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Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/36367
Title: Evidence of plasmodium falciparum malaria multidrug resistance to artemisinin and piperaquine in Western Cambodia: Dihydroartemisinin-piperaquine open-label multicenter clinical assessment
Authors: Rithea Leang
Walter R.J. Taylor
Denis Mey Bouth
Lijiang Song
Joel Tarning
Meng Chuor Char
Saorin Kim
Benoit Witkowski
Valentine Duru
Anais Domergue
Nimol Khim
Pascal Ringwald
Didier Menard
National Centre for Parasitology, Entomology and Malaria Control
Hopitaux universitaires de Geneve
Organisation Mondiale de la Sante
Mahidol University
University of Oxford
Institut Pasteur du Cambodge
Keywords: Medicine
Issue Date: 1-Aug-2015
Citation: Antimicrobial Agents and Chemotherapy. Vol.59, No.8 (2015), 4719-4726
Abstract: Copyright © 2015, American Society for Microbiology. All Rights Reserved. Western Cambodia is recognized as the epicenter of Plasmodium falciparum multidrug resistance. Recent reports of the efficacy of dihydroartemisinin (DHA)-piperaquine (PP), the latest of the artemisinin-based combination therapies (ACTs) recommended by the WHO, have prompted further investigations. The clinical efficacy of dihydroartemisinin-piperaquine in uncomplicated falciparum malaria was assessed in western and eastern Cambodia over 42 days. Day 7 plasma piperaquine concentrations were measured and day 0 isolates tested for in vitro susceptibilities to piperaquine and mefloquine, polymorphisms in the K13 gene, and the copy number of the Pfmdr-1 gene. A total of 425 patients were recruited in 2011 to 2013. The proportion of patients with recrudescent infections was significantly higher in western (15.4%) than in eastern (2.5%) Cambodia (P <10-3). Day 7 plasma PP concentrations and median 50% inhibitory concentrations (IC50) of PP were independent of treatment outcomes, in contrast to median mefloquine IC50, which were found to be lower for isolates from patients with recrudescent infections (18.7 versus 39.7 nM; P = 0.005). The most significant risk factor associated with DHA-PP treatment failure was infection by parasites carrying the K13 mutant allele (odds ratio [OR], 17.5; 95% confidence interval [CI], 1 to 308; P = 0.04). Our data show evidence of P. falciparum resistance to PP in western Cambodia, an area of widespread artemisinin resistance. New therapeutic strategies, such as the use of triple ACTs, are urgently needed and must be tested. (This study has been registered at the Australian New Zealand Clinical Trials Registry under registration no. ACTRN12614000344695.)
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84939832774&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/36367
ISSN: 10986596
00664804
Appears in Collections:Scopus 2011-2015

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