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107 results for “Cardiac mechanics”
Four-Chamber Human Heart Model for the Simulation of Cardiac Electrophysiology and Cardiac Mechanics
<p><strong>Changes in version 1.1 compared to version 1.0:</strong></p> <ul> <li>Ventricular fiber orientation changed to 66° on the endocardial and −41° on the epicardial surface</li> <li>Electrophysiology mesh was resampled</li> <li>Updated material tags in EP mesh</li> <li>Further details can be found in the <a href="https://github.com/KIT-IBT/CardioMechanics/tree/main">CardioMechanics GitHub repository</a> new reference paper:</li> </ul> <blockquote> <p>Gerach, T.; Loewe, A. Differential effects of mechano-electric feedback mechanisms on whole-heart activation, repolarization, and tension. <em>The Journal of Physiology</em> <strong>2024. </strong>https://doi.org/10.1113/JP285022 </p> </blockquote> <p>This repository contains a four-chamber model of the human heart which is ready to use for simulations of cardiac electrophysiology and cardiac mechanics problems. When using this dataset, please also cite the accompanying paper</p> <blockquote> <p>Gerach, T.; Schuler, S.; Fröhlich, J.; Lindner, L.; Kovacheva, E.; Moss, R.; Wülfers, E.M.; Seemann, G.; Wieners, C.; Loewe, A. Electro-Mechanical Whole-Heart Digital Twins: A Fully Coupled Multi-Physics Approach. <em>Mathematics</em> <strong>2021</strong>, <em>9</em>, 1247. https://doi.org/10.3390/math9111247</p> </blockquote> <p>The cardiac anatomy was manually segmented from magnetic resonance imaging (MRI) data of a 33 year old male volunteer. The volunteer provided informed consent and the study was approved by the IRB of Heidelberg University Hospital (Fritz et al., 2014).<br>The MRI data were acquired using a 1.5 T MR tomography system and consist of a static whole heart image stack taken during diastasis as well as time-resolved images in several long and short axis slices. Based on the segmentation, we first labeled the atria and the ventricles. The geometry was extended by a representation of the mitral valve, the tricuspid valve, the aortic valve and the pulmonary valve. Additionally, we closed the endo- and epicardial surfaces of the atria and added truncated pulmonary veins, vena cavae as well as the ascending aorta and pulmonary artery. Furthermore, we added a concentric layer of tissue around the entire heart which phenomenologically represents the influence of the pericardium and the surrounding tissue.</p> <p>Two tetrahedral meshes were created using Gmsh (Geuzaine et al., 2009): (1) the mechanical reference domain (<strong>M.vtu</strong>) with 128,976 elements (on average 3.17 mm edge length) and (2) the electrophysiological reference domain (<strong>EP.vtu</strong>) as a subset of M with 50,058,295 elements (on average 0.4 mm edge length).<br>We used rule-based methods to assign the myofiber orientation on EP: Wachter et al. (2015) was used for the atria and Bayer et al. (2012) for the ventricles. The fiber angle in the ventricles was chosen as +60° and -60° on the endocardial and epicardial surface, respectively. The sheet angle was set to -65° on the endocardium and 25° on the epicardium. Github repositories to these fiber generation tools are given in the sidebar. All geometry files are given in millimeter (mm).</p> <ul> <li><strong>Data:</strong><br>We provide time resolved data evaluated from cine MRI data, which can be used for model calibration. <ul> <li>Wall thickening (<strong>17AHA_WT.txt</strong>) / fractional wall thickening (<strong>17AHA_fractionalWT.txt</strong>) in the 17 AHA segments of the left ventricle</li> <li>Atrioventricular plane displacement (<strong>AVPD.txt</strong>) and velocity (<strong>AVPV.txt</strong>) as well as the displacement of all tracked points used for AVPD calculation (<strong>AVPD_trackedPoints.txt</strong>)</li> <li>Left and right ventricular volume (<strong>Volume_LV_RV.txt</strong>). RV volume is only available for end-diastole and end systole.