Publications des scientifiques de l'IRD

Mairet-Khedim M., Nsango S., Ngou C., Menard S., Roesch C., Khim N., Srun S., Iriart X., Lanot T., Otam L., Abega F., Ayong L., Morlais Isabelle, Gandia P., Witkowski B., Berry A. (2021). Efficacy of dihydroartemisinin/piperaquine in patients with non-complicated Plasmodium falciparum malaria in Yaounde, Cameroon. Journal of Antimicrobial Chemotherapy, 76 (11), p. 3037-3044. ISSN 0305-7453.

Titre du document
Efficacy of dihydroartemisinin/piperaquine in patients with non-complicated Plasmodium falciparum malaria in Yaounde, Cameroon
Année de publication
2021
Type de document
Article référencé dans le Web of Science WOS:000737577800041
Auteurs
Mairet-Khedim M., Nsango S., Ngou C., Menard S., Roesch C., Khim N., Srun S., Iriart X., Lanot T., Otam L., Abega F., Ayong L., Morlais Isabelle, Gandia P., Witkowski B., Berry A.
Source
Journal of Antimicrobial Chemotherapy, 2021, 76 (11), p. 3037-3044 ISSN 0305-7453
Background: Dihydroartemisinin/piperaquine is increasingly used for the treatment of uncomplicated Plasmodium falciparum malaria in Africa. The efficacy of this combination in Cameroon is poorly documented, while resistance to dihydroartemisinin/piperaquine readily spreads in Southeast Asia. Objectives: This study evaluated the clinical efficacy of dihydroartemisinin/piperaquine in Cameroon, as well as the molecular profile and phenotypic susceptibility of collected isolates to dihydroartemisinin and piperaquine. Patients and methods: Dihydroartemisinin/piperaquine efficacy in 42days was followed-up for 138 patients presenting non-complicated falciparum malaria. Piperaquine concentration was determined at day 7 for 124 patients. kelch13 gene polymorphisms (n=150) and plasmepsin2 gene amplification (n=148) were determined as molecular markers of resistance to dihydroartemisinin and piperaquine, respectively. Parasite susceptibility to dihydroartemisinin and piperaquine was determined using validated in vitro survival assays. Results: The efficacy of dihydroartemisinin/piperaquine treatment was 100% after PCR correction. The reinfections were not associated with a variation of piperaquine concentration at day 7. Ninety-six percent (144/150) of the samples presented a WT allele of the kelch13 gene. Two percent (3/150) presented the non-synonymous mutation A578S, which is not associated with resistance to dihydroartemisinin. No duplication of the plasmepsin2 gene was observed (0/148). All the samples tested in vitro by survival assays (n=87) were susceptible to dihydroartemisinin and piperaquine. Conclusions: Dihydroartemisinin/piperaquine has demonstrated excellent therapeutic efficacy with no evidence of emerging artemisinin or piperaquine resistance in Yaounde, Cameroon. This observation suggests that dihydroartemisinin/piperaquine could be a sustainable therapeutic solution for P. falciparum malaria if implemented in areas previously free of artemisinin- and piperaquine-resistant parasites, unlike Southeast Asia.
Plan de classement
Santé : généralités [050] ; Entomologie médicale / Parasitologie / Virologie [052]
Description Géographique
CAMEROUN ; YAOUNDE
Localisation
Fonds IRD
Identifiant IRD
PAR00023799
Contact