Evidence map›Paper›PMID 28750860›Full record

ArticleEBioMedicine2017

Impaired Barrier Function and Autoantibody Generation in Malnutrition Enteropathy in Zambia.

Beatrice Amadi, Ellen Besa, Kanekwa Zyambo, Patrick Kaonga, John Louis-Auguste, Kanta Chandwe, Phillip I Tarr, Donna M Denno, James P Nataro, William Faubion and 7 more

Open access · goldAbstract read
In one paragraph

Article in EBioMedicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
4.3field-weighted citation impact, top 5% 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

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Testosterone administration partially modulates gut microbiota responses to severe energy deficit.American journal of physiology. Endocrinology and metabolism · 2026
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4 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 3 countries.

Beatrice AmadiDepartment of Paediatrics, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia; Tropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia.
Ellen BesaTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia.
Kanekwa ZyamboTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia.
Patrick KaongaTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia.
John Louis-AugusteTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia; Blizard Institute, Barts & The London School of Medicine, Queen Mary University of London, London, UK.
Kanta ChandweDepartment of Paediatrics, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia.
Phillip I TarrDepartment of Pediatrics, Washington University School of Medicine, St Louis, MO, USA.
Donna M DennoDepartment of Pediatrics, University of Washington, Seattle, USA.
James P NataroDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, USA.
William FaubionMayo Clinic, Rochester, MN, USA.
Anne SailerDepartments of Pathology and Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Sunil YeruvaDepartments of Pathology and Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Tricia BrantnerMayo Clinic, Rochester, MN, USA.
Joseph MurrayMayo Clinic, Rochester, MN, USA.
Andrew J PrendergastBlizard Institute, Barts & The London School of Medicine, Queen Mary University of London, London, UK.
Jerrold R TurnerDepartments of Pathology and Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Paul KellyTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Nationalist Road, Lusaka, Zambia; Blizard Institute, Barts & The London School of Medicine, Queen Mary University of London, London, UK. Electronic address: m.p.kelly@qmul.ac.uk.
University of Zambia · ZMBrigham and Women's Hospital · USMayo Clinic in Arizona · USQueen Mary University of London · GBUniversity of Virginia · USUniversity of Washington · USWashington University in St. Louis · US

Funding

ZO-1-MEDIATED PROTEIN INTERACTIONS: REGULATORS AND INTEGRATORS OF DIVERSE EPITHELIAL FUNCTIONS IN HEALTH AND DISEASER01DK061931 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2001 to 2026
$15.0M
Therapeutic targeting of protein interactions to reverse MLCK1-mediated intestinal barrier loss and ameliorate disease.R01DK068271 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2005 to 2026
$11.3M
Translational Approaches to Develop Drug Therapy for DiarrheaR24DK099803 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI DONOWITZ, MARK · 2014 to 2019
$8.9M
Medical Research Council MR/K012711/1NIDDK NIH HHS R01 DK061931NIDDK NIH HHS R01 DK068271NIDDK NIH HHS R24 DK099803
6 · The paper itself

Abstract

Intestinal damage in malnutrition constitutes a threat to the survival of many thousands of children globally. We studied children in Lusaka, Zambia, with severe acute malnutrition (SAM) and persistent diarrhea using endoscopy, biopsy and analysis of markers and protective proteins in blood and intestinal secretions. We carried out parallel investigations in apparently healthy adults, and analyzed biomarkers only in apparently healthy children. Villus height and crypt depth did not differ in children with SAM and adult controls, but epithelial surface was reduced in children with SAM (median 445, interquartile range (IQR) 388, 562μm per 100μm muscularis mucosae) compared to adults (578, IQR 465,709; P=0.004). Histological lesions and disruptions of claudin-4 and E-cadherin were most pronounced in children with SAM. Circulating lipopolysaccharide, a marker of bacterial translocation, was higher in malnourished children (251, IQR 110,460EU/ml) than in healthy children (51, IQR 0,111; P=0.0001). Other translocation markers showed similar patterns. Anti-Deamidated Gliadin Peptide IgG concentrations, although within the normal range, were higher in children with SAM (median 2.7U/ml, IQR 1.5-8.6) than in adults (1.6, 1.4-2.1; P=0.005), and were inversely correlated with villus height (ρ=-0.79, n=13, P=0.001). Malnutrition enteropathy is associated with intestinal barrier failure and immune dysregulation.

Indexed as

Antigens, CDAutoantibodiesBiomarkersBiopsyCadherinsChildChild, PreschoolClaudin-4Cross-Sectional StudiesDiarrheaEndoscopy, GastrointestinalFemaleHumansLipopolysaccharidesMaleSevere Acute MalnutritionAntigens, CDAutoantibodiesBiomarkersCadherinsCDH1 protein, humanClaudin-4CLDN4 protein, humanLipopolysaccharidesAutoantibodiesEnteropathyEnvironmental enteric dysfunctionGlucagon-like peptide 2HIVMalnutritionMicrobial translocationTissue transglutaminase serology, deamidated gliadin peptide serology

Identifiers

PMID28750860
PMCPMC5552244
OpenAlexW2737322495

What OpenQuestion holds

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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.