%0 Journal Article
%9 ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES
%A Ndounga, M.
%A Tahar, Rachida
%A Basco, Leonardo
%A Casimiro, P. N.
%A Malonga, D. A.
%A Ntoumi, F.
%T Therapeutic efficacy of sulfadoxine-pyrimethamine and the prevalence of molecular markers of resistance in under 5-year olds in Brazzaville, Congo
%D 2007
%L fdi:010040923
%G ENG
%J Tropical Medicine and International Health
%@ 1360-2276
%K plasmodium falciparum ; sulfadoxine pyrimethamine ; efficacy ; treatment failures ; dihydro folate ; reductase ; dihydropteroate synthase ; Brazzaville
%K CONGO
%K BRAZZAVILLE
%M ISI:000250920300005
%N 10
%P 1164-1171
%R 10.1111/j.1365-3156.2007.01904.x
%U https://www.documentation.ird.fr/hor/fdi:010040923
%> https://horizon.documentation.ird.fr/exl-doc/pleins_textes/2023-08/010040923.pdf
%V 12
%W Horizon (IRD)
%X OBJECTIVE To test the efficacy of sulfadoxine-pyremethamine (SP) monotherapy and establish the prevalence of mutations in dhfr and dhps in Brazzaville, Congo. METHOD We recruited 97 patients aged 6-59 months with uncomplicated malaria who attended Tenrikyo public health Centre. Eighty-three were followed until day 28. SP efficacy was determined by the WHO 28-day test and analysis of mutations in the Plasmodium falciparum dihydrofolate reductase (pfdhfr) and clihydropteroate synthase (pfhbps) genes. RESULTs There were seven (8.4%) early treatment failures, 23 late treatment failures (27.7%), nine (10.8%) late parasitological failures and 44 (53%) adequate clinical and parasitological responses (ACPR). After polymerase chain reaction (PCR) analysis of 64 available samples, the corrected results there were 44 (68.8%) ACPR and 19 recrudescent cases (31.2%). Approximately, 97.5% of samples bore the Asn51lle mutation, 66.2% the Cys59Arg mutation and 98.8% the Ser108Asn mutation. Mutations of dhps at positions 437 (Ala-Gly) and 436 (Ser-Ala) were found in 85% and 12.5% of samples. Quadruple mutations (pfdhfr triple mutations in codons 51, 59 and 108+ pfdhps mutation in 437) were found in 42 samples (52.5%) and associated with treatment failures. CONCLUSION This high level of treatment failures and mutations in both genes calls for the urgent application of the new policy for malaria treatment to delay the spread of SP resistance.
%$ 050 ; 052