The time-dependent reproduction number for epidemics in heterogeneous populations

The time-dependent reproduction number [Formula: see text] can be used to track pathogen transmission and to assess the efficacy of interventions. This quantity can be estimated by fitting renewal equation models to time series of infectious disease case counts. These models almost invariably assume a homogeneous population. Individuals are assumed not to differ systematically in the rates at which they come into contact with others. It is also assumed that the typical time that elapses between one case and those it causes (known as the generation-time distribution) does not differ across groups. But contact patterns are known to widely differ by age and according to other demographic groupings, and infection risk and transmission rates have been shown to vary across groups for a range of directly transmitted diseases. Here, we derive from first principles a renewal equation framework which accounts for these differences in transmission across groups. We use a generalization of the classic M'Kendrick-von Foerster equation to handle populations structured into interacting groups. This system of partial differential equations allows us to derive a simple analytical expression for [Formula: see text], which involves only group-level contact patterns and infection risks. We show that the same expression emerges from both deterministic and stochastic discrete-time versions of the model and demonstrate through simulations that our [Formula: see text] expression governs the long-run fate of epidemics. Our renewal equation model provides a basis from which to account for more realistic, diverse populations in epidemiological models and opens the door to inferential approaches which use known group characteristics to estimate [Formula: see text].

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Publication Details

Journal
Journal of The Royal Society Interface
Published
2025-07-01
DOI
https://doi.org/10.1098/rsif.2025.0095
Citations
1
Primary Topic
COVID-19 epidemiological studies
Type
article
Field-Weighted Citation Impact
1.37

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article

The time-dependent reproduction number for epidemics in heterogeneous populations

David J. Gavaghan, Robin N. Thompson, Ioana Bouros, Ben C. Lambert
1 citations
Journal of The Royal Society Interface
COVID-19 epidemiological studies
1.37
article

The time-dependent reproduction number for epidemics in heterogeneous populations

David J. Gavaghan, Robin N. Thompson, Ioana Bouros, Ben C. Lambert
article en
1 citations

Abstract

The time-dependent reproduction number [Formula: see text] can be used to track pathogen transmission and to assess the efficacy of interventions. This quantity can be estimated by fitting renewal equation models to time series of infectious disease case counts. These models almost invariably assume a homogeneous population. Individuals are assumed not to differ systematically in the rates at which they come into contact with others. It is also assumed that the typical time that elapses between one case and those it causes (known as the generation-time distribution) does not differ across groups. But contact patterns are known to widely differ by age and according to other demographic groupings, and infection risk and transmission rates have been shown to vary across groups for a range of directly transmitted diseases. Here, we derive from first principles a renewal equation framework which accounts for these differences in transmission across groups. We use a generalization of the classic M'Kendrick-von Foerster equation to handle populations structured into interacting groups. This system of partial differential equations allows us to derive a simple analytical expression for [Formula: see text], which involves only group-level contact patterns and infection risks. We show that the same expression emerges from both deterministic and stochastic discrete-time versions of the model and demonstrate through simulations that our [Formula: see text] expression governs the long-run fate of epidemics. Our renewal equation model provides a basis from which to account for more realistic, diverse populations in epidemiological models and opens the door to inferential approaches which use known group characteristics to estimate [Formula: see text].

Journal of The Royal Society InterfaceVol. 22(228)
University of Oxford (GB), Mathematical Institute of the Slovak Academy of Sciences (SK)
Engineering and Physical Sciences Research Council
Good health and well-being
Openalex Percentile: Top 19%
COVID-19 epidemiological studies
1.37
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