Evidence map›Paper›PMID 42251899›Full record

Observational studyThe Journal of nutrition2026

Intestinal Permeability Is Associated with Mortality and Readmission in Children Hospitalized with Severe Acute Malnutrition.

Jonathan P Sturgeon, Bernard Chasekwa, Joice Tome, Cherlynn Dumbura, Florence D Majo, Deophine Ngosa, Kuda Mutasa, Ellen Besa, Kusum J Nathoo, Claire D Bourke and 6 more

Abstract readObservational Study
In one paragraph

Observational study in The Journal of nutrition, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Jonathan P SturgeonZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, United Kingdom; Department of Infectious Disease, Section of Paediatric Infectious Disease, Faculty of Medicine, Imperial College London, United Kingdom. Electronic address: jpsturgeon@cantab.net.
Bernard ChasekwaZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Joice TomeZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Cherlynn DumburaZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Florence D MajoZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Deophine NgosaTropical Gastroenterology and Nutrition Group, University of Zambia, Lusaka, Zambia.
Kuda MutasaZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Ellen BesaTropical Gastroenterology and Nutrition Group, University of Zambia, Lusaka, Zambia.
Kusum J NathooDepartment of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Claire D BourkeZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, United Kingdom.
Tafhima HaiderCentre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, United Kingdom.
Robert NtoziniZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe.
Mutsa Bwakura-DangarembiziZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe; Department of Paediatrics and Child Health, Faculty of Medicine and Health Sciences, University of Zimbabwe, Harare, Zimbabwe.
Beatrice AmadiTropical Gastroenterology and Nutrition Group, University of Zambia, Lusaka, Zambia.
Paul KellyCentre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, United Kingdom; Tropical Gastroenterology and Nutrition Group, University of Zambia, Lusaka, Zambia.
Andrew J PrendergastZvitambo Institute for Maternal and Child Health Research, Harare, Zimbabwe; Centre for Genomics and Child Health, Blizard Institute, Queen Mary University of London, London, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSevere acute malnutrition (SAM) is the most critical form of undernutrition, associated with high inpatient and postdischarge mortality. It is hypothesized that malnutrition enteropathy contributes to systemic inflammation by allowing translocation of intestinal pathogen-associated molecular patterns across the damaged epithelium.

objectivesAssess intestinal permeability, markers of bacterial translocation, and correlate these with inflammatory markers in children admitted with SAM and during 1 y after discharge.

methodsIn a substudy of the longitudinal Health Outcomes, Pathogenesis and Epidemiology of Severe Acute Malnutrition observational study, we recruited 264 children with complicated SAM on admission to hospital at 3 centers in Zimbabwe and Zambia. We measured gut permeability by urinary lactulose:mannitol ratio (LMR); plasma lipopolysaccharide (LPS) using the limulus amoebocyte lysate assay; and plasma inflammatory biomarkers by enzyme-linked immunosorbent assay and Luminex, at admission, discharge, 12- and 48-wk postdischarge. Values were compared with 173 adequately nourished community controls. Data were analyzed using mixed effects models for longitudinal data, regression for associations between groups, and Cox proportional hazards models for survival.

resultsGut permeability, as measured by LMR, was 2.5-fold higher in children with SAM compared with community controls [95% confidence interval (CI): 1.4, 4.5], and only resolved by 48-wk postdischarge. Higher inpatient gut permeability was associated with increased risk of death or readmission over the following year [hazard ratio 6.14 (95% CI: 1.03, 36.8) per 10-fold increase in LMR]. Children with high gut permeability had higher levels of the intestinal biomarker glucagon-like peptide-2 and lower L-selectin. Children with higher plasma LPS had independently higher concentrations of circulating inflammatory markers [tumor necrosis factor-α, interleukin (IL)-6, IL-1ra, C-reactive protein, IL-8, chemokine ligand 3, and chemokine ligand 4].

conclusionsCollectively, these results highlight the central role of the gut in children with SAM. Malnutrition enteropathy may represent a suitable target for therapeutic interventions to improve clinical outcomes in this high-risk population.

Indexed as

Intestinal MucosaIntestinesPatient ReadmissionSevere Acute MalnutritionBacterial TranslocationBiomarkersChild, PreschoolFemaleHospitalizationHumansInfantIntestinal Barrier FunctionLactuloseLipopolysaccharidesLongitudinal StudiesMaleBiomarkersLactuloseLipopolysaccharidesMannitolintestinal permeabilityLPSmalnutrition enteropathysevere acute malnutritionsystemic inflammation

Identifiers

PMID42251899
PMCPMC13494158

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Registered trials

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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.