Evidence map›Paper›PMID 28712360›Full record

ArticleBMC medicine2017

Resisting and tolerating P. falciparum in pregnancy under different malaria transmission intensities.

Nicaise Tuikue Ndam, Emmanuel Mbuba, Raquel González, Pau Cisteró, Simon Kariuki, Esperança Sevene, María Rupérez, Ana Maria Fonseca, Anifa Vala, Sonia Maculuve and 15 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00811421 (Evaluation of the Safety and Efficacy of Mefloquine as Intermittent Preventive Treatment of Malaria in Pregnancy), which is not on this map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.7field-weighted citation impact, top 23% 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.

NCT00811421 nacompletednot on this map

Evaluation of the Safety and Efficacy of Mefloquine as Intermittent Preventive Treatment of Malaria in Pregnancy

TypeinterventionalSponsorHospital Clinic of BarcelonaRan2009 to 2013Enrolled5,820ConditionsPregnancy, Malaria, HIV InfectionsArmsSulphadoxine-pyrimethamine, Mefloquine (full dose), Mefloquine (split dose), placebo, mefloquine
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 15 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. The Effects of Malaria in Pregnancy on Neurocognitive Development in Children at 1 and 6 Years of Age in Benin: A Prospective Mother-Child Cohort.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Trial
  4. Prenatal Hemoglobin Concentration and Long-Term Child Neurocognitive Development.The American journal of tropical medicine and hygiene · 2025
    Article
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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

25 authors at 11 institutions in 11 countries.

Nicaise Tuikue NdamInstitut de Recherche pour le Développement (IRD), Paris, France.
Emmanuel MbubaIfakara Health Institute (IHI), Bagamoyo Research and Training Centre (BRTC), Bagamoyo, Tanzania.
Raquel GonzálezISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Pau CisteróISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Simon KariukiKenya Medical Research Institute (KEMRI)/Centre for Global Health Research, Kisumu, Kenya.
Esperança SeveneCentro de Investigação em Saúde da Manhiça (CISM), Maputo, Mozambique.
María RupérezISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Ana Maria FonsecaISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Anifa ValaCentro de Investigação em Saúde da Manhiça (CISM), Maputo, Mozambique.
Sonia MaculuveCentro de Investigação em Saúde da Manhiça (CISM), Maputo, Mozambique.
Alfons JiménezISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Llorenç QuintóFaculté des Sciences de la Santé (FSS), Université d'Aboméy Calavi, Cotonou, Benin.
Peter OumaKenya Medical Research Institute (KEMRI)/Centre for Global Health Research, Kisumu, Kenya.
Michael RamharterInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
John J AponteISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Arsenio NhacoloCentro de Investigação em Saúde da Manhiça (CISM), Maputo, Mozambique.
Achille MassougbodjiFaculté des Sciences de la Santé (FSS), Université d'Aboméy Calavi, Cotonou, Benin.
Valerie BriandInstitut de Recherche pour le Développement (IRD), Paris, France.
Peter G KremsnerInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Ghyslain Mombo-NgomaInstitute of Tropical Medicine, University of Tübingen, Tübingen, Germany.
Meghna DesaiMalaria Branch, Division of Parasitic Diseases and Malaria, Center for Global Health, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Eusebio MaceteCentro de Investigação em Saúde da Manhiça (CISM), Maputo, Mozambique.
Michel CotInstitut de Recherche pour le Développement (IRD), Paris, France.
Clara MenéndezISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain.
Alfredo MayorISGlobal, Barcelona Ctr. Int. Health Res. (CRESIB), Hospital Clínic - Universitat de Barcelona, Barcelona, Spain. alfredo.mayor@isglobal.org.
Manhiça Health Research Centre · MZCentre de Recherche Médicales de Lambaréné · GABarcelona Institute for Global Health · ESInstitut de Recherche pour le Développement · FRKenya Medical Research Institute · KEUniversité d'Abomey-Calavi · BJCenters for Disease Control and Prevention · USEduardo Mondlane University · MZIfakara Health Institute · TZUniversidade do Porto · PTUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundResistance and tolerance to Plasmodium falciparum can determine the progression of malaria disease. However, quantitative evidence of tolerance is still limited. We investigated variations in the adverse impact of P. falciparum infections among African pregnant women under different intensities of malaria transmission.

methodsP. falciparum at delivery was assessed by microscopy, quantitative PCR (qPCR) and placental histology in 946 HIV-uninfected and 768 HIV-infected pregnant women from Benin, Gabon, Kenya and Mozambique. Resistance was defined by the proportion of submicroscopic infections and the levels of anti-parasite antibodies quantified by Luminex, and tolerance by the relationship of pregnancy outcomes with parasite densities at delivery.

resultsP. falciparum prevalence by qPCR in peripheral and/or placental blood of HIV-uninfected Mozambican, Gabonese and Beninese women at delivery was 6% (21/340), 11% (28/257) and 41% (143/349), respectively. The proportion of peripheral submicroscopic infections was higher in Benin (83%) than in Mozambique (60%) and Gabon (55%; P = 0.033). Past or chronic placental P. falciparum infection was associated with an increased risk of preterm birth in Mozambican newborns (OR = 7.05, 95% CI 1.79 to 27.82). Microscopic infections were associated with reductions in haemoglobin levels at delivery among Mozambican women (-1.17 g/dL, 95% CI -2.09 to -0.24) as well as with larger drops in haemoglobin levels from recruitment to delivery in Mozambican (-1.66 g/dL, 95% CI -2.68 to -0.64) and Gabonese (-0.91 g/dL, 95% CI -1.79 to -0.02) women. Doubling qPCR-peripheral parasite densities in Mozambican women were associated with decreases in haemoglobin levels at delivery (-0.16 g/dL, 95% CI -0.29 to -0.02) and increases in the drop of haemoglobin levels (-0.29 g/dL, 95% CI -0.44 to -0.14). Beninese women had higher anti-parasite IgGs than Mozambican women (P < 0.001). No difference was found in the proportion of submicroscopic infections nor in the adverse impact of P. falciparum infections in HIV-infected women from Kenya (P. falciparum prevalence by qPCR: 9%, 32/351) and Mozambique (4%, 15/417).

conclusionsThe lowest levels of resistance and tolerance in pregnant women from areas of low malaria transmission were accompanied by the largest adverse impact of P. falciparum infections. Exposure-dependent mechanisms developed by pregnant women to resist the infection and minimise pathology can reduce malaria-related adverse outcomes. Distinguishing both types of defences is important to understand how reductions in transmission can affect malaria disease.

trial registrationClinicalTrials.gov NCT00811421 . Registered 18 December 2008.

Indexed as

Pregnancy Complications, InfectiousAdultDelivery, ObstetricFemaleGabonHIV InfectionsHumansInfant, NewbornKenyaMalaria, FalciparumMicroscopyMozambiqueParturitionPlacentaPlasmodium falciparumPregnancyImmunityMalariaPregnancyResistanceTolerance

Identifiers

PMID28712360
PMCPMC5513247
OpenAlexW2724382180

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.