Evidence map›Paper›PMID 30532206›Full record

ArticlePLoS computational biology2018

Projecting social contact matrices to different demographic structures.

Sergio Arregui, Alberto Aleta, Joaquín Sanz, Yamir Moreno

Abstract read
In one paragraph

Article in PLoS computational biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing 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

47 citing papers in PubMed.

  1. Article
  2. Assessing the costs and benefits of non-pharmaceutical pandemic measures using the economic values of social contacts.The European journal of health economics : HEPAC : health economics in prevention and care · 2026
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  6. TheCommunications physics · 2026
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  15. Infectious Disease Modelling · 2024
    Review
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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

4 authors.

Sergio ArreguiInstitute for Biocomputation and Physics of Complex Systems (BIFI), University of Zargoza, Zargoza, Spain.ORCID 0000-0002-7478-4894
Alberto AletaInstitute for Biocomputation and Physics of Complex Systems (BIFI), University of Zargoza, Zargoza, Spain.ORCID 0000-0002-1192-8707
Joaquín SanzDepartment of Genetics. Saint-Justine Hospital Research Center, Montreal, Canada.
Yamir MorenoInstitute for Biocomputation and Physics of Complex Systems (BIFI), University of Zargoza, Zargoza, Spain.ORCID 0000-0002-0895-1893

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The modeling of large-scale communicable epidemics has greatly benefited in the last years from the increasing availability of highly detailed data. Particullarly, in order to achieve quantitative descriptions of the evolution of epidemics, contact networks and mixing patterns are key. These heterogeneous patterns depend on several factors such as location, socioeconomic conditions, time, and age. This last factor has been shown to encapsulate a large fraction of the observed inter-individual variation in contact patterns, an observation validated by different measurements of age-dependent contact matrices. Recently, several works have studied how to project those matrices to areas where empirical data are not available. However, the dependence of contact matrices on demographic structures and their time evolution has been largely neglected. In this work, we tackle the problem of how to transform an empirical contact matrix that has been obtained for a given demographic structure into a different contact matrix that is compatible with a different demography. The methodology discussed here allows to extrapolate a contact structure measured in a particular area to any other whose demographic structure is known, as well as to obtain the time evolution of contact matrices as a function of the demographic dynamics of the populations they refer to. To quantify the effect of considering time-dynamics of contact patterns on disease modeling, we implemented a Susceptible-Exposed-Infected-Recovered (SEIR) model on 16 different countries and regions and evaluated the impact of neglecting the temporal evolution of mixing patterns. Our results show that simulated disease incidence rates, both at the aggregated and age-specific levels, are significantly dependent on contact structures variation driven by demographic evolution. The present work opens the path to eliminate technical biases from model-based impact evaluations of future epidemic threats and warns against the use of contact matrices to model diseases without correcting for demographic evolution or geographic variations.

Indexed as

Models, StatisticalBiasComputational BiologyContact TracingDemographyEpidemicsHumansSocial Behavior

Identifiers

PMID30532206
PMCPMC6300299

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LicenceCC BY
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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.