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Introduction Entropy for coronary heart... Entropy for hypertension Entropy for analyzing cardiac... Conclusion and Future Aspect Abbreviations Acknowledgements References International Journal of Medical Sciences Journal of Bone and Joint Infection (JBJI) |
Int J Biol Sci 2017; 13(10):1320-1328. doi:10.7150/ijbs.19462 Review Complexity Change in Cardiovascular Disease 1. Faculty of Health Sciences, University of Macau, Taipa, Macau; This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
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Chen C, Jin Y, Lo IL, Zhao H, Sun B, Zhao Q, Zheng J, Zhang XD. Complexity Change in Cardiovascular Disease. Int J Biol Sci 2017; 13(10):1320-1328. doi:10.7150/ijbs.19462. Available from http://www.ijbs.com/v13p1320.htm AbstractWith the fast development of wearable medical device in recent years, it becomes critical to conduct research on continuously measured physiological signals. Entropy is a key metric for quantifying the irregularity and/or complexity contained in human physiological signals. In this review, we focus on exploring how entropy changes in various physiological signals in cardiovascular diseases. Our review concludes that the direction of entropy change relies on the physiological signals under investigation. For heart rate variability and pulse index, the entropy of a healthy person is higher than that of a patient with cardiovascular diseases. For diastolic period variability and diastolic heart sound, the direction of entropy change is reversed. Our conclusion should not only give valuable guidance for further research on the application of entropy in cardiovascular diseases but also provide a foundation for using entropy to analyze the irregularity and/or complexity of physiological signals measured by wearable medical device. Keywords: entropy, physiological signal, cardiovascular disease, irregularity, complexity. IntroductionCardiovascular disease has become a major disease that threats to our human life. Although diabetes, hypertension and other diseases can't immediately lead to death, but the autonomic nervous system disorders caused by them also have a huge threat to our human life. So how to detect cardiovascular disease becomes very important. The commonly used detection methods including dynamic blood pressure detection technology, dynamic electrocardiogram detection technology, cardiovascular ultrasound technology, positron emission computed tomography and so on. Following the fast development of wearable medical device, entropy based on continuously measured physiological signals could become a tool for disease detection because of its capacity of capturing the feature of nonlinear dynamics. Entropy was proposed by the German physicist Clausius in 1865. Entropy was originally used to describe a state of substance: "energy degradation". It has a wide range of applications in thermodynamics. At that time entropy is only a physical quantity that can be measured by the change of heat and its meaning is not clear. Until the development of the statistical physics and information theory [1], the meaning of entropy was gradually explained clearly: entropy is the "internal chaos" of a system. Now, entropy has important applications in cybernetics [2], probability theory [3], number theory [4], astrophysics [5], life sciences [6] and other fields [7], and it has also been extended to the more specific definition in different specific disciplines. In biological dynamics, entropy can measure the irregularity or complexity of a person's physiological signals. In this area, approximate entropy [8, 9] and sample entropy [6, 10] are the most commonly used although other entropies, such as fuzzy entropy [11], tone entropy [12, 50] and so on, have been proposed for some specific situations. Multi-scale entropy has been proposed to measure the entropy in different levels or scales of data [6]. For research in diseases, entropy is most commonly used to assess the irregularity and/or complexity of heart rate variability (HRV) [13] which is measured by electrocardiogram (ECG) although it can also be used to measure that of magnetocardiography (MCG), pulse, diastolic heart sound and other physiological signals. HRV is the physiological phenomenon of variation in the time interval between heartbeats (i.e., R-R interval) [14]. HRV represents a quantitative measure which uses the mean and standard deviation of a continuous normal R-R interval to reflect the degree and regularity of changes in heart rate. It determines heart rate's effect on cardiovascular activity [15]. At present, the analysis methods of HRV mainly include linear analysis (time domain analysis [16], frequency domain analysis [17]) and nonlinear analysis. The time domain analysis mainly analyzes the mean and standard deviation of the R-R period. Frequency domain analysis mainly uses Fourier transform and automatic regression analysis model to analyze the high frequency band and low frequency band. Nonlinear analysis of HRV is much more complicated. It is under fast development recently. Entropy analysis belongs to the nonlinear analysis. Currently, there are many researches on the application of entropy in the irregularity or complexity of heart rate. Early research in this area focused on healthy subjects. For example, Ryan et al. [18] used approximate entropy to find that women's heart rate is higher than the men's in the same conditions. Pikkujamsa et al. [19] used approximate entropy to study the impact of age on the heart rate, and concluded that the heart rate complexity of young people is higher than that of the elderly. Costa et al. [20] also