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Sensitivity of temporal heart rate variability in Poincaré plot to changes in parasympathetic nervous system activity

  • Chandan K Karmakar1,
  • Ahsan H Khandoker1Email author,
  • Andreas Voss2 and
  • Marimuthu Palaniswami1
BioMedical Engineering OnLine201110:17

https://doi.org/10.1186/1475-925X-10-17

©  Karmakar et al; licensee BioMed Central Ltd. 2011

Received: 19 January 2011

Accepted: 3 March 2011

Published: 3 March 2011

Abstract

Background

A novel descriptor (Complex Correlation Measure (CCM)) for measuring the variability in the temporal structure of Poincaré plot has been developed to characterize or distinguish between Poincaré plots with similar shapes.

Methods

This study was designed to assess the changes in temporal structure of the Poincaré plot using CCM during atropine infusion, 70° head-up tilt and scopolamine administration in healthy human subjects. CCM quantifies the point-to-point variation of the signal rather than gross description of the Poincaré plot. The physiological relevance of CCM was demonstrated by comparing the changes in CCM values with autonomic perturbation during all phases of the experiment. The sensitivities of short term variability (SD 1), long term variability (SD 2) and variability in temporal structure (CCM) were analyzed by changing the temporal structure by shuffling the sequences of points of the Poincaré plot. Surrogate analysis was used to show CCM as a measure of changes in temporal structure rather than random noise and sensitivity of CCM with changes in parasympathetic activity.

Results

CCM was found to be most sensitive to changes in temporal structure of the Poincaré plot as compared to SD 1 and SD 2. The values of all descriptors decreased with decrease in parasympathetic activity during atropine infusion and 70° head-up tilt phase. In contrast, values of all descriptors increased with increase in parasympathetic activity during scopolamine administration.

Conclusions

The concordant reduction and enhancement in CCM values with parasympathetic activity indicates that the temporal variability of Poincaré plot is modulated by the parasympathetic activity which correlates with changes in CCM values. CCM is more sensitive than SD 1 and SD 2 to changes of parasympathetic activity.

Keywords

Heart Rate VariabilityScopolamineTemporal StructureParasympathetic ActivityHeart Rate Variability Signal

Background

Heart rate variability (HRV) is a powerful non-invasive method for analyzing the function of the autonomic nervous system. It is useful to understand the interplay between the sympathetic and parasympathetic autonomic nervous system, which serves to speed up and slow down the heart rate, respectively [1]. HRV, the variation of the time period between consecutive heart beats, is thought to reflect the heart's adaptability to the changing physiological conditions. It is dependent predominantly on the extrinsic regulation of the heart rate [2]. Assessment of HRV provides quantitative information about the modulation of heart rate (HR) by sympathetic nervous system (SNS) and parasympathetic nervous system (PNS). Interactions of SNS and PNS using HRV signal have been well studied and their importance established with a number of cardiac diseases including myocardial infarction [3], patients with congestive heart failure [4], patients at risk of sudden cardiac death [5, 6] and patients with hypertension [7, 8]. There are two main approaches to the analysis of HRV: time-domain and frequency-domain analysis. Time-domain indices (i.e., Mean, standard deviation (SD), standard deviation of normal RR intervals (SDNN), standard deviation of averaged normal RR intervals (SDANN) [9]) are derived from simple statistical calculations based on interbeat intervals (RR intervals). These indices are sensitive to transients and trends in the sample of heartbeats, and as such provide estimates of overall and beat-to-beat variability [10]. Frequency-domain analysis, which is based on the power spectral density of the heart rate time series, highlights the issue of the underlying rhythms of the mechanisms controlling heart rate (HR) and identified three major spectral peaks (high frequency (HF: 0.15-0.4 Hz), low frequency (LF: 0.04-0.15 Hz) and very low frequency (VLF: below 0.04 Hz)) in the adult HR spectrum [1]. These measurements can be derived from short-term (i.e 5 to 30 minutes) or long-term ECG recordings (i.e. 24 hours). HRV has been used as a non-invasive marker of the activity of the autonomic nervous system for over two decades. The necessary guidelines for comparing different studies of HRV have been established by the Task force of ESC and NPSE [9]. In [9], it has been suggested that the time-domain methods are ideal for the analysis of long-term HRV signal. Poincaré plot is one of the popular time domain HRV analysis techniques which is used both for short term (i.e. 5 to 30 minutes) or long term (ie. 24 hours) analysis.

