Renyi entropy in identification of cardiac autonomic neuropathy in diabetes (original) (raw)
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Using Renyi entropy to detect early cardiac autonomic neuropathy
Conference proceedings : ... Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual Conference, 2013
Cardiac Autonomic Neuropathy (CAN) is a disease that involves nerve damage leading to abnormal control of heart rate. CAN affects the correct operation of the heart and in turn leads to associated arrhythmias and heart attack. An open question is to what extent this condition is detectable by the measurement of Heart Rate Variability (HRV). An even more desirable option is to detect CAN in its early, preclinical stage, to improve treatment and outcomes. In previous work we have shown a difference in the Renyi spectrum between participants identified with well-defined CAN and controls. In this work we applied the multi-scale Renyi entropy for identification of early CAN in diabetes patients. Results suggest that Renyi entropy derived from a 20 minute, Lead-II ECG recording, forms a useful contribution to the detection of CAN even in the early stages of the disease. The positive α parameters (1 ≤ α ≤ 5) associated with the Renyi distribution indicated a significant difference (p < ...
Frontiers in bioengineering and biotechnology, 2014
Cardiac autonomic neuropathy (CAN) is a disease that involves nerve damage leading to an abnormal control of heart rate. An open question is to what extent this condition is detectable from heart rate variability (HRV), which provides information only on successive intervals between heart beats, yet is non-invasive and easy to obtain from a three-lead ECG recording. A variety of measures may be extracted from HRV, including time domain, frequency domain, and more complex non-linear measures. Among the latter, Renyi entropy has been proposed as a suitable measure that can be used to discriminate CAN from controls. However, all entropy methods require estimation of probabilities, and there are a number of ways in which this estimation can be made. In this work, we calculate Renyi entropy using several variations of the histogram method and a density method based on sequences of RR intervals. In all, we calculate Renyi entropy using nine methods and compare their effectiveness in separ...
2015
In this work we compare three multiscale measures for their ability to discriminate between participants having cardiac autonomic neuropathy (CAN) and aged controls. CAN is a disease that involves nerve damage leading to an abnormal control of heart rate, so one would expect disease progression to manifest in changes to heart rate variability (HRV). We applied multiscale entropy (MSE), multi fractal detrended fluctuation analysis (MFDFA), and Renyi entropy (RE) to recorded datasets of RR intervals. The latter measure provided the best separation (lowest p-value in Mann-Whitney tests) between classes of participants having CAN, early CAN or no CAN (controls). This comparison suggests the efficacy of RE as a measure for diagnosis of CAN and its progression, when compared to the other multiscale measures.
Entropy, 2015
In this work we compare three multiscale measures for their ability to discriminate between participants having cardiac autonomic neuropathy (CAN) and aged controls. CAN is a disease that involves nerve damage leading to an abnormal control of heart rate, so one would expect disease progression to manifest in changes to heart rate variability (HRV). We applied multiscale entropy (MSE), multi fractal detrended fluctuation analysis (MFDFA), and Renyi entropy (RE) to recorded datasets of RR intervals. The latter measure provided the best separation (lowest p-value in Mann-Whitney tests) between classes of participants having CAN, early CAN or no CAN (controls). This comparison suggests the efficacy of RE as a measure for diagnosis of CAN and its progression, when compared to the other multiscale measures.
Entropy
The time series of interbeat intervals of the heart reveals much information about disease and disease progression. An area of intense research has been associated with cardiac autonomic neuropathy (CAN). In this work we have investigated the value of additional information derived from the magnitude, sign and acceleration of the RR intervals. When quantified using an entropy measure, these time series show statistically significant differences between disease classes of Normal, Early CAN and Definite CAN. In addition, pathophysiological characteristics of heartbeat dynamics provide information not only on the change in the system using the first difference but also the magnitude and direction of the change measured by the second difference (acceleration) with respect to sequence length. These additional measures provide disease categories to be discriminated and could prove useful for non-invasive diagnosis and understanding changes in heart rhythm associated with CAN.
