Evidence map›Paper›PMID 28594879›Full record

ArticlePloS one2017

Molecular surveillance of Plasmodium falciparum resistance to artemisinin-based combination therapies in the Democratic Republic of Congo.

Dieudonné Makaba Mvumbi, Thierry Lengu Bobanga, Jean-Marie Ntumba Kayembe, Georges Lelo Mvumbi, Hippolyte Nani-Tuma Situakibanza, Françoise Benoit-Vical, Pierrette Melin, Patrick De Mol, Marie-Pierre Hayette

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 3 pooled it
4.7field-weighted citation impact, top 5% 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, 3 syntheses or guidelines pooled it, 32 citations in OpenAlex.

  1. Pooled it
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  12. Evolutionary bioinformatics online · 2021
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  17. Mutations inProceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  18. Multiple Phenotypic and Genotypic Artemisinin Sensitivity Evaluation of MalianThe American journal of tropical medicine and hygiene · 2018
    Article
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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

9 authors at 3 institutions in 3 countries.

Dieudonné Makaba MvumbiBiochemistry and Molecular Biology Unit, Department of Basic Sciences, School of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.ORCID http://orcid.org/0000-0001-6991-5178
Thierry Lengu BobangaDepartment of Parasitology and Tropical Medicine, School of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Jean-Marie Ntumba KayembeDepartment of Internal Medicine, School of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Georges Lelo MvumbiBiochemistry and Molecular Biology Unit, Department of Basic Sciences, School of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Hippolyte Nani-Tuma SituakibanzaDepartment of Parasitology and Tropical Medicine, School of Medicine, University of Kinshasa, Kinshasa, Democratic Republic of Congo.
Françoise Benoit-VicalCNRS, LCC (Laboratoire de Chimie de Coordination), Toulouse et Université de Toulouse, UPS, France.
Pierrette MelinDepartment of Clinical Microbiology, University Hospital of Liege, Liege, Belgium.
Patrick De MolDepartment of Clinical Microbiology, University Hospital of Liege, Liege, Belgium.
Marie-Pierre HayetteDepartment of Clinical Microbiology, University Hospital of Liege, Liege, Belgium.
University of Kinshasa · CDUniversity of Liège · BECentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malaria is a major public health problem in the Democratic Republic of Congo. Despite progress achieved over the past decade in the fight against malaria, further efforts have to be done such as in the surveillance and the containment of Plasmodium falciparum resistant strains. We investigated resistance to artemisinin-based combination therapies currently in use in Democratic Republic of Congo by surveying molecular polymorphisms in three genes: pfcrt, pfmdr1 and pfk13 to explore possible emergence of amodiaquine, lumefantrine or artemisinin resistance in Democratic Republic of Congo. This study essentially revealed that resistance to chloroquine is still decreasing while polymorphism related to amodiaquine resistance seems to be not present in Democratic Republic of Congo, that three samples, located in the east of the country, harbor Pfmdr1 amplification and that none of the mutations found in South-East Asia correlated with artemisinine resistance have been found in Democratic Republic of Congo. But new mutations have been identified, especially the M476K, occurred in the same position that the M476I previously identified in the F32-ART strain, strongly resistant to artemisinine. Antimalarial first-line treatments currently in use in Democratic Republic of Congo are not associated with emergence of molecular markers of resistance.

Indexed as

ArtemisininsDemocratic Republic of the CongoDrug ResistanceDrug Therapy, CombinationGene DosageGenetic MarkersGeographyHaplotypesHumansMalaria, FalciparumMutationPlasmodium falciparumPolymorphism, GeneticProtozoan ProteinsArtemisininsGenetic MarkersProtozoan Proteins

Identifiers

PMID28594879
PMCPMC5464640
OpenAlexW2622921261

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.