Poincaré plot is a visual presentation of time series signal to recognize the hidden patterns. It is also a quantitative technique in the sense that it has various parameters (ex: short-term variability (SD 1) and long-term variability (SD 2)) to quantify the information from the plot. The Poincaré plot of HRV signal is constructed by plotting consecutive points of RR interval time series (i.e., lag-1 plot). It is a representation of HRV signal on phase space or Cartesian plane [11], which is commonly used to asses the dynamics of the HRV [12–15] signal, describe the sympathetic and parasympathetic modulation of heart rate [16, 17] and in various clinical settings like diabetes [18], chronic heart failure [19], chronic renal failure [15] and sleep apnea syndrome [20].

The popular technique used to quantify the Poincaré plot is fitting an ellipse to the shape of the Poincaré plot and measure the dispersion along the major and minor axis of the ellipse. This technique was first proposed by Tulppo et. al. [12] in which they have defined two standard descriptors of the plot SD 1 and SD 2 for quantification of the Poincaré plot geometry. Later, the description of SD 1 and SD 2 in terms of linear statistics, given by Brennan et. al. [21], showed that the standard descriptors guide the visual inspection of the distribution. In case of HRV, it reveals a useful visual pattern of the RR interval data by representing both short and long term variations of the signal [12, 21]. The primary limitation of the standard descriptors used for quantifying Poincaré plot is the lack of embedding temporal information. The standard descriptors, SD 1 and SD 2, represent the distribution of signal in 2 D space and carries only information of width and length. As shown in Figure 1, Poincaré plots of similar SD 1 and SD 2 values can have completely different underlying temporal dynamics.
Figure 1
Figure 1

Poincaré plots with similar SD 1 and SD 2 having different temporal dynamics. Two different RR interval time series of length N (N = 2000) with similar SD 1 and SD 2 values having different temporal dynamics (first 20 points) are shown in top and bottom panel.

To overcome this limitation, in our previous study [22], we developed a novel measure, complex correlation measure (CCM), to quantify the temporal variation of the Poincaré plot. In that study, it was shown that CCM is more sensitive to changes in temporal structure of the signal than SD 1 and SD 2. In [22], it was reported that it is possible to have two Poincaré plots with similar SD 1 and SD 2 having varied temporal structure. In such a scenario, CCM can be used to successfully distinguish two Poincaré plots. CCM was also shown as a measurement from a series of lagged Poincaré plots (multiple lag correlation) which can potentially provide more information about the behavior of Poincaré plot than the conventional lag-1 plot measurements (SD 1 and SD 2). Moreover, CCM has shown to have better generalization capability over different pathology than SD 1 and SD 2, and it was reported as a novel parameter to characterize the variability in the temporal structure of the Poincaré plot.

Use of Poincaré plot of successive RR intervals to study the heart rate behavior during accentuated sympathovagal interaction has been reported in several studies [12, 13, 16]. In this study we demonstrate the physiological significance of the novel measure CCM by analyzing the effects of perturbations of autonomic function on Poincaré plot descriptors (SD 1 and SD 2) in young healthy subjects caused by the 70° head-up tilt test, atropine infusion and transdermal scopolamine patch. We also analyze the characteristics of the responses of CCM to changes in sequences of points in Poincaré plot by surrogate analysis, which provides insight into the variability in temporal structure of the Poincaré plot.

Methods

Complex Correlation Measure (CCM)

The CCM measures the point-to-point variation of the signal rather than gross description of the Poincaré plot. It is computed in a windowed manner which embeds the temporal information of the signal. A moving window of three consecutive points from the Poincaré plot are considered and the temporal variation of the points are measured. If three points are aligned on a line then the value of the variation is zero, which represents the linear alignment of the points. Moreover, since the individual measure involves three points of the two dimensional Poincaré plot, it is comprised of at least four different points of the time series for lag m = 1 and at most six points in case of lag m ≥ 3. Hence the measure conveys information about four different lag correlations of the signal. If the Poincaré plot is composed of N points then the temporal variation of the plot, termed as CCM , is composed of all overlapping three point windows and can be calculated as:
C C M ( m ) = 1 C n ( N − 2 ) ∑ i = 1 N − 2 ‖ A ( i ) ‖
(1)

where m represents lag of Poincaré plot, A(i) represents area of the i-th triangle and C n is the normalizing constant which is defined as, C n = π * SD 1 * SD 2, represents the area of the fitted ellipse over Poincaré plot at lag-m. The length of major and minor axis of the ellipse are 2SD 1, 2SD 2, where SD 1, SD 2 are the dispersion perpendicular to the line of identity (minor axis) and along the line of identity (major axis) respectively. The detail mathematical formulation of CCM is reported in our previous study [22].

