Abstract | BACKGROUND: METHODS: Between 2009 and 2011, delivering women without human immunodeficiency virus infection were enrolled in an observational study of IPTp-SP effectiveness in Malawi. Parasites were detected by polymerase chain reaction (PCR); positive samples were sequenced to genotype the dhfr and dhps loci. The presence of K540 E: in dhps was used as a marker for the quintuple mutant. RESULTS: Samples from 1809 women were analyzed by PCR; 220 (12%) were positive for P. falciparum. A total of 202 specimens were genotyped at codon 581 of dhps; 17 (8.4%) harbored the sextuple mutant. The sextuple mutant was associated with higher risks of patent infection in peripheral blood (adjusted prevalence ratio [aPR], 2.76; 95% confidence interval [CI], 1.82-4.18) and placental blood (aPR 3.28; 95% CI, 1.88-5.78) and higher parasite densities. Recent SP use was not associated with increased parasite densities or placental pathology overall and among women with parasites carrying dhps A581 G: . CONCLUSIONS: IPTp-SP failed to inhibit parasite growth but did not exacerbate pathology among women infected with sextuple-mutant parasites. New interventions to prevent malaria during pregnancy are needed urgently.
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Authors | Julie Gutman, Linda Kalilani, Steve Taylor, Zhiyong Zhou, Ryan E Wiegand, Kyaw L Thwai, Dyson Mwandama, Carole Khairallah, Mwayi Madanitsa, Ebbie Chaluluka, Fraction Dzinjalamala, Doreen Ali, Don P Mathanga, Jacek Skarbinski, Ya Ping Shi, Steve Meshnick, Feiko O ter Kuile |
Journal | The Journal of infectious diseases
(J Infect Dis)
Vol. 211
Issue 12
Pg. 1997-2005
(Jun 15 2015)
ISSN: 1537-6613 [Electronic] United States |
PMID | 25564249
(Publication Type: Journal Article, Observational Study, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Copyright | Published by Oxford University Press on behalf of the Infectious Diseases Society of America 2015. This work is written by (a) US Government employee(s) and is in the public domain in the US. |
Chemical References |
- DNA, Protozoan
- Drug Combinations
- fanasil, pyrimethamine drug combination
- Sulfadoxine
- Tetrahydrofolate Dehydrogenase
- Dihydropteroate Synthase
- Pyrimethamine
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Topics |
- DNA, Protozoan
(chemistry, genetics)
- Dihydropteroate Synthase
(genetics)
- Drug Combinations
- Drug Resistance
- Female
- Genotype
- Humans
- Infant, Newborn
- Malaria, Falciparum
(parasitology, prevention & control)
- Malawi
- Mutation, Missense
- Plasmodium falciparum
(enzymology, genetics, isolation & purification)
- Point Mutation
- Polymerase Chain Reaction
- Pregnancy
- Pyrimethamine
(pharmacology, therapeutic use)
- Sequence Analysis, DNA
- Sulfadoxine
(pharmacology, therapeutic use)
- Tetrahydrofolate Dehydrogenase
(genetics)
- Treatment Outcome
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