Journal Article

Increasing Prevalence of Artemisinin-Resistant HRP2-Negative Malaria in Eritrea

Campagne, Pascal, Legrand, Eric, Warsame, Marian, Zehaie Kassahun, Assefash, Ringwald, Pascal, Platon, Lucien, Fidock, David A., Mihreteab, Selam, Ward, Kurt E., Ménard, Didier, Ma, Laurence, Stokes, Barbara H., Petiot, Nathalie, Berhane, Araia, Criscuolo, Alexis, Doderer-Lang, Cécile

2023

Overview

Although the clinical efficacy of antimalarial artemisinin-based combination therapies in Africa remains high, the recent emergence of partial resistance to artemisinin in on the continent is troubling, given the lack of alternative treatments. In this study, we used data from drug-efficacy studies conducted between 2016 and 2019 that evaluated 3-day courses of artemisinin-based combination therapy (artesunate-amodiaquine or artemether-lumefantrine) for uncomplicated malaria in Eritrea to estimate the percentage of patients with day-3 positivity (i.e., persistent parasitemia 3 days after the initiation of therapy). We also assayed parasites for mutations in as predictive markers of partial resistance to artemisinin and screened for deletions in and that result in variable performance of histidine rich protein 2 (HRP2)-based rapid diagnostic tests for malaria. We noted an increase in the percentage of patients with day-3 positivity from 0.4% (1 of 273) in 2016 to 1.9% (4 of 209) in 2017 and 4.2% (15 of 359) in 2019. An increase was also noted in the prevalence of the R622I mutation, which was detected in 109 of 818 isolates before treatment, from 8.6% (24 of 278) in 2016 to 21.0% (69 of 329) in 2019. The odds of day-3 positivity increased by a factor of 6.2 (95% confidence interval, 2.5 to 15.5) among the patients with 622I variant parasites. Partial resistance to artemisinin, as defined by the World Health Organization, was observed in Eritrea. More than 5% of the patients younger than 15 years of age with day-3 positivity also had parasites that carried R622I. In vitro, the R622I mutation conferred a low level of resistance to artemisinin when edited into NF54 and Dd2 parasite lines. Deletions in both and were identified in 16.9% of the parasites that carried the R622I mutation, which made them potentially undetectable by HRP2-based rapid diagnostic tests. The emergence and spread of lineages with both -mediated partial resistance to artemisinin and deletions in and in Eritrea threaten to compromise regional malaria control and elimination campaigns. (Funded by the Bill and Melinda Gates Foundation and others; Australian New Zealand Clinical Trials Registry numbers, ACTRN12618001223224, ACTRN12618000353291, and ACTRN12619000859189.).

• Publisher: Massachusetts Medical Society
• Subject: Amodiaquine / Amodiaquine - administration & dosage / Amodiaquine - pharmacology / Amodiaquine - therapeutic use / Antimalarials - pharmacology / Antimalarials - therapeutic use / Artemether / Artemether, Lumefantrine Drug Combination - pharmacology / Artemether, Lumefantrine Drug Combination - therapeutic use / Artemisinin / Artemisinins - administration & dosage / Artemisinins - pharmacology / Artemisinins - therapeutic use / Artesunate / Clinical Medicine / Clinical trials / Confidence intervals / Diagnostic tests / Diagnostics / Drug efficacy / Drug Resistance - genetics / Eritrea - epidemiology / Genetic testing / Genetics / Genetics General / Genomes / Genotype & phenotype / Global Health / Health facilities / Histidine / Humans / Hypothesis testing / Infections / Infectious Disease / Infectious Disease General / Klinisk medicin / Life Sciences / Malaria / Malaria, Falciparum - drug therapy / Malaria, Falciparum - epidemiology / Malaria, Falciparum - genetics / Malaria, Falciparum - parasitology / Mutation / Parasite resistance / Parasitemia / Parasites / Parasitic Infections / Patients / Plasmodium falciparum / Plasmodium falciparum - drug effects / Plasmodium falciparum - genetics / Prevalence