86 research outputs found

    Tissue Doppler, Strain and Strain Rate in ischemic heart disease “How I do it”

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    Echocardiography is the standard method for assessing myocardial function in patients with ischemic heart disease. The acquisition and interpretation of echocardiographic images, however, remains a highly specialized task which often relies entirely on the subjective visual assessment of the reader and requires therefore, particular training and expertise. Myocardial deformation imaging allows quantifying myocardial function far beyond what can be done with sole visual assessment. It can improve the interpretation of regional dysfunction and offers sensitive markers of induced ischemia which can be used for stress tests. In the following, we recapitulate shortly the pathophysiological and technical basics and explain in a practical manner how we use this technique in investigating patients with ischemic heart disease

    Sheep can be used as animal model of regional myocardial remodeling and controllable work

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    Background: Pacing the right heart has been shown to induce reversible conduction delay and subse­quent asymmetric remodeling of the left ventricle (LV) in dogs and pigs. Both species have disadvantages in animal experiments. Therefore the aim of this study was to develop a more feasible and easy-to-use animal model in sheep. Methods: Dual-chamber (DDD) pacemakers with epicardial leads on the right atrium and right ven­tricular free wall were implanted in 13 sheep. All animals underwent 8 weeks of chronic rapid pacing at 180 bpm. Reported observations were made at 110 bpm. Results: DDD pacing acutely induced a left bundle branch block (LBBB) — like pattern with almost doubling in QRS width and the appearance of a septal flash, indicating mechanical dyssynchrony. Atrial pacing (AAI) resulted in normal ventricular conduction and function. During 8 weeks of rapid DDD pacing, animals developed LV remodeling (confirmed with histology) with septal wall thinning (–30%, p < 0.05), lateral wall thickening (+22%, p < 0.05), LV volume increase (+32%, p < 0.05), decrease of LV ejection fraction (–31%, p < 0.05), and functional mitral regurgitation. After 8 weeks, segmental pressure-strain-loops, representing regional myocardial work, were recorded. Switching from AAI to DDD pacing decreased immediately work in the septum and increased it in the lateral wall (–69 and +41%, respectively, p < 0.05). Global LV stroke work and dP/dtmax decreased (–27% and -25%, respectively, p < 0.05). Conclusions: This study presents the development a new sheep model with an asymmetrically remod­eled LV. Simple pacemaker programing allows direct modulation of regional myocardial function and work. This animal model provides a new and valuable alternative for canine or porcine models and has the potential to become instrumental for investigating regional function and loading conditions on regional LV remodeling

    Simplicial Complex based Point Correspondence between Images warped onto Manifolds

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    Recent increase in the availability of warped images projected onto a manifold (e.g., omnidirectional spherical images), coupled with the success of higher-order assignment methods, has sparked an interest in the search for improved higher-order matching algorithms on warped images due to projection. Although currently, several existing methods "flatten" such 3D images to use planar graph / hypergraph matching methods, they still suffer from severe distortions and other undesired artifacts, which result in inaccurate matching. Alternatively, current planar methods cannot be trivially extended to effectively match points on images warped onto manifolds. Hence, matching on these warped images persists as a formidable challenge. In this paper, we pose the assignment problem as finding a bijective map between two graph induced simplicial complexes, which are higher-order analogues of graphs. We propose a constrained quadratic assignment problem (QAP) that matches each p-skeleton of the simplicial complexes, iterating from the highest to the lowest dimension. The accuracy and robustness of our approach are illustrated on both synthetic and real-world spherical / warped (projected) images with known ground-truth correspondences. We significantly outperform existing state-of-the-art spherical matching methods on a diverse set of datasets.Comment: Accepted at ECCV 202

