Evidence map›Paper›PMID 38685382›Full record

ArticleThe American journal of clinical nutrition2024

Duodenal quantitative mucosal morphometry in children with environmental enteric dysfunction: a cross-sectional multicountry analysis.

Lubaina Ehsan, David Coomes, Paul Kelly, Adam R Greene, S Asad Ali, Chola Mulenga, Donna M Denno, Kelley VanBuskirk, Muhammad Faraz Raghib, Mustafa Mahfuz and 7 more

Abstract readMulticenter Study
In one paragraph

Article in The American journal of clinical nutrition, 2024. 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
–field-weighted citation impact
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.

  1. Article
  2. Mild Duodenal Mucosal Injury and Increased Type I Interferon Signaling Are Preludes to Celiac Disease.Laboratory investigation; a journal of technical methods and pathology · 2025
    Article
  3. Article
  4. Article
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

17 authors.

Lubaina EhsanDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Virginia, Charlottesville, VA, United States.
David CoomesDepartment of Epidemiology, University of Washington, Seattle, WA, United States.
Paul KellyBlizard Institute, Barts and The London School of Medicine, Queen Mary University of London, London, United Kingdom.
Adam R GreeneDivision of Pediatric Gastroenterology, Hepatology, and Nutrition, Department of Pediatrics, University of Virginia, Charlottesville, VA, United States.
S Asad AliDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Chola MulengaTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Lusaka, Zambia.
Donna M DennoDepartment of Pediatrics, University of Washington, Seattle, WA, United States.
Kelley VanBuskirkDepartment of Global Health, University of Washington, Seattle, WA, United States.
Muhammad Faraz RaghibDepartment of Pediatrics, University of Virginia, Charlottesville, VA, United States.
Mustafa MahfuzNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Sean R MooreDepartment of Pediatrics, University of Virginia, Charlottesville, VA, United States.
Md Shabab HossainNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Tahmeed AhmedNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Peter B SullivanDepartment of Paediatrics, Children's Hospital, University of Oxford, Oxford, United Kingdom.
Christopher A MoskalukDepartment of Pathology, University of Virginia, Charlottesville, VA, United States.
Sana SyedDepartment of Pediatrics, University of Virginia, Charlottesville, VA, United States. Electronic address: ss8xj@virginia.edu.
EEDBI Consortium

Funding

Computational Characterization of Environmental EnteropathyK23DK117061 · NIDDK · UNIVERSITY OF VIRGINIA · PI SYED, SANA · 2019 to 2023
$964k
NIDDK NIH HHS K23 DK117061
6 · The paper itself

Abstract

backgroundEnvironmental enteric dysfunction (EED), a chronic inflammatory condition of the small intestine, is an important driver of childhood malnutrition globally. Quantifying intestinal morphology in EED allows for exploration of its association with functional and disease outcomes.

objectivesWe sought to define morphometric characteristics of childhood EED and determine whether morphology features were associated with disease pathophysiology.

methodsMorphometric measurements and histology were assessed on duodenal biopsy slides for this cross-sectional study from children with EED in Bangladesh, Pakistan, and Zambia (n = 69), and those with no pathologic abnormality (NPA; n = 8) or celiac disease (n = 18) in North America. Immunohistochemistry was also conducted on 46, 8, and 18 biopsy slides, respectively. Linear mixed-effects regression models were used to reveal morphometric differences between EED compared with NPA or celiac disease and identify associations between morphometry and histology or immunohistochemistry among children with EED.

resultsIn duodenal biopsies, median EED villus height (248 μm), crypt depth (299 μm), and villus:crypt (V:C) ratio (0.9) values ranged between those of NPA (396 μm villus height; 246 μm crypt depth; 1.6 V:C ratio) and celiac disease (208 μm villus height; 365 μm crypt depth; 0.5 V:C ratio). Among EED biopsy slides, morphometric assessments were not associated with histologic parameters or immunohistochemical markers, other than pathologist-determined subjective semiquantitative villus architecture.

conclusionsMorphometric analysis of duodenal biopsy slides across geographies identified morphologic features of EED, specifically short villi, elongated crypts, and a smaller V:C ratio relative to NPA slides, although not as severe as in celiac slides. Morphometry did not explain other EED features, suggesting that EED histopathologic processes may be operating independently of morphology. Although acknowledging the challenges with obtaining relevant tissue, these data form the basis for further assessments of the role of morphometry in EED.

Indexed as

DuodenumIntestinal MucosaBangladeshBiopsyCeliac DiseaseChildChild, PreschoolCross-Sectional StudiesFemaleHumansInfantMalePakistanZambiacryptgastrointestinal morphologyglobal healthpediatricvilli

Identifiers

PMID38685382
PMCPMC11562031

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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.