Evidence map›Paper›PMID 27756395›Full record

Trial reportMalaria journal2016

Geographical patterns of malaria transmission based on serological markers for falciparum and vivax malaria in Ratanakiri, Cambodia.

Karen Kerkhof, Vincent Sluydts, Somony Heng, Saorin Kim, Myrthe Pareyn, Laura Willen, Lydie Canier, Siv Sovannaroth, Didier Ménard, Tho Sochantha and 2 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Malaria journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. The American journal of tropical medicine and hygiene · 2018
    Trial
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  6. Using Serological Markers for the Surveillance ofPathogens (Basel, Switzerland) · 2023
    Article
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  8. Serological surveillance on potentialFrontiers in cellular and infection microbiology · 2023
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  9. Review
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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 4 institutions in 2 countries.

Karen KerkhofDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium. kkerkhof@itg.be.ORCID http://orcid.org/0000-0002-2208-9902
Vincent SluydtsDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Somony HengNational Centre for Parasitology, Entomology and Malaria Control, Phnom Penh, Cambodia.
Saorin KimMolecular Epidemiology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Myrthe PareynDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Laura WillenDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Lydie CanierMolecular Epidemiology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Siv SovannarothNational Centre for Parasitology, Entomology and Malaria Control, Phnom Penh, Cambodia.
Didier MénardMolecular Epidemiology Unit, Institut Pasteur du Cambodge, Phnom Penh, Cambodia.
Tho SochanthaNational Centre for Parasitology, Entomology and Malaria Control, Phnom Penh, Cambodia.
Marc CoosemansDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
Lies DurnezDepartment of Biomedical Sciences, Institute of Tropical Medicine, Antwerp, Belgium.
University of Antwerp · BECambodia National Malaria Center · KHInstitut Pasteur du Cambodge · KHInstituut voor Tropische Geneeskunde · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMalaria transmission is highly heterogeneous, especially in low endemic countries, such as Cambodia. This results in geographical clusters of residual transmission in the dry, low transmission season, which can fuel the transmission to wider areas or populations during the wet season. A better understanding of spatial clustering of malaria can lead to a more efficient, targeted strategy to reduce malaria transmission. This study aims to evaluate the potential of the use of serological markers to define spatial patterns in malaria exposure.

methodsBlood samples collected in a community-based randomized trial performed in 98 high endemic communities in Ratanakiri province, north-eastern Cambodia, were screened with a multiplex serological assay for five serological markers (three Plasmodium falciparum and two Plasmodium vivax). The antibody half-lives range from approximately six months until more than two years. Geographical heterogeneity in malaria transmission was examined using a spatial scan statistic on serology, PCR prevalence and malaria incidence rate data. Furthermore, to identify behavioural patterns or intrinsic factors associated with malaria exposure (antibody levels), risk factor analyses were performed by using multivariable random effect logistic regression models. The serological outcomes were then compared to PCR prevalence and malaria incidence data.

resultsA total of 6502 samples from two surveys were screened in an area where the average parasite prevalence estimated by PCR among the selected villages is 3.4 %. High-risk malaria pockets were observed adjacent to the 'Tonle San River' and neighbouring Vietnam for all three sets of data (serology, PCR prevalence and malaria incidence rates). The main risk factors for all P. falciparum antigens and P. vivax MSP1.19 are age, ethnicity and staying overnight at the plot hut.

conclusionIt is possible to identify similar malaria pockets of higher malaria transmission together with the potential risk factors by using serology instead of PCR prevalence or malaria incidence data. In north-eastern Cambodia, the serological markers show that malaria transmission occurs mainly in adults staying overnight in plot huts in the field. Pf.GLURP.R2 showed a shrinking pocket of malaria transmission over time, and Pf.MSP1.19, CSP, PvAMA1 were also informative for current infection to a lesser extent. Therefore, serology could contribute in future research. However, further in-depth research in selecting the best combination of antigens is required.

Indexed as

Disease Transmission, InfectiousTopography, MedicalAdolescentAdultAntibodies, ProtozoanCambodiaChildChild, PreschoolCluster AnalysisCross-Sectional StudiesFemaleHumansIncidenceMalaria, FalciparumMalaria, VivaxMaleAntibodies, ProtozoanCambodiaGeographical patternsHeterogeneous transmissionMalariaMalaria pocketsSerological markers

Identifiers

PMID27756395
PMCPMC5069850
OpenAlexW2533007924

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.