</li> </ul> </li> <li><strong>Surfaces:</strong><br>This directory contains *.stl files with triangulated surfaces on which boundary conditions can be applied. <ul> <li><strong>cavityXX.stl</strong>: blood volume of the LV, RV, LA, RA</li> <li><strong>epicard.stl</strong>: the whole epicardium</li> <li><strong>outerPeri.stl</strong> and <strong>outerTrunks.stl</strong>: surfaces for Dirichlet boundary conditions</li> <li><strong>master.stl </strong>and <strong>slave.stl</strong>: surfaces used for the frictionless contact problem described in Fritz et al. (2014)</li> </ul> </li> <li><strong>TetGen:</strong><br>Contains the geometry <strong>M.vtu</strong> in the TetGen file format. T4 mesh with 4 node tetrahedrons and 3 node triangles. <ul> <li>.bases: fiber, sheet, and normal orientation at quadrature points of all elements</li> <li>.node: vertex coordinates</li> <li>.ele: list of tetrahedra</li> <li>.sur: list of triangles</li> </ul> </li> <li><strong>EP.vtu:</strong><br>Contains the cell arrays Fiber and Material.</li> <li><strong>M.vtu:</strong><br>Contains the cell arrays Fiber, Sheet, Sheetnormal, Material, and Label.</li> <li><strong>LabelIDs.txt:</strong><br>List of Label and Material identification numbers and corresponding anatomical structures.</li> </ul> <p> </p>
An integrated approach including docking, MD simulations, and network analysis highlights the action mechanism of the cardiac hERG activator RPR260243
<p>500 ns MD trajectories of the hERG bound states (protein and ligand) used for the analyses discussed in the paper. There are three replica for each system. The trajectories can be visualized using molecular visualization programs such as Pymol or VMD uploading the PDB and the DCD file.</p> <p>The PDB and the topology files of the hERG bound state (protein, membrane, ions and ligand) are also included.</p> <p>An example of input file used for the production step of the dynamics has been provided (production_1.conf). </p>
PLOS Comput. Biol. "Biophysically detailed mathematical models of multiscale cardiac active mechanics": datasets
<p>This repository contains the data accompanying the PLOS Computational Biology paper "<em>Biophysically detailed mathematical models of multiscale cardiac active mechanics</em>", by Francesco Regazzoni, Luca Dedè and Alfio Quarteroni.</p> <p>It contains the following datasets:</p> <ul> <li><strong>steady_state.csv</strong>: steady-state active tension for constant calcium concentration and sarcomere length (Figs. 11, 12, 13 ,14).</li> <li><strong>isometric_twitches.csv</strong>: active tension transients in isometric conditions (Figs. 15, 16, 17).</li> <li><strong>force_velocity_relationship.csv</strong>: force-velocity relationship at different calcium concentrations and sarcomere lenghts (Fig. 18).</li> <li><strong>fast_transient_response.csv</strong>: tension-elongation curve after a fast step in length (Fig. 19).</li> </ul> <p>CSV headers refer to the following variables (and measure units):</p> <ul> <li><strong>Ca</strong> (<em>μM</em>): intracellular calcium concentration.</li> <li><strong>SL</strong> (<em>μm</em>): sarcomere length.</li> <li><strong>active_tension</strong> (<em>kPa</em>): active tension.</li> <li><strong>Delta_L</strong> (<em>nm/hs</em>): step length.</li> <li><strong>velocity</strong> (<em>hs/s</em>): shortening velocity.</li> <li><strong>time</strong> (<em>s</em>): time.</li> </ul>
Data From: Emulation of Cardiac Mechanics using Graph Neural Networks
<p>Contains simulation results of the forward displacement from beginning to end-diastole for approximately 3000 synthetically generated left ventricle geometries.</p> <p>The simulation results are split into training, validation and test data.</p> <p>The data is described in detail in a forthcoming publication in <em>Computer Methods in Applied Mechanics and Engineering</em> - further information will be provided upon publication. A GitHub repository will also be made available, with code for processing the simulation data and training a Graph Neural Network emulator.</p>
Dataset related to the article "Cardiac Biomarkers and Autoantibodies in Endurance Athletes: Potential Similarities with Arrhythmogenic Cardiomyopathy Pathogenic Mechanisms"