summarizes the rule that the heart rate complexity measured by multi-scale sample entropy decreases with the increase of age or with disease. With further development and application of entropy, researchers have applied entropy for disease diagnosis, prognosis and related problems, so that entropy and other nonlinear dynamic indicators can be used as a diagnosis tool in cardiovascular disease, respiratory disease, diabetes mellitus and other disease. There are many articles applying entropy on cardiovascular diseases, covering a wide range from disease detection, classification to prognosis and so on. They used different physiological signals and different entropy calculation methods. For example, many ECG data and latest entropy articles can be found in the website http://physionet.org/. Although there are many studies in this area, the present review mainly classifies the linear index of HRV [17, 21], introduces the nonlinear index of HRV [22, 23], or focuses the application of entropy for the research of aging and aging related diseases [24]. They don't summarize the application of entropy in cardiovascular disease in detail, especially in terms of disease classification. Our review focuses on the application of entropy for the cardiovascular diseases diagnosis. We aim at addressing the question about how the entropy changes in cardiovascular diseases and come out summarized results in general. Specifically, we focus on three categories: coronary artery disease (CAD), hypertension, and diabetic complications. For different diseases, we discuss whether we can have a general summarized result on the entropy feature of the disease. For this review, we searched EMBASE, PubMed, and Google Scholar for the application of entropy in cardiovascular disease until January 2017. The key words for searching were entropy, coronary heart disease, hypertension, diabetes, cardiovascular. Then we selected the articles with the disease diagnosis for the review. After duplication removed, a total of 191 potentially relevant articles in the initial database search were identified. Finally, 25 studies met the selection criteria, including 12 studies for CAD, 7 studies for hypotension, 6 studies for diabetes (Figure 1). Entropy for coronary heart diseaseThe artery atherosclerotic lesion causes stenosis or obstruction of the blood vessel lumen. It will result in myocardial ischemia, hypoxia or necrosis, which leads to heart disease finally. CAD also includes cardiovascular stenosis or occlusion caused by inflammation, embolism. CAD diagnosis depends on the typical clinical symptoms. Combined with myocardial injury markers and auxiliary examination, the doctors found evidence of myocardial ischemia or coronary artery occlusion and determined whether there is myocardial necrosis. The most commonly used methods of detecting myocardial ischemia include routine ECG [25], ECG loading tests and radionuclide myocardial imaging. The further examination includes coronary angiography, intravascular ultrasound and so on. Entropy and other kinetic parameters can be used as an aid to detect coronary artery disease and surgical prognosis. Combined with other nonlinear kinetic parameters, entropy can be used to distinguish patients with CAD from healthy people and roughly determine the severity of the disease in the early detection of CAD. Some literatures attempted to use entropy for automatic classification of CAD [26]. Some literatures compared the autonomic function of patients with CAD, diabetes and healthy control group. These literatures found that the patients have more cardiac autonomic neuropathy (CAN) than the healthy control group. In the distinction between patients with CAD and healthy people, there are many physiological signals and many types of entropy to use (Table 1). From Table 1 we can see that the most frequently measured physiological signal is HRV (mainly measured by ECG). Wang et al. [27], Acharya et al. [28] and Makikallio et al. [29, 30] Pivatelli et al. [31] all used electrocardiogram data to derive heart rate variability and draw relevant conclusion. However, they used different methods to calculate entropy on HRV, where Wang et al. [27] used multi-scale sample entropy, Acharya et al. [28] used sample entropy, and Makikallio et al. [29, 30], Pivatelli et al. [31] used approximate entropy. They all got the conclusion that the entropy of HRV in patients with coronary heart diseases is lower than the healthy people. This trend of change is also displayed in Figure 1 with data extracted from the studies in five articles [17, 28, 29, 30, 31]. Guo Rui et al. [32, 33] measured the pulse of the experimental subjects. Their first article used the sample entropy based on the test pattern decomposition and their second article used the sample entropy based on 45° diagonal distribution's recursive quantitative analysis. They measured the pulse of people with coronary heart disease and those without disease. Their first article directly reached the result that the pulse entropy of patients with coronary heart diseases is less than that of healthy people, thus the pulse irregularity decreased after the illness. In their second article, the sample entropy of patients with coronary heart disease based on diagonal-recursive graph is higher than that of the healthy control group. It means that CAD patients' recursive map entropy has more diagonal structure than that of the control group. They have higher regularity and certainty. It shows that, when the entropy of the physiological system decreased, regularity increased. Table 1
Entropy studies for comparison between healthy people and the patients with coronary artery disease.
