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Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali

BACKGROUND: Intermittent preventive treatment in infants (IPTi) with sulphadoxine-pyrimethamine (SP) given during routine vaccinations is efficacious in preventing malaria disease and shows no interaction with the vaccines. However, there is a fear that IPTi may result in a rapid increase of parasit...

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Autores principales: Dicko, Alassane, Sagara, Issaka, Djimdé, Abdoulaye A, Touré, Sidy O, Traore, Mariam, Dama, Souleymane, Diallo, Abdoulbaki I, Barry, Amadou, Dicko, Mohamed, Coulibaly, Oumar M, Rogier, Christophe, de Sousa, Alexandra, Doumbo, Ogobara K
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820043/
https://www.ncbi.nlm.nih.gov/pubmed/20064223
http://dx.doi.org/10.1186/1475-2875-9-9
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author Dicko, Alassane
Sagara, Issaka
Djimdé, Abdoulaye A
Touré, Sidy O
Traore, Mariam
Dama, Souleymane
Diallo, Abdoulbaki I
Barry, Amadou
Dicko, Mohamed
Coulibaly, Oumar M
Rogier, Christophe
de Sousa, Alexandra
Doumbo, Ogobara K
author_facet Dicko, Alassane
Sagara, Issaka
Djimdé, Abdoulaye A
Touré, Sidy O
Traore, Mariam
Dama, Souleymane
Diallo, Abdoulbaki I
Barry, Amadou
Dicko, Mohamed
Coulibaly, Oumar M
Rogier, Christophe
de Sousa, Alexandra
Doumbo, Ogobara K
author_sort Dicko, Alassane
collection PubMed
description BACKGROUND: Intermittent preventive treatment in infants (IPTi) with sulphadoxine-pyrimethamine (SP) given during routine vaccinations is efficacious in preventing malaria disease and shows no interaction with the vaccines. However, there is a fear that IPTi may result in a rapid increase of parasite resistance to SP. METHODS: To evaluate the impact of IPTi on SP-resistance point mutations, the 22 health sub-districts in the district of Kolokani, Mali, were randomized in a 1:1 ratio and starting in December 2006, IPTi with SP was implemented in 11 health sub-districts (intervention zone), while the other 11 health sub-districts served as the control (non-intervention zone). Blood smears and blood dots on filter paper were obtained from children aged 0-5 years, randomly selected in each of heath sub-districts during two cross-sectional surveys. The first survey was conducted in May 2007 before the start of the transmission season to collect baseline prevalence of the molecular markers of resistance to SP and the second in December 2007 after the end of the transmission season and one year after implementation of IPTi. A total of 427 and 923 randomly selected blood samples from the first and second surveys respectively were analysed by PCR for dhfr and dhps mutations. RESULTS: Each of the three dhfr mutations at codons 51, 59 and 108 was present in 35% and 57% of the samples during the two surveys with no significant differences between the two zones. Dhps mutations at codons 437 and 540 were present respectively in about 20% and 1% of the children during the two surveys in both zones at similar proportion. The prevalence of quadruple mutants (triple dhfr-mutants + dhps-437G) associated with in-vivo resistance to SP in Mali after one year implementation of IPTi was also similar between the two zones (11.6% versus 11.2%, p = 0.90) and to those obtained at baseline survey (10.3% versus 8.1%). CONCLUSION: This study shows no increase in the frequency of molecular markers of SP resistance in areas where IPTi with SP was implemented for one year.
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spelling pubmed-28200432010-02-11 Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali Dicko, Alassane Sagara, Issaka Djimdé, Abdoulaye A Touré, Sidy O Traore, Mariam Dama, Souleymane Diallo, Abdoulbaki I Barry, Amadou Dicko, Mohamed Coulibaly, Oumar M Rogier, Christophe de Sousa, Alexandra Doumbo, Ogobara K Malar J Research BACKGROUND: Intermittent preventive treatment in infants (IPTi) with sulphadoxine-pyrimethamine (SP) given during routine vaccinations is efficacious in preventing malaria disease and shows no interaction with the vaccines. However, there is a fear that IPTi may result in a rapid increase of parasite resistance to SP. METHODS: To evaluate the impact of IPTi on SP-resistance point mutations, the 22 health sub-districts in the district of Kolokani, Mali, were randomized in a 1:1 ratio and starting in December 2006, IPTi with SP was implemented in 11 health sub-districts (intervention zone), while the other 11 health sub-districts served as the control (non-intervention zone). Blood smears and blood dots on filter paper were obtained from children aged 0-5 years, randomly selected in each of heath sub-districts during two cross-sectional surveys. The first survey was conducted in May 2007 before the start of the transmission season to collect baseline prevalence of the molecular markers of resistance to SP and the second in December 2007 after the end of the transmission season and one year after implementation of IPTi. A total of 427 and 923 randomly selected blood samples from the first and second surveys respectively were analysed by PCR for dhfr and dhps mutations. RESULTS: Each of the three dhfr mutations at codons 51, 59 and 108 was present in 35% and 57% of the samples during the two surveys with no significant differences between the two zones. Dhps mutations at codons 437 and 540 were present respectively in about 20% and 1% of the children during the two surveys in both zones at similar proportion. The prevalence of quadruple mutants (triple dhfr-mutants + dhps-437G) associated with in-vivo resistance to SP in Mali after one year implementation of IPTi was also similar between the two zones (11.6% versus 11.2%, p = 0.90) and to those obtained at baseline survey (10.3% versus 8.1%). CONCLUSION: This study shows no increase in the frequency of molecular markers of SP resistance in areas where IPTi with SP was implemented for one year. BioMed Central 2010-01-10 /pmc/articles/PMC2820043/ /pubmed/20064223 http://dx.doi.org/10.1186/1475-2875-9-9 Text en Copyright ©2010 Dicko et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Dicko, Alassane
Sagara, Issaka
Djimdé, Abdoulaye A
Touré, Sidy O
Traore, Mariam
Dama, Souleymane
Diallo, Abdoulbaki I
Barry, Amadou
Dicko, Mohamed
Coulibaly, Oumar M
Rogier, Christophe
de Sousa, Alexandra
Doumbo, Ogobara K
Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title_full Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title_fullStr Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title_full_unstemmed Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title_short Molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in Mali
title_sort molecular markers of resistance to sulphadoxine-pyrimethamine one year after implementation of intermittent preventive treatment of malaria in infants in mali
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2820043/
https://www.ncbi.nlm.nih.gov/pubmed/20064223
http://dx.doi.org/10.1186/1475-2875-9-9
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