are not limited to, image noise and inhomogeneity, nonlinear signal intensity changes of the images over the time course of data acquisition, appearances and shape changes (deformations) of the organ-of-interest during data acquisition, determination of the best features (indexes) that describe the perfusion of a contrast agent (CA) into the tissue. To address these challenges, this dissertation focuses on building new mathematical models and learning techniques that facilitate accurate analysis of CAs perfusion in living organs and include: (i) accurate mathematical models for the segmentation of the object-of-interest, which integrate object shape and appearance features in terms of pixel/voxel-wise image intensities and their spatial interactions; (ii) motion correction techniques that combine both global and local models, which exploit geometric features, rather than image intensities to avoid problems associated with nonlinear intensity variations of the CE images; (iii) fusion of multiple features using the genetic algorithm. The proposed techniques have been integrated into CAD systems that have been tested in, but not limited to, three clinical studies. First, a noninvasive CAD system is proposed for the early and accurate diagnosis of acute renal transplant rejection using dynamic contrast-enhanced MRI (DCE-MRI). Acute rejection–the immunological response of the human immune system to a foreign kidney–is the most sever cause of renal dysfunction among other diagnostic possibilities, including acute tubular necrosis and immune drug toxicity. In the U.S., approximately 17,736 renal transplants are performed annually, and given the limited number of donors, transplanted kidney salvage is an important medical concern. Thus far, biopsy remains the gold standard for the assessment of renal transplant dysfunction, but only as the last resort because of its invasive nature, high cost, and potential morbidity rates. The diagnostic results of the proposed CAD system, based on the analysis of 50 independent in-vivo cases were 96% with a 95% confidence interval. These results clearly demonstrate the promise of the proposed image-based diagnostic CAD system as a supplement to the current technologies, such as nuclear imaging and ultrasonography, to determine the type of kidney dysfunction. Second, a comprehensive CAD system is developed for the characterization of myocardial perfusion and clinical status in heart failure and novel myoregeneration therapy using cardiac first-pass MRI (FP-MRI). Heart failure is considered the most important cause of morbidity and mortality in cardiovascular disease, which affects approximately 6 million U.S. patients annually. Ischemic heart disease is considered the most common underlying cause of heart failure. Therefore, the detection of the heart failure in its earliest forms is essential to prevent its relentless progression to premature death. While current medical studies focus on detecting pathological tissue and assessing contractile function of the diseased heart, this dissertation address the key issue of the effects of the myoregeneration therapy on the associated blood nutrient supply. Quantitative and qualitative assessment in a cohort of 24 perfusion data sets demonstrated the ability of the proposed framework to reveal regional perfusion improvements with therapy, and transmural perfusion differences across the myocardial wall; thus, it can aid in follow-up on treatment for patients undergoing the myoregeneration therapy. Finally, an image-based CAD system for early detection of prostate cancer using DCE-MRI is introduced. Prostate cancer is the most frequently diagnosed malignancy among men and remains the second leading cause of cancer-related death in the USA with more than 238,000 new cases and a mortality rate of about 30,000 in 2013. Therefore, early diagnosis of prostate cancer can improve the effectiveness of treatment and increase the patient’s chance of survival. Currently, needle biopsy is the gold standard for the diagnosis of prostate cancer. However, it is an invasive procedure with high costs and potential morbidity rates. Additionally, it has a higher possibility of producing false positive diagnosis due to relatively small needle biopsy samples. Application of the proposed CAD yield promising results in a cohort of 30 patients that would, in the near future, represent a supplement of the current technologies to determine prostate cancer type. The developed techniques have been compared to the state-of-the-art methods and demonstrated higher accuracy as shown in this dissertation. The proposed models (higher-order spatial interaction models, shape models, motion correction models, and perfusion analysis models) can be used in many of today’s CAD applications for early detection of a variety of diseases and medical conditions, and are expected to notably amplify the accuracy of CAD decisions based on the automated analysis of CE images

