Evidence map›Paper›PMID 19905933›Full record

Trial reportThe Journal of infectious diseases2009

Selection of parasites with diminished drug susceptibility by amodiaquine-containing antimalarial regimens in Uganda.

Fatima Nawaz, Samuel L Nsobya, Moses Kiggundu, Moses Joloba, Philip J Rosenthal

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in The Journal of infectious diseases, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Changing Antimalarial Drug Sensitivities in Uganda.Antimicrobial agents and chemotherapy · 2017
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  6. Molecular Surveillance andFrontiers in cellular and infection microbiology · 2021
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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

5 authors at 2 institutions in 2 countries.

Fatima NawazDepartment of Medicine, University of California, San Francisco, CA, USA.
Samuel L Nsobya
Moses Kiggundu
Moses Joloba
Philip J Rosenthal
University of California, San Francisco · USMakerere University · UG

Funding

Resistance of Malaria Parasites to Artemisinin-Based TherapiesR01AI075045 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENTHAL, PHILIP JON · 2009 to 2024
$8.4M
Clinical &Molecular Studies of Drug Resistant MalariaU01AI052142 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ROSENTHAL, PHILIP JON · 2003 to 2008
$4.4M
TRAINING IN MALARIA RESEARCH IN UGANDAD43TW001506 · FIC · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI ROSENTHAL, PHILIP JON · 2000 to 2004
$900k
FIC NIH HHS D43 TW001506NIAID NIH HHS AI52142NIAID NIH HHS R01 AI075045NIAID NIH HHS U01 AI052142
6 · The paper itself

Abstract

backgroundAmodiaquine (AQ) is paired with artesunate (AS) or sulfadoxine-pyrimethamine (SP) in recommended antimalarial regimens. It is unclear how readily AQ resistance will be selected with combination chemotherapy.

methodsWe collected 61 Plasmodium falciparum samples from a cohort of Ugandan children randomized for treatment with AQ-SP, AS-AQ, or artemether-lumefantrine (AL) for uncomplicated malaria. In vitro susceptibility to monodesethylamodiaquine (MDAQ) was measured with a histidine-rich protein 2-based enzyme-linked immunosorbent assay, and potential resistance-mediating polymorphisms in pfmdr1 were evaluated.

resultsParasites collected from patients treated with AQ-SP or AS-AQ within the prior 12 weeks were less susceptible to MDAQ (n = 18; mean of the median inhibitory concentration [IC(50)], 62.9 nmol/L; range, 12.7-158.3 nmol/L) than were parasites from those not treated within 12 weeks (n = 43; mean IC(50), 37.5 nmol/L; range, 6.3-184.7 nmol/L; P=.009) or only from those patients in the treatment arm that did not receive AQ (n = 12; mean IC(50), 28.8 nmol/L; range, 6.3-121.8 nmol/L; P = .004). The proportion of strains with polymorphisms expected to mediate diminished response to AQ (pfmdr1 86Y and 1246Y) increased after AQ therapy, although differences were not statistically significant.

conclusionsPrior therapy selected for diminished response to MDAQ, which suggests that AQ-containing regimens may rapidly lose efficacy in Africa. The mechanism of diminished MDAQ response is not fully explained by known mutations in pfmdr1.

Indexed as

Amino Acid SequenceAmodiaquineAntimalarialsArtemether, Lumefantrine Drug CombinationArtemisininsArtesunateATP-Binding Cassette, Sub-Family C ProteinsChildChild, PreschoolCohort StudiesDrug CombinationsDrug ResistanceEthanolaminesFluorenesHumansInfantAmodiaquineAntimalarialsArtemether, Lumefantrine Drug CombinationArtemisininsArtesunateATP-Binding Cassette, Sub-Family C ProteinsdesethylamodiaquineDrug CombinationsEthanolaminesfanasil, pyrimethamine drug combinationFluorenesMdr1 protein, Plasmodium falciparumPyrimethamineSulfadoxine

Identifiers

PMID19905933
PMCPMC2782860
OpenAlexW2100435538

What OpenQuestion holds

Textmetadata
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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.