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Modeling, Inference, and Prediction in Mobility-Based Compartmental Models for Epidemiology

Ning Jiang, Weiqi Chu, Yao Li

TL;DR

This work tackles the overestimation problem of classical homogeneous epidemiological models by introducing mobility-based heterogeneity into compartmental dynamics. It builds a density-based SIRS framework with mobility-resolved compartments $S(m,t)$, $I(m,t)$, and $R(m,t)$ driven by a population mobility distribution $f(m)$, yielding an infinite-dimensional system whose infection term couples across mobility levels. The authors derive a mobility-aware basic reproduction number $\mathcal{R}_0 = \frac{\beta}{\gamma} \langle m^2 f \rangle$ via the next-generation operator and show that the final pandemic size $R_\infty$ is maximized by a Dirac delta mobility, implying heterogeneity reduces final size for the same $\mathcal{R}_0$. They establish identifiability of the mobility distribution from the infected-time-series data and propose a neural-network-based inverse problem framework trained on Gaussian-mixture mobilities to recover $f(m)$ from real data, including COVID-19 datasets, demonstrating that polarized mobility leads to smaller outbreaks than homogeneous assumptions. Overall, this mobility-based approach provides more accurate forecasts and a principled way to infer population mobility from infection data, with potential extensions to richer compartments and policy-adaptation strategies.

Abstract

Classical compartmental models in epidemiology often assume a homogeneous population for simplicity, which neglects the inherent heterogeneity among individuals. This assumption frequently leads to inaccurate predictions when applied to real-world data. For example, evidence has shown that classical models overestimate the final pandemic size in the H1N1-2009 and COVID-19 outbreaks. To address this issue, we introduce individual mobility as a key factor in disease transmission and control. We characterize disease dynamics using mobility distribution functions for each compartment and propose a mobility-based compartmental model that incorporates population heterogeneity. Our results demonstrate that, for the same basic reproduction number, our mobility-based model predicts a smaller final pandemic size compared to the classical models, effectively addressing the common overestimation problem. Additionally, we infer mobility distributions from the time series of the infected population. We provide sufficient conditions for uniquely identifying the mobility distribution from a dataset and propose a machine-learning-based approach to learn mobility from both synthesized and real-world data.

Modeling, Inference, and Prediction in Mobility-Based Compartmental Models for Epidemiology

TL;DR

This work tackles the overestimation problem of classical homogeneous epidemiological models by introducing mobility-based heterogeneity into compartmental dynamics. It builds a density-based SIRS framework with mobility-resolved compartments , , and driven by a population mobility distribution , yielding an infinite-dimensional system whose infection term couples across mobility levels. The authors derive a mobility-aware basic reproduction number via the next-generation operator and show that the final pandemic size is maximized by a Dirac delta mobility, implying heterogeneity reduces final size for the same . They establish identifiability of the mobility distribution from the infected-time-series data and propose a neural-network-based inverse problem framework trained on Gaussian-mixture mobilities to recover from real data, including COVID-19 datasets, demonstrating that polarized mobility leads to smaller outbreaks than homogeneous assumptions. Overall, this mobility-based approach provides more accurate forecasts and a principled way to infer population mobility from infection data, with potential extensions to richer compartments and policy-adaptation strategies.

Abstract

Classical compartmental models in epidemiology often assume a homogeneous population for simplicity, which neglects the inherent heterogeneity among individuals. This assumption frequently leads to inaccurate predictions when applied to real-world data. For example, evidence has shown that classical models overestimate the final pandemic size in the H1N1-2009 and COVID-19 outbreaks. To address this issue, we introduce individual mobility as a key factor in disease transmission and control. We characterize disease dynamics using mobility distribution functions for each compartment and propose a mobility-based compartmental model that incorporates population heterogeneity. Our results demonstrate that, for the same basic reproduction number, our mobility-based model predicts a smaller final pandemic size compared to the classical models, effectively addressing the common overestimation problem. Additionally, we infer mobility distributions from the time series of the infected population. We provide sufficient conditions for uniquely identifying the mobility distribution from a dataset and propose a machine-learning-based approach to learn mobility from both synthesized and real-world data.
Paper Structure (13 sections, 8 theorems, 69 equations, 8 figures)

This paper contains 13 sections, 8 theorems, 69 equations, 8 figures.

Key Result

Theorem 1

The basic reproduction number $\mathcal{R}_0$ of the mobility-based SIRS model eq: densitySIRS is

Figures (8)

  • Figure 1: A schematic diagram to show the transition between three compartments and the transition rates in the mobility-based compartments models.
  • Figure 2: Evolution dynamics of the mobility-based SIRS model \ref{['eq: SIRf']}, with parameter $\beta=0.1,\varepsilon=0.01$, $\gamma=0.3$ and initial $S(m,0)=0.99,I(m,0)=0.01,R(m,0)=0$ for (a) the susceptible population $S(m,t)$, (b) the infected population $I(m,t)$, and (c) the recovered population $R(m,t)$.
  • Figure 3: Time evolution of the ratios of three compartments in the mobility-based SIRS model \ref{['eq: SIRf']}, with parameters $\beta=1.5$, $\gamma=0.13$, $\varepsilon=0.001$ and the proportional initial condition with $I_0=1\text{e-}4$ in \ref{['eq: homogeneous_initial']}.
  • Figure 4: Time evolution of the mean mobility of three compartments in the mobility-based SIR model \ref{['eq: densitySIR']} with parameters $\beta=1.5$, $\gamma=0.13$, $I_0=0.0001$, and $f=f_1$ in \ref{['eq: initial']}. The mean mobility of the susceptible population decreases strictly over time, while the mean mobility of the infected and the recovered populations increases first and then decreases as time progresses.
  • Figure 5: A partition of intervals due to the sign of \ref{['eq: difference']}.
  • ...and 3 more figures

Theorems & Definitions (16)

  • Theorem 1
  • proof
  • Theorem 2
  • proof
  • Theorem 3
  • proof
  • Theorem 4
  • Lemma 5
  • proof
  • proof
  • ...and 6 more