Automatic Spatiotemporal Analysis of Cardiac Image Series

RÉSUMÉ À ce jour, les maladies cardiovasculaires demeurent au premier rang des principales causes de décès en Amérique du Nord. Chez l’adulte et au sein de populations de plus en plus jeunes, la soi-disant épidémie d’obésité entraînée par certaines habitudes de vie tels que la mauvaise alimentation, le manque d’exercice et le tabagisme est lourde de conséquences pour les personnes affectées, mais aussi sur le système de santé. La principale cause de morbidité et de mortalité chez ces patients est l’athérosclérose, une accumulation de plaque à l’intérieur des vaisseaux sanguins à hautes pressions telles que les artères coronaires. Les lésions athérosclérotiques peuvent entraîner l’ischémie en bloquant la circulation sanguine et/ou en provoquant une thrombose. Cela mène souvent à de graves conséquences telles qu’un infarctus. Outre les problèmes liés à la sténose, les parois artérielles des régions criblées de plaque augmentent la rigidité des parois vasculaires, ce qui peut aggraver la condition du patient. Dans la population pédiatrique, la pathologie cardiovasculaire acquise la plus fréquente est la maladie de Kawasaki. Il s’agit d’une vasculite aigüe pouvant affecter l’intégrité structurale des parois des artères coronaires et mener à la formation d’anévrismes. Dans certains cas, ceux-ci entravent l’hémodynamie artérielle en engendrant une perfusion myocardique insuffisante et en activant la formation de thromboses. Le diagnostic de ces deux maladies coronariennes sont traditionnellement effectués à l’aide d’angiographies par fluoroscopie. Pendant ces examens paracliniques, plusieurs centaines de projections radiographiques sont acquises en séries suite à l’infusion artérielle d’un agent de contraste. Ces images révèlent la lumière des vaisseaux sanguins et la présence de lésions potentiellement pathologiques, s’il y a lieu. Parce que les séries acquises contiennent de l’information très dynamique en termes de mouvement du patient volontaire et involontaire (ex. battements cardiaques, respiration et déplacement d’organes), le clinicien base généralement son interprétation sur une seule image angiographique où des mesures géométriques sont effectuées manuellement ou semi-automatiquement par un technicien en radiologie. Bien que l’angiographie par fluoroscopie soit fréquemment utilisé partout dans le monde et souvent considéré comme l’outil de diagnostic “gold-standard” pour de nombreuses maladies vasculaires, la nature bidimensionnelle de cette modalité d’imagerie est malheureusement très limitante en termes de spécification géométrique des différentes régions pathologiques. En effet, la structure tridimensionnelle des sténoses et des anévrismes ne peut pas être pleinement appréciée en 2D car les caractéristiques observées varient selon la configuration angulaire de l’imageur. De plus, la présence de lésions affectant les artères coronaires peut ne pas refléter la véritable santé du myocarde, car des mécanismes compensatoires naturels (ex. vaisseaux----------ABSTRACT Cardiovascular disease continues to be the leading cause of death in North America. In adult and, alarmingly, ever younger populations, the so-called obesity epidemic largely driven by lifestyle factors that include poor diet, lack of exercise and smoking, incurs enormous stresses on the healthcare system. The primary cause of serious morbidity and mortality for these patients is atherosclerosis, the build up of plaque inside high pressure vessels like the coronary arteries. These lesions can lead to ischemic disease and may progress to precarious blood flow blockage or thrombosis, often with infarction or other severe consequences. Besides the stenosis-related outcomes, the arterial walls of plaque-ridden regions manifest increased stiffness, which may exacerbate negative patient prognosis. In pediatric populations, the most prevalent acquired cardiovascular pathology is Kawasaki disease. This acute vasculitis may affect the structural integrity of coronary artery walls and progress to aneurysmal lesions. These can hinder the blood flow’s hemodynamics, leading to inadequate downstream perfusion, and may activate thrombus formation which may lead to precarious prognosis. Diagnosing these two prominent coronary artery diseases is traditionally performed using fluoroscopic angiography. Several hundred serial x-ray projections are acquired during selective arterial infusion of a radiodense contrast agent, which reveals the vessels’ luminal area and possible pathological lesions. The acquired series contain highly dynamic information on voluntary and involuntary patient movement: respiration, organ displacement and heartbeat, for example. Current clinical analysis is largely limited to a single angiographic image where geometrical measures will be performed manually or semi-automatically by a radiological technician. Although widely used around the world and generally considered the gold-standard diagnosis tool for many vascular diseases, the two-dimensional nature of this imaging modality is limiting in terms of specifying the geometry of various pathological regions. Indeed, the 3D structures of stenotic or aneurysmal lesions may not be fully appreciated in 2D because their observable features are dependent on the angular configuration of the imaging gantry. Furthermore, the presence of lesions in the coronary arteries may not reflect the true health of the myocardium, as natural compensatory mechanisms may obviate the need for further intervention. In light of this, cardiac magnetic resonance perfusion imaging is increasingly gaining attention and clinical implementation, as it offers a direct assessment of myocardial tissue viability following infarction or suspected coronary artery disease. This type of modality is plagued, however, by motion similar to that present in fluoroscopic imaging. This issue predisposes clinicians to laborious manual intervention in order to align anatomical structures in sequential perfusion frames, thus hindering automation o

