Evidence map›Paper›PMID 36169721›Full record

ArticleJournal of mathematical biology2022

From individual-based epidemic models to McKendrick-von Foerster PDEs: a guide to modeling and inferring COVID-19 dynamics.

Félix Foutel-Rodier, François Blanquart, Philibert Courau, Peter Czuppon, Jean-Jil Duchamps, Jasmine Gamblin, Élise Kerdoncuff, Rob Kulathinal, Léo Régnier, Laura Vuduc and 2 more

Abstract read
In one paragraph

Article in Journal of mathematical biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Félix Foutel-RodierDépartement de Mathématiques, Université du Québec á Montréal, Montréal, QC, Canada. felix.foutel-rodier@college-de-france.fr.ORCID 0000-0002-2751-1324
François BlanquartInfection, Antimicrobials, Modeling, Evolution UMR 1137, Université de Paris, INSERM, Paris, France.
Philibert CourauSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Peter CzupponSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Jean-Jil DuchampsLaboratoire de mathématiques de Besançon UMR 6623, Université Bourgogne Franche-Comté, CNRS, F-25000, Besançon, France.
Jasmine GamblinSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Élise KerdoncuffSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Rob KulathinalDepartment of Biology, Temple University, Philadelphia, PA, USA.
Léo RégnierSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Laura VuducSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Amaury LambertSMILE Group, Center for Interdisciplinary Research in Biology UMR 7241, Collège de France, CNRS, INSERM U 1050, PSL Research University, Paris, France.
Emmanuel SchertzerFaculty of Mathematics, University of Vienna, Oskar-Morgenstern-Platz 1, 1090, Wien, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present a unifying, tractable approach for studying the spread of viruses causing complex diseases requiring to be modeled using a large number of types (e.g., infective stage, clinical state, risk factor class). We show that recording each infected individual's infection age, i.e., the time elapsed since infection, has three benefits. First, regardless of the number of types, the age distribution of the population can be described by means of a first-order, one-dimensional partial differential equation (PDE) known as the McKendrick-von Foerster equation. The frequency of type i is simply obtained by integrating the probability of being in state i at a given age against the age distribution. This representation induces a simple methodology based on the additional assumption of Poisson sampling to infer and forecast the epidemic. We illustrate this technique using French data from the COVID-19 epidemic. Second, our approach generalizes and simplifies standard compartmental models using high-dimensional systems of ordinary differential equations (ODEs) to account for disease complexity. We show that such models can always be rewritten in our framework, thus, providing a low-dimensional yet equivalent representation of these complex models. Third, beyond the simplicity of the approach, we show that our population model naturally appears as a universal scaling limit of a large class of fully stochastic individual-based epidemic models, where the initial condition of the PDE emerges as the limiting age structure of an exponentially growing population starting from a single individual.

Indexed as

COVID-19EpidemicsForecastingHumansModels, BiologicalProbability35Q9260J8562P10Primary 53D35Secondary 60J80

Identifiers

PMID36169721
PMCPMC9517997

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.