Evidence map›Paper›PMID 41843937›Full record

ArticleThe American journal of tropical medicine and hygiene2026

Geographical Heterogeneity in Antimalarial Resistance Markers by Genomic Surveillance in Angola, 2023.

Maria Florinda João, Andrés Aranda-Díaz, Faith De Amaral, Takalani I Makhanthisa, Sonja B Lauterbach, Mukosha Chisenga, Brighton Mangena, Paulo Maquina, Isobel Routledge, Chadwick Sikaala and 6 more

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Article in The American journal of tropical medicine and hygiene, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Maria Florinda JoãoPrograma Nacional do Controlo da Malária, Luanda, Angola.
Andrés Aranda-DíazEPPIcenter Research Program, Department of Medicine, University of California, San Francisco, California.
Faith De AmaralEPPIcenter Research Program, Department of Medicine, University of California, San Francisco, California.
Takalani I MakhanthisaLaboratory for Antimalarial Resistance Monitoring and Malaria Operational Research, Centre of Emerging Zoonotic and Parasitic Diseases, National Institute for Communicable Diseases, Johannesburg, South Africa.
Sonja B LauterbachLaboratory for Antimalarial Resistance Monitoring and Malaria Operational Research, Centre of Emerging Zoonotic and Parasitic Diseases, National Institute for Communicable Diseases, Johannesburg, South Africa.
Mukosha ChisengaSADC Malaria Elimination Eight Secretariat, Windhoek, Namibia.
Brighton MangenaSADC Malaria Elimination Eight Secretariat, Windhoek, Namibia.
Paulo MaquinaSADC Malaria Elimination Eight Secretariat, Windhoek, Namibia.
Isobel RoutledgeMalaria Elimination Initiative, Global Health Group, University of California, San Francisco, California.
Chadwick SikaalaSADC Malaria Elimination Eight Secretariat, Windhoek, Namibia.
John ChimumbwaSADC Malaria Elimination Eight Secretariat, Windhoek, Namibia.
Domingos JandondoInstituto Nacional de Investigação em Saúde, Luanda, Angola.
José Franco MartinsPrograma Nacional do Controlo da Malária, Luanda, Angola.
Jaishree RamanLaboratory for Antimalarial Resistance Monitoring and Malaria Operational Research, Centre of Emerging Zoonotic and Parasitic Diseases, National Institute for Communicable Diseases, Johannesburg, South Africa.
Jennifer L SmithMalaria Elimination Initiative, Global Health Group, University of California, San Francisco, California.
Pedro Rafael DimbuPrograma Nacional do Controlo da Malária, Luanda, Angola.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Plasmodium falciparum malaria remains a leading cause of mortality in Angola, with emerging antimalarial resistance threatening treatment and prevention strategies. Efficacy of artemether-lumefantrine has been reported below 90% in two provinces, underscoring the need for routine resistance surveillance. This study aimed to provide a geographically comprehensive and up-to-date overview of antimalarial drug resistance markers in Angola. Between March and July 2023, dried blood spots and demographic data were collected from P. falciparum-positive participants at 14 health facilities across 7 provinces. Multiplexed amplicon sequencing was used to characterize single nucleotide polymorphisms in 12 genes linked with resistance, estimate allele frequencies, and detect coinfecting non-falciparum Plasmodium species. Sequence data from 820 samples revealed significant geographic variation in resistance markers. In the southeast, artemisinin partial resistance markers (k13 P574L, P441L) were detected at very low prevalence (<0.1%), whereas the quintuple dhps/dhfr haplotype, linked to sulfadoxine-pyrimethamine resistance, was very prevalent (>35% of samples). In the northwest, the sextuple dhps/dhfr haplotype, a marker of higher sulfadoxine-pyrimethamine resistance, was most prevalent in the Zaire province (14.2%). The chloroquine resistance marker crt C72/V73/M74I/N75E/K76T (CVIET) haplotype had a national prevalence of 17.7%, detected in over 48% of samples from the northern sites. The mdr1 N86 genotype, linked to reduced lumefantrine susceptibility, was detected in 99.2% of samples. Coinfections of P. falciparum and non-falciparum species were rare, with no Plasmodium vivax coinfections detected. These findings highlight the need for continued monitoring to safeguard treatment efficacy, reinforcing the importance of molecular surveillance in malaria control strategies.

Identifiers

PMID41843937

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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.