Analysis of cardiac motion using MRI and nonrigid image registration

Imperial Users onl

Multidimensional image analysis of cardiac function in MRI

Cardiac morphology is a key indicator of cardiac health. Important metrics that are currently in clinical use are left-ventricle cardiac ejection fraction, cardiac muscle (myocardium) mass, myocardium thickness and myocardium thickening over the cardiac cycle. Advances in imaging technologies have led to an increase in temporal and spatial resolution. Such an increase in data presents a laborious task for medical practitioners to analyse. In this thesis, measurement of the cardiac left-ventricle function is achieved by developing novel methods for the automatic segmentation of the left-ventricle blood-pool and the left ventricle myocardium boundaries. A preliminary challenge faced in this task is the removal of noise from Magnetic Resonance Imaging (MRI) data, which is addressed by using advanced data filtering procedures. Two mechanisms for left-ventricle segmentation are employed. Firstly segmentation of the left ventricle blood-pool for the measurement of ejection fraction is undertaken in the signal intensity domain. Utilising the high discrimination between blood and tissue, a novel methodology based on a statistical partitioning method offers success in localising and segmenting the blood pool of the left ventricle. From this initialisation, the estimation of the outer wall (epi-cardium) of the left ventricle can be achieved using gradient information and prior knowledge. Secondly, a more involved method for extracting the myocardium of the leftventricle is developed, that can better perform segmentation in higher dimensions. Spatial information is incorporated in the segmentation by employing a gradient-based boundary evolution. A level-set scheme is implemented and a novel formulation for the extraction of the cardiac muscle is introduced. Two surfaces, representing the inner and the outer boundaries of the left-ventricle, are simultaneously evolved using a coupling function and supervised with a probabilistic model of expertly assisted manual segmentations

The anthropometric, environmental and genetic determinants of right ventricular structure and function

BACKGROUND Measures of right ventricular (RV) structure and function have significant prognostic value. The right ventricle is currently assessed by global measures, or point surrogates, which are insensitive to regional and directional changes. We aim to create a high-resolution three-dimensional RV model to improve understanding of its structural and functional determinants. These may be particularly of interest in pulmonary hypertension (PH), a condition in which RV function and outcome are strongly linked. PURPOSE To investigate the feasibility and additional benefit of applying three-dimensional phenotyping and contemporary statistical and genetic approaches to large patient populations. METHODS Healthy subjects and incident PH patients were prospectively recruited. Using a semi-automated atlas-based segmentation algorithm, 3D models characterising RV wall position and displacement were developed, validated and compared with anthropometric, physiological and genetic influences. Statistical techniques were adapted from other high-dimensional approaches to deal with the problems of multiple testing, contiguity, sparsity and computational burden. RESULTS 1527 healthy subjects successfully completed high-resolution 3D CMR and automated segmentation. Of these, 927 subjects underwent next-generation sequencing of the sarcomeric gene titin and 947 subjects completed genotyping of common variants for genome-wide association study. 405 incident PH patients were recruited, of whom 256 completed phenotyping. 3D modelling demonstrated significant reductions in sample size compared to two-dimensional approaches. 3D analysis demonstrated that RV basal-freewall function reflects global functional changes most accurately and that a similar region in PH patients provides stronger survival prediction than all anthropometric, haemodynamic and functional markers. Vascular stiffness, titin truncating variants and common variants may also contribute to changes in RV structure and function. CONCLUSIONS High-resolution phenotyping coupled with computational analysis methods can improve insights into the determinants of RV structure and function in both healthy subjects and PH patients. Large, population-based approaches offer physiological insights relevant to clinical care in selected patient groups.Open Acces