Linear and nonlinear heart rate variability indexes in clinical practice

Buccelletti Francesco, Bocci Maria Grazia, Gilardi Emanuele, Fiore Valentina, Calcinaro Sara, Fragnoli Chiara, Maviglia Riccardo, Franceschi Francesco, Buccelletti Francesco, Bocci Maria Grazia, Gilardi Emanuele, Fiore Valentina, Calcinaro Sara, Fragnoli Chiara, Maviglia Riccardo, Franceschi Francesco

Abstract

Biological organisms have intrinsic control systems that act in response to internal and external stimuli maintaining homeostasis. Human heart rate is not regular and varies in time and such variability, also known as heart rate variability (HRV), is not random. HRV depends upon organism's physiologic and/or pathologic state. Physicians are always interested in predicting patient's risk of developing major and life-threatening complications. Understanding biological signals behavior helps to characterize patient's state and might represent a step toward a better care. The main advantage of signals such as HRV indexes is that it can be calculated in real time in noninvasive manner, while all current biomarkers used in clinical practice are discrete and imply blood sample analysis. In this paper HRV linear and nonlinear indexes are reviewed and data from real patients are provided to show how these indexes might be used in clinical practice.

Figures

Figure 1
Figure 1
Series Standard Deviation (Frequentist Statistics). SDNN index displayed as mean (circles) and 95% confidential interval (Bars). Healthy subjects showed a higher degree of dispersion around the mean (higher variability) compared to critically ill patients, P = 0.10 using Mann-Witney U-test. ED: Emergency Department.
Figure 2
Figure 2
Fast Fourier Transform Analysis. Black dots represent healthy patients and empty squares ICU cases. Dashed and continuous lines reflect LF/HF ratio after adjusting for other clinical comorbidities along with 95% confidential intervals (curved lines). x-axis represents age in years. The two groups did not differ in term of LF/HF ratio (P = 0.82).
Figure 3
Figure 3
Detrended Fluctuation Analysis (DFA). Black dots represent healthy patients and empty squares ICU cases. Dashed and continuous lines reflect predicted values (adjusted for comorbidities) for the respective group along with 95% confidential intervals (curved lines). x-axis represents years. It is to be noted that DFA index was significantly different between the two groups even when adjusted for other comorbidities and age (P = 0.02). Age affects DFA index in both groups.

References

    1. Gallagher R, Appenzeller T. Beyond reductionism. Science. 1999;284(5411):p. 79.
    1. Goldberger AL. Fractal variability versus pathologic periodicity: complexity loss and stereotypy in disease. Perspectives in Biology and Medicine. 1997;40(4):543–561.
    1. Vaillancourt DE, Newell KM. Changing complexity in human behavior and physiology through aging and disease. Neurobiology of Aging. 2002;23(1):1–11.
    1. Que CL, Kenyon CM, Olivenstein R, Macklem PT, Maksym GN. Homeokinesis and short-term variability of human airway caliber. Journal of Applied Physiology. 2001;91(3):1131–1141.
    1. Seely AJ, Macklem PT. Complex systems and the technology of variability analysis. Critical Care. 2004;8(6):R367–R384.
    1. Seely AJE, Christou NV. Multiple organ dysfunction syndrome: exploring the paradigm of complex nonlinear systems. Critical Care Medicine. 2000;28(7):2193–2200.
    1. Cohen MJ, Grossman AD, Morabito D, Knudson MM, Butte AJ, Manley GT. Identification of complex metabolic states in critically injured patients using bioinformatic cluster analysis. Critical Care. 2010;14(1, article R10)
    1. Pikkujämsä SM, Mäkikallio TH, Sourander LB, et al. Cardiac interbeat interval dynamics from childhood to senescence: comparison of conventional and new measures based on fractals and chaos theory. Circulation. 1999;100(4):393–399.
    1. Buccelletti F, Gilardi E, Scaini E, et al. Heart rate variability and myocardial infarction: systematic literature review and metanalysis. European Review for Medical and Pharmacological Sciences. 2009;13(4):299–307.
    1. Malik M. Heart rate variability: standards of measurement, physiological interpretation, and clinical use. Circulation. 1996;93(5):1043–1065.
    1. Tapanainen JM, Thomsen PEB, Køber L, et al. Fractal analysis of heart rate variability and mortality after an acute myocardial infarction. American Journal of Cardiology. 2002;90(4):347–352.
    1. Gisiger T. Scale invariance in biology: coincidence or footprint of a universal mechanism? Biological Reviews of the Cambridge Philosophical Society. 2001;76(2):161–209.
    1. Mandelbrot B. The Fractal Geometry of Nature. New York, NY, USA: W. H. Freeman; 1983.
    1. Pincus SM. Approximate entropy as a measure of system complexity. Proceedings of the National Academy of Sciences of the United States of America. 1991;88(6):2297–2301.
    1. Peng CK, Havlin S, Stanley HE, Goldberger AL. Quantification of scaling exponents and crossover phenomena in nonstationary heartbeat time series. Chaos. 1995;5(1):82–87.
    1. Huikuri HV, Mäkikallio TH. Heart rate variability in ischemic heart disease. Autonomic Neuroscience. 2001;90(1-2):95–101.
    1. Win NN, Fukayama H, Kohase H, Umino M. The different effects of intravenous propofol and midazolam sedation on hemodynamic and heart rate variability. Anesthesia and Analgesia. 2005;101(1):97–102.
    1. Kanaya N, Hirata N, Kurosawa S, Nakayama M, Namiki A. Differential effects of propofol and sevoflurane on heart rate variability. Anesthesiology. 2003;98(1):34–40.
    1. Sroka K, Peimann CJ, Seevers H. Heart rate variability in myocardial ischemia during daily life. Journal of Electrocardiology. 1997;30(1):45–56.

Source: PubMed

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