Techniques for ventricular repolarization instability assessment from the ECG

Instabilities in ventricular repolarization have been documented to be tightly linked to arrhythmia vulnera- bility. Translation of the information contained in the repolar- ization phase of the electrocardiogram (ECG) into valuable clinical decision-making tools remains challenging. This work aims at providing an overview of the last advances in the pro- posal and quantification of ECG-derived indices that describe repolarization properties and whose alterations are related with threatening arrhythmogenic conditions. A review of the state of the art is provided, spanning from the electrophysio- logical basis of ventricular repolarization to its characteriza- tion on the surface ECG through a set of temporal and spatial risk markers

A study on stability analysis of atrial repolarization variability using ARX model in sinus rhythm and atrial tachycardia ECGs

© 2016 Elsevier Ireland Ltd Background The interaction between the PTa and PP interval dynamics from the surface ECG is seldom explained. Mathematical modeling of these intervals is of interest in finding the relationship between the heart rate and repolarization variability. Objective The goal of this paper is to assess the bounded input bounded output (BIBO) stability in PTa interval (PTaI) dynamics using autoregressive exogenous (ARX) model and to investigate the reason for causing instability in the atrial repolarization process. Methods Twenty-five male subjects in normal sinus rhythm (NSR) and ten male subjects experiencing atrial tachycardia (AT) were included in this study. Five minute long, modified limb lead (MLL) ECGs were recorded with an EDAN SE-1010 PC ECG system. The number of minute ECGs with unstable segments (N us ) and the frequency of premature activation (PA) (i.e. atrial activation) were counted for each ECG recording and compared between AT and NSR subjects. Results The instability in PTaI dynamics was quantified by measuring the numbers of unstable segments in ECG data for each subject. The unstable segments in the PTaI dynamics were associated with the frequency of PA. The presence of PA is not the only factor causing the instability in PTaI dynamics in NSR subjects, and it is found that the cause of instability is mainly due to the heart rate variability (HRV). C onclusion The ARX model showed better prediction of PTa interval dynamics in both groups. The frequency of PA is significantly higher in AT patients than NSR subjects. A more complex model is needed to better identify and characterize healthy heart dynamics

A Time-Varying Non-Parametric Methodology for Assessing Changes in QT Variability Unrelated to Heart Rate Variability

OBJECTIVE: To propose and test a novel methodology to measure changes in QT interval variability (QTV) unrelated to RR interval variability (RRV) in non-stationary conditions. METHODS: Time-frequency coherent and residual spectra representing QTV related (QTVrRRV) and unrelated (QTVuRRV) to RRV, respectively, are estimated using time-frequency Cohen's class distributions. The proposed approach decomposes the non-stationary output spectrum of any two-input one-output model with uncorrelated inputs into two spectra representing the information related and unrelated to one of the two inputs, respectively. An algorithm to correct for the bias of the time-frequency coherence function between QTV and RRV is proposed to provide accurate estimates of both QTVuRRV and QTVrRRV. Two simulation studies were conducted to assess the methodology in challenging non-stationary conditions and data recorded during head-up tilt in 16 healthy volunteers were analyzed. RESULTS: In the simulation studies, QTVuRRV changes were tracked with only a minor delay due to the filtering necessary to estimate the non-stationary spectra. The correlation coefficient between theoretical and estimated patterns was >0.92 even for extremely noisy recordings (SNR in QTV =-10dB). During head-up tilt, QTVrRRV explained the largest proportion of QTV, whereas QTVuRRV showed higher relative increase than QTV or QTVrRRV in all spectral bands (P<0.05 for most pairwise comparisons). CONCLUSION: The proposed approach accurately tracks changes in QTVuRRV. Head-up tilt induced a slightly greater increase in QTVuRRV than in QTVrRRV. SIGNIFICANCE: The proposed index QTVuRRV may represent an indirect measure of intrinsic ventricular repolarization variability, a marker of cardiac instability associated with sympathetic ventricular modulation and sudden cardiac death

Arrhythmic risk prediction based on the analysis of ventricular repolarization markers from surface ECG

