Evidence map›Paper›PMID 42467715›Full record

ArticlePLOS global public health2026

Estimating the basic reproduction number of measles in low-and middle-income settings using 172 seroprevalence studies: A modelling approach.

Han Fu, Alyssa N Sbarra, Timothy Russell, Kaja Abbas, Megan Auzenbergs, Mark Jit

Abstract read
In one paragraph

Article in PLOS global public health, 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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0cells of the map it votes in
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

6 authors.

Han FuDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.ORCID https://orcid.org/0000-0002-8934-7347
Alyssa N SbarraDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.
Timothy RussellDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.
Kaja AbbasDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.ORCID https://orcid.org/0000-0003-0563-1576
Megan AuzenbergsDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.
Mark JitDepartment of Infectious Disease Epidemiology and Dynamics, London School of Hygiene and Tropical Medicine, United Kingdom.

Funding

Research in practice: translating infectious disease epidemiology RIP-TIDET32AI165369 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WILLIAM J MOSS · 2022 to 2026
$1.5M
Development and application of subnational measles incidence and mortality estimates in high burden and incidence settingsF31AI167535 · NIAID · LONDON SCH/HYGIENE & TROPICAL MEDICINE · PI SBARRA, ALYSSA NICOLE · 2022 to 2023
$72k
Bill & Melinda Gates Foundation INV-009125NIAID NIH HHS F31 AI167535NIAID NIH HHS T32 AI165369
6 · The paper itself

Abstract

The basic reproduction number, R0, is an epidemiological measure to describe the transmissibility of infectious diseases and evaluate the potential effect of interventions. Measles R0 has historically been considered to be between 12-18, with contextual factors contributing to its heterogeneity, but has rarely been estimated using data across multiple countries. Our study aims to estimate measles R0 in low- and middle-income countries using a standardised database of population-based serosurveys. We fitted an age-structured compartmental model of measles transmission dynamics and vaccination (DynaMICE) to the age-specific seroprevalence data extracted from a recent systematic review. Using Markov Chain Monte Carlo, we estimated setting-specific posterior distributions of R0 in 172 studies with unique survey years and locations from 57 countries. Bootstrapped samples of R0 estimates were pooled by study characteristics, including survey period, geography, and overall bias in sampling, measurement, and reporting results. Measles R0 estimates varied substantially across serostudies, ranging from 0.93 (95% credible interval (CrI): 0.70-1.00) to 147 (95% CrI: 76.5-208), with fewer than 13% of studies having median R0 values in the range of 12-18. Pooled R0 estimates showed smaller medians and variation in serostudies conducted after 2000 or including the adult population, while no distinguishable variation was identified across the World Health Organization regions. Our revised estimates demonstrated the wide range of measles R0 across low- and middle-income settings and highlighted the importance of considering the heterogeneity in measles transmissibility when modelling epidemics and planning interventions and vaccination strategies.

Identifiers

PMID42467715
PMCPMC13378968

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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.