Ji et al. [11] found that for short-term HRV sequence, entropy can't distinguish healthy people from sick patients well. Consequently he used diastolic period variability (DPV) and refined fuzzy entropy to get the result that the patients with coronary heart diseases have higher DPV entropy. The reason is explained as follows: the increased Fuzzy Entropy of DPV might suggest abnormal beat-to-beat systolic intervals fluctuations in patients with coronary artery stenosis which leads to irregularity in the DPV series. Akay et al. [34] used approximate entropy to measure diastolic heart sound of patients and obtained the conclusion that the entropy of diastolic heart sound in patients with coronary heart diseases is higher than that in healthy people. In fact, the diastolic sound of healthy people should be stable. If the heart sound intensity has a great volatility and high entropy, the heart has the disease. The sensitivity of this method is 77%, indicating that entropy of diastolic heart sound can be used to differentiate healthy subjects from patients with coronary heart disease. Griffel et al. [35] applied the Path Length Entropy to the same measurements, and the same conclusion was reached. They used cardiac diastolic sounds because the diastolic period is much longer than the systolic period in the heartbeat of the cardiac cycle and it is easier to measure. Gapelyuk et al. [36] used relative entropy [37] to study the myocardial magnetic field localization, and obtained the result that, for the heart magnetic map, the relative entropy of the healthy human is lower than that of the sick person. Since the relative entropy represents the degree of fitting of the two distributions, the distribution of the measured RQS or STT interval waves is closer to the standard normal wave and the relative entropy is lower. This is different from other entropy measurements. They got the results: the relative entropy of healthy people is close to 0, while the relative entropy of the patient is in the vicinity of 0.2. The result is the same as what should come out theoretically. Steinisch et al. [26] also explored the entropy of the magnetic map data, but used sample entropy instead of relative entropy. It is worth noting that entropy is part of the nonlinear dynamic index. Entropy can be used in a wide range including ECG data, MCG data and so on, but its calculation methods are diverse, such as sample entropy, approximate entropy and so on. Different methods may be suitable for different physiological signals. We also see in the previous literature that it can't directly conclude that low entropy means healthy, so we need a concrete analysis of the situation. Through our review on the entropy studies, we obtain the following summarized results. For the studies on HRV and pulse, the entropy in a healthy person is higher than that in a patient. For the DPV and diastolic heart sound, the entropy in a healthy person is lower than that of a patient. For the magnetic cardiogram, we need to distinguish the type of entropy: the relative entropy is higher in patients, the sample entropy is higher in healthy people. Entropy for hypertensionHypertension is a common chronic disease. It's also the most important risk factors of cardiovascular disease. Hypertension is divided into primary hypertension and secondary hypertension. In this review, we focus on the primary hypertension and its complications. We mainly compared the special populations: pregnant women with hyperthyroidism and their neonatal cardiac entropy. We also compared the entropy of the autonomic dysfunction caused by hypertension. For hypertension and diabetes, the researchers compared the cardiac entropy in a specific population (pregnant women and their newborns). Park et al. [38] calculated the HRV through approximate entropy and compared with pregnant women with pregnancy-induced hypertension, gestational diabetes mellitus, anemia and healthy pregnant women's heart rate entropy. They found that the heart rate entropy of pregnant women is lower than healthy pregnant women. If the pregnant women bore newborns, the babies' heart rate entropy was also lower than normal. The anemia patients had the lowest cardiac entropy. Table 2
Entropy studies for comparison between healthy people and the patients with hypertension