Sensitivity to changes in temporal structure

Literally the sensitivity is defined as the rate of change of the value due to the change in temporal structure of the signal. The change in temporal structure of the signal in a window is achieved by surrogating the signal (i.e, data points) in that window. In our previous study [22], we studied the temporal nature of sensitivity of CCM by changing the temporal structure of the signal using a moving fixed length window. In this study, the sensitivity of CCM was analyzed in order to define how it was affected by increasing amount of change in temporal structure. By increasing the number of surrogating points we have increased the probability of the amount of change in temporal structure of time-series signal. At each step the number of surrogated points is increased by 50, which gives enough resolution to understand the overall pattern. We calculated SD 1, SD 2 and CCM of a RR interval signal by increasing the number of surrogating points at a time. For a selected number of surrogating points, we have shuffled the points for 30 times and calculated all descriptors each time after shuffling. Finally the surrogated values of descriptors were taken as a mean of the calculated values. Finally, the sensitivity of descriptors ΔSD 1 j , ΔSD 2 j and ΔCCM j was calculated using equations 2-4:
Δ S D 1 j = S D 1 j − S D 1 0 S D 1 0
(2)
Δ S D 2 j = S D 2 j − S D 2 0 S D 2 0
(3)
Δ C C M j = C C M j − C C M 0 C C M 0
(4)

where SD 10, SD 20 and CCM 0 were the parameters measured for the original data set without surrogation and j represents the window number whose data was surrogated. Moreover, SD 1 j, SD 2 j and CCM j represent the SD 1, SD 2 and CCM values respectively after surrogation of j th step.

Surrogate analysis

To show statistically that CCM is a measure of temporal variation rather than the outcome of a random process with no temporal variations, we adapted one method of surrogate data introduced by Theiler et al. [23]. We have used this method to prove, the hypothesis that the correlation properties of RR interval were distinguishable from uncorrelated random noise. This also indicates that the effect of surrogation is higher in case of a strongly correlated signal. In this study, 30 surrogate RR interval series were generated for each RR interval time series by shuffling the original RR interval time series. Each of the surrogated RR interval series had the identical statistical distribution (mean, SD, higher moments) as surrogation differed only in the temporal sequence from the original time series. The effect of surrogation on the Poincaré plot was then measured by calculating SD 1, SD 2 and CCM for each surrogated time series and the means of the surrogated values (MeanSD 1 s , MeanSD 2 s and MeanCCM s ) were then calculated for 30 surrogated time series and compared to the SD 1 i , SD 2 i and CCM i of original time series to determine the sensitivity of all parameters. The test of the hypothesis was performed by computing the relative changes of SD 1, SD 2 and CCM values (SD 1 R , SD 2 R and CCM R respectively) between original and the mean of surrogated time series. That is, for i th time series it was defined as:
S D 1 R = ‖ ( S D 1 i − M e a n S D 1 s ) ‖ S D 1 i
(5)
S D 2 R = ‖ ( S D 2 i − M e a n S D 2 s ) ‖ S D 2 i
(6)
C C M R = ‖ ( C C M i − M e a n C C M s ) ‖ C C M i
(7)

Subjects and Study design

In this study, five subjects with normal sinus rhythm, did not smoke, had no cardiovascular abnormalities and were not taking any medications were studied. Subjects were aged between 20 and 40 years (30.2 ± 7.2 year). All subjects had provided fully informed consent and ethical approval was granted by the Austin Hospital Committee of Ethics in Human Research.

All studies were performed at the same time of the day without any disturbances. No respiration control was performed because all phases of the study were conducted in the resting state. An intravenous cannula was inserted into an antecubital vein and subjects then rested for 20 minutes before commencement of data collection. The length of the study varies from 10 to 20 minutes. For autonomic perturbations the following sequence of protocol was performed. At least 20 minutes was allowed between each phase to permit the heart rate to return baseline. The sequence of phases was maintained strictly as follows:

Baseline study

All baseline studies were conducted in subjects in the post-absorptive state after resting for 10 minutes in the supine position.

Seventy degree head-up tilt

Data were collected after subjects were tilted 70° on a motorized table. This maneuver increases sympathetic and decreases parasympathetic nervous system activity [24]. To permit the heart rate to stabilize at the new position, data were collected 5 minutes after the subjects were tilted.

Atropine infusion

Atropine sulphate (1.2 mg) was added to 50 ml of intravenous dextrose and infused at a rate of 0.12 mg/min for 5 minutes and then at a rate of 0.24 mg/min until completion of this phase of study. Use of this dose regimen reduces parasympathetic nervous system activity significantly [25]. After 10 minutes of infusion of atropine, the data collection started.