La dependencia de la duración del potencial de acción (APD, del inglés "Action Potential Duration") con el ritmo cardiaco (HR, del inglés "Heart Rate"), también conocida como cinética de restitución, es crítica a la hora de generar inestabilidades eléctricas en el corazón y proporciona información relevante en la estratificación del riesgo a sufrir arritmias ventriculares. La curva dinámica de restitución del APD (APDR, del inglés "APD restitution") cuantifica la relación entre el APD y el intervalo RR (inverso de HR) en condiciones estacionarias. Heterogeneidades en el ventrículo dan lugar a propiedades de la restitución no uniformes, haciendo que las curvas APDR presenten variaciones espaciales. La dispersión es una medida de dicha variación espacial. Recientemente se propuso en la literatura un índice derivado del electrocardiograma (ECG), Δα, que cuantifica la dispersión en las pendientes de las curvas dinámicas de APDR mediante la caracterización de la relación entre los intervalos del pico al final de la onda T (Tpe) y RR bajo condiciones estacionarias diferentes. En este Trabajo Fin de Máster (TFM) se ha desarrollado un método automático para obtener y evaluar, a partir de registros ambulatorios, Δα, como predictor independiente de muerte súbita cardiaca (SCD, del inglés "Sudden Cardiac Death") en pacientes con fallo cardiaco crónico (CHF, del inglés "Chronic Heart Failure"). Pacientes con CHF sintomático formaron parte del estudio "MUSIC" (MUerte Súbita en Insuficiencia Cardiaca). La base de datos contenía los registros Holter de 609 pacientes (48 víctimas de SCD, 64 de otras causas cardiacas, 25 de causas no cardiacas y 472 supervivientes) con ritmo sinusal. El preprocesado de las señales ECG realizado en este TFM consistió en un filtrado paso bajo a 40 Hz, interpolación de splines cúbicos y un detector de latidos ectópicos. Se aplicó una técnica de delineación "uniderivacional más reglas a posteriori" para seleccionar las muestras pertenecientes a la onda T y realizar un análisis de componentes principales. A continuación, se delineó la primera componente principal mediante una técnica uniderivacional y, a partir de las marcas de delineación, se obtuvieron las series de los intervalos RR y Tpe. Posteriormente, se interpolaron a una frecuencia de muestreo fs = 1 Hz. Como cada valor de la curva APDR está medido a un valor específico de RR, el índice de ECG Δα debería calcularse usando segmentos de ECG de ritmos cardiacos estables. Dichos segmentos son difíciles de conseguir en la práctica clínica y por lo tanto se modeló la dependencia del intervalo Tpe con una historia de intervalos previos de RR y se compensó por el retardo de memoria de Tpe. La relación entre Tpe y RR se caracterizó en los registros completos de ECG. Un umbral fijado en Δα>0.046 discriminó los pacientes en alto y bajo riesgo a sufrir SCD (p-valor = 0.003). El tiempo hasta el evento (SCD) fue aproximadamente el doble en los pacientes con Δα0.046 (p-valor = 0.001). Al combinar Δα con el índice de media de alternancias de onda T se mejoró la estratificación del riesgo a sufrir SCD (p-valor<0.001). Este estudio demuestra que la dispersión en APDR, cuantificada a partir de registros ECG Holter, es un predictor de SCD fuerte e independiente en pacientes con CHF. Estos resultados apoyan la hipótesis de que una dispersión de APDR elevada refleja un funcionamiento cardiaco anormal, con predisposición a sufrir SCD

QT interval time lag in response to heart rate changes during stress test for Coronary Artery Disease diagnosis

Background: Slow adaptation of the QT interval to abrupt changes in heart rate (HR) can enhance ventricular heterogeneity and has been suggested as a marker of arrhythmic risk. Most investigations on QT rate adaptation lag have been performed in response to step-like HR changes. However, abrupt HR changes are difficult to induce or observe in ECG recordings under ambulatory conditions. Objective: We aim to evaluate the power of indices related to the QT lag in response to ramp-like HR changes in stress test to assess CAD risk. Methods: We quantified the lag between the actual QT series and the memoryless expected QT series, which was obtained by fitting a hyperbolic regression model to the instantaneous QT and HR measurements in stages where their behavior could be assumed stationary. The proposed methodology was applied to analyze ECG stress tests of a subset of 448 patients presenting different risk levels for Coronary Artery Disease (CAD). The QT lag was estimated separately in the exercise and recovery phases. Results: An increase in the estimated QT lag during exercise (from 25 to 36 s) and a decrease during recovery (from 57 to 39 s) were associated with higher CAD risk. The difference between these lags showed significant capacity for CAD risk stratification. Conclusion: The QT lag in response to HR changes can be quantified from a stress test. QT lag values in response to ramp-like HR changes are in ranges comparable to those quantified from abrupt HR changes and show clinical significance to stratify CAD risk

