Effects of artemisinin derivatives on malaria transmissibility

Background. On the western border of Thailand the efficacy of mefloquine in the treatment of falciparum malaria has declined while gametocyte carriage rates have increased, which suggests increased transmissibility of these resistant infections. We compared the following antimalarial drugs in relati...

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Main Authors: R. N. Price, F. Nosten, C. Luxemburger, F. O. Ter Kuile, L. Paiphun, T. Chongsuphajaisiddhi, N. J. White
Other Authors: Shoklo Malaria Research Unit
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Published: 2018
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Online Access:https://repository.li.mahidol.ac.th/handle/123456789/17727
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spelling th-mahidol.177272018-07-04T14:29:13Z Effects of artemisinin derivatives on malaria transmissibility R. N. Price F. Nosten C. Luxemburger F. O. Ter Kuile L. Paiphun T. Chongsuphajaisiddhi N. J. White Shoklo Malaria Research Unit Mahidol University John Radcliffe Hospital University of Amsterdam Medicine Background. On the western border of Thailand the efficacy of mefloquine in the treatment of falciparum malaria has declined while gametocyte carriage rates have increased, which suggests increased transmissibility of these resistant infections. We compared the following antimalarial drugs in relation to subsequent Plasmodium falciparum gametocyte carriage: mefloquine, halofantrine, quinine, and the artemisinin derivatives. Methods. Between 1990 and 1995 we assessed gametocytaemia in a series of prospective studies of antimalarial drug treatment in 5193 adults and children with acute uncomplicated falciparum malaria in an area of malarious hill forest on the western border of Thailand. Weekly parasite counts from thick and thin blood films were done during the 4-week (1990-93) or 9-week (1993-95) follow-up period. Gametocyte positivity rates and person gametocyte week (PGW) rates were calculated to measure gametocyte carriage and transmission potential. Findings. In primary P falciparum infections the gametocyte carriage rate was significantly higher after treatment with mefloquine than after treatment with the artemisinin derivatives (PGW 34.1 [95% CI 25.2-42.9] vs 3.9 [1.9-5.9] per 1000 person weeks; relative risk 8.0 [4.1-15.6]; p < 0.0001). Recrudescent infections were associated with increased gametocyte carrier rates (relative risk 2.2 [1.6-3.0]; p < 0.0001), but retreatment with artemisinin derivatives reduced subsequent gametocyte carriage 18.5 fold [3.5-98] compared with mefloquine retreatment and 6.8 fold (3.1-15.1) compared with quinine retreatment (p < 0.001). The introduction of the artemisinin derivatives in routine treatment at this study site in mid 1994 was associated with a reduction in the subsequent incidence of falciparum malaria of 47 (25-69)%. Interpretation. Although environmental changes affect vector numbers, and hence malaria incidence, artemisinin derivatives were found to reduce the transmission potential of falciparum malaria, Widespread introduction of artemisinin derivatives in the treatment of falciparum malaria may prevent the spread of multidrug resistance. 2018-07-04T07:29:13Z 2018-07-04T07:29:13Z 1996-06-15 Article Lancet. Vol.347, No.9016 (1996), 1654-1658 10.1016/S0140-6736(96)91488-9 01406736 2-s2.0-0029948433 https://repository.li.mahidol.ac.th/handle/123456789/17727 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0029948433&origin=inward
institution Mahidol University
building Mahidol University Library
continent Asia
country Thailand
Thailand
content_provider Mahidol University Library
collection Mahidol University Institutional Repository
topic Medicine
spellingShingle Medicine
R. N. Price
F. Nosten
C. Luxemburger
F. O. Ter Kuile
L. Paiphun
T. Chongsuphajaisiddhi
N. J. White
Effects of artemisinin derivatives on malaria transmissibility
description Background. On the western border of Thailand the efficacy of mefloquine in the treatment of falciparum malaria has declined while gametocyte carriage rates have increased, which suggests increased transmissibility of these resistant infections. We compared the following antimalarial drugs in relation to subsequent Plasmodium falciparum gametocyte carriage: mefloquine, halofantrine, quinine, and the artemisinin derivatives. Methods. Between 1990 and 1995 we assessed gametocytaemia in a series of prospective studies of antimalarial drug treatment in 5193 adults and children with acute uncomplicated falciparum malaria in an area of malarious hill forest on the western border of Thailand. Weekly parasite counts from thick and thin blood films were done during the 4-week (1990-93) or 9-week (1993-95) follow-up period. Gametocyte positivity rates and person gametocyte week (PGW) rates were calculated to measure gametocyte carriage and transmission potential. Findings. In primary P falciparum infections the gametocyte carriage rate was significantly higher after treatment with mefloquine than after treatment with the artemisinin derivatives (PGW 34.1 [95% CI 25.2-42.9] vs 3.9 [1.9-5.9] per 1000 person weeks; relative risk 8.0 [4.1-15.6]; p < 0.0001). Recrudescent infections were associated with increased gametocyte carrier rates (relative risk 2.2 [1.6-3.0]; p < 0.0001), but retreatment with artemisinin derivatives reduced subsequent gametocyte carriage 18.5 fold [3.5-98] compared with mefloquine retreatment and 6.8 fold (3.1-15.1) compared with quinine retreatment (p < 0.001). The introduction of the artemisinin derivatives in routine treatment at this study site in mid 1994 was associated with a reduction in the subsequent incidence of falciparum malaria of 47 (25-69)%. Interpretation. Although environmental changes affect vector numbers, and hence malaria incidence, artemisinin derivatives were found to reduce the transmission potential of falciparum malaria, Widespread introduction of artemisinin derivatives in the treatment of falciparum malaria may prevent the spread of multidrug resistance.
author2 Shoklo Malaria Research Unit
author_facet Shoklo Malaria Research Unit
R. N. Price
F. Nosten
C. Luxemburger
F. O. Ter Kuile
L. Paiphun
T. Chongsuphajaisiddhi
N. J. White
format Article
author R. N. Price
F. Nosten
C. Luxemburger
F. O. Ter Kuile
L. Paiphun
T. Chongsuphajaisiddhi
N. J. White
author_sort R. N. Price
title Effects of artemisinin derivatives on malaria transmissibility
title_short Effects of artemisinin derivatives on malaria transmissibility
title_full Effects of artemisinin derivatives on malaria transmissibility
title_fullStr Effects of artemisinin derivatives on malaria transmissibility
title_full_unstemmed Effects of artemisinin derivatives on malaria transmissibility
title_sort effects of artemisinin derivatives on malaria transmissibility
publishDate 2018
url https://repository.li.mahidol.ac.th/handle/123456789/17727
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