Transdermal scopolamine

One week after the above studies, a low-dose transdermal scopolamine patch (hyoscine 1.5 mg) was applied overnight to an undamaged hair free area of skin behind the ear. The patch remained in situ for the duration of this period of the study. It has been shown in [26] that low-dose transermal scopolamine increases parasympathetic nervous system activity.

Details of the study design and data collection were published in [16].

Results

In Figure 2, the RR intervals and the corresponding Poincaré plot for all four phases of the experiment with the same subject are shown. From figure it is eminent that the atropine infusion strongly reduces the size of plot by reducing both the RR interval (increase in heart rate) and its variation. Whereas, the head-up tilt position reduces the RR interval (increase in heart rate) variability markedly with respect to the baseline. In contrast, use of low-dose transdermal scopolamine increases the RR interval (reduces heart rate) and its variability resulted into a wider Poincaré plot in terms of width in both direction (perpendicular to line of identity and along the line of identity).
Figure 2
Figure 2

RR intervals and Poincaré plots during autonomic perturbations. RR interval time series for single subject from all four phases of study with corresponding Poincaré plot.

Table 1 summarizes the mean and standard deviation of heart rate variability features of all subjects in all four phases. Short-term variability (SD 1) was increased in Scopolamine phase and decreased in Atropine phase. A similar trend was also found for long-term variability (SD 2). Changes of SD 1 values from phase to phase was much higher than that of SD 2. CCM value was also minimum in Atropine phase and maximum at Scopolamine phase. Changes in mean values of CCM between study phases were higher than both SD 1 and SD 2 (Table 1). Moreover, change in CCM values in Atropine, 70° head-up tilt and Scopolamine phases from Baseline are found significant (p < 0.01). SD 1 values were significantly different in Atropine and Scopolamine phases and SD 2 values differ only in Atropine phase.
Table 1

MEAN and Standard deviation SD of values of all descriptors for lag-1 Poincaré plot

Feature

SD1

SD2

CCM

 

(mean ± sd) (ms)

(mean ± sd) (ms)

(mean ± sd)

Atropine

4.45 ± 2.45*

43.11 ± 13.79*

3.88E-02 ± 1.05E − 02*

Head-up tilt

11.96 ± 5.47

70.77 ± 13.98

6.29E-02 ± 2.08E − 02*

Baseline

28.74 ± 9.28

85.94 ± 11.27

1.50E-01 ± 3.40E-02

Scopolamine

69.90 ± 21.25*

103.05 ± 20.05

2.75E-01 ± 2.14E − 02*

SD 1, SD 2 and CCM values of all subjects (N = 5) were calculated for four phases as described in section.

* indicates the value of the feature in corresponding phase is significantly (p < 0.01) different from baseline phase using Wilcoxon rank sum test.

The errorbars of log-scaled SD 1, SD 2 and CCM values for four groups of subjects are shown in Figure 3. The atropine administration resulted into reduction in mean value of SD 1 (SD of ΔRR) for all subjects. The similar effect was also found for SD 2 and CCM . The use of scopolamine patch increased both the width and height of the Poincaré plot which resulted into increase in mean values of CCM as well as SD 1, SD 2. All subjects have shown a marked reduction in SD 1, SD 2 and CCM values in 70° head-up tilt phase compared to the baseline.
Figure 3
Figure 3

Errorbars of SD 1, SD 2 and CCM. Errorbar (n = 5) of log(SD 1), log(SD 2) and log(CCM) for Atropine, 70° head-up tilt, baseline and scopolamine phase. All values were calculated for short segment (~ 20 minutes) RR interval time series signal.

Figure 4 represented the change of descriptors SD 1, SD 2 and CCM with increasing number of shuffled RR intervals. From Figure 4 it is obvious that the rate of change with number of shuffled RR intervals was highest for CCM at any point than SD 1 and SD 2.
Figure 4
Figure 4

Sensitivity of SD 1, SD 2 and CCM with changes in temporal dynamics. Sensitivity of SD 1, SD 2 and CCM with number of shuffled points N s . At each step the number of shuffled points increased by 50. Each time the signal has been shuffled for 30 times and its mean has been taken to calculated the sensitivity.

