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Detecting critical slowing down in high-dimensional epidemiological systems

Despite medical advances, the emergence and re-emergence of infectious diseases continue to pose a public health threat. Low-dimensional epidemiological models predict that epidemic transitions are preceded by the phenomenon of critical slowing down (CSD). This has raised the possibility of anticipa...

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Autores principales: Brett, Tobias, Ajelli, Marco, Liu, Quan-Hui, Krauland, Mary G., Grefenstette, John J., van Panhuis, Willem G., Vespignani, Alessandro, Drake, John M., Rohani, Pejman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082051/
https://www.ncbi.nlm.nih.gov/pubmed/32150536
http://dx.doi.org/10.1371/journal.pcbi.1007679
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author Brett, Tobias
Ajelli, Marco
Liu, Quan-Hui
Krauland, Mary G.
Grefenstette, John J.
van Panhuis, Willem G.
Vespignani, Alessandro
Drake, John M.
Rohani, Pejman
author_facet Brett, Tobias
Ajelli, Marco
Liu, Quan-Hui
Krauland, Mary G.
Grefenstette, John J.
van Panhuis, Willem G.
Vespignani, Alessandro
Drake, John M.
Rohani, Pejman
author_sort Brett, Tobias
collection PubMed
description Despite medical advances, the emergence and re-emergence of infectious diseases continue to pose a public health threat. Low-dimensional epidemiological models predict that epidemic transitions are preceded by the phenomenon of critical slowing down (CSD). This has raised the possibility of anticipating disease (re-)emergence using CSD-based early-warning signals (EWS), which are statistical moments estimated from time series data. For EWS to be useful at detecting future (re-)emergence, CSD needs to be a generic (model-independent) feature of epidemiological dynamics irrespective of system complexity. Currently, it is unclear whether the predictions of CSD—derived from simple, low-dimensional systems—pertain to real systems, which are high-dimensional. To assess the generality of CSD, we carried out a simulation study of a hierarchy of models, with increasing structural complexity and dimensionality, for a measles-like infectious disease. Our five models included: i) a nonseasonal homogeneous Susceptible-Exposed-Infectious-Recovered (SEIR) model, ii) a homogeneous SEIR model with seasonality in transmission, iii) an age-structured SEIR model, iv) a multiplex network-based model (Mplex) and v) an agent-based simulator (FRED). All models were parameterised to have a herd-immunity immunization threshold of around 90% coverage, and underwent a linear decrease in vaccine uptake, from 92% to 70% over 15 years. We found evidence of CSD prior to disease re-emergence in all models. We also evaluated the performance of seven EWS: the autocorrelation, coefficient of variation, index of dispersion, kurtosis, mean, skewness, variance. Performance was scored using the Area Under the ROC Curve (AUC) statistic. The best performing EWS were the mean and variance, with AUC > 0.75 one year before the estimated transition time. These two, along with the autocorrelation and index of dispersion, are promising candidate EWS for detecting disease emergence.
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spelling pubmed-70820512020-03-24 Detecting critical slowing down in high-dimensional epidemiological systems Brett, Tobias Ajelli, Marco Liu, Quan-Hui Krauland, Mary G. Grefenstette, John J. van Panhuis, Willem G. Vespignani, Alessandro Drake, John M. Rohani, Pejman PLoS Comput Biol Research Article Despite medical advances, the emergence and re-emergence of infectious diseases continue to pose a public health threat. Low-dimensional epidemiological models predict that epidemic transitions are preceded by the phenomenon of critical slowing down (CSD). This has raised the possibility of anticipating disease (re-)emergence using CSD-based early-warning signals (EWS), which are statistical moments estimated from time series data. For EWS to be useful at detecting future (re-)emergence, CSD needs to be a generic (model-independent) feature of epidemiological dynamics irrespective of system complexity. Currently, it is unclear whether the predictions of CSD—derived from simple, low-dimensional systems—pertain to real systems, which are high-dimensional. To assess the generality of CSD, we carried out a simulation study of a hierarchy of models, with increasing structural complexity and dimensionality, for a measles-like infectious disease. Our five models included: i) a nonseasonal homogeneous Susceptible-Exposed-Infectious-Recovered (SEIR) model, ii) a homogeneous SEIR model with seasonality in transmission, iii) an age-structured SEIR model, iv) a multiplex network-based model (Mplex) and v) an agent-based simulator (FRED). All models were parameterised to have a herd-immunity immunization threshold of around 90% coverage, and underwent a linear decrease in vaccine uptake, from 92% to 70% over 15 years. We found evidence of CSD prior to disease re-emergence in all models. We also evaluated the performance of seven EWS: the autocorrelation, coefficient of variation, index of dispersion, kurtosis, mean, skewness, variance. Performance was scored using the Area Under the ROC Curve (AUC) statistic. The best performing EWS were the mean and variance, with AUC > 0.75 one year before the estimated transition time. These two, along with the autocorrelation and index of dispersion, are promising candidate EWS for detecting disease emergence. Public Library of Science 2020-03-09 /pmc/articles/PMC7082051/ /pubmed/32150536 http://dx.doi.org/10.1371/journal.pcbi.1007679 Text en © 2020 Brett et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Brett, Tobias
Ajelli, Marco
Liu, Quan-Hui
Krauland, Mary G.
Grefenstette, John J.
van Panhuis, Willem G.
Vespignani, Alessandro
Drake, John M.
Rohani, Pejman
Detecting critical slowing down in high-dimensional epidemiological systems
title Detecting critical slowing down in high-dimensional epidemiological systems
title_full Detecting critical slowing down in high-dimensional epidemiological systems
title_fullStr Detecting critical slowing down in high-dimensional epidemiological systems
title_full_unstemmed Detecting critical slowing down in high-dimensional epidemiological systems
title_short Detecting critical slowing down in high-dimensional epidemiological systems
title_sort detecting critical slowing down in high-dimensional epidemiological systems
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082051/
https://www.ncbi.nlm.nih.gov/pubmed/32150536
http://dx.doi.org/10.1371/journal.pcbi.1007679
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