Evidence map›Paper›PMID 28454537›Full record

ArticleMalaria journal2017

Increase in the prevalence of mutations associated with sulfadoxine-pyrimethamine resistance in Plasmodium falciparum isolates collected from early to late pregnancy in Nanoro, Burkina Faso.

Esmée Ruizendaal, Marc C Tahita, Ronald B Geskus, Inge Versteeg, Susana Scott, Umberto d'Alessandro, Palpouguini Lompo, Karim Derra, Maminata Traore-Coulibaly, Menno D de Jong and 3 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Malaria journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04147546 (Operational Feasibility, Impact of Additional Screening Using Highly-sensitives RDTs Combined With High Coverage of IPTp on Placental Malaria and Low Birth Weight), which is not on this map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04147546 phase3completednot on this mapstarted 2020, after this paper: background citation

Operational Feasibility, Impact of Additional Screening Using Highly-sensitives RDTs Combined With High Coverage of IPTp on Placental Malaria and Low Birth Weight

TypeinterventionalSponsorInstitut de Recherche en Sciences de la Sante, Burkina FasoRan2020 to 2021Enrolled340ConditionsPlasmodium Falciparum Malaria, Malaria DiagnosisArmsAdditional screening using ultra sensitive RDTs, Dihydroartemisinin-piperaquin, Reminders
3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Observational
  15. Article
  16. Article
  17. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 5 countries.

Esmée RuizendaalDepartment of Medical Microbiology, Academic Medical Centre, Amsterdam, The Netherlands. esmee.ruizendaal@gmail.com.ORCID 0000-0001-8087-4477
Marc C TahitaInstitut de Recherche en Sciences de la Santé-Unité de Recherche Clinique de Nanoro, (IRSS-URCN), Nanoro, Burkina Faso.
Ronald B GeskusDepartment of Clinical Epidemiology, Biostatistic and Bioinformatics, Academic Medical Centre, Amsterdam, The Netherlands.
Inge VersteegKoninklijk Instituut voor de Tropen, Amsterdam, The Netherlands.
Susana ScottDepartment of Infectious Disease Epidemiology, London School of Hygiene and Tropical Medicine, London, UK.
Umberto d'AlessandroDisease Control and Elimination, Medical Research Council Unit, Fajara, Gambia.
Palpouguini LompoInstitut de Recherche en Sciences de la Santé-Unité de Recherche Clinique de Nanoro, (IRSS-URCN), Nanoro, Burkina Faso.
Karim DerraInstitut de Recherche en Sciences de la Santé-Unité de Recherche Clinique de Nanoro, (IRSS-URCN), Nanoro, Burkina Faso.
Maminata Traore-CoulibalyInstitut de Recherche en Sciences de la Santé-Unité de Recherche Clinique de Nanoro, (IRSS-URCN), Nanoro, Burkina Faso.
Menno D de JongDepartment of Medical Microbiology, Academic Medical Centre, Amsterdam, The Netherlands.
Henk D F H SchalligDepartment of Medical Microbiology, Academic Medical Centre, Amsterdam, The Netherlands.
Halidou TintoInstitut de Recherche en Sciences de la Santé-Unité de Recherche Clinique de Nanoro, (IRSS-URCN), Nanoro, Burkina Faso.
Petra F MensDepartment of Medical Microbiology, Academic Medical Centre, Amsterdam, The Netherlands.
Amsterdam UMC Location University of Amsterdam · NLInstitut de Recherche en Sciences de la Santé · BFLondon School of Hygiene & Tropical Medicine · GBMRC Unit the Gambia · GMRoyal Tropical Institute · NL

Funding

Medical Research Council MC_UP_A900_1119
6 · The paper itself

Abstract

backgroundPregnant women are a high-risk group for Plasmodium falciparum infections, which may result in maternal anaemia and low birth weight newborns, among other adverse birth outcomes. Intermittent preventive treatment with sulfadoxine-pyrimethamine during pregnancy (IPTp-SP) is widely implemented to prevent these negative effects of malaria. However, resistance against SP by P. falciparum may decrease efficacy of IPTp-SP. Combinations of point mutations in the dhps (codons A437, K540) and dhfr genes (codons N51, C59, S108) of P. falciparum are associated with SP resistance. In this study the prevalence of SP resistance mutations was determined among P. falciparum found in pregnant women and the general population (GP) from Nanoro, Burkina Faso and the association of IPTp-SP dosing and other variables with mutations was studied.

methodsBlood spots on filter papers were collected from pregnant women at their first antenatal care visit (ANC booking) and at delivery, from an ongoing trial and from the GP in a cross-sectional survey. The dhps and dhfr genes were amplified by nested PCR and products were sequenced to identify mutations conferring resistance (ANC booking, n = 400; delivery, n = 223; GP, n = 400). Prevalence was estimated with generalized estimating equations and for multivariate analyses mixed effects logistic regression was used.

resultsThe prevalence of the triple dhfr mutation was high, and significantly higher in the GP and at delivery than at ANC booking, but it did not affect birth weight. Furthermore, quintuple mutations (triple dhfr and double dhps mutations) were found for the first time in Burkina Faso. IPTp-SP did not significantly affect the occurrence of any of the mutations, but high transmission season was associated with increased mutation prevalence in delivery samples. It is unclear why the prevalence of mutations was higher in the GP than in pregnant women at ANC booking.

conclusionThe high number of mutants and the presence of quintuple mutants in Burkina Faso confirm concerns about the efficacy of IPTp-SP in the near future. Other drug combinations to tackle malaria in pregnancy should, therefore, be explored. An increase in mutation prevalence due to IPTp-SP dosing could not be confirmed.

Indexed as

Drug ResistanceMutationAdolescentAdultAntimalarialsBurkina FasoChildChild, PreschoolCross-Sectional StudiesDrug CombinationsFemaleHumansLongitudinal StudiesMalaria, FalciparumMalePlasmodium falciparumAntimalarialsDrug Combinationsfanasil, pyrimethamine drug combinationPyrimethamineSulfadoxineMutationsPlasmodium falciparumPregnancyResistanceSulfadoxine–pyrimethamine

Identifiers

PMID28454537
PMCPMC5410088
OpenAlexW2608049415

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.