Surrogate data testing was performed to test if CCM can represent a measure of temporal dynamics of RR intervals and quantify sensitivity of those parameters to relative changes. For each subject at all four phases, relative changes in SD 1, SD 2 and CCM values of the RR interval signal were calculated. Figure 5 shows the log scaled values of relative changes in SD 1, SD 2 and CCM at all four phases of the study using SD errorbar. Relative changes in CCM values were higher compared to relative changes in SD 1 and SD 2 values due to shuffling the sequences of data series (Figure 5). Moreover, the relative changes were found to be lowest for SD 2 for all four phases.
Figure 5
Figure 5

Changes in SD 1, SD 2 and CCM values for all phases. SD 1 R , SD 2 R and CCM R is the change between original and surrogated values of SD 1, SD 2 and CCM (given by number of original Mean). RR interval signal of each subject for four different phases was randomly shuffled 30 times then SD 1, SD 2 and CCM was calculated each time. Mean of each descriptor (SD 1, SD 2 and CCM) of these 30 data sets was compared to value of corresponding descriptor (SD 1, SD 2 and CCM) of originally ordered RR interval signal.

Discussion

Heart rate variability time series were analyzed using a variety of linear methods, most commonly using HRV descriptive statistics in the time and frequency domains [1, 10, 12, 14, 16]. The potential use of Poincaré plot as a serial correlation technique has also been explored to quantify autonomic activity [16, 27]. In this study, we have shown that CCM (a measure of temporal dynamics) for Poincaré plot provides a dynamical way to quantify autonomic activity. In addition to this, CCM has been shown to be a more sensitive parameter compared to SD 1 and SD 2 to any changes of dynamics in autonomic activity.

Physiological relevance of CCM

Quantitative Poincaré plot analysis was used to assess the changes in HRV during parasympathetic blockade [12] and compared the results with power spectral analysis of HRV, which was the commonly used method in the measurement of sympathovagal interaction [1, 12, 28, 29]. It was also reported that Poincaré analysis method can provide the heart rate dynamics that is not detected by the conventional time domain methods [12]. The present quantitative analysis was performed to measure the instantaneous beat-to-beat variance of RR intervals (SD 1), the long term continuous variance of all RR intervals (SD 2) and the variation in temporal structure of all RR intervals (CCM). Instantaneous changes in RR intervals are mediated by vagal efferent activity, because vagal effects on the sinus node are known to develop faster than sympathetically mediated effects [30, 31]. The maximum reduction in SD 1 during atropine infusion compared to baseline values, confirming that SD 1 quantifies the vagal modulation of heart rate, which was also reported by Kamen et. al. [16] and Tulppo et. al. [12]. Similar reduction in CCM value could be observed (Table 1 and Figure 3), which indicates that CCM might correlate the parasympathetic nervous system activity. The lowest value of CCM has also been found during atropine infusion which reduced the parasympathetic activity and reduces instantaneous changes in HRV signal. Moreover, significant (p < 0.01) change in CCM values in all phases from Baseline phase compared to SD 1 and SD 2 indicates that CCM is more sensitive to changes in parasympathetic activity (Table 1). On the contrary, changes in SD 1 values are insignificant in 70° Head-up tilt phase and changes in SD 2 values are insignificant both in 70° Head-up tilt as well as Scopolamine phases.

Reciprocal changes in sympathetic and parasympathetic activity occurs during head-up tilt phase. The RR interval and the high-frequency power of RR intervals decreases during the head up tilt phase as evidence of withdrawal of vagal activity (decrease in parasympathetic activity) [32–34]. The short term variability measure of Poincaré plot (SD 1) also decreases and correlates with high-frequency power as reported by Kamen et. al. [16]. In this study, SD 1 value decreased during 70° head-up tilt phase compared to baseline, which supports the results reported by previous studies [16, 24]. The CCM value has also decreased in 70° head-up tilt phase compared to baseline, which indicates that CCM value is modulated by the vagal tone (parasympathetic activity). Therefore, changes in autonomic regulation caused by 70° head-up tilt phase resulted in concordant changes in the temporal structure of the Poincaré plot of RR intervals.

The low-dose transdermal scopolamine patch (hyoscine 1.5 mg) may decrease heart rate by a paradoxical vagomimetic effect [26]. Delivery by transdermal patch substantially increases both baseline and reflexly augmented levels of cardiac parasympathetic activity over 24 hours in normal subjects [35, 36]. Both time-domain HRV (Mean, SD) and frequency domain HRV (high frequency power) increased to a greater extent during administration of low-dose scopolamine, which indicates the increase in parasympathetic activity [26]. The increase in parasympathetic activity decreases the heart rate and increases the RR interval as well as instantaneous variance in the RR, as measured by SD 1 of Poincaré plot. The increased value of SD1 correlates with increased high frequency power and is supported by the previous study reported by Kamen et. al. [16]. In this study, the variability in the temporal structure of the Poincaré plot (measured as CCM) was also found to be increased with increase in parasympathetic activity during administration of low-dose scopolamine (Figure 3, Table 1). The increase in CCM value indicates that it reflects the change in parasympathetic activity harmoniously.

