Evidence map›Paper›PMID 29615044›Full record

ArticleMalaria journal2018

Simulation models predict that school-age children are responsible for most human-to-mosquito Plasmodium falciparum transmission in southern Malawi.

Jenna E Coalson, Lauren M Cohee, Andrea G Buchwald, Andrew Nyambalo, John Kubale, Karl B Seydel, Don Mathanga, Terrie E Taylor, Miriam K Laufer, Mark L Wilson

Abstract read
In one paragraph

Article in Malaria journal, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 2 pooled it
–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

45 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  14. Serological evidence of continued exposure toFrontiers in microbiology · 2025
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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

10 authors.

Jenna E CoalsonDepartment of Epidemiology, School of Public Health, University of Michigan, M5507 SPH II, 1415 Washington Heights, Ann Arbor, MI, 48109, USA. jcoalson@gmail.com.ORCID http://orcid.org/0000-0002-8591-5642
Lauren M CoheeDivision of Malaria Research, Institute of Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Andrea G BuchwaldDivision of Malaria Research, Institute of Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Andrew NyambaloBlantyre Malaria Project, University of Malawi College of Medicine, Blantyre, Malawi.
John KubaleDepartment of Epidemiology, School of Public Health, University of Michigan, M5507 SPH II, 1415 Washington Heights, Ann Arbor, MI, 48109, USA.
Karl B SeydelCollege of Osteopathic Medicine, Michigan State University, East Lansing, USA.
Don MathangaMalaria Alert Centre, University of Malawi College of Medicine, Blantyre, Malawi.
Terrie E TaylorCollege of Osteopathic Medicine, Michigan State University, East Lansing, USA.
Miriam K LauferDivision of Malaria Research, Institute of Global Health, University of Maryland School of Medicine, Baltimore, MD, USA.
Mark L WilsonDepartment of Epidemiology, School of Public Health, University of Michigan, M5507 SPH II, 1415 Washington Heights, Ann Arbor, MI, 48109, USA. wilsonml@umich.edu.

Funding

POST DOCTORAL EXCELLENCE IN RESEARCH AND TEACHINGK12GM000708 · NIGMS · UNIVERSITY OF ARIZONA · PI STRAUSFELD, NICHOLAS J · 2000 to 2018
$21.5M
The role of monocytes in the pathology of severe malaria.U19AI089683 · NIAID · MICHIGAN STATE UNIVERSITY · PI MATHANGA, DON P · 2010 to 2023
$21.4M
FELLOWSHIP TRAINING PROGRAM IN VACCINOLOGYT32AI007524 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Marcelo B. Sztein · 1997 to 2026
$6.4M
Asymptomatic Gametocytemia and Malaria: Implications for Plasmodium TransmissionR21AI107421 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI WILSON, MARK L · 2014 to 2015
$446k
National Institute of Allergy and Infectious Diseases R21AI107421National Institute of Allergy and Infectious Diseases U19AI089683National Institute of General Medical Sciences K12 GM000708NIAID NIH HHS R21 AI107421NIAID NIH HHS T32 AI007524NIAID NIH HHS U19 AI089683NIGMS NIH HHS K12 GM000708
6 · The paper itself

Abstract

backgroundMalaria persists in some high-transmission areas despite extensive control efforts. Progress toward elimination may require effective targeting of specific human populations that act as key transmission reservoirs.

methodsParameterized using molecular-based Plasmodium falciparum infection data from cross-sectional community studies in southern Malawi, a simulation model was developed to predict the proportions of human-to-mosquito transmission arising from (a) children under 5 years old (U5s), (b) school-age children (SAC, 5-15 years), (c) young adults (16-30 years), and (d) adults > 30 years. The model incorporates mosquito biting heterogeneity and differential infectivity (i.e. probability that a blood-fed mosquito develops oocysts) by age and gametocyte density.

resultsThe model predicted that SAC were responsible for more than 60% of new mosquito infections in both dry and rainy seasons, even though they comprise only 30% of this southern Malawi population. Young adults were the second largest contributors, while U5s and adults over 30 were each responsible for < 10% of transmission. While the specific predicted values are sensitive to the relative infectiousness of SAC, this group remained the most important contributor to mosquito infections under all realistic estimates.

conclusionsThese results suggest that U5 children play a small role compared to SAC in maintaining P. falciparum transmission in southern Malawi. Models that assume biting homogeneity overestimate the importance of U5s. To reduce transmission, interventions will need to reach more SAC and young adults. This publicly available model can be used by others to estimate age-specific transmission contributions in epidemiologically similar sites with local parameter estimates of P. falciparum prevalence and bed net use.

Indexed as

AdolescentAdultAgedAge FactorsAnimalsAnophelesChildChild, PreschoolHumansInfantInfant, NewbornMalaria, FalciparumMalawiMiddle AgedModels, TheoreticalPlasmodium falciparumGametocytesMalariaPlasmodium falciparumSchool-age childrenSimulation modelTransmission reservoirs

Identifiers

PMID29615044
PMCPMC5883608

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.