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Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance

BACKGROUND: Spreading Plasmodium falciparum artemisinin drug resistance threatens global malaria public health gains. Limited data exist to define the extent of P. falciparum artemisinin resistance southeast of the Greater Mekong region in Malaysia. METHODS: A clinical efficacy study of oral artesun...

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Autores principales: Grigg, Matthew J., William, Timothy, Piera, Kim A., Rajahram, Giri S., Jelip, Jenarun, Aziz, Ammar, Menon, Jayaram, Marfurt, Jutta, Price, Ric N., Auburn, Sarah, Barber, Bridget E., Yeo, Tsin W., Anstey, Nicholas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287347/
https://www.ncbi.nlm.nih.gov/pubmed/30526613
http://dx.doi.org/10.1186/s12936-018-2593-x
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author Grigg, Matthew J.
William, Timothy
Piera, Kim A.
Rajahram, Giri S.
Jelip, Jenarun
Aziz, Ammar
Menon, Jayaram
Marfurt, Jutta
Price, Ric N.
Auburn, Sarah
Barber, Bridget E.
Yeo, Tsin W.
Anstey, Nicholas M.
author_facet Grigg, Matthew J.
William, Timothy
Piera, Kim A.
Rajahram, Giri S.
Jelip, Jenarun
Aziz, Ammar
Menon, Jayaram
Marfurt, Jutta
Price, Ric N.
Auburn, Sarah
Barber, Bridget E.
Yeo, Tsin W.
Anstey, Nicholas M.
author_sort Grigg, Matthew J.
collection PubMed
description BACKGROUND: Spreading Plasmodium falciparum artemisinin drug resistance threatens global malaria public health gains. Limited data exist to define the extent of P. falciparum artemisinin resistance southeast of the Greater Mekong region in Malaysia. METHODS: A clinical efficacy study of oral artesunate (total target dose 12 mg/kg) daily for 3 days was conducted in patients with uncomplicated falciparum malaria and a parasite count < 100,000/µL admitted to 3 adjacent district hospitals in Sabah, East Malaysia. On day 3 and 4 all patients were administered split dose mefloquine (total dose 25 mg/kg) and followed for 28 days. Twenty-one kelch13 polymorphisms associated with P. falciparum artemisinin resistance were also evaluated in P. falciparum isolates collected from patients presenting to health facilities predominantly within the tertiary referral area of western Sabah between 2012 and 2016. RESULTS: In total, 49 patients were enrolled and treated with oral artesunate. 90% (44/49) of patients had cleared their parasitaemia by 48 h and 100% (49/49) within 72 h. The geometric mean parasite count at presentation was 9463/µL (95% CI 6757–13,254), with a median time to 50% parasite clearance of 4.3 h (IQR 2.0–8.4). There were 3/45 (7%) patients with a parasite clearance slope half-life of ≥ 5 h. All 278 P. falciparum isolates evaluated were wild-type for kelch13 markers. CONCLUSION: There is no suspected or confirmed evidence of endemic artemisinin-resistant P. falciparum in this pre-elimination setting in Sabah, Malaysia. Current guidelines recommending first-line treatment with ACT remain appropriate for uncomplicated malaria in Sabah, Malaysia. Ongoing surveillance is needed southeast of the Greater Mekong sub-region. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2593-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-62873472018-12-14 Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance Grigg, Matthew J. William, Timothy Piera, Kim A. Rajahram, Giri S. Jelip, Jenarun Aziz, Ammar Menon, Jayaram Marfurt, Jutta Price, Ric N. Auburn, Sarah Barber, Bridget E. Yeo, Tsin W. Anstey, Nicholas M. Malar J Research BACKGROUND: Spreading Plasmodium falciparum artemisinin drug resistance threatens global malaria public health gains. Limited data exist to define the extent of P. falciparum artemisinin resistance southeast of the Greater Mekong region in Malaysia. METHODS: A clinical efficacy study of oral artesunate (total target dose 12 mg/kg) daily for 3 days was conducted in patients with uncomplicated falciparum malaria and a parasite count < 100,000/µL admitted to 3 adjacent district hospitals in Sabah, East Malaysia. On day 3 and 4 all patients were administered split dose mefloquine (total dose 25 mg/kg) and followed for 28 days. Twenty-one kelch13 polymorphisms associated with P. falciparum artemisinin resistance were also evaluated in P. falciparum isolates collected from patients presenting to health facilities predominantly within the tertiary referral area of western Sabah between 2012 and 2016. RESULTS: In total, 49 patients were enrolled and treated with oral artesunate. 90% (44/49) of patients had cleared their parasitaemia by 48 h and 100% (49/49) within 72 h. The geometric mean parasite count at presentation was 9463/µL (95% CI 6757–13,254), with a median time to 50% parasite clearance of 4.3 h (IQR 2.0–8.4). There were 3/45 (7%) patients with a parasite clearance slope half-life of ≥ 5 h. All 278 P. falciparum isolates evaluated were wild-type for kelch13 markers. CONCLUSION: There is no suspected or confirmed evidence of endemic artemisinin-resistant P. falciparum in this pre-elimination setting in Sabah, Malaysia. Current guidelines recommending first-line treatment with ACT remain appropriate for uncomplicated malaria in Sabah, Malaysia. Ongoing surveillance is needed southeast of the Greater Mekong sub-region. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12936-018-2593-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-10 /pmc/articles/PMC6287347/ /pubmed/30526613 http://dx.doi.org/10.1186/s12936-018-2593-x Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Grigg, Matthew J.
William, Timothy
Piera, Kim A.
Rajahram, Giri S.
Jelip, Jenarun
Aziz, Ammar
Menon, Jayaram
Marfurt, Jutta
Price, Ric N.
Auburn, Sarah
Barber, Bridget E.
Yeo, Tsin W.
Anstey, Nicholas M.
Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title_full Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title_fullStr Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title_full_unstemmed Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title_short Plasmodium falciparum artemisinin resistance monitoring in Sabah, Malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
title_sort plasmodium falciparum artemisinin resistance monitoring in sabah, malaysia: in vivo therapeutic efficacy and kelch13 molecular marker surveillance
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287347/
https://www.ncbi.nlm.nih.gov/pubmed/30526613
http://dx.doi.org/10.1186/s12936-018-2593-x
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