Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar

被引:165
作者
Kyaw, Myat P. [1 ]
Nyunt, Myat H. [1 ]
Chit, Khin [1 ]
Aye, Moe M. [1 ]
Aye, Kyin H. [1 ]
Aye, Moe M. [1 ]
Lindegardh, Niklas [2 ,3 ]
Tarning, Joel [2 ,3 ]
Imwong, Mallika [4 ]
Jacob, Christopher G. [5 ]
Rasmussen, Charlotte [6 ]
Perin, Jamie [7 ]
Ringwald, Pascal [6 ]
Nyunt, Myaing M. [7 ,8 ]
机构
[1] Dept Med Res Lower Myanmar, Yangon, Myanmar
[2] Mahidol Univ, Mahidol Oxford Trop Med Res Unit, Bangkok 10700, Thailand
[3] Univ Oxford, Nuffield Dept Clin Med, Ctr Trop Med, Oxford, England
[4] Mahidol Univ, Dept Mol Trop Med & Genet, Bangkok 10700, Thailand
[5] Univ Maryland, Sch Med, Howard Hughes Med Inst, Ctr Vaccine Dev,Malaria Grp, Baltimore, MD 21201 USA
[6] WHO, Global Malaria Programme, Drug Resistance & Containment Unit, CH-1211 Geneva, Switzerland
[7] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Int Hlth, Baltimore, MD 21218 USA
[8] Johns Hopkins Univ, Sch Med, Div Clin Pharmacol, Baltimore, MD USA
来源
PLOS ONE | 2013年 / 8卷 / 03期
关键词
ARTEMISININ-RESISTANT MALARIA; PARASITE CLEARANCE; NO EVIDENCE; DIHYDROARTEMISININ; BIOAVAILABILITY; PROVINCE; SPREAD;
D O I
10.1371/journal.pone.0057689
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Plasmodium falciparum resistance to artemisinins, the first line treatment for malaria worldwide, has been reported in western Cambodia. Resistance is characterized by significantly delayed clearance of parasites following artemisinin treatment. Artemisinin resistance has not previously been reported in Myanmar, which has the highest falciparum malaria burden among Southeast Asian countries. Methods: A non-randomized, single-arm, open-label clinical trial of artesunate monotherapy (4 mg/kg daily for seven days) was conducted in adults with acute blood-smear positive P. falciparum malaria in Kawthaung, southern Myanmar. Parasite density was measured every 12 hours until two consecutive negative smears were obtained. Participants were followed weekly at the study clinic for three additional weeks. Co-primary endpoints included parasite clearance time (the time required for complete clearance of initial parasitemia), parasite clearance half-life (the time required for parasitemia to decrease by 50% based on the linear portion of the parasite clearance slope), and detectable parasitemia 72 hours after commencement of artesunate treatment. Drug pharmacokinetics were measured to rule out delayed clearance due to suboptimal drug levels. Results: The median (range) parasite clearance half-life and time were 4.8 (2.1-9.7) and 60 (24-96) hours, respectively. The frequency distributions of parasite clearance half-life and time were bimodal, with very slow parasite clearance characteristic of the slowest-clearing Cambodian parasites (half-life longer than 6.2 hours) in approximately 1/3 of infections. Fourteen of 52 participants (26.9%) had a measurable parasitemia 72 hours after initiating artesunate treatment. Parasite clearance was not associated with drug pharmacokinetics. Conclusions: A subset of P. falciparum infections in southern Myanmar displayed markedly delayed clearance following artemisinin treatment, suggesting either emergence of artemisinin resistance in southern Myanmar or spread to this location from its site of origin in western Cambodia. Resistance containment efforts are underway in Myanmar.
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