Automatic Spatiotemporal Analysis of Cardiac Image Series

RÉSUMÉ À ce jour, les maladies cardiovasculaires demeurent au premier rang des principales causes de décès en Amérique du Nord. Chez l’adulte et au sein de populations de plus en plus jeunes, la soi-disant épidémie d’obésité entraînée par certaines habitudes de vie tels que la mauvaise alimentation, le manque d’exercice et le tabagisme est lourde de conséquences pour les personnes affectées, mais aussi sur le système de santé. La principale cause de morbidité et de mortalité chez ces patients est l’athérosclérose, une accumulation de plaque à l’intérieur des vaisseaux sanguins à hautes pressions telles que les artères coronaires. Les lésions athérosclérotiques peuvent entraîner l’ischémie en bloquant la circulation sanguine et/ou en provoquant une thrombose. Cela mène souvent à de graves conséquences telles qu’un infarctus. Outre les problèmes liés à la sténose, les parois artérielles des régions criblées de plaque augmentent la rigidité des parois vasculaires, ce qui peut aggraver la condition du patient. Dans la population pédiatrique, la pathologie cardiovasculaire acquise la plus fréquente est la maladie de Kawasaki. Il s’agit d’une vasculite aigüe pouvant affecter l’intégrité structurale des parois des artères coronaires et mener à la formation d’anévrismes. Dans certains cas, ceux-ci entravent l’hémodynamie artérielle en engendrant une perfusion myocardique insuffisante et en activant la formation de thromboses. Le diagnostic de ces deux maladies coronariennes sont traditionnellement effectués à l’aide d’angiographies par fluoroscopie. Pendant ces examens paracliniques, plusieurs centaines de projections radiographiques sont acquises en séries suite à l’infusion artérielle d’un agent de contraste. Ces images révèlent la lumière des vaisseaux sanguins et la présence de lésions potentiellement pathologiques, s’il y a lieu. Parce que les séries acquises contiennent de l’information très dynamique en termes de mouvement du patient volontaire et involontaire (ex. battements cardiaques, respiration et déplacement d’organes), le clinicien base généralement son interprétation sur une seule image angiographique où des mesures géométriques sont effectuées manuellement ou semi-automatiquement par un technicien en radiologie. Bien que l’angiographie par fluoroscopie soit fréquemment utilisé partout dans le monde et souvent considéré comme l’outil de diagnostic “gold-standard” pour de nombreuses maladies vasculaires, la nature bidimensionnelle de cette modalité d’imagerie est malheureusement très limitante en termes de spécification géométrique des différentes régions pathologiques. En effet, la structure tridimensionnelle des sténoses et des anévrismes ne peut pas être pleinement appréciée en 2D car les caractéristiques observées varient selon la configuration angulaire de l’imageur. De plus, la présence de lésions affectant les artères coronaires peut ne pas refléter la véritable santé du myocarde, car des mécanismes compensatoires naturels (ex. vaisseaux----------ABSTRACT Cardiovascular disease continues to be the leading cause of death in North America. In adult and, alarmingly, ever younger populations, the so-called obesity epidemic largely driven by lifestyle factors that include poor diet, lack of exercise and smoking, incurs enormous stresses on the healthcare system. The primary cause of serious morbidity and mortality for these patients is atherosclerosis, the build up of plaque inside high pressure vessels like the coronary arteries. These lesions can lead to ischemic disease and may progress to precarious blood flow blockage or thrombosis, often with infarction or other severe consequences. Besides the stenosis-related outcomes, the arterial walls of plaque-ridden regions manifest increased stiffness, which may exacerbate negative patient prognosis. In pediatric populations, the most prevalent acquired cardiovascular pathology is Kawasaki disease. This acute vasculitis may affect the structural integrity of coronary artery walls and progress to aneurysmal lesions. These can hinder the blood flow’s hemodynamics, leading to inadequate downstream perfusion, and may activate thrombus formation which may lead to precarious prognosis. Diagnosing these two prominent coronary artery diseases is traditionally performed using fluoroscopic angiography. Several hundred serial x-ray projections are acquired during selective arterial infusion of a radiodense contrast agent, which reveals the vessels’ luminal area and possible pathological lesions. The acquired series contain highly dynamic information on voluntary and involuntary patient movement: respiration, organ displacement and heartbeat, for example. Current clinical analysis is largely limited to a single angiographic image where geometrical measures will be performed manually or semi-automatically by a radiological technician. Although widely used around the world and generally considered the gold-standard diagnosis tool for many vascular diseases, the two-dimensional nature of this imaging modality is limiting in terms of specifying the geometry of various pathological regions. Indeed, the 3D structures of stenotic or aneurysmal lesions may not be fully appreciated in 2D because their observable features are dependent on the angular configuration of the imaging gantry. Furthermore, the presence of lesions in the coronary arteries may not reflect the true health of the myocardium, as natural compensatory mechanisms may obviate the need for further intervention. In light of this, cardiac magnetic resonance perfusion imaging is increasingly gaining attention and clinical implementation, as it offers a direct assessment of myocardial tissue viability following infarction or suspected coronary artery disease. This type of modality is plagued, however, by motion similar to that present in fluoroscopic imaging. This issue predisposes clinicians to laborious manual intervention in order to align anatomical structures in sequential perfusion frames, thus hindering automation o

