Evidence map›Paper›PMID 35659301›Full record

ArticleInfectious diseases of poverty2022

Leveraging mathematical models of disease dynamics and machine learning to improve development of novel malaria interventions.

Monica Golumbeanu, Guo-Jing Yang, Flavia Camponovo, Erin M Stuckey, Nicholas Hamon, Mathias Mondy, Sarah Rees, Nakul Chitnis, Ewan Cameron, Melissa A Penny

Open access · goldAbstract read
In one paragraph

Article in Infectious diseases of poverty, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.8field-weighted citation impact, top 3% of its field
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

17 citing papers in PubMed, 31 citations in OpenAlex.

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  7. Gaussian Process Emulation for Exploring Complex Infectious Disease Models.medRxiv : the preprint server for health sciences · 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 at 5 institutions in 5 countries.

Monica Golumbeanu *Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
Guo-Jing Yang *Swiss Tropical and Public Health Institute, Allschwil, Switzerland.
Flavia CamponovoSwiss Tropical and Public Health Institute, Allschwil, Switzerland.
Erin M StuckeyThe Bill & Melinda Gates Foundation, Seattle, WA, USA.
Nicholas HamonInnovative Vector Control Consortium, Liverpool, UK.
Mathias MondyInnovative Vector Control Consortium, Liverpool, UK.
Sarah ReesInnovative Vector Control Consortium, Liverpool, UK.
Nakul ChitnisSwiss Tropical and Public Health Institute, Allschwil, Switzerland.
Ewan CameronMalaria Atlas Project, Big Data Institute, University of Oxford, Oxford, UK.
Melissa A PennySwiss Tropical and Public Health Institute, Allschwil, Switzerland. melissa.penny@unibas.ch.ORCID http://orcid.org/0000-0002-4972-593X
Swiss Tropical and Public Health Institute · CHInnovative Vector Control Consortium · GBCenter for Disease Dynamics, Economics & Policy · USGates Foundation · USThe Kids Research Institute Australia · AU

Funding

Bill and Melinda Gates Foundation OPP1170505Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung PP00P3_170702
6 · The paper itself

Abstract

backgroundSubstantial research is underway to develop next-generation interventions that address current malaria control challenges. As there is limited testing in their early development, it is difficult to predefine intervention properties such as efficacy that achieve target health goals, and therefore challenging to prioritize selection of novel candidate interventions. Here, we present a quantitative approach to guide intervention development using mathematical models of malaria dynamics coupled with machine learning. Our analysis identifies requirements of efficacy, coverage, and duration of effect for five novel malaria interventions to achieve targeted reductions in malaria prevalence.

methodsA mathematical model of malaria transmission dynamics is used to simulate deployment and predict potential impact of new malaria interventions by considering operational, health-system, population, and disease characteristics. Our method relies on consultation with product development stakeholders to define the putative space of novel intervention specifications. We couple the disease model with machine learning to search this multi-dimensional space and efficiently identify optimal intervention properties that achieve specified health goals.

resultsWe apply our approach to five malaria interventions under development. Aiming for malaria prevalence reduction, we identify and quantify key determinants of intervention impact along with their minimal properties required to achieve the desired health goals. While coverage is generally identified as the largest driver of impact, higher efficacy, longer protection duration or multiple deployments per year are needed to increase prevalence reduction. We show that interventions on multiple parasite or vector targets, as well as combinations the new interventions with drug treatment, lead to significant burden reductions and lower efficacy or duration requirements.

conclusionsOur approach uses disease dynamic models and machine learning to support decision-making and resource investment, facilitating development of new malaria interventions. By evaluating the intervention capabilities in relation to the targeted health goal, our analysis allows prioritization of interventions and of their specifications from an early stage in development, and subsequent investments to be channeled cost-effectively towards impact maximization. This study highlights the role of mathematical models to support intervention development. Although we focus on five malaria interventions, the analysis is generalizable to other new malaria interventions.

Indexed as

MalariaHumansMachine LearningModels, TheoreticalPrevalenceInfectious diseasesMachine learningMalariaMathematical modellingNovel interventions

Identifiers

PMID35659301
PMCPMC9167503
OpenAlexW4281640023

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.