Sensitivity of CCM due to changes in dynamics

In this study, we have found that CCM correlates with the parasympathetic activity similar to SD 1 [16]. In [22], we have shown that CCM is sensitive to change in temporal structure of the signal irrespective of temporal position of the signal. In that study, we had used simulated RR interval signal to prove our hypothesis. In line with the previous finding [22], in this study the relation of CCM with increasing number of shuffled RR intervals has been studied. The highest rate of change of CCM with number of shuffled RR intervals (Figure 4) at any point represents the maximum sensitivity of CCM with respect to change in temporal structure of the Poincaré plot. Therefore, we can conclude that CCM is much more sensitive than SD 1 and SD 2 with respect to change in temporal structure or the change in autocorrelation of the signal which was earlier reported in [22]. Moreover, sensitivity of CCM with small number of RR intervals increases its applicability to short length HRV signal analysis. However, it is not possible to determine the value of minimum number of required RR interval for all biomedical application as it will be problem specific rather than a global one.

The impact of changes in parasympathetic activity on temporal structure of the Poincaré plot is obvious from Figure 5. The changes due to surrogating are the highest for CCM in all phases, which might indicate that CCM is a measure of temporal structure of the plot and more sensitive to it than SD 1 and SD 2. Moreover, the change in its value between before and after surrogating is the highest for atropine phase which might indicate the reducing parasympathetic activity and its impact on the temporal structure of the plot better manifest in CCM value. In atropine phase, since the parasympathetic activity is reduced, variability decreases (low SD 1 values) which is reflected by substantially linear temporal structure of the plot (lower CCM values). After surrogating, the correlation among the signal vanishes and as a result, uncorrelated or random temporal structure increased the CCM value. Therefore, the difference between original and surrogate value indicates that CCM depends on the correlation properties of the RR interval and it can be used to distinguish the HRV signal from uncorrelated random noise. Moreover, the difference between original and surrogate value also indicates the sensitivity of the CCM increases with degree of blocking parasympathetic activity by 70° head-up tilt and atropine infusion. On the other hand, the sensitivity of CCM decreases with enhancement of parasympathetic activity by scopolamine administration.

Conclusion

By using the quantitative Poincaré plot analysis of HRV signal, we observed that atropine infusion, 70° head-up tilt and scopolamine administration result in changes in heart rate variability [short term variation (SD 1) as well as long term variation (SD 2)] and heart rate dynamics [temporal structure (CCM) values]. Subtle differences in dynamics of HRV signal were detected by CCM in all phases of the study. These observations provide some novel information on the physiological relevance of CCM for Poincaré plot analysis: 1) The variability of temporal structure of Poincaré plot of HRV, quantified using CCM, correlates the parasympathetic activity 2) CCM is highly sensitive to changes in parasympathetic activity (vagal tone) as compared to SD 1 and SD 2. Although CCM captures temporal variation of Poincaré plot, it fails if the RR intervals are aligned on a line. However, existence of few zero area patterns does not affect the overall CCM value as it is measured using a moving window of three consecutive points. Further studies of CCM of HRV signal with changes in sympathetic activity may give the complete physiological explanation of CCM with respect to sympathovagal activity. Moreover, due to well published changes in autonomic regulation between men and women and in different age groups [37], and investigation of gender and age effects on CCM would be of interest in further studies.

Declarations

Authors’ Affiliations

(1)
Department of Electrical and Electronic Engineering, The University of Melbourne, Parkville, Australia
(2)
Department of Medical Engineering & Biotechnology, University of Applied Sciences Jena, Germany

