Evidence map›Paper›PMID 42374417›Full record

ArticleMalaria journal2026

Prevalence of antimalarial drug resistance markers and factors associated with Plasmodium falciparum infection in asymptomatic children prior to rectal artesunate implementation in Kapolowe Health District, Democratic Republic of the Congo.

Flory Luzolo Khote, Madalena Raposo, Tafadzwa Maseko, Deborah Kanyamukenge, Sebastian Hachizovu, Geofrey Makenga, Eric Mukomena, Aimé Kakudji, Augustin Mutombo, Ghislain Kikunda and 13 more

Abstract read
In one paragraph

Article in Malaria journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

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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

23 authors.

Flory Luzolo KhoteDepartment of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo. luzolokhote@gmail.com.
Madalena RaposoCenter for Translational Medicine and Parasitology, Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Tafadzwa MasekoGlobal Health Institute, University of Antwerp, Antwerp, Belgium.
Deborah KanyamukengeGlobal Health Institute, University of Antwerp, Antwerp, Belgium.
Sebastian HachizovuGlobal Health Institute, University of Antwerp, Antwerp, Belgium.
Geofrey MakengaGlobal Health Institute, University of Antwerp, Antwerp, Belgium.
Eric MukomenaUniversity of Lubumbashi, Lubumbashi, Democratic Republic of the Congo.
Aimé KakudjiUniversity of Lubumbashi, Lubumbashi, Democratic Republic of the Congo.
Augustin MutomboUniversity of Lubumbashi, Lubumbashi, Democratic Republic of the Congo.
Ghislain KikundaUniversity of Lubumbashi, Lubumbashi, Democratic Republic of the Congo.
Jérémie SombolaDepartment of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Vivi MaketaDepartment of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.
Michael NamboziNational Health Research and Training Institute, Ndola, Zambia.
Stephan DuparcMMV Medicines for Malaria Venture, Geneva, Switzerland.
Hans RietveldMMV Medicines for Malaria Venture, Geneva, Switzerland.
Michael AlifrangisCenter for Translational Medicine and Parasitology, Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Helle HanssonCenter for Translational Medicine and Parasitology, Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Louise WellmannCenter for Translational Medicine and Parasitology, Department of Immunology and Microbiology, University of Copenhagen, Copenhagen, Denmark.
Nathalie OuareClinical Research Unit of Nanoro, Nanoro, Burkina Faso.
Christine ManyandoNational Health Research and Training Institute, Ndola, Zambia.
J P Van GeertruydenGlobal Health Institute, University of Antwerp, Antwerp, Belgium.
Vito Baraka *Tanga Centre, National Institute for Medical Research, Hospital Street, P O Box 5004, Tanga, United Republic of Tanzania.
Hypolite Muhindo Mavoko *Department of Tropical Medicine, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.

Funding

The European and Developing Countries Clinical Trials Partnerships (EDCTP) 101103191 [HORIZON-JU-GH-EDCTP3-2022-01]
6 · The paper itself

Abstract

backgroundIn remote areas where access to parenteral treatment for severe malaria or referral is limited, rectal artesunate (RAS) followed by a full course of artemisinin-based combination therapy (ACT) provided by community health workers would be a pragmatic solution. However, concerns remain that its expanded use may select for artemisinin-resistant Plasmodium falciparum strains. This baseline study assessed the presence of molecular markers of resistance to artemisinin and partner drugs and investigated factors associated with Plasmodium falciparum infection prior to RAS implementation.

methodsA community-based cross-sectional survey was conducted in remote areas of the Kapolowe health district, Democratic Republic of the Congo, in March-April 2024. Dried blood spot samples were collected from asymptomatic children aged 6-59 months. Molecular markers of antimalarial drug resistance in P. falciparum were analyzed using targeted next-generation sequencing, focusing on the Pfkelch13, Pfcoronin, Pfubp1, Pfmdr1, and Pfcrt genes.

resultsAmong 1242 children screened in 906 households, 656 (53%, 95% CI: 50-55%) were P. falciparum malaria rapid diagnostic test-positive, of which 646 samples were available for analyses. Factors associated with reduced odds of asymptomatic P. falciparum infection included higher household socio-economic status and non-agricultural sources of income, whereas children from households where malaria was perceived as treatable had increased odds of infection. No validated Pfkelch13 mutations associated with artemisinin partial resistance were detected. Several non-synonymous Pfkelch13 mutations were observed more than once, including A578S (7/395, 1.8%). Two Pfubp1 mutations associated with reduced dihydroartemisinin susceptibility, D1525E (88/354, 24.9%) and E1528D (62/354, 17.5%) were observed. No resistance-associated Pfcoronin mutations were detected. The wild-type Pfcrt CVMNK haplotype predominated, while the Pfmdr1 NFSND haplotype (57/379, 15.0%) associated with reduced lumefantrine susceptibility was identified.

conclusionsThe absence of Pfkelch13 mutations and a full reversal to wild-type Pfcrt are reassuring for directly guiding the implementation strategies of RAS and continued effectiveness of current ACTs. However, the detection of the Pfmdr1 single mutant NFSND haplotype highlights the need for continued monitoring of lumefantrine susceptibility.

Indexed as

AntimalarialsArtesunateDrug ResistanceMalaria, FalciparumPlasmodium falciparumArtemisininsAsymptomatic InfectionsChild, PreschoolCross-Sectional StudiesDemocratic Republic of the CongoFemaleHumansInfantMalePrevalenceAntimalarialsArtemisininsArtesunateArtemisinin-based combination therapyDemocratic Republic of the CongoDrug resistanceMalariaMolecular markersPfkelch13Plasmodium falciparumRectal artesunate

Identifiers

PMID42374417
PMCPMC13584420

What Socratic holds

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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 Socratic graph.