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Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar

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...

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Autores principales: Kyaw, Myat P., Nyunt, Myat H., Chit, Khin, Aye, Moe M., Aye, Kyin H., Lindegardh, Niklas, Tarning, Joel, Imwong, Mallika, Jacob, Christopher G., Rasmussen, Charlotte, Perin, Jamie, Ringwald, Pascal, Nyunt, Myaing M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592920/
https://www.ncbi.nlm.nih.gov/pubmed/23520478
http://dx.doi.org/10.1371/journal.pone.0057689
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author Kyaw, Myat P.
Nyunt, Myat H.
Chit, Khin
Aye, Moe M.
Aye, Kyin H.
Aye, Moe M.
Lindegardh, Niklas
Tarning, Joel
Imwong, Mallika
Jacob, Christopher G.
Rasmussen, Charlotte
Perin, Jamie
Ringwald, Pascal
Nyunt, Myaing M.
author_facet Kyaw, Myat P.
Nyunt, Myat H.
Chit, Khin
Aye, Moe M.
Aye, Kyin H.
Aye, Moe M.
Lindegardh, Niklas
Tarning, Joel
Imwong, Mallika
Jacob, Christopher G.
Rasmussen, Charlotte
Perin, Jamie
Ringwald, Pascal
Nyunt, Myaing M.
author_sort Kyaw, Myat P.
collection PubMed
description 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. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ACTRN12610000896077
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spelling pubmed-35929202013-03-21 Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar Kyaw, Myat P. Nyunt, Myat H. Chit, Khin Aye, Moe M. Aye, Kyin H. Aye, Moe M. Lindegardh, Niklas Tarning, Joel Imwong, Mallika Jacob, Christopher G. Rasmussen, Charlotte Perin, Jamie Ringwald, Pascal Nyunt, Myaing M. PLoS One Research Article 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. TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry ACTRN12610000896077 Public Library of Science 2013-03-08 /pmc/articles/PMC3592920/ /pubmed/23520478 http://dx.doi.org/10.1371/journal.pone.0057689 Text en © 2013 Kyaw et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Kyaw, Myat P.
Nyunt, Myat H.
Chit, Khin
Aye, Moe M.
Aye, Kyin H.
Aye, Moe M.
Lindegardh, Niklas
Tarning, Joel
Imwong, Mallika
Jacob, Christopher G.
Rasmussen, Charlotte
Perin, Jamie
Ringwald, Pascal
Nyunt, Myaing M.
Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title_full Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title_fullStr Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title_full_unstemmed Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title_short Reduced Susceptibility of Plasmodium falciparum to Artesunate in Southern Myanmar
title_sort reduced susceptibility of plasmodium falciparum to artesunate in southern myanmar
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3592920/
https://www.ncbi.nlm.nih.gov/pubmed/23520478
http://dx.doi.org/10.1371/journal.pone.0057689
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