Assessment of cardiac function and early detection of abnormality play an essential role in the diagnosis, treatment, and control of several heart diseases. Visual assessment of cardiac function may result in higher inter- and intra-observer variability. Alternatively, automating abnormality scoring and producing clinically relevant quantitative measurements are desirable to facilitate the disease diagnosis. Due to the similarity between the statistical information associated with normal and abnormal heart motions, the heart motion abnormality detection is acknowledged as a difficult problem, which has recently bestirred a significant research attention. Our study investigates several fundamental problems related to cardiac images acquired in regular clinical routine. First, this study investigates automating the analysis of global cardiac function, and proposes effective measures to process the information from the data. Then, it addresses the problem of uncertainties associated with cardiac motion and proposes solutions based on a more complex motion models. Finally, a solution to the regional myocardial abnormality analysis is developed in accordance with the clinical standard issued by the American Heart Association.
There are a significant number of problems that exhibit a large range of physical scales but none so prominent in the 21st Century as that exemplified within the biological sciences. In the major arterial networks the blood flow dynamic scales are of the order of 1mm (cerebral vessels) up to 25mm (ascending aorta). Downstream of any major vessel exists a substantial network of arteries, arterioles and capillaries whose characteristic length scales reach the order of 10-20 microns. Within the walls of these cylindrical vessels lie ion channels consisting of proteins (100 nanometers and smaller) folded in such a way as to allow only certain molecules through the membrane. One can now of course ask the question as to why all these scales should be integrated into a single model.
To investigate the way in which the brain responds to variations in pressure and yet maintains a virtually constant supply of blood to the tissue numerical models need to be able to have a representation of not only the vascular tree but also a dynamic model of how the small arteries constrict and dilate. Simulating this phenomenon as a "lumped" connection of arteries is insufficient since different parts of the arterial tree respond differently. Thus we have a range of scales from the major arteries down to the arteriolar bed. The combination of a 3D model taken from MR data coupled with an autoregulation model with a fully populated arterial tree able to regulate dynamically remains a relatively unexplored field. This particular talk will outline the reasons for investigating multiple scales and their particular constraints with special reference to the autoregulation of blood in the cerebro-vasculature and outline a possible solution.
Neurodegenerative diseases afflict a significant portion of the world's aging population, with Alzheimer's disease (AD) alone affecting close to 500,000 Canadians. Non-invasive magnetic resonance imaging has shown potential to detect structural changes at an earlier stage than neuropsychological or cognitive evaluations, however, the high degree of anatomical variability among our brains has proven to be a challenge in developing general computational methods. Neuroanatomical registration and segmentation are fundamental components of many structural and functional analysis techniques, thus advances here can lead to the development of biomarkers for early disease progression. In this presentation I will present methods for improved accuracy and robustness using context-specific anatomical guidance in registration and intelligent atlas selection in multi-atlas segmentation, then demonstrate applications of these in shape analysis of the hippocampus in AD.

