Evidence map›Paper›PMID 36197916›Full record

ArticlePLoS neglected tropical diseases2022

The role of environmental enteric dysfunction in the pathogenesis of Schistosoma mansoni-associated morbidity in school-aged children.

Jacqueline Araújo Fiuza, Susannah Colt, Letícia Gambogi de Ornellas, Leonardo Ferreira Matoso, Andrea Gazzinelli, Jennifer F Friedman, Rodrigo Corrêa-Oliveira

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

7 authors at 3 institutions in 2 countries.

Jacqueline Araújo FiuzaGrupo de Imunologia Celular e Molecular, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, Brazil.
Susannah ColtCenter for International Health Research, Rhode Island Hospital, Providence, Rhode Island, United States of America.ORCID 0000-0002-1935-4197
Letícia Gambogi de OrnellasGrupo de Imunologia Celular e Molecular, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, Brazil.
Leonardo Ferreira MatosoEscola de Enfermagem, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Andrea GazzinelliEscola de Enfermagem, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Jennifer F FriedmanCenter for International Health Research, Rhode Island Hospital, Providence, Rhode Island, United States of America.
Rodrigo Corrêa-OliveiraGrupo de Imunologia Celular e Molecular, Instituto René Rachou, Fundação Oswaldo Cruz, Belo Horizonte, Minas Gerais, Brazil.
Fundação Oswaldo Cruz · BRBrown University · USUniversidade Federal de Minas Gerais · BR

Funding

Modeling Drug Induced Resistance in S. mansoni Endemic AreasP50AI098507 · NIAID · FOUNDATION FOR RESEARCH DEVELOPMENT · PI OLIVEIRA, GUILHERME C · 2012 to 2016
$1.5M
NIAID NIH HHS P50 AI098507
6 · The paper itself

Abstract

backgroundStudies have implicated schistosomiasis as a cause of intestinal barrier disruption, a salient feature of environmental enteric dysfunction (EED), as eggs translocate from the sterile bloodstream through the gut wall. We examined the longitudinal impact of praziquantel (PZQ) treatment on a) EED biomarkers and b) Insulin growth factor I (IGF-1), a key driver of childhood linear growth, since EED has been implicated in linear growth stunting. METHODOLOGY: 290 children infected with S. mansoni in Brazil were treated with PZQ at baseline. EED biomarkers lipopolysaccharide (LPS) and intestinal fatty acid binding-protein (I-FABP) were measured, as well as IGF-1 at baseline, 6 and 12-months. Multivariate regression analysis was applied to assess associations between S. mansoni intensity and plasma biomarkers (LPS, I-FABP, and IGF-1), controlling for potential confounding variables. PRINCIPAL

findingsAt baseline, S. mansoni infection intensities were 27.2% light, 46.9% moderate, and 25.9% heavy. LPS concentrations were significantly reduced at the 12-month visit compared to baseline (p = 0.0002). No longitudinal changes were observed for I-FABP or IGF-1 in the 6- or 12-month periods following baseline treatment. After 6-months, I-FABP concentration was significantly higher in high vs low intensity (p = 0.0017). IGF-1 concentrations were significantly lower among children with high and moderate vs low intensity infections at each study visit. CONCLUSIONS/SIGNIFICANCE: We report that S. mansoni infection impacts LPS, I-FABP and IGF-1. These findings suggest a mechanistic role for EED in schistosomiasis-related morbidities, particularly linear growth.

Indexed as

AnthelminticsInsulinsSchistosomiasisSchistosomiasis mansoniAnimalsChildFatty AcidsHumansInsulin-Like Growth Factor ILipopolysaccharidesMorbidityPraziquantelSchistosoma mansoniAnthelminticsFatty AcidsInsulin-Like Growth Factor IInsulinsLipopolysaccharidesPraziquantel

Identifiers

PMID36197916
PMCPMC9576041
OpenAlexW4302275562

What OpenQuestion 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 OpenQuestion graph.