Evidence map›Paper›PMID 33422068›Full record

ArticleMalaria journal2021

Persistence of mRNA indicative of Plasmodium falciparum ring-stage parasites 42 days after artemisinin and non-artemisinin combination therapy in naturally infected Malians.

Almahamoudou Mahamar, Kjerstin Lanke, Wouter Graumans, Halimatou Diawara, Koualy Sanogo, Kalifa Diarra, Sidi Mohamed Niambele, Roly Gosling, Chris Drakeley, Ingrid Chen and 3 more

Open access · goldAbstract read
In one paragraph

Article in Malaria journal, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Isolation and characterization ofAntimicrobial agents and chemotherapy · 2025
    Article
  3. Article
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

13 authors at 3 institutions in 3 countries.

Almahamoudou MahamarMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Kjerstin LankeRadboud Institute for Health Sciences, Radboud University Medical Center, Geert Grooteplein Zuid 26-28, PO Box 9101, 6525GA, Nijmegen, The Netherlands.
Wouter GraumansRadboud Institute for Health Sciences, Radboud University Medical Center, Geert Grooteplein Zuid 26-28, PO Box 9101, 6525GA, Nijmegen, The Netherlands.
Halimatou DiawaraMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Koualy SanogoMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Kalifa DiarraMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Sidi Mohamed NiambeleMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Roly GoslingGlobal Health Group, Malaria Elimination Initiative, University of California, San Francisco, CA, USA.
Chris DrakeleyDepartment of Infection & Immunity, London School of Hygiene & Tropical Medicine, London, UK.
Ingrid ChenGlobal Health Group, Malaria Elimination Initiative, University of California, San Francisco, CA, USA.
Alassane DickoMalaria Research and Training Centre, Faculty of Pharmacy, Medicine, and Dentistry, University of Science, Techniques, and Technologies of Bamako, Bamako, Mali.
Teun BousemaRadboud Institute for Health Sciences, Radboud University Medical Center, Geert Grooteplein Zuid 26-28, PO Box 9101, 6525GA, Nijmegen, The Netherlands. teun.bousema@radboudumc.nl.ORCID http://orcid.org/0000-0003-2666-094X
Michelle E RohGlobal Health Group, Malaria Elimination Initiative, University of California, San Francisco, CA, USA.
Radboud University Nijmegen · NLUniversity of California, San Francisco · USLondon School of Hygiene & Tropical Medicine · GB

Funding

Bill and Melinda Gates Foundation OPP1089413Bill and Melinda Gates Foundation OPP1173572H2020 European Research Council ERC-2014-StG 639776
6 · The paper itself

Abstract

backgroundMalaria control in sub-Saharan Africa relies upon prompt case management with artemisinin-based combination therapy (ACT). Ring-stage parasite mRNA, measured by sbp1 quantitative reverse-transcriptase PCR (qRT-PCR), was previously reported to persist after ACT treatment and hypothesized to reflect temporary arrest of the growth of ring-stage parasites (dormancy) following exposure to artemisinins. Here, the persistence of ring-stage parasitaemia following ACT and non-ACT treatment was examined.

methodsSamples were used from naturally infected Malian gametocyte carriers who received dihydroartemisinin-piperaquine (DP) or sulfadoxine-pyrimethamine (SP-AQ) with or without gametocytocidal drugs. Gametocytes and ring-stage parasites were quantified by qRT-PCR during 42 days of follow-up.

resultsAt baseline, 89% (64/73) of participants had measurable ring-stage parasite mRNA. Following treatment, the proportion of ring-stage parasite-positive individuals and estimated densities declined for all four treatment groups. Ring-stage parasite prevalence and density was generally lower in arms that received DP compared to SP-AQ. This finding was most apparent days 1, 2, and 42 of follow-up (p < 0.01). Gametocytocidal drugs did not influence ring-stage parasite persistence. Ring-stage parasite density estimates on days 14 and 28 after initiation of treatment were higher among individuals who subsequently experienced recurrent parasitaemia compared to those who remained free of parasites until day 42 after initiation of treatment (p

conclusionsThe current findings of lower ring-stage persistence after ACT without an effect of gametocytocidal partner drugs affirms the use of sbp1 as ring-stage marker. Lower persistence of ring-stage mRNA after ACT treatment suggests the marker may not reflect dormant parasites whilst it was predictive of re-appearance of parasitaemia.

Indexed as

AdolescentAdultAntimalarialsArtemisininsChildDrug CombinationsHumansMaleMiddle AgedPiperazinesPlasmodium falciparumPyrimethamineQuinolinesRNA, MessengerRNA, ProtozoanSulfadoxineAntimalarialsArtemisininsartenimolDrug Combinationsfanasil, pyrimethamine drug combinationpiperaquinePiperazinesPyrimethamineQuinolinesRNA, MessengerRNA, ProtozoanSulfadoxineArtemisinin-based combination therapyDormancyGametocytesPersistencePlasmodium falciparumRecrudescenceResistance

Identifiers

PMID33422068
PMCPMC7797096
OpenAlexW3120168175

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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 OpenQuestion graph.