Abstract
Dysregulation of the inflammatory response is a critical component of many clinically challenging disorders such as sepsis. Inflammation is a biological process designed to lead to healing and recovery, ultimately restoring homeostasis; however, the failure to fully achieve those beneficial results can leave a patient in a dangerous persistent inflammatory state. One of the primary challenges in developing novel therapies in this area is that inflammation is comprised of a complex network of interacting pathways. Here, we discuss our approaches towards addressing this problem through computational systems biology, with a particular focus on how the presence of biological rhythms and the disruption of these rhythms in inflammation may be applied in a translational context. By leveraging the information content embedded in physiologic variability, ranging in scale from oscillations in autonomic activity driving short-term heart rate variability to circadian rhythms in immunomodulatory hormones, there is significant potential to gain insight into the underlying physiology. © 2012 Springer Science+Business Media New York.
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Scheff, J. D., Mavroudis, P. D., Calvano, S. E., & Androulakis, I. P. (2013). Translational applications of evaluating physiologic variability in human endotoxemia. Journal of Clinical Monitoring and Computing, 27(4), 405–415. https://doi.org/10.1007/s10877-012-9418-1
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