    Graph similarity through entropic manifold alignment

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    In this paper we decouple the problem of measuring graph similarity into two sequential steps. The first step is the linearization of the quadratic assignment problem (QAP) in a low-dimensional space, given by the embedding trick. The second step is the evaluation of an information-theoretic distributional measure, which relies on deformable manifold alignment. The proposed measure is a normalized conditional entropy, which induces a positive definite kernel when symmetrized. We use bypass entropy estimation methods to compute an approximation of the normalized conditional entropy. Our approach, which is purely topological (i.e., it does not rely on node or edge attributes although it can potentially accommodate them as additional sources of information) is competitive with state-of-the-art graph matching algorithms as sources of correspondence-based graph similarity, but its complexity is linear instead of cubic (although the complexity of the similarity measure is quadratic). We also determine that the best embedding strategy for graph similarity is provided by commute time embedding, and we conjecture that this is related to its inversibility property, since the inverse of the embeddings obtained using our method can be used as a generative sampler of graph structure.The work of the first and third authors was supported by the projects TIN2012-32839 and TIN2015-69077-P of the Spanish Government. The work of the second author was supported by a Royal Society Wolfson Research Merit Award

    An Analysis of Errors in Graph-Based Keypoint Matching and Proposed Solutions

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    International audienceAn error occurs in graph-based keypoint matching when key-points in two different images are matched by an algorithm but do not correspond to the same physical point. Most previous methods acquire keypoints in a black-box manner, and focus on developing better algorithms to match the provided points. However to study the complete performance of a matching system one has to study errors through the whole matching pipeline, from keypoint detection, candidate selection to graph optimisation. We show that in the full pipeline there are six different types of errors that cause mismatches. We then present a matching framework designed to reduce these errors. We achieve this by adapting keypoint detectors to better suit the needs of graph-based matching, and achieve better graph constraints by exploiting more information from their keypoints. Our framework is applicable in general images and can handle clutter and motion discontinuities. We also propose a method to identify many mismatches a posteriori based on Left-Right Consistency inspired by stereo matching due to the asymmetric way we detect keypoints and define the graph

    Simultaneous Optimization of Both Node and Edge Conservation in Network Alignment via WAVE

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    Network alignment can be used to transfer functional knowledge between conserved regions of different networks. Typically, existing methods use a node cost function (NCF) to compute similarity between nodes in different networks and an alignment strategy (AS) to find high-scoring alignments with respect to the total NCF over all aligned nodes (or node conservation). But, they then evaluate quality of their alignments via some other measure that is different than the node conservation measure used to guide the alignment construction process. Typically, one measures the amount of conserved edges, but only after alignments are produced. Hence, a recent attempt aimed to directly maximize the amount of conserved edges while constructing alignments, which improved alignment accuracy. Here, we aim to directly maximize both node and edge conservation during alignment construction to further improve alignment accuracy. For this, we design a novel measure of edge conservation that (unlike existing measures that treat each conserved edge the same) weighs each conserved edge so that edges with highly NCF-similar end nodes are favored. As a result, we introduce a novel AS, Weighted Alignment VotEr (WAVE), which can optimize any measures of node and edge conservation, and which can be used with any NCF or combination of multiple NCFs. Using WAVE on top of established state-of-the-art NCFs leads to superior alignments compared to the existing methods that optimize only node conservation or only edge conservation or that treat each conserved edge the same. And while we evaluate WAVE in the computational biology domain, it is easily applicable in any domain.Comment: 12 pages, 4 figure

    Shape description and matching using integral invariants on eccentricity transformed images

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    Matching occluded and noisy shapes is a problem frequently encountered in medical image analysis and more generally in computer vision. To keep track of changes inside the breast, for example, it is important for a computer aided detection system to establish correspondences between regions of interest. Shape transformations, computed both with integral invariants (II) and with geodesic distance, yield signatures that are invariant to isometric deformations, such as bending and articulations. Integral invariants describe the boundaries of planar shapes. However, they provide no information about where a particular feature lies on the boundary with regard to the overall shape structure. Conversely, eccentricity transforms (Ecc) can match shapes by signatures of geodesic distance histograms based on information from inside the shape; but they ignore the boundary information. We describe a method that combines the boundary signature of a shape obtained from II and structural information from the Ecc to yield results that improve on them separately

    The Roles of the Dystrophin-Associated Glycoprotein Complex at the Synapse

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