Entropy Measures in Heart Rate Variability Data
Lecture Notes in Computer Science, 2000
Standard parameters of heart rate variability are restricted in measuring linear effects, whereas nonlinear descriptions often suffer from the curse of dimensionality. An approach which might be capable of assessing complex properties is the calculation of entropy measures from normalised periodograms. Two concepts, both based on autoregressive spectral estimations are introduced here. To test the hypothesis that these entropy measures may improve the result of high risk stratification, they were applied to a clinical pilot study and to the data of patients with different cardiac diseases. The study shows that the entropy measures discussed here are useful tools to estimate the individual risk of patients suffering from heart failure. Further, the results demonstrate that the combination of different heart rate variability parameters leads to a better classification of cardiac diseases than single parameters.
Physiological Measurement, 2011
Approximate entropy (ApEn) is widely accepted as a complexity measure of the heart rate variability (HRV) signal, but selecting the criteria for the threshold value r is controversial. This paper aims to verify whether Chon's method of forecasting the r max is an appropriate one for the HRV signal. The standard limb lead ECG signals of 120 subjects were recorded for 10 min in a supine position. The subjects were divided into two groups: the heart failure (22 females and 38 males, median age 62.4 ± 12.6) and healthy control group (33 females and 27 males, median age 51.5 ± 16.9). Three types of ApEn were calculated: the ApEn 0.2 using the recommended constant r = 0.2, the ApEn chon using Chon's method and the ApEn max using the true r max . A Wilcoxon rank sum test showed that the ApEn 0.2 (p = 0.267) and the ApEn max (p = 0.813) had no statistical differences between the two groups, while the ApEn chon (p = 0.040) had. We generated a synthetic database to study the effect of two influential factors (the signal length N and the ratio of short-and long-term variability sd 1 /sd 2 ) on the empirical formula in Chon's method (Chon et al 2009 IEEE Eng. Med. Biol. Mag. 28 18-23). The results showed that the empirical formula proposed by Chon et al is a good method for analyzing the random signal, but not an appropriate tool for analyzing nonlinear signals, such as the logistic or HRV signals.
2010
In this work, Refined Multiscale Entropy (RMSE) was applied to characterize risk of cardiac death in ischemic cardiomyopathy patients, analyzing heart rate variability (HRV) by means of RR series during daytime and nighttime. RMSE approach measures an entropy rate in different time scales of a series, giving a multiscale characterization of complexity of that series. RMSE showed statistically significant differences (p<0.05) during daytime and nighttime only in middle time scales (τ=4–15 and τ=3–16, respectively). For these scales, RMSE was higher in low risk (SV) than in high risk (CM) group of cardiac death, indicating a reduction of the entropy-based complexity in CM when it was compared with SV. No statistical differences between risk groups were presented at time scale τ=1 (unfiltered original RR series). It can be concluded that the dynamics in middle time scales should be considered to better describe the HRV of patients with cardiac death.
Physiological Measurement, 2008
Multiscale entropy (MSE) analysis provides information about complexity on various time scales. The aim of this study was to test whether MSE is able to detect autonomic dysregulation in young patients with diabetes mellitus (DM). We analyzed heart rate (HR) oscillations, systolic (SBP) and diastolic blood pressure (DBP) signals in 14 patients with DM type 1 and 14 age-and sexmatched healthy controls. SampEn values (scales 1-10) and linear measures were computed. HR: among the linear measures of heart rate variability significant differences between groups were only found for RMSSD ( p = 0.043). MSE was significantly reduced on scales 2 and 3 in DM ( p = 0.023 and 0.010, respectively). SBP and DBP: no significant differences were detected with linear measures. In contrast, MSE analysis revealed significantly lower SampEn values in DM on scale 3 ( p = 0.039 for SBP; p = 0.015 for DBP). No significant correlations were found between MSE and linear measures. In conclusion, MSE analysis of HR, SBP and DBP oscillations is able to detect subtle abnormalities in cardiovascular control in young patients with DM and is independent of standard linear measures.
Atypical Cardiac Autonomic Neuropathy Identified with Entropy Measures
Cardiology and Angiology: An International Journal, 2015
Aims: To identify Cardiac Autonomic Neuropathy (CAN) from a range of measures extracted from Heart Rate Variability (HRV), including higher moments of RR intervals and a spectrum of entropy measures of RR intervals. Study Design: Analysis of HRV measured from participants at a diabetes screening clinic. Groups were compared using t-tests to identify variables that provide separation between groups.