Abstract
Uncertainty can be classified as either aleatoric (intrinsic randomness) or epistemic (imperfect knowledge of parameters). The majority of frameworks assessing infectious disease risk consider only epistemic uncertainty. We only ever observe a single epidemic, and therefore cannot empirically determine aleatoric uncertainty. Here, we characterise both epistemic and aleatoric uncertainty using a time-varying general branching process. Our framework explicitly decomposes aleatoric variance into mechanistic components, quantifying the contribution to uncertainty produced by each factor in the epidemic process, and how these contributions vary over time. The aleatoric variance of an outbreak is itself a renewal equation where past variance affects future variance. We find that, superspreading is not necessary for substantial uncertainty, and profound variation in outbreak size can occur even without overdispersion in the offspring distribution (i.e. the distribution of the number of secondary infections an infected person produces). Aleatoric forecasting uncertainty grows dynamically and rapidly, and so forecasting using only epistemic uncertainty is a significant underestimate. Therefore, failure to account for aleatoric uncertainty will ensure that policymakers are misled about the substantially higher true extent of potential risk. We demonstrate our method, and the extent to which potential risk is underestimated, using two historical examples.
Originalsprog | Engelsk |
---|---|
Artikelnummer | 146 |
Tidsskrift | Communications Physics |
Vol/bind | 6 |
Udgave nummer | 1 |
Antal sider | 9 |
ISSN | 2399-3650 |
DOI | |
Status | Udgivet - 2023 |
Bibliografisk note
Funding Information:S.B., C.A.D. and D.J.L. acknowledge support from the MRC Centre for Global Infectious Disease Analysis (MR/R015600/1), jointly funded by the UK Medical Research Council (MRC) and the UK Foreign, Commonwealth & Development Office (FCDO), under the MRC/FCDO Concordat agreement, and also part of the EDCTP2 programme supported by the European Union. S.B. acknowledges support from the Novo Nordisk Foundation via The Novo Nordisk Young Investigator Award (NNF20OC0059309), which also supports S.M.. S.B. acknowledges support from the Danish National Research Foundation via a chair position. S.B. and C.M. acknowledges support from The Eric and Wendy Schmidt Fund For Strategic Innovation via the Schmidt Polymath Award (G-22-63345). S.B. acknowledges support from the National Institute for Health Research (NIHR) via the Health Protection Research Unit in Modelling and Health Economics. D.J.L. acknowledges funding from Vaccine Efficacy Evaluation for Priority Emerging Diseases (VEEPED) grant, (ref. NIHR:PR-OD-1017-20002) from the National Institute for Health Research. M.J.P. acknowledges funding from a EPSRC DTP Studentship. C.W. acknowledges support from the Wellcome Trust.
Publisher Copyright:
© 2023, The Author(s).