Evidence map›Paper›PMID 32178706›Full record

ArticleParasites & vectors2020

Parasite associations predict infection risk: incorporating co-infections in predictive models for neglected tropical diseases.

Nicholas J Clark, Kei Owada, Eugene Ruberanziza, Giuseppina Ortu, Irenee Umulisa, Ursin Bayisenge, Jean Bosco Mbonigaba, Jean Bosco Mucaca, Warren Lancaster, Alan Fenwick and 2 more

Open access · goldAbstract read
In one paragraph

Article in Parasites & vectors, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
5.9field-weighted citation impact, top 4% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  3. Coinfection by multipleMicrobiology and molecular biology reviews : MMBR · 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

12 authors at 3 institutions in 3 countries.

Nicholas J ClarkUQ Spatial Epidemiology Laboratory, School of Veterinary Science, The University of Queensland, Gatton, QLD, 4343, Australia. n.clark@uq.edu.au.ORCID http://orcid.org/0000-0001-7131-3301
Kei OwadaUQ Spatial Epidemiology Laboratory, School of Veterinary Science, The University of Queensland, Gatton, QLD, 4343, Australia.
Eugene RuberanzizaNeglected Tropical Diseases and Other Parasitic Diseases Unit, Malaria and Other Parasitic Diseases Division, Rwanda Biomedical Center, Kigali, Rwanda.
Giuseppina OrtuSchistosomiasis Control Initiative (SCI), Department of Infectious Diseases Epidemiology, Imperial College, London, UK.
Irenee UmulisaNeglected Tropical Diseases and Other Parasitic Diseases Unit, Malaria and Other Parasitic Diseases Division, Rwanda Biomedical Center, Kigali, Rwanda.
Ursin BayisengeNeglected Tropical Diseases and Other Parasitic Diseases Unit, Malaria and Other Parasitic Diseases Division, Rwanda Biomedical Center, Kigali, Rwanda.
Jean Bosco MbonigabaNeglected Tropical Diseases and Other Parasitic Diseases Unit, Malaria and Other Parasitic Diseases Division, Rwanda Biomedical Center, Kigali, Rwanda.
Jean Bosco MucacaMicrobiology Unit, National Reference Laboratory (NRL) Division, Rwanda Biomedical Center, Ministry of Health, Kigali, Rwanda.
Warren LancasterThe END Fund, 2 Park Avenue, 18th Floor, New York, NY, 10016, USA.
Alan FenwickSchistosomiasis Control Initiative (SCI), Department of Infectious Diseases Epidemiology, Imperial College, London, UK.
Ricardo J Soares MagalhãesUQ Spatial Epidemiology Laboratory, School of Veterinary Science, The University of Queensland, Gatton, QLD, 4343, Australia.
Aimable MbituyumuremyiMalaria and Other Parasitic Diseases Division, Rwanda Biomedical Center, Ministry of Health, Kigali, Rwanda.
Rwanda Biomedical Center · RWThe University of Queensland · AUImperial College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSchistosomiasis and infection by soil-transmitted helminths are some of the world's most prevalent neglected tropical diseases. Infection by more than one parasite (co-infection) is common and can contribute to clinical morbidity in children. Geostatistical analyses of parasite infection data are key for developing mass drug administration strategies, yet most methods ignore co-infections when estimating risk. Infection status for multiple parasites can act as a useful proxy for data-poor individual-level or environmental risk factors while avoiding regression dilution bias. Conditional random fields (CRF) is a multivariate graphical network method that opens new doors in parasite risk mapping by (i) predicting co-infections with high accuracy; (ii) isolating associations among parasites; and (iii) quantifying how these associations change across landscapes.

methodsWe built a spatial CRF to estimate infection risks for Ascaris lumbricoides, Trichuris trichiura, hookworms (Ancylostoma duodenale and Necator americanus) and Schistosoma mansoni using data from a national survey of Rwandan schoolchildren. We used an ensemble learning approach to generate spatial predictions by simulating from the CRF's posterior distribution with a multivariate boosted regression tree that captured non-linear relationships between predictors and covariance in infection risks. This CRF ensemble was compared against single parasite gradient boosted machines to assess each model's performance and prediction uncertainty.

resultsParasite co-infections were common, with 19.57% of children infected with at least two parasites. The CRF ensemble achieved higher predictive power than single-parasite models by improving estimates of co-infection prevalence at the individual level and classifying schools into World Health Organization treatment categories with greater accuracy. The CRF uncovered important environmental and demographic predictors of parasite infection probabilities. Yet even after capturing demographic and environmental risk factors, the presences or absences of other parasites were strong predictors of individual-level infection risk. Spatial predictions delineated high-risk regions in need of anthelminthic treatment interventions, including areas with higher than expected co-infection prevalence.

conclusionsMonitoring studies routinely screen for multiple parasites, yet statistical models generally ignore this multivariate data when assessing risk factors and designing treatment guidelines. Multivariate approaches can be instrumental in the global effort to reduce and eventually eliminate neglected helminth infections in developing countries.

Indexed as

AdolescentAncylostomatoideaAnimalsAnthelminticsAscaris lumbricoidesChildCoinfectionFecesFemaleHumansMaleNeglected DiseasesParasitic DiseasesPrevalenceRegression AnalysisRisk FactorsAnthelminticsConditional random fieldsNeglected tropical diseaseParasite co-infectionSchistosoma mansoniSoil-transmitted helminthsSpatial epidemiology

Identifiers

PMID32178706
PMCPMC7077138
OpenAlexW3012148133

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.