Abstract

BackgroundDrug resistance in Plasmodiumfalciparum has posed an obstacle to effective treatment and challenges many malaria control programmes in endemic areas. In Angola, until 2003, chloroquine (CQ) was used as first-line therapy for uncomplicated malaria. It was replaced initially by amodiaquine and, in 2006, by artemisinin-based combination therapy (ACT) with artemether-lumefantrine (AL, Coartem®). Efficacy study of ACT, conducted in Angola between 2004 and 2005, showed a baseline efficacy of ≈99 %.Methods103 malaria patients were enrolled according to WHO proceedings. Patients were followed up with clinical and parasitological evaluations for 28 days, parasite density and identification was evaluated by microscopy, the pfmsp2 were genotyped by nested-PCR, to distinguish parasite recrudescence from new infections; the polymorphisms at codons 86 and 1246 of pfmdr1 gene, and 769 of pfatp6 gene were assessed by PCR–RFLP and sequencing for pfk13-propeller genotype.ResultsThe cure rate was 91.3 %. The obtained results showed that from 103 patients, 12.6 % (n = 13) still had parasitaemia 1 day after the treatment was finished. On day 0, of the 94 evaluated samples, wild-type alleles were identified in 73.4 % (n = 69) for pfmdr1 N86Y position and only one sample carried the mutant allele (Y) for pfmdr1 1246; 14 % of these samples showed increased pfmdr1 copy number; 100 % (n = 21) had wild-type allele of k13 gene in all the studied positions.DiscussionThese results showed changes in parasite profile susceptibility to AL in comparison to the baseline data from 2002 to 2004 and on the genotyping characteristics; the clinical outcome after treatment with AL did not link a particular genotype with treatment failure; observed changes do not provide sufficient evidence for a treatment policy change, but they suggest that a carefully monitoring is needed in this area.

Highlights

  • Drug resistance in Plasmodium falciparum has posed an obstacle to effective treatment and challenges many malaria control programmes in endemic areas

  • The present study aims to evaluate the therapeutic efficacy of Coartem® for the treatment of uncomplicated P. falciparum infection, in Luanda, Angola, and to analyse the polymorphisms in pfmdr1, pfatp6, and K13 genes previously associated to susceptibility to AL, 6 years after its introduction on this area

  • The cure rate (91.2 %) found in this study suggests that, in accordance with World Health Organization (WHO) parameters, AL is still effective as first-line drug for uncomplicated malaria treatment in Angola, but an regular monitoring is necessary

Read more

Summary

Introduction

Drug resistance in Plasmodium falciparum has posed an obstacle to effective treatment and challenges many malaria control programmes in endemic areas. According to an unpublished report (2014) of National Malaria Control Programme (NMCP), between 2010 and 2012 deaths attributed to malaria decreased from 8114 to 5736, but in 2013, 1,999,868 cases and 7300 deaths due to malaria were reported [2]. In this endemic country, malaria infection is still the major cause of morbidity and mortality, accounting for 25 % of health care demands, 20 % of hospitalization requirements, 40 % of perinatal death, 25 % of maternal death and is the main reason of absenteeism, both at work and in schools [5]

Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call