Evidence map›Paper›PMID 42611995›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2026

Characterizing the impact of incorporating spatially aggregated human mobility data into infectious disease models.

Ronan Corgel, Kyra H Grantz, Lauren Gardner, Derek A T Cummings, Harendra de Silva, Thilini Somaratne, Dhammika Silva, LakKumar Fernando, Amy Wesolowski

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Ronan CorgelDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205.ORCID 0009-0000-2845-5427
Kyra H GrantzDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205.
Lauren GardnerDepartment of Civil and Systems Engineering, Johns Hopkins Whiting School of Engineering, Baltimore, MD 21218.ORCID 0000-0003-1083-3850
Derek A T CummingsDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205.ORCID 0000-0002-9437-1907
Harendra de SilvaFaculty of Medicine, Department of Paediatrics, University of Colombo, Colombo 00800, Sri Lanka.
Thilini SomaratneCentre for Clinical Management of Dengue and Dengue Hemorrhagic Fever, Negombo General Hospital, Negombo 11500, Sri Lanka.ORCID 0000-0002-8529-3177
Dhammika SilvaCentre for Clinical Management of Dengue and Dengue Hemorrhagic Fever, Negombo General Hospital, Negombo 11500, Sri Lanka.
LakKumar FernandoCentre for Clinical Management of Dengue and Dengue Hemorrhagic Fever, Negombo General Hospital, Negombo 11500, Sri Lanka.ORCID 0000-0001-8645-3497
Amy WesolowskiDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205.

Funding

Human mobility models to forecast disease dynamics and the effectiveness of public health interventionsR01AI160780 · NIAID · JOHNS HOPKINS UNIVERSITY · PI CUMMINGS, DEREK A, WESOLOWSKI, AMY · 2021 to 2025
$3.3M
HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID) 1R01AI160780NIAID NIH HHS R01 AI160780
6 · The paper itself

Abstract

Models of infectious disease dynamics should align the spatial scale of mobility data to the scale of travel relevant to inferring disease introduction events and subsequent local transmission. Despite this, the biases of spatially aggregating mobility data on model inferences are rarely explored. Here, we examine the sensitivity of infectious disease modeling results to different spatial scales of human mobility by integrating multiscale mobility data from Sri Lanka into Susceptible, Exposed, Infected, Recovered (SEIR) metapopulation models. Aggregated mobility data were obtained from mobile phone records at three increasingly coarser spatial scales to simulate epidemic spread of an emerging acute respiratory infection. We found that travel was not evenly distributed among nested spatial scales when data were disaggregated, with subunits close to borders exhibiting higher levels of travel relative to the unit. In simulations of disease transmission, these different scales of mobility aggregation had potential to yield wide variations in the estimated spatial invasion timing but not in final epidemic size. Modeled differences in spatial invasion time depended on disease transmission intensity and exogenous factors like the initial seeding location. Our results carry implications for infectious disease modeling best practices and public health response, particularly the policy decisions made from model inferences that were or were not informed by the relevant spatial scale of mobility data such as intervention timing, risk communication, and resource allocation.

Indexed as

Communicable DiseasesModels, BiologicalTravelHumansSri Lankadenguehuman mobilityspatial

Identifiers

PMID42611995
PMCPMC13506029

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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.