Tejera et al. [39] calculated both approximate entropy and sample entropy of HRV. They compared the cardiac entropy of pregnant women with pregnancy-induced hypertension, congenital eclampsia, and healthy pregnant women. The results confirmed that for pregnant women with the same time of pregnancy, healthy pregnant women have the highest entropy and congenital eclampsia patients have the lowest entropy. Kul Yum et al. [40] calculated the approximate entropy of HRV in newborns with pulmonary hypertension and normal neonates. The entropy in the newborns with neonatal pulmonary hypertension is lower than that in normal neonates. They associated pulmonary artery pressure with it, and found that pulmonary hypertension induced by left- to-right shunt lesions suppresses both periodic and complex heart rate oscillation. The mean pulmonary artery pressure can be predicted by calculating the approximate entropy of heart rate variability. For the CAN caused by hypertension, many articles investigated the autonomic nervous function in patients with essential hypertension. They took the R-R interval power spectrum analysis, and used the ECG method to obtain low-frequency band (LFB) and high frequency band (HFB) through the maximum entropy every 10 minutes [41]. The LFB and HFB represent parasympathetic activity, sympathetic nerve activity and parasympathetic activities respectively. From Table 2, Kohara et al. [42] aimed at middle-aged patients and young patients. Both LFB and HFB were significantly lower in elderly hypertensive patients than that in middle-aged patients. They also aimed at non-dipper patients and dipper patients [43]. The findings indicate that compared with dipper patients, non-dipper hypertensive patients were characterized with a decreased physiological circadian fluctuation on autonomic functions. Kawamura et al. [44] did the same research for Kazak non-dipper patients and dipper patients, and got the same conclusion. Kohara et al. also used maximum entropy power spectrum to compare the patients with essential hypertension relationship between autonomic nervous activity and the left ventricular mass index [45]. The conclusion is that the left ventricular mass index is negatively correlated with the total low frequency and total high frequency. The general conclusion is: when calculating the HFB and LFB by using the maximum entropy power spectrum, the lower the frequency means the worse the autonomic nerve function. The older people are worse than the young people; the patients with dipper hypertension are worse than the non-dipper patients; patients with a high left ventricular mass index (indicative a severe cardiovascular disease) are worse than those with a low left ventricular mass index. Entropy for analyzing cardiac autonomic never function damage caused by diabetesStrictly speaking, diabetes is not a cardiovascular disease. In this review, we mainly focus on one of the most important complications of diabetes: cardiac autonomic nervous system dysfunction. This is related to cardiovascular activity and there are many relevant research literature, so we also discussed it in this review. The present article mainly uses the diabetes' HRV data to analyze the cardiac autonomic nerve function damage caused by diabetes. From the Table 3, we can see that Souza et al. [46], Marwaha et al. [47], and Li et al. [48] measured the HRV data in diabetic patients and healthy people as experimental and control groups, but they used different entropy: Shannon entropy, improved multiscale sample entropy, approximate entropy, respectively. They got the same conclusion: the HRV entropy of diabetic patients is lower than the healthy control group. Combined as other nonlinear dynamical parameters, entropy can be served as an additional supplemental tool for the conventional autonomic tests. Then Wu et al. [49] and Karmakar et al. [50] focused on diabetic patients with mild and severe diabetes, but they use different entropy and different measurement data. In the end, they got the same conclusion. Wu measured the pulse conduction time. They used multiscale cross-approximate entropy for their analysis, whereas Karmakar measured ECG data by using tone entropy. Their conclusion is: with the increase in the severity of disease, the HRV entropy is significantly lower. Khandoker et al. [51] used sample entropy to calculate the entropy of HRV. They found the same conclusion. In summary, although the calculation method of entropy is different, the results are similar. That is, for entropy of HRV, higher entropy value means healthier people. We further display this feature by extracting summarized data from the 5 articles [46-50] and drawing a figure (Figure 3). From Figure 3, we can see clearly that no matter what the type of entropy is, the entropy of HRV in a healthy person is higher than that in a patient with diabetes. Table 3
Entropy studies for comparison between healthy people and the patients with diabetes-induced cardiac autonomic neuropathy (CAN).
