Examining the controllability of sepsis using genetic algorithms on an agent-based model of systemic inflammation
Authored by Gary An, Robert Chase Cockrell
Date Published: 2018
DOI: 10.1371/journal.pcbi.1005876
Sponsors:
United States Department of Energy (DOE)
Platforms:
C++
Model Documentation:
Other Narrative
Flow charts
Model Code URLs:
https://bitbucket.org/cockrell/iirabm_public
Abstract
Sepsis, a manifestation of the body's inflammatory response to injury
and infection, has a mortality rate of between 28\%-50\% and affects
approximately 1 million patients annually in the United States.
Currently, there are no therapies targeting the cellular/molecular
processes driving sepsis that have demonstrated the ability to control
this disease process in the clinical setting. We propose that this is in
great part due to the considerable heterogeneity of the clinical
trajectories that constitute clinical ``sepsis,{''} and that determining
how this system can be controlled back into a state of health requires
the application of concepts drawn from the field of dynamical systems.
In this work, we consider the human immune system to be a random
dynamical system, and investigate its potential controllability using an
agent-based model of the innate immune response (the Innate Immune
Response ABM or IIRABM) as a surrogate, proxy system. Simulation
experiments with the IIRABM provide an explanation as to why
single/limited cytokine perturbations at a single, or small number of,
time points is unlikely to significantly improve the mortality rate of
sepsis. We then use genetic algorithms (GA) to explore and characterize
multi-targeted control strategies for the random dynamical immune system
that guide it from a persistent, non-recovering inflammatory state
(functionally equivalent to the clinical states of systemic inflammatory
response syndrome (SIRS) or sepsis) to a state of health. We train the
GA on a single parameter set with multiple stochastic replicates, and
show that while the calculated results show good generalizability, more
advanced strategies are needed to achieve the goal of adaptive
personalized medicine. This work evaluating the extent of interventions
needed to control a simplified surrogate model of sepsis provides
insight into the scope of the clinical challenge, and can serve as a
guide on the path towards true ``precision control{''} of sepsis.
Tags
evolutionary algorithms