Objective Assessment of Image Quality: Extension of Numerical Observer Models to Multidimensional Medical Imaging Studies

Encompassing with fields on engineering and medical image quality, this dissertation proposes a novel framework for diagnostic performance evaluation based on objective image-quality assessment, an important step in the development of new imaging devices, acquisitions, or image-processing techniques being used for clinicians and researchers. The objective of this dissertation is to develop computational modeling tools that allow comprehensive evaluation of task-based assessment including clinical interpretation of images regardless of image dimensionality. Because of advances in the development of medical imaging devices, several techniques have improved image quality where the format domain of the outcome images becomes multidimensional (e.g., 3D+time or 4D). To evaluate the performance of new imaging devices or to optimize various design parameters and algorithms, the quality measurement should be performed using an appropriate image-quality figure-of-merit (FOM). Classical FOM such as bias and variance, or mean-square error, have been broadly used in the past. Unfortunately, they do not reflect the fact that the average performance of the principal agent in medical decision-making is frequently a human observer, nor are they aware of the specific diagnostic task. The standard goal for image quality assessment is a task-based approach in which one evaluates human observer performance of a specified diagnostic task (e.g. detection of the presence of lesions). However, having a human observer performs the tasks is costly and time-consuming. To facilitate practical task-based assessment of image quality, a numerical observer is required as a surrogate for human observers. Previously, numerical observers for the detection task have been studied both in research and industry; however, little research effort has been devoted toward development of one utilized for multidimensional imaging studies (e.g., 4D). Limiting the numerical observer tools that accommodate all information embedded in a series of images, the performance assessment of a particular new technique that generates multidimensional data is complex and limited. Consequently, key questions remain unanswered about how much the image quality improved using these new multidimensional images on a specific clinical task. To address this gap, this dissertation proposes a new numerical-observer methodology to assess the improvement achieved from newly developed imaging technologies. This numerical observer approach can be generalized to exploit pertinent statistical information in multidimensional images and accurately predict the performance of a human observer over the complexity of the image domains. Part I of this dissertation aims to develop a numerical observer that accommodates multidimensional images to process correlated signal components and appropriately incorporate them into an absolute FOM. Part II of this dissertation aims to apply the model developed in Part I to selected clinical applications with multidimensional images including: 1) respiratory-gated positron emission tomography (PET) in lung cancer (3D+t), 2) kinetic parametric PET in head-and-neck cancer (3D+k), and 3) spectral computed tomography (CT) in atherosclerotic plaque (3D+e). The author compares the task-based performance of the proposed approach to that of conventional methods, evaluated based on a broadly-used signal-known-exactly /background-known-exactly paradigm, which is in the context of the specified properties of a target object (e.g., a lesion) on highly realistic and clinical backgrounds. A realistic target object is generated with specific properties and applied to a set of images to create pathological scenarios for the performance evaluation, e.g., lesions in the lungs or plaques in the artery. The regions of interest (ROIs) of the target objects are formed over an ensemble of data measurements under identical conditions and evaluated for the inclusion of useful information from different complex domains (i.e., 3D+t, 3D+k, 3D+e). This work provides an image-quality assessment metric with no dimensional limitation that could help substantially improve assessment of performance achieved from new developments in imaging that make use of high dimensional data

Left Ventricular Viability Maps : Fusion of Multimodal Images of Coronary Morphology and Functional Information

