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Am J Trop Med Hyg ; 111(1): 43-47, 2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38806022

ABSTRACT

Increasing antimicrobial resistance (AMR) is a global public health emergency. Although chemoprevention has improved malaria-related pregnancy outcomes, the downstream effects on AMR have not been characterized. We compared the abundance of 10 AMR genes in stool samples from pregnant women receiving sulfadoxine-pyrimethamine (SP) as intermittent preventive treatment against malaria in pregnancy (IPTp) to that in samples from women receiving dihydroartemisinin-piperaquine (DP) for IPTp. All participants had at least one AMR gene at baseline. Mean quantities of the antifolate gene dfrA17 were increased after two or more doses of SP (mean difference = 1.6, 95% CI: 0.4-2.7, P = 0.008). Antimicrobial resistance gene abundance tended to increase from baseline in SP recipients compared with a downward trend in the DP group. Overall, IPTp-SP had minimal effects on the abundance of antifolate resistance genes (except for dfrA17), potentially owing to a high starting prevalence. However, the trend toward increasing AMR in SP recipients warrants further studies.


Subject(s)
Antimalarials , Artemisinins , Drug Combinations , Feces , Pyrimethamine , Quinolines , Sulfadoxine , Humans , Female , Pyrimethamine/therapeutic use , Pyrimethamine/administration & dosage , Pyrimethamine/pharmacology , Sulfadoxine/therapeutic use , Sulfadoxine/administration & dosage , Sulfadoxine/pharmacology , Pregnancy , Antimalarials/therapeutic use , Antimalarials/pharmacology , Antimalarials/administration & dosage , Quinolines/therapeutic use , Quinolines/administration & dosage , Artemisinins/therapeutic use , Artemisinins/pharmacology , Artemisinins/administration & dosage , Adult , Feces/microbiology , Young Adult , Pregnancy Complications, Parasitic/prevention & control , Pregnancy Complications, Parasitic/drug therapy , Drug Resistance/genetics , Malaria, Falciparum/prevention & control , Malaria, Falciparum/epidemiology , Plasmodium falciparum/drug effects , Plasmodium falciparum/genetics , Piperazines
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