<p>This record contains raw data related to the article “Cardiac Biomarkers and Autoantibodies in Endurance Athletes: Potential Similarities with Arrhythmogenic Cardiomyopathy Pathogenic Mechanisms". </p> <p>The "Extreme Exercise Hypothesis" states that when individuals perform training beyond the ideal exercise dose, a decline in the beneficial effects of physical activity occurs. This is due to significant changes in myocardial structure and function, such as hemodynamic alterations, cardiac chamber enlargement and hypertrophy, myocardial inflammation, oxidative stress, fibrosis, and conduction changes. In addition, an increased amount of circulating biomarkers of exercise-induced damage has been reported. Although these changes are often reversible, long-lasting cardiac damage may develop after years of intense physical exercise. Since several features of the athlete's heart overlap with arrhythmogenic cardiomyopathy (ACM), the syndrome of "exercise-induced ACM" has been postulated. Thus, the distinction between ACM and the athlete's heart may be challenging. Recently, an autoimmune mechanism has been discovered in ACM patients linked to their characteristic junctional impairment. Since cardiac junctions are similarly impaired by intense physical activity due to the strong myocardial stretching, we propose in the present work the novel hypothesis of an autoimmune response in endurance athletes. This investigation may deepen the knowledge about the pathological remodeling and relative activated mechanisms induced by intense endurance exercise, potentially improving the early recognition of whom is actually at risk.</p>
Spliced isoforms of the cardiac Nav1.5 channel modify channel activation by distinct structural mechanisms: Molecular dynamics coordinate and trajectory files
<p>Molecular dynamics files associated with the publication: Spliced isoforms of the cardiac Nav1.5 channel modify channel activation by distinct structural mechanisms</p>
Cardiac Mechanics by Speckle Tracking as a Prognostic Predictor in Patients With Chagas Cardiomyopathy
ClinicalTrials.gov study NCT06806722. IPD Sharing: NO. Countries: 1. Publications: 2.
Molecular Mechanisms of Volume Overload-Aim 1(SCCOR in Cardiac Dysfunction and Disease)
ClinicalTrials.gov study NCT01052428. IPD Sharing: Not stated. Countries: 1. Publications: 36.
Study on the Efficacy and Mechanism of Cardiac Rehabilitation for Stem Cell Mobilization and Heart Failure Improvement
ClinicalTrials.gov study NCT00154466. IPD Sharing: Not stated. Countries: 1. Publications: 1.
A Publicly Available Virtual Cohort of Four-chamber Heart Meshes for Cardiac Electro-mechanics Simulations
<p><strong>Motivation: </strong> Computational models of the heart are increasingly being used in the development of devices, patient diagnosis and therapy guidance. While software techniques have been developed for simulating single hearts, there remain significant challenges in simulating cohorts of virtual hearts from multiple patients.</p> <p><strong>Dataset Description: </strong>We present the first database of four-chamber heart models suitable for electro-mechanical simulations. Our database consists of twenty-four four-chamber heart models generated from end-diastolic CT acquired from heart failure patients recruited for cardiac resynchronization therapy upgrade. We also provide a higher resolution version for each of the twenty-four meshes.</p> <p>We segmented end-diastolic CT. The segmentation was then upsampled and smoothed. The final multi-label segmentation was used to generate a tetrahedral mesh. The resulting meshes had an average edge length of 1.1mm. The elements of all the twenty-four meshes are labelled as follows: 1) Left ventricle myocardium 2) Right ventricle myocardium 3) Left atrium myocardium 4) Right atrium myocardium 5) Aorta wall 6) Pulmonary artery wall 7) Left atrium appendage ring 8) Left superior pulmonary vein ring 9) Left inferior pulmonary vein ring 10) Right inferior pulmonary vein ring 11) Right superior pulmonary vein ring 12) Superior vena cava ring 13) Inferior vena cava ring 14) Mitral valve plane 15) Tricuspid valve plane 16) Aortic valve plane 17) Pulmonary valve plane 18) Left atrial appendage valve plane 19) Left superior pulmonary vein valve plane 20) Left inferior pulmonary vein valve plane 21) Right inferior pulmonary vein valve plane 22) Right superior pulmonary vein valve plane 23) Superior vena cava valve plane 24) Inferior vena cava valve plane.