RÉSUMÉ Les maladies coronariennes demeurent encore la première cause de décès aux Etats-Unis étant donné que le taux de mortalité lié à ces maladies enregistré en 2005 est d’une personne sur cinq. Les sténoses (obstructions des artères coronaires) se manifestent par un rétrécissement du diamètre des coronaires, produisant une ischémie soit une réduction du flot sanguin vers le myocarde (le muscle cardiaque). Dans les cas les plus graves, les cellules qui composent le myocarde meurent définitivement et perdent leur fonction contractile. En présence de cette maladie les cliniciens ont recours à l’imagerie médicale pour étudier l’état du myocarde afin de déterminer si les cellules qui le composent sont mortes ou non ainsi que pour diagnostiquer les sténoses dans les coronaires. Actuellement, le clinicien utilise l’imagerie nucléaire pour étudier la perfusion du myocarde afin de déterminer son état. Une projection de cette information sur un modèle segmenté du myocarde, soit le modèle à 17-segments, établie le lien entre les zones atteintes et les coronaires qui sont les plus responsables de leur irrigation. Ce n’est que par la suite, lors d’une angiographie, que le clinicien pourra identifier les sténoses et possiblement intervenir par revascularisation. Une autre méthode de visualisation de la structure coronarienne et de la présence de sténoses est la méthode Green Lane. Le clinicien reproduit la structure des coronaires sur une carte circulaire en se basant sur l’angiographie. L’objectif de notre projet de recherche est de créer un modèle spécifique au patient où il serait possible de voir les territoires coronariens sur la surface du myocarde fusionnés avec la viabilité myocardique. Ce modèle s’adapterait au patient et permettrait l’étude d’autres groupes de coronaires, ce qui n’est pas possible avec le modèle à 17-segments qui est fixe et ne présente que les trois groupes principaux de coronaires (coronaire droite, gauche et circonflexe). De plus, ce modèle divise la surface de l’épicarde en segments à partir de données statistiques qui sont limitées par la nature et la représentativité de l’échantillon de la population considérée et ne permet pas de visualiser la distribution de perte de viabilité sur la surface épicardique.---------- ABSTRACT Coronary heart disease (CHD) can be attributed to the build up of plaque in the coronary arteries (atherosclerosis) which leads to ischemia, an insufficient supply of blood to the heart wall, which results in myocardial dysfunction. When ischemia remains untreated an infarction may appear (areas of necrosis in cardiac tissues) and consequently the heart’s contractility is affected, which may lead to death. This disease is the basis of one of every five deaths in the United States during 2005, elevating this disease to the largest cause of death in United States. In standard clinical practice, perfusion and viability studies allow clinicians to examine the extent and the severity of CHD over the myocardium. Then, by consulting a population-based coronary territory model, such as the 17-segment model, the clinician mentally integrates affected areas of myocardium, found in nuclear or magnetic resonance imaging, to coronaries that typically irrigate this region with blood. However, population-based models do not fit every patient. There are individuals whose coronary tree structure deviates from that of the majority of the population. In addition, the 17-segment model limits the number of coronary groups to three: left coronary artery (LAD), right coronary artery (RCA) and left circumflex (LCX). Moreover this map is not continuous; it divides the myocardial surface in segments.Our objective is therefore to create a patient-specific map explicitly combining coronary territories and myocardial viability. This continuous model would adapt to the patient and allow the study of groups of coronary unavailable with standard models. After having identified loss of viability, the clinician would use this model to infer the most likely obstructed coronary artery responsible for myocardial damage. Visualization of the loss of viability along with coronary structure would replace the physician’s task of mentally integrating information from various sources

Automated segmentation and characterisation of white matter hyperintensities

Neuroimaging has enabled the observation of damage to the white matter that occurs frequently in elderly population and is depicted as hyperintensities in specific magnetic resonance images. Since the pathophysiology underlying the existence of these signal abnormalities and the association with clinical risk factors and outcome is still investigated, a robust and accurate quantification and characterisation of these observations is necessary. In this thesis, I developed a data-driven split and merge model selection framework that results in the joint modelling of normal appearing and outlier observations in a hierarchical Gaussian mixture model. The resulting model can then be used to segment white matter hyperintensities (WMH) in a post-processing step. The validity of the method in terms of robustness to data quality, acquisition protocol and preprocessing and its comparison to the state of the art is evaluated in both simulated and clinical settings. To further characterise the lesions, a subject-specific coordinate frame that divides the WM region according to the relative distance between the ventricular surface and the cortical sheet and to the lobar location is introduced. This coordinate frame is used for the comparison of lesion distributions in a population of twin pairs and for the prediction and standardisation of visual rating scales. Lastly the cross-sectional method is extended into a longitudinal framework, in which a Gaussian Mixture model built on an average image is used to constrain the representation of the individual time points. The method is validated through a purpose-build longitudinal lesion simulator and applied to the investigation of the relationship between APOE genetic status and lesion load progression