Javascript must be enabled to continue!
Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment
View through CrossRef
Abstract
Background
Artemisinin-based combinations differ in their impact on gametocyte prevalence and density. This study assessed female and male gametocyte dynamics after treating children with uncomplicated Plasmodium falciparum malaria with either pyronaridine–artesunate (PA) or artemether–lumefantrine (AL).
Methods
Kenyan children with uncomplicated Plasmodium falciparum malaria were included and randomly assigned to PA or AL treatment. Filter paper blood samples were collected as a source of RNA for quantitative reverse-transcription PCR (qRT-PCR) and nucleic acid sequence based amplification (QT-NASBA) to detect female gametocytes (targeting Pfs25 mRNA). Male gametocytes were detected by qRT-PCR (targeting PfMGET mRNA). Duration of gametocyte carriage, the female and male gametocyte response and the agreement between qRT-PCR and QT-NASBA were determined.
Results
The mean duration of female gametocyte carriage was significantly longer for PA (4.9 days) than for AL (3.8 days) as estimated by QT-NASBA (P = 0.036), but this difference was less clear when determined by Pfs25 qRT-PCR (4.5 days for PA and 3.7 for AL, P = 0.166). qRT-PCR based female gametocyte prevalence decreased from 100% (75/75) at baseline to 6.06% (4/66) at day 14 in the AL group and from 97.7% (83/85) to 13.9% (11/79) in the PA group. Male gametocyte prevalence decreased from 41.3% (31/75) at baseline to 19.7% (13/66) at day 14 in the AL group and from 35.3% (30/85) to 22.8% (18/79) in the PA group. There was good agreement between Pfs25 qRT-PCR and QT-NASBA female gametocyte prevalence (0.85, 95% CI 0.82–0.87).
Conclusions
This study indicates that female gametocyte clearance may be slightly faster after AL compared to PA. Male gametocytes showed similar post-treatment clearance between study arms. Future studies should further address potential differences between the post-treatment transmission potential after PA compared to AL.
Trial registration This study is registered at clinicaltrials.gov under NCT02411994. Registration date: 8 April 2015. https://clinicaltrials.gov/ct2/show/NCT02411994?term=pyronaridine-artesunate&cond=Malaria&cntry=KE&rank=1
Springer Science and Business Media LLC
Title: Plasmodium falciparum gametocyte dynamics after pyronaridine–artesunate or artemether–lumefantrine treatment
Description:
Abstract
Background
Artemisinin-based combinations differ in their impact on gametocyte prevalence and density.
This study assessed female and male gametocyte dynamics after treating children with uncomplicated Plasmodium falciparum malaria with either pyronaridine–artesunate (PA) or artemether–lumefantrine (AL).
Methods
Kenyan children with uncomplicated Plasmodium falciparum malaria were included and randomly assigned to PA or AL treatment.
Filter paper blood samples were collected as a source of RNA for quantitative reverse-transcription PCR (qRT-PCR) and nucleic acid sequence based amplification (QT-NASBA) to detect female gametocytes (targeting Pfs25 mRNA).
Male gametocytes were detected by qRT-PCR (targeting PfMGET mRNA).
Duration of gametocyte carriage, the female and male gametocyte response and the agreement between qRT-PCR and QT-NASBA were determined.
Results
The mean duration of female gametocyte carriage was significantly longer for PA (4.
9 days) than for AL (3.
8 days) as estimated by QT-NASBA (P = 0.
036), but this difference was less clear when determined by Pfs25 qRT-PCR (4.
5 days for PA and 3.
7 for AL, P = 0.
166).
qRT-PCR based female gametocyte prevalence decreased from 100% (75/75) at baseline to 6.
06% (4/66) at day 14 in the AL group and from 97.
7% (83/85) to 13.
9% (11/79) in the PA group.
Male gametocyte prevalence decreased from 41.
3% (31/75) at baseline to 19.
7% (13/66) at day 14 in the AL group and from 35.
3% (30/85) to 22.
8% (18/79) in the PA group.
There was good agreement between Pfs25 qRT-PCR and QT-NASBA female gametocyte prevalence (0.
