In advanced arrhythmogenic cardiomyopathy, regional RVfw contractile function and compliance decreased significantly, showing 17% vs. 8% and 18% vs. 10% respectively (P < 0.01).
Can patient-specific computer simulations based on echocardiographic deformation data non-invasively estimate myocardial tissue substrates in arrhythmogenic cardiomyopathy mutation carriers?
Patient-specific computer simulations using echocardiographic data can non-invasively identify regional right ventricular contractile and compliance abnormalities in arrhythmogenic cardiomyopathy.
Absolute Event Rate: 0% vs 0%
Abstract Aims Arrhythmogenic cardiomyopathy (AC) is an inherited cardiac disease, characterized by life-threatening ventricular arrhythmias and progressive cardiac dysfunction. The aim of this study is to use computer simulations to non-invasively estimate the individual patient’s myocardial tissue substrates underlying regional right ventricular (RV) deformation abnormalities in a cohort of AC mutation carriers. Methods and results In 68 AC mutation carriers and 20 control subjects, regional longitudinal deformation patterns of the RV free wall (RVfw), interventricular septum (IVS), and left ventricular free wall (LVfw) were obtained using speckle-tracking echocardiography. We developed and used a patient-specific parameter estimation protocol based on the multi-scale CircAdapt cardiovascular system model to create virtual AC subjects. Using the individual’s deformation data as model input, this protocol automatically estimated regional RVfw and global IVS and LVfw tissue properties. The computational model was able to reproduce clinically measured regional deformation patterns for all subjects, with highly reproducible parameter estimations. Simulations revealed that regional RVfw heterogeneity of both contractile function and compliance were increased in subjects with clinically advanced disease compared to mutation carriers without clinically established disease (17 ± 13% vs. 8 ± 4%, P = 0.01 and 18 ± 11% vs. 10 ± 7%, P 0.01, respectively). No significant difference in activation delay was found. Conclusion Regional RV deformation abnormalities in AC mutation carriers were related to reduced regional contractile function and tissue compliance. In clinically advanced disease stages, a characteristic apex-to-base heterogeneity of tissue abnormalities was present in the majority of the subjects, with most pronounced disease in the basal region of the RVfw.
Osta et al. (Mon,) reported a other. In advanced arrhythmogenic cardiomyopathy, regional RVfw contractile function and compliance decreased significantly, showing 17% vs. 8% and 18% vs. 10% respectively (P < 0.01).