| Mamoudou Cisse, Gordon A Awandare, Alamissa Soulama, Halidou Tinto, Marie-Pierre Hayette, Robert T Guiguemdé Recent uptake of intermittent preventive treatment during pregnancy with sulfadoxine-pyrimethamine is associated with increased prevalence of Pfdhfr mutations in Bobo-Dioulasso, Burkina Faso (Journal Article) In: Malar. J., vol. 16, no. 1, pp. 38, 2017, ISSN: 1475-2875. @article{Cisse2017-td,
title = {Recent uptake of intermittent preventive treatment during pregnancy with sulfadoxine-pyrimethamine is associated with increased prevalence of Pfdhfr mutations in Bobo-Dioulasso, Burkina Faso},
author = {Mamoudou Cisse and Gordon A Awandare and Alamissa Soulama and Halidou Tinto and Marie-Pierre Hayette and Robert T Guiguemd\'{e}},
doi = {10.1186/s12936-017-1695-1},
issn = {1475-2875},
year = {2017},
date = {2017-01-01},
urldate = {2017-01-01},
journal = {Malar. J.},
volume = {16},
number = {1},
pages = {38},
abstract = {BACKGROUND: The impact of sulfadoxine-pyrimethamine (SP) used as
intermittent preventive treatment during pregnancy (IPTp-SP) on
mutant parasite selection has been poorly documented in Burkina
Faso. This study sought first to explore the relationship between
IPTp-SP and the presence of mutant parasites. Second, to assess
the relationship between the mutant parasites and adverse
pregnancy outcomes. METHODS: From September to December 2010,
dried blood spots (DBS) were collected during antenatal care
visits and at delivery from 109 pregnant women with
microscopically confirmed falciparum malaria infection. DBS were
analysed by PCR-restriction fragment length polymorphism
(PCR-RFLP) for the polymorphisms at codons 51, 59, 108, and 164
of the Pfdhfr gene and codons 437 and 540 in the Pfdhps gene.
RESULTS: Both the Pfdhfr and Pfdhps genes were successfully
genotyped in 92.7% (101/109) of the samples. The prevalence of
Pfdhfr mutations N51I, C59R and S108N was 71.3, 42.6 and 64.4%,
respectively. Overall, 80.2% (81/101) of samples carried the
Pfdhps A437G mutation. None of the samples had the Pfdhfr I164L
and the Pfdhps K540E mutations. The prevalence of the triple
mutation N51I + C59R + S108N was 25.7% (26/101). The use of
IPTp-SP was associated with a threefold increased odds of Pfdhfr
C59R mutation [crude OR 3.29; 95% CI (1.44-7.50)]. Pregnant
women with recent uptake of IPTp-SP were at higher odds of both
the Pfdhfr C59R mutation [adjusted OR 4.26; 95% CI (1.64-11.07)]
and the Pfdhfr intermediate-to-high resistance, i.e., $geq$ 2
Pfdhfr mutations [adjusted OR 3.45; 95% CI (1.18-10.07)]. There
was no statistically significant association between the presence
of the Pfdhfr intermediate-to-high resistance and parasite
densities or both maternal haemoglobin level and anaemia.
CONCLUSION: The data indicate that despite the possibility that
IPTp-SP contributes to the selection of resistant parasites, it
did not potentiate pregnancy-associated malaria morbidity,
suggesting the continuation of SP use as IPTp in Burkina Faso.},
keywords = {Burkina Faso; Drug resistance; Malaria; Pregnancy; Sulfadoxine-pyrimethamine},
pubstate = {published},
tppubtype = {article}
}
BACKGROUND: The impact of sulfadoxine-pyrimethamine (SP) used as
intermittent preventive treatment during pregnancy (IPTp-SP) on
mutant parasite selection has been poorly documented in Burkina
Faso. This study sought first to explore the relationship between
IPTp-SP and the presence of mutant parasites. Second, to assess
the relationship between the mutant parasites and adverse
pregnancy outcomes. METHODS: From September to December 2010,
dried blood spots (DBS) were collected during antenatal care
visits and at delivery from 109 pregnant women with
microscopically confirmed falciparum malaria infection. DBS were
analysed by PCR-restriction fragment length polymorphism
(PCR-RFLP) for the polymorphisms at codons 51, 59, 108, and 164
of the Pfdhfr gene and codons 437 and 540 in the Pfdhps gene.
RESULTS: Both the Pfdhfr and Pfdhps genes were successfully
genotyped in 92.7% (101/109) of the samples. The prevalence of
Pfdhfr mutations N51I, C59R and S108N was 71.3, 42.6 and 64.4%,
respectively. Overall, 80.2% (81/101) of samples carried the
Pfdhps A437G mutation. None of the samples had the Pfdhfr I164L
and the Pfdhps K540E mutations. The prevalence of the triple
mutation N51I + C59R + S108N was 25.7% (26/101). The use of
IPTp-SP was associated with a threefold increased odds of Pfdhfr
C59R mutation [crude OR 3.29; 95% CI (1.44-7.50)]. Pregnant
women with recent uptake of IPTp-SP were at higher odds of both
the Pfdhfr C59R mutation [adjusted OR 4.26; 95% CI (1.64-11.07)]
and the Pfdhfr intermediate-to-high resistance, i.e., $geq$ 2
Pfdhfr mutations [adjusted OR 3.45; 95% CI (1.18-10.07)]. There
was no statistically significant association between the presence
of the Pfdhfr intermediate-to-high resistance and parasite
densities or both maternal haemoglobin level and anaemia.
CONCLUSION: The data indicate that despite the possibility that
IPTp-SP contributes to the selection of resistant parasites, it
did not potentiate pregnancy-associated malaria morbidity,
suggesting the continuation of SP use as IPTp in Burkina Faso. |