Ionic Mechanisms of Action Potential Rate Dependence, Conduction and Block in Normal Epicardium and in Remodeled Epicardium Post-Infarction

In this work, detailed computational models are used to study the electrophysiology of normal epicardium and the arrhythmogenic effects of epicardial cell remodeling post-infarction. The canine epicardial myocyte model described here reproduces a wide range of experimentally observed rate dependent phenomena in cell and tissue. Model behavior depends on updated formulations for the 4-AP sensitive transient outward current: Ito1), the slow component of the delayed rectifier potassium current: IKs), the L-type Ca2+ channel: ICa,L) and the sodium-potassium pump: INaK) fit to data from canine ventricular myocytes. The model shows that Ito1 plays a limited role in potentiating peak ICa,L and Ca2+ release for propagated action potentials: APs), but modulates the time course of action potential duration: APD) restitution. IKs plays an important role in APD shortening at short diastolic intervals but a limited role in AP repolarization at longer cycle lengths. In addition, simulations demonstrate that ICa,L, INaK and [Na+]i play critical roles in APD accommodation and the rate dependence of APD restitution. Starting from the ionic model of a normal epicardial cell described above, an epicardial border zone: EBZ) model was developed based on available remodeling data. Ionic models of normal zone: NZ) and EBZ myocytes were incorporated into one-dimensional models of propagation to gain mechanistic insight into how ion channel remodeling affects APD and refractoriness, vulnerability to conduction block and conduction safety post-infarction. Simulations of EBZ APD restitution show that remodeled INa and ICaL promote increased effective refractory period: ERP) and prolonged APD at short diastolic interval: DI). Heterogeneous tissue simulations show that increased post-repolarization refractoriness and altered restitution lead to a large rate dependent vulnerable window for conduction block. In simulations of conduction post-infarction, EBZ IK1 remodeling partially offsets the reduction in conduction safety due to altered INa, while Ito1 and ICaL have a negligible effect on conduction. Further simulations show that injection of skeletal muscle sodium channel SkM1-INa, a recently proposed anti-arrhythmic therapy, has several desirable effects including normalization of EBZ ERP and APD restitution, elimination of vulnerability to conduction block and normalization of conduction in uncoupled tissue

The role of ß-adrenergic stimulation in QT interval adaptation to heart rate during stress test

The adaptation lag of the QT interval after heart rate (HR) has been proposed as an arrhythmic risk marker. Most studies have quantified the QT adaptation lag in response to abrupt, step-like changes in HR induced by atrial pacing, in response to tilt test or during ambulatory recordings. Recent studies have introduced novel methods to quantify the QT adaptation lag to gradual, ramp-like HR changes in stress tests by evaluating the differences between the measured QT series and an estimated, memoryless QT series obtained from the instantaneous HR. These studies have observed the QT adaptation lag to progressively reduce when approaching the stress peak, with the underlying mechanisms being still unclear. This study analyzes the contribution of β-adrenergic stimulation to QT interval rate adaptation in response to gradual, ramp-like HR changes. We first quantify the QT adaptation lag in Coronary Artery Disease (CAD) patients undergoing stress test. To uncover the involved mechanisms, we use biophysically detailed computational models coupling descriptions of human ventricular electrophysiology and β-adrenergic signaling, from which we simulate ventricular action potentials and ECG signals. We characterize the adaptation of the simulated QT interval in response to the HR time series measured from each of the analyzed CAD patients. We show that, when the simulated ventricular tissue is subjected to a time-varying β-adrenergic stimulation pattern, with higher stimulation levels close to the stress peak, the simulated QT interval presents adaptation lags during exercise that are more similar to those measured from the patients than when subjected to constant β-adrenergic stimulation. During stress test recovery, constant and time-varying β-adrenergic stimulation patterns render similar adaptation lags, which are generally shorter than during exercise, in agreement with results from the patients. In conclusion, our findings support the role of time-varying β-adrenergic stimulation in contributing to QT interval adaptation to gradually increasing HR changes as those seen during the exercise phase of a stress test

