2024年9月30日星期一

Evidence of Artemisinin-Resistant Malaria in Africa_ A Growing Concern


Evidence of Artemisinin-Resistant Malaria in Africa: A Growing Concern

The emergence of artemisinin-resistant malaria in Africa is a critical public health concern that threatens to undermine decades of progress in malaria control and elimination efforts. While artemisinin resistance was first documented in Southeast Asia, recent evidence suggests that it has now taken hold in parts of Africa, the continent with the highest malaria burden. This development poses a significant challenge to global malaria control strategies and highlights the urgent need for enhanced surveillance, research, and intervention measures.

Key evidence of artemisinin-resistant malaria in Africa includes:



Rwanda Study (2020): A landmark study published in The Lancet Infectious Diseases reported the first evidence of artemisinin resistance in Africa. Researchers identified mutations in the Plasmodium falciparum kelch13 gene, specifically the R561H mutation, which is associated with delayed parasite clearance. This mutation was found in 19 of 257 (7.4%) patients in Masaka, Rwanda.



Uganda Findings (2021): A subsequent study in Uganda, published in the New England Journal of Medicine, identified the emergence of artemisinin resistance markers in northern Uganda. The study found a substantial increase in the prevalence of parasites carrying mutations in the kelch13 gene, particularly the A675V mutation.



Multicountry Surveillance Data: The WHO's antimalarial drug efficacy and resistance database has reported sporadic cases of delayed parasite clearance in several African countries, including Burkina Faso, Cameroon, and Mali. While these cases do not yet constitute widespread resistance, they highlight the need for continued vigilance.



Molecular Marker Studies: Various research groups have conducted molecular surveillance studies across Africa, identifying low-frequency kelch13 mutations associated with artemisinin resistance. While many of these mutations differ from those seen in Southeast Asia, their presence is concerning.



Ex vivo and In vitro Studies: Laboratory studies using parasites isolated from African patients have shown reduced susceptibility to artemisinin in some samples, corroborating clinical and molecular findings.



Treatment Failure Reports: Although not definitively linked to artemisinin resistance, there have been increasing reports of artemisinin-based combination therapy (ACT) treatment failures in some African countries. While these could be due to various factors, they warrant close monitoring.



Genomic Evidence: Whole-genome sequencing studies have revealed evidence of selection pressure on P. falciparum populations in some African regions, suggesting adaptation to artemisinin exposure.



The evidence of artemisinin-resistant malaria in Africa, while still localized, is deeply concerning to the global health community. It underscores the need for:


Enhanced surveillance systems to monitor drug efficacy and resistance markers across the continent.

Increased investment in research to understand the mechanisms and spread of resistance in African parasite populations.

Development of new antimalarial drugs and combination therapies to stay ahead of evolving resistance.

Strengthening of malaria control programs, including vector control and rapid diagnosis and treatment initiatives.

Exploration of strategies to prolong the efficacy of existing ACTs, such as triple artemisinin combination therapies (TACTs).

Continued global collaboration and knowledge sharing to address this emerging threat effectively.


The situation remains dynamic, and ongoing research and surveillance efforts are crucial to fully understand and address the threat of artemisinin resistance in Africa. 

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