Evidence map›Paper›PMID 39300664›Full record

ArticleThe American journal of clinical nutrition2024

Anthropometry relationship with duodenal histologic features of children with environmental enteric dysfunction: a multicenter cross-sectional study.

Zehra Jamil, Kelley VanBuskirk, Monica Mweetwa, Samer Mouksassi, Gerald Smith, Tahmeed Ahmed, Kanta Chandwe, Donna M Denno, S Mohammad Fahim, Paul Kelly 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 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. 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
  4. Article
  5. 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.

Zehra JamilDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Kelley VanBuskirkDepartment of Global Health, University of Washington School of Public Health, Seattle, WA, United States.
Monica MweetwaTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Lusaka, Zambia.
Samer MouksassiCertara, Princeton, NJ, United States.
Gerald SmithCytel, Vancouver, British Columbia, Canada.
Tahmeed AhmedNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Kanta ChandweTropical Gastroenterology and Nutrition Group, University of Zambia School of Medicine, Lusaka, Zambia.
Donna M DennoDepartment of Pediatrics, University of Washington School of Medicine, Seattle, WA, United States.
S Mohammad FahimNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Paul KellyBlizard Institute, Barts & The London School of Medicine, Queen Mary University of London, London, United Kingdom.
Mustafa MahfuzNutrition Research Division, International Centre for Diarrhoeal Disease Research, Bangladesh, Dhaka, Bangladesh.
Indika MallawaarachchiDepartment of Public Health Sciences, University of Virginia School of Medicine, Charlottesville, VA, United States.
Chelsea MarieDepartment of Medicine, University of Virginia School of Medicine, Charlottesville, VA, United States.
Sean R MooreDepartment of Pediatrics, University of Virginia School of Medicine, Charlottesville, VA, United States.
William A PetriDepartment University of Virginia, Charlottesville, VA, United States.
S Asad AliDepartment of Paediatrics and Child Health, Aga Khan University, Karachi, Pakistan. Electronic address: asad.ali@aku.edu.
EEDBI Consortium

Funding

Washington University DDRCC Supplemental Equipment RequestP30DK052574 · NIDDK · WASHINGTON UNIVERSITY · PI Jeffrey Wade Brown · 2000 to 2026
$30.8M
NIDDK NIH HHS P30 DK052574
6 · The paper itself

Abstract

backgroundEnvironmental enteric dysfunction (EED) is a precursor of growth faltering in children living in impoverished conditions who are frequently exposed to environmental toxins and enteropathogens, leading to small bowel inflammatory, malabsorptive, and permeability derangements and low-grade chronic systemic inflammation.

objectivesWe explored the association between anthropometrics and duodenal histologic features of EED among children from 3 lower middle-income country centers.

methodsIn this cross-sectional study, Pakistani children (n = 63) with wasting, Bangladesh children (n = 116) with stunting or at risk for stunting (height-for-age Z score [HAZ] <-1 but ≥-2), and Zambian children (n = 108) with wasting or stunting received nutritional intervention. Children with anthropometric status refractory to intervention underwent endoscopy. Linear regression models included anthropometric around endoscopy, scores of histology parameters, and a global index score of EED-the total score percent-5 (TSP-5). Multivariable models were adjusted for center, age, sex, and histology slide quality.

resultsIntersite variation was observed while exploring the association between anthropometrics and the TSP-5; for example, Pakistani children had the worst HAZ, yet their median TSP-5 score was lower than that of the other 2 centers. Even within each site, no overall pattern of higher TSP-5 score was observed with worsening HAZ. During univariate analysis, TSP-5 (coefficient: 0.01; 95% confidence interval [CI]: 0, 0.02), goblet cell depletion (coefficient: 0.22; 95% CI: 0.06, 0.37), and Paneth cell depletion (coefficient: 0.14; 95% CI: 0.01, 0.27) were associated with HAZ scores; however, they lost statistical significance in the multivariable models, with study center most strongly confounding the relationships seen in univariate models between anthropometry and histology.

conclusionsThis study contributes a crucial negative finding that duodenal morphological features did not associate with anthropometric phenotypes; hence, anthropometric measurements may not be a suitable outcome measure for use in EED trials. Trial outcomes may need to be defined by combining the functional and structural elements of the gut to monitor EED.

Indexed as

AnthropometryDuodenumBangladeshChildChild, PreschoolCross-Sectional StudiesFemaleGrowth DisordersHumansInfantMalePakistanZambiaanthropometryduodenal histologyenvironmental enteric dysfunctionstuntingwasting

Identifiers

PMID39300664
PMCPMC13168959

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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.