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Analysis of physiologic signals often tends to focus on average quantities, with comparisons of means and variances (so-called time domain statistics). Additional analyses based on frequency domain techniques involving spectral analysis are also sometimes applied. The utility of newer measures based on fractal analysis and nonlinear dynamics (chaos theory and complexity) remains uncertain, however. Further, these techniques are largely unknown to most investigators involved in physiologic data analysis. A key question, therefore, is whether techniques based on dynamical analysis add information to conventional statistics. If so, what are the appropriate applications and limitations of such techniques? For example, does the use of metrics based on chaos theory add diagnostic or prognostic information to biomedical time series analysis? Does such analysis provide insight into the underlying physiologic control mechanisms?
In this self-guided exploration of the dynamics of physiologic time series, we encourage you to focus on the analysis of actual time series derived from human subjects (1-16). Two classes of ``real world'' physiologic signals are available here, one related to human gait, and the other related to human heartbeat. The accompanying datasets are provided to allow you to begin to explore these and related questions. The datasets are described below. As a starting point, we suggest the following general approach:
These questions may help to guide your explorations:
As noted, there are many different ways of approaching such datasets, and this short list of techniques only begins to scratch the surface of the analytic possibilities. You may also wish to test other algorithms based directly on chaos theory, including assessment of fractal dimensions, plots of phase-space trajectories, and so forth, using any of a variety of suggested approaches. A key issue, and perhaps the most important one, is how any of these algorithms are limited in their applications, and what the potential pitfalls may be when these tests are applied. Does the statistical test actually yield meaningful information? Are the datasets of sufficient length, and do they meet criteria for stationarity, if that is required by the given statistical test? If the data are non-stationary, what is the nature of the non-stationarity? How does one quantify it, and how does one analyze datasets for which one or more statistical properties are changing over time?
Gait is a complex process with multiple inputs and numerous outputs. One of the final outputs of this highly integrated, multi-layered system is the gait cycle duration. Also known as the stride interval, this quantity reflects the rhythm of the locomotor system, and study of the temporal fluctuations in the stride interval can provide a non-invasive, quantitative window into neural control of locomotion and its changes with aging and disease.
The Gait in Aging and Disease Database contains stride interval time series collected from healthy young and old volunteers, and patients with Parkinson's disease.
Five young (21-34 years old) and five elderly (68-81 years old) rigorously-screened healthy subjects underwent 120 minutes of continuous supine resting while continuous electrocardiographic (ECG) signals were collected (7).
All subjects remained in a resting state in sinus rhythm while watching the movie Fantasia (Disney) to help maintain wakefulness. The continuous ECG was digitized at 250 Hz. Each heartbeat was annotated using an automated arrhythmia detection algorithm, and each beat annotation was verified by visual inspection. The R-R interval (interbeat interval) time series for each subject was then computed. The Fantasia Database provides these time series as one-column data files with the interbeat intervals in seconds.
Here are two techniques that can be used to explore these databases:
Approximate entropy (ApEn) measures the unpredictability of fluctuations in a time series. (At the request of S.M. Pincus, who first defined approximate entropy, software for calculation of ApEn has not been posted here. It is not difficult to implement the calculation in about 10 lines of code, however, using the detailed description of the algorithm for computing ApEn given here. If you do this, be sure to check your implementation using the example data provided.)
Detrended Fluctuation Analysis (DFA) can reveal the presence of long-term correlations (self-similarity) even when embedded in non-stationary time series.
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This collection of tutorial materials, software, and data was constructed as a teaching resource for an intensive course (``The Modern Science of Human Aging,'' conducted at MIT in October, 1999 under the auspices of NECSI). As such, this specific collection is not intended for basic research or publications. It may be useful, however, in other classroom or tutorial settings, and for self-guided explorations into the world of biologic complexity. For a large selection of research databases, please visit PhysioBank. |
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Updated Thursday, 08-Feb-2001 23:24:21 EST