85, 95% CI 0.
82–0.
87).
Conclusions
This study indicates that female gametocyte clearance may be slightly faster after AL compared to PA.
Male gametocytes showed similar post-treatment clearance between study arms.
Future studies should further address potential differences between the post-treatment transmission potential after PA compared to AL.
Trial registration This study is registered at clinicaltrials.
gov under NCT02411994.
Registration date: 8 April 2015.
https://clinicaltrials.
gov/ct2/show/NCT02411994?term=pyronaridine-artesunate&cond=Malaria&cntry=KE&rank=1.
Related Results
Efficacy and Safety of Pyronaridine-Artesunate Versus Artemether-Lumefantrine in the Treatment of Acute Uncomplicated Malaria in Children in South-West Nigeria: An open- labelled randomized controlled trial
Efficacy and Safety of Pyronaridine-Artesunate Versus Artemether-Lumefantrine in the Treatment of Acute Uncomplicated Malaria in Children in South-West Nigeria: An open- labelled randomized controlled trial
Abstract
Background: Declining responsiveness to artemether-lumefantrine (AL), the ACT of choice since 2005, has been reported in Nigeria. Pyronaridine-artesunate (PA) is a...
Population pharmacokinetics of artemether–lumefantrine plus amodiaquine in patients with uncomplicated
Plasmodium falciparum
malaria
Population pharmacokinetics of artemether–lumefantrine plus amodiaquine in patients with uncomplicated
Plasmodium falciparum
malaria
Aims
Resistance to the artemisinins and the artemisinin‐based combination therapy (ACT) partner drugs has developed in Southeast Asia, and artemisinin resistanc...
Possible mechanisms of the hypoglycaemic effect of artesunate: Gender implication
Possible mechanisms of the hypoglycaemic effect of artesunate: Gender implication
Abstract
Background
Artesunate is an antimalarial drug that affects glucose homeostasis but the mechanism of its glucose-modulating effect is not fully understood especial...
Efficacy and tolerability of artemether–lumefantrine and pyronaridine-artesunate for uncomplicated Plasmodium falciparum malaria in Niger
Efficacy and tolerability of artemether–lumefantrine and pyronaridine-artesunate for uncomplicated Plasmodium falciparum malaria in Niger
Abstract
Background
Following the WHO recommendation for the use of Artemisinin based combination for treatment of uncomplicate...
Gametocyte clearance in children, from western Kenya, with uncomplicated Plasmodium falciparum malaria after artemether–lumefantrine or dihydroartemisinin–piperaquine treatment
Gametocyte clearance in children, from western Kenya, with uncomplicated Plasmodium falciparum malaria after artemether–lumefantrine or dihydroartemisinin–piperaquine treatment
Abstract
Background
The efficacy and safety of artemether–lumefantrine (AL) and dihydroartemisinin–piperaquine (DP) against asexual parasites population has been documented. Howeve...
Therapeutic Efficacy of Artemether-Lumefantrine (AL) plus Single Low Dose Primaquine for the treatment of uncomplicated
falciparum
malaria in a high transmission setting, Western Ethiopia
Therapeutic Efficacy of Artemether-Lumefantrine (AL) plus Single Low Dose Primaquine for the treatment of uncomplicated
falciparum
malaria in a high transmission setting, Western Ethiopia
Abstract
Background
The development and spread of drug-resistant parasites continue to threaten the move t...
In vitro study of the interaction between artemether-lumefantrine and ciprofloxacin/metronidazole
In vitro study of the interaction between artemether-lumefantrine and ciprofloxacin/metronidazole
This study investigated the in vitro interactions between artemether-lumefantrine and ciprofloxacin or metronidazole in their co-administration. Commercial brands of artemether-lum...
Improved antimalarial activity of caprol-based nanostructured lipid carriers encapsulating artemether-lumefantrine for oral administration
Improved antimalarial activity of caprol-based nanostructured lipid carriers encapsulating artemether-lumefantrine for oral administration
Background: Artemether and lumefantrine display low aqueous solubility leading to poor release profile; hence the need for the use of lipid-based systems to improve their oral bioa...

