Evidence map›Paper›PMID 41429846›Full record

ArticleScientific reports2025

Development of a dynamical model to enhance understanding of epidemiology of schistosomiasis in school-aged-children.

Amber L Reed, Sekeleghe A Kayuni, Janelisa Musaya, J Russell Stothard, Claudio Fronterre, Chris Jewell

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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.

Amber L ReedLancaster Medical School, Lancaster University, Bailrigg House, Bailrigg, Lancaster, LA1 4YE, UK. amberreed21@hotmail.com.
Sekeleghe A KayuniTropical Disease Biology, Liverpool School of Tropical Medicine, Pembroke PI, Liverpool, L3 5QA, UK.
Janelisa MusayaMalawi Liverpool Wellcome Trust Programme of Clinical Tropical Research, Queen Elizabeth Central Hospital, College of Medicine, P.O.Box 30096, Blantyre, Malawi.
J Russell StothardTropical Disease Biology, Liverpool School of Tropical Medicine, Pembroke PI, Liverpool, L3 5QA, UK.
Claudio FronterreDepartment of Applied Health Sciences, School of Health Sciences, College of Medicine and Health, University of Birmingham, Birmingham, UK.
Chris JewellMathematics and Statistics, Lancaster University, Bailrigg House, Bailrigg, Lancaster, LA1 4YE, UK.

Funding

Medical Research Council MR/N013514/1
6 · The paper itself

Abstract

School-aged-children are most vulnerable to schistosomiasis as exemplified by age-prevalence profiles although current understanding of these patterns needs improvement. Using epidemiological data from the southern shoreline of Lake Malawi, we investigated the dynamics of Schistosoma transmission and the main determinants of Schistosoma infection risk using a transmission dynamic model, considering urogenital and intestinal schistosomiasis respectively. Specifically, we assessed whether the proximity of primary schools to the immediate shoreline was a major geospatial and epidemiological determinant. Cross-sectional parasitology and malacological data previously collected and analysed was used, including age-infection profiles and interpolated predicted snail distributions for the southern part of Lake Malawi shoreline. A disease SEIRS ordinary differential equation model was created, and an observation prevalence model was formed using a binomial sampling distribution using the already published dataset. An optimisation using L-BFGS-B algorithm with upper/lower bounded box constraints was carried out to calibrate the model to find the best parameter values for each infection state transition given the disease model and dataset. The aim was to recapture the age-structure dynamics shown in the observation model representing the already published age-infection profiles. Concerning intestinal schistosomiasis, the best model for Biomphalaria sp. was the use of a single transmission rate for all the school's and no spatial effect. By contrast, for urogenital schistosomiasis, the best model for Bulinus spp. was found when using an independent transmission rate for each school and no spatial effect. There was some evidence that we were able to capture the age-structured dynamics of infection in SAC despite the expected outcome differing to statistical output due to sparse data. Within our study area, we found there was no significant effect on SAC exposure to Schistosoma infection risk based on school distance from the shoreline. Further, there was heterogeneity between schools in transmission rates estimated, although these did not have significantly different confidence intervals. However, schools considered in our study were all relatively close to cercaria infested shorelines. Further studies using a longitudinal cohort study could improve understanding of Schistosoma infection dynamics and allow for improved control method application.

Indexed as

SchistosomiasisAdolescentAnimalsBiomphalariaChildCross-Sectional StudiesFemaleHumansMalawiMalePrevalenceSchistosomiasis haematobiaSchoolsBiomphalariaBulinusOptimisationSchistosomiasisTransmission dynamics

Identifiers

PMID41429846
PMCPMC12749467

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.