References

  1. Akselrod S, Gordon D, Ubel F, Shannon D, Berger A, Cohen R: Power spectrum analysis of heart rate fluctuation: a quantitative probe of beat-to-beat cardiovascular control. Science 1981, 213(4504):220–222. 10.1126/science.6166045View ArticleGoogle Scholar
  2. Acharya UR, Joseph KP, Kannathal N, Lim CM, Suri JS: Heart rate variability: a review. Medical and Biological Engineering and Computing 2006, 44(12):1031–1051. 10.1007/s11517-006-0119-0View ArticleGoogle Scholar
  3. Carney RM, Blumenthal JA, Stein PK, Watkins L, Catellier D, Berkman LF: Depression, heart rate variability, and acute myocardial infarction. Circulation 2001, 104: 2024–2028. 10.1161/hc4201.097834View ArticleGoogle Scholar
  4. Aronson D, Burger AJ: Effect of beta-blockade on heart rate variability in decompensated heart failure. Int J Cardiol 2001, 79: 31–39. 10.1016/S0167-5273(01)00401-6View ArticleGoogle Scholar
  5. Corr PB, Pitt B, Natelson BH, J RD, Shine KI, Skinner JE: Sudden cardiac death Neural-chemical interactions. Circulation 1987, 76(Suppl I):208–214.Google Scholar
  6. Makikallio TH, Seppanen T, Airaksinen KE, Koistinen J, Tulppo MP, Peng CK, Goldberger AL, Huikuri HV: Dynamic analysis of heart rate may predict subsequent ventricular tachycardia after myocardial infarction. Am J Cardiol 1997, 80: 779–783. 10.1016/S0002-9149(97)00516-XView ArticleGoogle Scholar
  7. Pagani M, Lucini D: Autonomic dysregulation in essential hypertension: insight from heart rate and arterial pressure variability. Auton Neurosci 2001, 90: 76–82. 10.1016/S1566-0702(01)00270-3View ArticleGoogle Scholar
  8. Takahashi N, Nakagawa M, Saikawa T, Ooie T, Yufu K, Shigematsu S: Effect of essential hypertension on cardiac autonomic function in type 2 diabetic patients. J Am Coll Cardiol 2001, 38: 232–237. 10.1016/S0735-1097(01)01363-8View ArticleGoogle Scholar
  9. Task Force of ESC and NASPE: Heart rate variability, standards of measurement, physiological interpretation, and clinical use. Circulation 1996, 93(5):1043–1065.View ArticleGoogle Scholar
  10. Rosenstock EG, Cassuto Y, Zmora E: Heart rate variability in the neonate and infant: analytical methods, physiological and clinical observations. Acta Paediatrica 1999, 88(5):477–482. 10.1080/08035259950169422View ArticleGoogle Scholar
  11. Liebovitch LS, Scheurle D: Two lessons from fractals and chaos. Complexity 2000, 5: 34–43. 10.1002/1099-0526(200003/04)5:4<34::AID-CPLX5>3.0.CO;2-3MathSciNetView ArticleGoogle Scholar
  12. Tulppo MP, Makikallio TH, Takala TES, Seppanen T, V HH: Quantitative beat-to-beat analysis of heart rate dynamics during exercise. Am J Physiol 1996, 271: H244-H252.Google Scholar
  13. Tulppo MP, Makikallio TH, Seppanen T, Airaksinen JKE, V HH: Heart rate dynamics during accentuated sympathovagal interaction. Am J Physiol 1998, 247: H810-H816.Google Scholar
  14. Toichi M, Sugiura T, Murai T, Sengoku A: A new method of assessing cardiac autonomic function and its comparison with spectral analysis and coefficient of variation of R-R interval. J Auton Nerv Syst 1997, 62: 79–84. 10.1016/S0165-1838(96)00112-9View ArticleGoogle Scholar
  15. Hayano J, Takahashi H, Toriyama T, Mukai S, Okada A, Sakata S, Yamada A, Ohte N, Kawahara H: Prognostic value of heart rate variability during long-term follow-up in chronic haemodialysis patiens with end-stage renal disease. Nephrol Dial Transplant 1999, 14: 1480–1488. 10.1093/ndt/14.6.1480View ArticleGoogle Scholar
  16. Kamen PW, Krum H, Tonkin AM: Poincaré plot of heart rate variability allows quantitative display of parasympathetic nervous activity in humans. Clinical Science 1996, 91: 201–208.View ArticleGoogle Scholar
  17. Brennan M, Palaniswami M, Kamen P: Poicare plot interpretation using a physiological model of HRV based on a network of oscillators. Am J Physiol Heart Circ Physiol 2002, 283: 1873–1886.View ArticleGoogle Scholar
  18. Guzik P, Bychowiec B, Piskorski J, Wegrzynowski A, Krauze T, Schneider R, Liszkowski P, Wykretowicz A, Wierusz-Wysocka B, Wysocki H: Heart rate variability by Poincaré plot and spectral analysis in young healthy subjects and patients with type 1 diabetes. Folia Cardiol 2005, 12(suppl D):64–67.Google Scholar
  19. Schechtman VL, Lee MY, Wilson AJ, Harper RM: Dynamics of respiratory patterning in normal infants and infants who subsequently died of the sudden infant death syndrome. Pediatric Research 1996, 40: 571–577. 10.1203/00006450-199610000-00010View ArticleGoogle Scholar