Figure 2
Entropy of heart rate variability in studies for coronary artery disease (CAD). In each bar, the standard error of the mean in each group is represented by the vertical line above the mean. Comparison 1 uses the multiscale sample entropy and doesn't have the data for standard error from the study in article [27]. Comparison 2 uses approximate entropy whereas comparison 3 uses sample entropy; both for the same data in the study in article [28]. Comparison 4 uses approximate entropy for the study in article [29]. Comparison 5 uses approximate entropy for the study in [31]. (Click on the image to enlarge.) Figure 3
Entropy of heart rate variability in studies for cardiac autonomic nervous system dysfunction of diabetes. In each bar, the standard error of the mean in each group is represented by the vertical line above the mean. Comparison 1 uses the Shannon entropy for the study in [46]. Comparison 2 uses the improved multiscale sample entropy for the study in [47]. Comparison 3 use the approximate entropy for the study in [48]. Comparison 4 use the multiscale cross approximate entropy for the study in [29]. Comparison 5 use the tone entropy for the study in [50]. Comparison 1 is for comparing type 1 diabetes with healthy people, and the remaining pairs are for comparing type 2 diabetes with healthy people. (Click on the image to enlarge.)Conclusion and Future AspectFor the upcoming era of digital medicine, the continuous monitoring of human's physiological signals and associated entropy analysis are getting more and more critical. Currently, there are many studies for cardiovascular diseases in this area [c.f., 6, 8-12, 24, 26, 27-50]. However, as far as we know, no one has published a sophisticated review specifically on the entropy analysis of cardiovascular diseases. There are key questions to be answered only through reviews on all available relevant studies. For example, one review focusing on the application of entropy for aging and aging related diseases [24] mentions that, for HRV, the entropy of a healthy person is higher than that of a patient with cardiovascular diseases in general? Is it true based on all the major related research in this area? How about the entropy of other physiological signals such as DPV and heart sound? Thus, in this article, we conduct a sophisticated review to address these key questions. Through our review, we obtained the following summarized results based on the available relevant studies that we searched through literature. For HRV, in the three major disease areas (i.e., coronary heart disease, hypertension, diabetes complications), no matter how the entropy calculation method is used (namely, whether Shannon entropy, sample entropy, approximate entropy, tone entropy or maximum entropy power spectrum is used), the entropy of healthy people is higher than that of the patients and the entropy decreases as the severity of the disease increases (Tables 1-3). For the pulse index, the results on the entropy analysis is the same as those for HRV. For DPV in CAD, the Fuzzy entropy of the healthy people is lower than that of the patients. For diastolic heart sound, the entropy of a healthy person is lower than that of a patient whether the entropy is assessed by approximate entropy or path length entropy. For MCG, whether a healthy person has a higher entropy value than a CAD patient relies on the used entropy. A healthy person has a higher entropy value when using sample entropy but a lower value when using relative entropy than a patient (Table 1). The explanation for the above summarized results can be complicated. One explanation for a higher entropy of HRV in a healthy person relative to a cardiovascular patient is to use heart autonomic nerve function: higher entropy, better heart autonomic nerve function [13]. One explanation for a lower entropy of DPV in a healthy person relative to a CAD patient is that CAD patients may have abnormal beat-to-beat systolic intervals fluctuations which leads to irregularity in the DPV series [11]. For MCG, the data are high-dimensional, consequently it must go through a process of dimensional reduction before entropy can be calculated. When the data is reduced to one dimension, sample entropy and similar entropy can be calculated. The entropy results are similar to those of HRV. Relative entropy is calculated in the case where the data are reduced to three dimensions as compared to a reference distribution coming from healthy people. If the distribution is similar to the reference