Determinants of primaquine and carboxyprimaquine exposures in children and adults with Plasmodium vivax malaria

Author:

Chu Cindy S,Watson James AORCID,Phyo Aung Pyae,Win Htun Htun,Yotyingaphiram Widi,Thinraow Suradet,Soe Nay Lin,Aung Aye Aye,Wilaisrisak Pornpimon,Puaprasert Kanokpich,Imwong MallikaORCID,Hanpithakpong Warunee,Blessborn Daniel,Tarning JoelORCID,Proux Stéphane,Ling Clare,Nosten François HORCID,White Nicholas J

Abstract

AbstractBackgroundPrimaquine is the only widely available drug for radical cure of Plasmodium vivax malaria. There is uncertainty whether the pharmacokinetic properties of primaquine are altered significantly in childhood or not.MethodsGlucose-6-phosphate dehydrogenase normal patients with uncomplicated P. vivax malaria were randomized to receive either chloroquine (25mg base/kg) or dihydroartemisinin-piperaquine (dihydroartemisinin 7mg/kg and piperaquine 55mg/kg) plus primaquine; given either as 0.5 mg base/kg/day for 14 days or 1 mg/kg/day for 7 days. Pre-dose day 7 venous plasma concentrations of chloroquine, desethylchloroquine, piperaquine, primaquine and carboxyprimaquine were measured. Methemoglobin levels were measured either daily or on days 1, 3, 6 and 13, and additionally on day 10 in the primaquine 14-day groups.ResultsDay 7 primaquine and carboxyprimaquine concentrations were available for 641 patients. After adjustment for the primaquine mg/kg daily dose, day of sampling, partner drug, and fever clearance, there was a significant non-linear relationship between age and trough primaquine and carboxyprimaquine concentrations, and day methemoglobin levels. Compared to adults 30 years of age, children 5 years of age had trough primaquine concentrations 0.53 (95% CI: 0.39-0.73) fold lower, trough carboxyprimaquine concentrations 0.45 (95% CI: 0.35-0.55) fold lower, and day 7 methemoglobin levels 0.87 (95% CI: 0.58-1.27) fold lower. Increasing concentrations of piperaquine and chloroquine and poor metabolizer CYP 2D6 alleles were associated with higher day 7 primaquine and carboxyprimaquine concentrations. Higher blood methemoglobin concentrations were associated with a lower risk of recurrence.ConclusionYoung children have lower primaquine and carboxyprimaquine exposures, and lower levels of methemoglobinemia, than adults. Young children may need higher weight adjusted primaquine doses than adults.

Publisher

Cold Spring Harbor Laboratory

Reference27 articles.

1. World Health Organization. 2015. Guidelines for the treatment of malaria, 3rd Edition. World Health Organization, Geneva.

2. Pharmacokinetic Properties of Single-Dose Primaquine in Papua New Guinean Children: Feasibility of Abbreviated High-Dose Regimens for Radical Cure of Vivax Malaria

3. Age, weight, and CYP2D6 genotype are major determinants of primaquine pharmacokinetics in African children;Antimicrob Agents Chemother Agents Chemother,2017

4. Doses of primaquine administered to children with Plasmodium vivax according to an age-based dose regimen;Pathog Glob Health,2020

5. Evaluation of pharmacokinetics of single-dose primaquine in undernourished versus normally nourished children diagnosed with Plasmodium vivax malaria in Mumbai;J Postgrad Med,2021

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