  20. Aljadeff G, Gozal D, Schechtman VL, Burrell B, Harper RM, Ward SL: Heart rate variability in children with obstructive sleep apnea. Sleep 1997, 20: 151–157.Google Scholar
  21. Brennan M, Palaniswami M, Kamen P: Do existing measures of poincare plot geometry reflect nonlinear features of heart rate variability. IEEE Trans on Biomed Engg 2001, 48: 1342–1347. 10.1109/10.959330View ArticleGoogle Scholar
  22. Karmakar C, Khandoker A, Gubbi J, Palaniswami M: Complex Correlation Measure: a novel descriptor for Poincaré plot. BioMedical Engineering OnLine 2009, 8: 17. 10.1186/1475-925X-8-17View ArticleGoogle Scholar
  23. Theiler J, S E, Longtin A, B G, Farmer J: Testing for nonlinearity in time series: the method of surrogate data. Physica 1992, 58: 77–94.MATHGoogle Scholar
  24. Vybrial T, Byrg RJ, Maddens ME, Boden WE: Effect of pasive tilt on sympathetic and parasympathetic components of heart rate variability oin normal subjects. Am J Cariol 1989, 63: 1117–1120. 10.1016/0002-9149(89)90089-1View ArticleGoogle Scholar
  25. Hayano J, Sakakibara Y, Yamada A: Accuracy of assessment of cardiac vagal tone by heart rate variability in normal subjects. Am J Cardiol 1991, 67: 199–204. 10.1016/0002-9149(91)90445-QView ArticleGoogle Scholar
  26. La Rovere MT, Mortara A, Pantaleo P, Maestri R, Cobelli F, Tavazzi L: Scopolamine improves autnomic balance in advanced congestive heart failure. Circulation 1994, 90(2):838–843.View ArticleGoogle Scholar
  27. Kamen PW, Tonkin AM: Application of the Poincaré plot to heart rate variability: A new measure of functional status in heart failure. Aust NZ J Med 1995, 25: 18–26.View ArticleGoogle Scholar
  28. Jaffe RS, Fung DL, Behrman KH: Optimal frequency ranges for extracting information on autonomic activity from the heart rate spectrogram. Journal of the autonomic nervous system 1994, 46(1–2):37–46. 10.1016/0165-1838(94)90142-2View ArticleGoogle Scholar
  29. Pagani M, Lombardi F, Guzzetti S, Rimoldi O, Furlan R, Pizzinelli P, Sandrone G, Malfatto G, Dell'Orto S, Piccaluga E: Power spectral analysis of heart rate and arterial pressure variabilities as a marker of sympatho-vagal interaction in man and conscious dog. Circ Res 1986, 59(2):178–193.View ArticleGoogle Scholar
  30. Berger RD, Saul JP, Cohen RJ: Transfer function analysis of autonomic regulation. I. Canine atrial rate response. Am J Physiol Heart Circ Physiol 1989, 256: H142–152.Google Scholar
  31. Rosenblueth A, A SF: The interrelations of vagal and accelerator effects on the cardiac rate. Am J PhysioZ 1934, 110: 42–55.Google Scholar
  32. Montano N, Ruscone T, Porta A, Lombardi F, Pagani M, Malliani A: Power spectrum analysis of heart rate variability to assess the changes in sympathovagal balance during graded orthostatic tilt. Circulation 1994, 90(4):1826–1831.View ArticleGoogle Scholar
  33. Nakamura Y, Yamamoto Y, Muraoka I: Autonomic control of heart rate during physical exercise and fractal dimension of heart rate variability. J Appl Physiol 1993, 74(2):875–881.Google Scholar
  34. Yamamoto Y, Hughson RL: Coarse-graining spectral analysis: new method for studying heart rate variability. J Appl Physiol 1991, 71(3):1143–1150.Google Scholar
  35. Dibner-Dunlap ME, Eckberg DL, Magid NM, Cintron-Trevino NM: The long-term increase of baseline and reflexly augmented levels of human vagal-cardiac nervous activity induced by scopolamine. Circulation 1985, 71(4):797–804.View ArticleGoogle Scholar
  36. Vybrial T, Byrg RJ, Maddens ME, Bhasin SS, Chronin WE, Boden WE, Lehmann MH: Effects of transdermal scopolamine on heart rate variability in normal subjects. Am J Cariol 1990, 65: 604–608. 10.1016/0002-9149(90)91038-8View ArticleGoogle Scholar
  37. Voss A, Schulz S, Schroeder R, Baumert M, Caminal P: Methods derived from nonlinear dynamics for analysing heart rate variability. Philosophical Transactions of the Royal Society A: Mathematical, Physical and Engineering Sciences 2009, 367(1887):277–296. 10.1098/rsta.2008.0232MATHView ArticleGoogle Scholar

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© Karmakar et al; licensee BioMed Central Ltd. 2011

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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