distribution, the relative entropy is low. If the two distributions are completely coincident, the entropy is 0. Thus, the relative entropy of a patient should at least no less than that of a healthy person [37]. Therefore, the relative entropy actually measures different things as sample entropy and other regular entropy does. With this in mind, the entropy results for MCG is actually similar to those for HRV. Multiple studies used entropy to distinguish between a healthy person and an ill person with good performance in some situations [cf. 26, 31, 34-36, 50-51]. For example, Akay et al. [34] used approximate entropy of diastolic heart sounds to distinguish between CAD and non-CAD patients and obtained sensitivity of 77%, a specificity of 80%, and an overall accuracy of 78%. Steinisch et al. [26] used sample entropy of MCG to distinguish between CAD patients and healthy people and obtained good performance: 99% sensitivity, 97% specificity, 98% accuracy, 96% and 99% positive and negative predictive values respectively [26]. To distinguish between CAN and non-CAN patients, Khandoker et al. [51] obtained 82.35% accuracy, 100% sensitivity and 62.5% specificity when using sample entropy of HRV alone and 88.24% accuracy, 100% sensitivity and 75% specificity when using the combination of sample entropy and Poincaré plot. However, the use of entropy for discrimination and classification does not have a broad utility yet based on all available literature. One reason may be that, although a variety of entropy measures have been proposed, none of them have a broad utility in all the major physiological signals. One of the entropy measures, sample entropy, tends to get more and more popular among all the available entropy measures. However, the calculation of sample entropy requires the adjustment of multiple parameters such as embedding dimension and tolerance and different settings on these parameters may lead to different results. Consequently, entropy alone can hardly be used as a clinically valid diagnosis tool at present. In addition, different entropies may be suitable for different physiological signals. Thus, currently, it is more practical to explore the overall trend of entropy change in different disease statuses as we did in this review. In the future, research can be conducted to explore better and more stable entropy measures with broader usage in various major physiological signals. In all, through the summarized results coming out of our review on the application of entropy in cardiovascular diseases, we conclude that the direction of entropy change heavily relies on the physiological signals under investigation. We confirmed that, for HRV, the entropy of a healthy person is higher than that of a patient with cardiovascular diseases in all existing literature that we have searched. This is also true for pulse index. However, for DPV and diastolic heart sound, the direction of entropy change is reversed: the entropy of a healthy person is lower than that of a CAD patient. These above results hold regardless of the different types of entropy to be used in the studies. For MCG, a healthy person has a higher entropy value than a CAD patient if using regular entropy such as sample entropy. Our conclusion should not only give valuable guidance for further research on the application of entropy in cardiovascular diseases but also provide a foundation for using entropy to analyze the entropy of physiological signals measured by wearable medical device. AbbreviationsHRV: heart rate variability; ECG: electrocardiogram; MCG: magnetocardiography; CAD: coronary artery disease; CAN: cardiac autonomic neuropathy; DPV: diastolic period variability; LFB: low-frequency band; HFB: high frequency band; CCM: complex correlation measure; DM: diabetes mellitus. AcknowledgementsThis work was supported by the Start-up Research Grant (SRG2016-00083-FHS) at University of Macau. Competing InterestsThe authors have declared that no competing interest exists. References1. Shannon CE, Weaver W. The Mathematical Theory of Information. Mathematical Gazette. 1949;97:170-80 2. Cibert C. Entropy and information in flagellar axoneme cybernetics: a radial spokes integrative function. Cell Motility & the Cytoskeleton. 2003;54:296-316 3. Dan V. The Analogues of Entropy and of Fisher's Information Measure in Free Probability Theory: VI. Liberation and Mutual Free Information. Communications in Mathematical Physics. 1993;155:71-92 4. Maslov VP, Maslova TV. 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