Evidence map›Paper›PMID 40885517›Full record

ReviewInternational journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases2025

Mapping Plasmodium falciparum mutations in Africa: A critical review of emerging drug resistance and implications for malaria control.

Pierre Gashema, James Kagame, Patrick Gad Iradukunda, Emmanuel Edwar Siddig, Sofonias Kifle Tessema, Merawi Aragaw Tegegne, Mazyanga Lucy Mazaba, Mosoka Fallah, Daniel Ngamije, Jean de Dieu Harelimana and 1 more

Abstract readReview
In one paragraph

Review in International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed, 2 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

4 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Assessing the threat of artemisinin resistance: seasonal and ecological patterns ofFrontiers in cellular and infection microbiology · 2026
    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

11 authors.

Pierre GashemaAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia; Repolicy research Centre, Kigali, Rwanda.
James KagameRwanda Biomedical Centre, Kigali, Rwanda.
Patrick Gad IradukundaRepolicy research Centre, Kigali, Rwanda; Rwanda Food Drugs and Authority, Kigali, Rwanda.
Emmanuel Edwar SiddigAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia.
Sofonias Kifle TessemaAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia.
Merawi Aragaw TegegneAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia.
Mazyanga Lucy MazabaAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia.
Mosoka FallahAfrica Centres for Disease Control and Prevention (Africa CDC), Addis Ababa, Ethiopia.
Daniel NgamijeWorld Health Organization, Geneva, Switzerland.
Jean de Dieu HarelimanaRwanda Biomedical Centre, Kigali, Rwanda.
Claude Mambo MuvunyiRwanda Biomedical Centre, Kigali, Rwanda. Electronic address: claude.muvunyi@rbc.gov.rw.

Funding

World Health Organization 001
6 · The paper itself

Abstract

Malaria remains a significant public health concern in Africa, with the efficacy of artemisinin-based combination therapies being threatened by the emergence of Plasmodium falciparum (Pf) kelch13 mutations. The current genetic diversity of Pf and associated contributing factors reported in Africa between 2019 and 2024 were reviewed. It was shown that validated kelch13 mutations are mainly distributed in east African regions, particularly, in Eritrea (R622I, 68%) and Uganda (R561H, 52%). Emerging Pf mutations have been documented in Rwanda (C469F, 36%), Uganda (C469F, 59% and P441L, 69%), and Tanzania (P441L, 20%). Resistance markers for partner drugs, including Pfcrt, Pfmdr1, Pfdhfr, and Pfdhps, were prevalent in eastern (30-38%) and western African regions (44-55%). The key factors contributing to the development of Pf mutations were identified as drug pressure (23-35%), misuse of antimalarial drugs (10-12.5%), and cross-border population movements (10%). This review posits a critical need to refine malaria control programs, crucially reinforcing drug regulations, enhancing community awareness on appropriate treatment practices, and integrating molecular epidemiologic surveillance systems.

Indexed as

AntimalarialsDrug ResistanceMalaria, FalciparumMutationPlasmodium falciparumAfricaHumansProtozoan ProteinsAntimalarialsProtozoan ProteinsAfricaArtemisininMutationsPlasmodium falciparumResistance

Identifiers

PMID40885517
PMCPMC12485076

What OpenQuestion holds

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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.