Long-term microgravity exposure increases ECG repolarization instability manifested by low-frequency oscillations of T-Wave vector

Ventricular arrhythmias and sudden cardiac death during long-term space missions are a major concern for space agencies. Long-duration spaceflight and its ground-based analog head-down bed rest (HDBR) have been reported to markedly alter autonomic and cardiac functioning, particularly affecting ventricular repolarization of the electrocardiogram (ECG). In this study, novel methods are developed, departing from previously published methodologies, to quantify the index of Periodic Repolarization Dynamics (PRD), an arrhythmic risk marker that characterizes sympathetically-mediated low-frequency oscillations in the T-wave vector. PRD is evaluated in ECGs from 42 volunteers at rest and during an orthostatic tilt table test recorded before and after 60-day –6° HDBR. Our results indicate that tilt test, on top of enhancing sympathetic regulation of heart rate, notably increases PRD, both before and after HDBR, thus supporting previous evidence on PRD being an indicator of sympathetic modulation of ventricular repolarization. Importantly, long-term microgravity exposure is shown to lead to significant increases in PRD, both when evaluated at rest and, even more notably, in response to tilt test. The extent of microgravity-induced changes in PRD has been associated with arrhythmic risk in prior studies. An exercise-based, but not a nutrition-based, countermeasure is able to partially reverse microgravity-induced effects on PRD. In conclusion, long-term exposure to microgravity conditions leads to elevated low-frequency oscillations of ventricular repolarization, which are potentiated following sympathetic stimulation and are related to increased risk for repolarization instabilities and arrhythmias. Tested countermeasures are only partially effective in counteracting microgravity effects

Time Course of Low-Frequency Oscillatory Behavior in Human Ventricular Repolarization Following Enhanced Sympathetic Activity and Relation to Arrhythmogenesis

Background and Objectives: Recent studies in humans and dogs have shown that ventricular repolarization exhibits a low-frequency (LF) oscillatory pattern following enhanced sympathetic activity, which has been related to arrhythmic risk. The appearance of LF oscillations in ventricular repolarization is, however, not immediate, but it may take up to some minutes. This study seeks to characterize the time course of the action potential (AP) duration (APD) oscillatory behavior in response to sympathetic provocations, unveil its underlying mechanisms and establish a potential link to arrhythmogenesis under disease conditions. Materials and Methods: A representative set of human ventricular computational models coupling cellular electrophysiology, calcium dynamics, β-adrenergic signaling, and mechanics was built. Sympathetic provocation was modeled via phasic changes in β-adrenergic stimulation (β-AS) and mechanical stretch at Mayer wave frequencies within the 0.03–0.15 Hz band. Results: Our results show that there are large inter-individual differences in the time lapse for the development of LF oscillations in APD following sympathetic provocation, with some cells requiring just a few seconds and other cells needing more than 3 min. Whereas, the oscillatory response to phasic mechanical stretch is almost immediate, the response to β-AS is much more prolonged, in line with experimentally reported evidences, thus being this component the one driving the slow development of APD oscillations following enhanced sympathetic activity. If β-adrenoceptors are priorly stimulated, the time for APD oscillations to become apparent is remarkably reduced, with the oscillation time lapse being an exponential function of the pre-stimulation level. The major mechanism underlying the delay in APD oscillations appearance is related to the slow IKs phosphorylation kinetics, with its relevance being modulated by the IKs conductance of each individual cell. Cells presenting short oscillation time lapses are commonly associated with large APD oscillation magnitudes, which facilitate the occurrence of pro-arrhythmic events under disease conditions involving calcium overload and reduced repolarization reserve. Conclusions: The time course of LF oscillatory behavior of APD in response to increased sympathetic activity presents high inter-individual variability, which is associated with different expression and PKA phosphorylation kinetics of the IKs current. Short time lapses in the development of APD oscillations are associated with large oscillatory magnitudes and pro-arrhythmic risk under disease conditions