</p> <p>Ventricular fibres were generated using a rule-based method, with a fibre orientation varying transmurally from endocardium to epicardium from 80˚ to -60˚, respectively. We defined a system of universal ventricular coordinates on the meshes, see Figure 1B: an apico-basal coordinate varying continuously from 0 at the apex to 1 at the base; a transmural coordinate varying continuously from 0 at the endocardium to 1 at the epicardium; a rotational coordinate varying continuously from – π at the left ventricular free wall, 0 at the septum and then back to + π at the left ventricular free wall; intra-ventricular coordinate defined at -1 at the left ventricle and +1 at the right ventricle. This coordinate system was assigned to the ventricles in the four-chamber meshes and all the other labels were assigned with -100. </p> <p>We also refined each mesh from 1.1mm resolution down to 0.39mm resolution. Each refined mesh has tags defined on its elements (same numbering as described above) and ventricular fibres.</p> <p><strong>Database format: </strong>We provide a zipped folder for each mesh. Each folder contains the coarse and the finer versions of the same mesh. All twenty-four 1mm-meshes are supplied in case format, readable with paraview. All binary files containing the meshes data (ens and geo formats) are provided within the zipped folder. Points coordinates are given in mm. Element tags are assigned to the elements of the mesh as well as fibres and sheet directions. Fibres and sheet directions are assigned to the ventricles according to a rule-based method, while non-ventricular elements are assigned with default vectors [1; 0; 0] and [0; 1; 0]. UVCs are assigned to the nodes of the meshes. We also provide the location of the cardiac resynchronisation therapy right-ventricular electrode used to initiate ventricular excitation. This is given as a label on the nodes called electrode endo rv, which is 1 at the stimulated nodes. Finer meshes are provided in vtk format, also readable in paraview. For these meshes, we provide element tags, fibres and sheet directions on the ventricles, all in the same file.</p>
Biology of Sex Differences Sex-linked differences in cardiac atrophy after mechanical unloading induced by heterotopic heart transplantation
<p>GraphPad prism dataset to support - Biology of Sex Differences Sex-linked differences in cardiac atrophy after mechanical unloading induced by heterotopic heart transplantation</p>
Cardiac, Pulmonary and Diaphragm Sonography for the Early Diagnosis of the Different Etiologies Underlying Failure of Weaning From Mechanical Ventilation
ClinicalTrials.gov study NCT03261440. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Mechanical Ventilation Controlled by the Electrical Activity of the Patient's Diaphragm - Effects on Cardiac Performance
ClinicalTrials.gov study NCT00647361. IPD Sharing: Not stated. Countries: 1. Publications: 2.
Assessment of the Mechanism of Non-cardiac Syncope
ClinicalTrials.gov study NCT05728255. IPD Sharing: NO. Countries: 5. Publications: 2.
Cardiac Performance in Mechanically Ventilated COVID-19 Patients
ClinicalTrials.gov study NCT04628195. IPD Sharing: UNDECIDED. Countries: 1. Publications: 20.
Mechanical Ventilation During Cardiac Surgery
ClinicalTrials.gov study NCT02090205. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Measure Cardiac Output Using Ultrasound Dilution in Mechanically Ventilated Children
ClinicalTrials.gov study NCT01662141. IPD Sharing: Not stated. Countries: 1. Publications: 1.
Maintaining Mechanical Ventilation During Cardiopulmonary Bypass for Cardiac Surgery
ClinicalTrials.gov study NCT03372174. IPD Sharing: NO. Countries: 1. Publications: 1.
Validation of Kinocardiography, a New Technology Measuring Cardiac Mechanical Activity Via Accelerometers and Gyroscopes
ClinicalTrials.gov study NCT04772807. IPD Sharing: UNDECIDED. Countries: 1. Publications: 4.
Effect of Mechanical Ventilation on Cardiac RF Ablation
ClinicalTrials.gov study NCT06986577. IPD Sharing: UNDECIDED. Countries: 1. Publications: 3.
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