Evidence map›Paper›PMID 34264936›Full record

ArticlePLoS neglected tropical diseases2021

Gut integrity and duodenal enteropathogen burden in undernourished children with environmental enteric dysfunction.

Zehra Jamil, Najeeha Talat Iqbal, Romana Idress, Zubair Ahmed, Kamran Sadiq, Indika Mallawaarachchi, Junaid Iqbal, Sana Syed, Aneeta Hotwani, Furqan Kabir and 8 more

Open access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
4.5field-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

13 citing papers in PubMed, 40 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

18 authors at 2 institutions in 2 countries.

Zehra JamilDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Najeeha Talat IqbalDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.ORCID 0000-0003-4026-5655
Romana IdressDepartment of Pathology & Laboratory Medicine, Aga Khan University, Karachi, Pakistan.ORCID 0000-0001-6980-0231
Zubair AhmedDepartment of Pathology & Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Kamran SadiqDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.ORCID 0000-0001-5103-4575
Indika MallawaarachchiDepartment of Public Health Sciences, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0002-4137-5728
Junaid IqbalDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Sana SyedDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Aneeta HotwaniDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Furqan KabirDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Kumail AhmedDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Sheraz AhmedDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.ORCID 0000-0003-2336-3165
Fayaz UmraniDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Jennie Z MaDepartment of Public Health Sciences, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0002-5839-2882
Fatima AzizDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Adil KalamDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Sean R MooreDivision of Pediatric Gastroenterology, Hepatology, and Nutrition; Department of Pediatrics, University of Virginia, Charlottesville, Virginia, United States of America.ORCID 0000-0003-1150-6632
Syed Asad AliDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.ORCID 0000-0001-5274-7665
Aga Khan University · PKUniversity of Virginia · US

Funding

Pediatric Infectious Diseases, Enteric Health and Malnutrition in Pakistan (PIDEMP) Research Training ProgramD43TW007585 · FIC · AGA KHAN UNIVERSITY (PAKISTAN) · PI ALI, SYED ASAD, MOORE, SEAN RYAN · 2006 to 2024
$3.7M
Computational Characterization of Environmental EnteropathyK23DK117061 · NIDDK · UNIVERSITY OF VIRGINIA · PI SYED, SANA · 2019 to 2023
$964k
Microbiota, Inflammation and Environmental Enteric Dysfunction (MiEED)K43TW010697 · FIC · AGA KHAN UNIVERSITY (PAKISTAN) · PI IQBAL, NAJEEHA TALAT · 2017 to 2019
$185k
FIC NIH HHS D43 TW007585FIC NIH HHS K43 TW010697NIDDK NIH HHS K23 DK117061
6 · The paper itself

Abstract

Environmental enteric dysfunction (EED) is a subclinical condition of intestinal inflammation, barrier dysfunction and malabsorption associated with growth faltering in children living in poverty. This study explores association of altered duodenal permeability (lactulose, rhamnose and their ratio) with higher burden of enteropathogen in the duodenal aspirate, altered histopathological findings and higher morbidity (diarrhea) that is collectively associated with linear growth faltering in children living in EED endemic setting. In a longitudinal birth cohort, 51 controls (WHZ > 0, HAZ > -1.0) and 63 cases (WHZ< -2.0, refractory to nutritional intervention) were recruited. Anthropometry and morbidity were recorded on monthly bases up to 24 months of age. Dual sugar assay of urine collected after oral administration of lactulose and rhamnose was assessed in 96 children from both the groups. Duodenal histopathology (n = 63) and enteropathogen analysis of aspirate via Taqman array card (n = 60) was assessed in only cases. Giardia was the most frequent pathogen and was associated with raised L:R ratio (p = 0.068). Gastric microscopy was more sensitive than duodenal aspirate in H. pylori detection. Microscopically confirmed H. pylori negatively correlated with HAZ at 24 months (r = -0.313, p = 0.013). Regarding histopathological parameters, goblet cell reduction significantly correlated with decline in dual sugar excretion (p< 0.05). Between cases and controls, there were no significant differences in the median (25th, 75th percentile) of urinary concentrations (μg/ml) of lactulose [27.0 (11.50, 59.50) for cases vs. 38.0 (12.0, 61.0) for controls], rhamnose [66.0 (28.0, 178.0) vs. 86.5 (29.5, 190.5)] and L:R ratio [0.47 (0.24, 0.90) vs. 0.51 (0.31, 0.71)] respectively. In multivariable regression model, 31% of variability in HAZ at 24 months of age among cases and controls was explained by final model including dual sugars. In conclusion, enteropathogen burden is associated with altered histopathological features and intestinal permeability. In cases and controls living in settings of endemic enteropathy, intestinal permeability test may predict linear growth. However, for adoption as a screening tool for EED, further validation is required due to its complex intestinal pathophysiology.

Indexed as

Case-Control StudiesChildChild Nutrition DisordersDuodenumHumansInflammationIntestinal DiseasesLactulosePakistanPermeabilityRhamnoseLactuloseRhamnose

Identifiers

PMID34264936
PMCPMC8352064
OpenAlexW3182019791

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.