Evidence map›Paper›PMID 35883064›Full record

ArticleBMC infectious diseases2022

Etramp5 as a useful serological marker in children to assess the immediate effects of mass drug campaigns for malaria.

T Druetz, L van den Hoogen, G Stresman, V Joseph, K E S Hamre, C Fayette, F Monestime, J Presume, I Romilus, G Mondélus and 11 more

Open access · goldAbstract read
In one paragraph

Article in BMC infectious diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 31% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

21 authors at 4 institutions in 3 countries.

T DruetzCenter for Applied Malaria Research and Evaluation, School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA. thomas.druetz@umontreal.ca.ORCID http://orcid.org/0000-0002-9234-4286
L van den HoogenCenter for Applied Malaria Research and Evaluation, School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA.
G StresmanDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, UK.
V JosephCenter for Applied Malaria Research and Evaluation, School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA.
K E S HamreMalaria Branch, Centers for Diseases Control and Prevention, Atlanta, USA.
C FayetteIMA World Health, Port-au-Prince, Haiti.
F MonestimeIMA World Health, Port-au-Prince, Haiti.
J PresumeLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
I RomilusLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
G MondélusLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
T ElisméLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
S CooperDepartment of Social and Preventive Medicine, School of Public Health, University of Montreal, Montreal, Canada.
D ImpoinvilMalaria Branch, Centers for Diseases Control and Prevention, Atlanta, USA.
R A AshtonCenter for Applied Malaria Research and Evaluation, School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA.
E RogierMalaria Branch, Centers for Diseases Control and Prevention, Atlanta, USA.
A ExisteLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
J BoncyLaboratoire National de Santé Publique, Port-au-Prince, Haiti.
M A ChangMalaria Branch, Centers for Diseases Control and Prevention, Atlanta, USA.
J F LemoineProgramme National de Contrôle du Paludisme, Port-au-Prince, Haiti.
C DrakeleyDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, UK.
T P EiseleCenter for Applied Malaria Research and Evaluation, School of Public Health and Tropical Medicine, Tulane University, New Orleans, USA.
Tulane University · USCenters for Disease Control and Prevention · USLondon School of Hygiene & Tropical Medicine · GBUniversité de Montréal · CA

Funding

Bill and Melinda Gates Foundation OPP1114297
6 · The paper itself

Abstract

introductionSerological methods provide useful metrics to estimate age-specific period prevalence in settings of low malaria transmission; however, evidence on the use of seropositivity as an endpoint remains scarce in studies to evaluate combinations of malaria control measures, especially in children. This study aims to evaluate the immediate effects of a targeted mass drug administration campaign (tMDA) in Haiti by using serological markers.

methodsThe tMDA was implemented in September-October 2018 using sulfadoxine-pyrimethamine and single low-dose primaquine. A natural quasi-experimental study was designed, using a pretest and posttest in a cohort of 754 randomly selected school children, among which 23% reported having received tMDA. Five antigens were selected as outcomes (MSP1-19, AMA-1, Etramp5 antigen 1, HSP40, and GLURP-R0). Posttest was conducted 2-6 weeks after the intervention.

resultsAt baseline, there was no statistical difference in seroprevalence between the groups of children that were or were not exposed during the posttest. A lower seroprevalence was observed for markers informative of recent exposure (Etramp5 antigen 1, HSP40, and GLURP-R0). Exposure to tMDA was significantly associated with a 50% reduction in the odds of seropositivity for Etramp5 antigen 1 and a 21% reduction in the odds of seropositivity for MSP119.

conclusionSerological markers can be used to evaluate the effects of interventions against malaria on the risk of infection in settings of low transmission. Antibody responses against Etramp5 antigen 1 in Haitian children were reduced in the 2-6 weeks following a tMDA campaign, confirming its usefulness as a short-term marker in child populations.

Indexed as

MalariaMalaria, FalciparumAntibodies, ProtozoanChildDrug CombinationsHaitiHumansPharmaceutical PreparationsPlasmodium falciparumSeroepidemiologic StudiesAntibodies, ProtozoanDrug CombinationsPharmaceutical PreparationsCohort studyEvaluationHaitiImpact assessmentMalariaMass drug administrationSerologySeropositivity

Identifiers

PMID35883064
PMCPMC9321307
OpenAlexW4288053950

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.