Evidence map›Paper›PMID 36913924›Full record

ArticleThe American journal of tropical medicine and hygiene2023

Quantitative Morphometry and Machine Learning Model to Explore Duodenal and Rectal Mucosal Tissue of Children with Environmental Enteric Dysfunction.

Marium Khan, Zehra Jamil, Lubaina Ehsan, Fatima Zulqarnain, Sanjana Srivastava, Saman Siddiqui, Philip Fernandes, Muhammad Raghib, Saurav Sengupta, Zia Mujahid and 12 more

Open access · hybridAbstract read
In one paragraph

Article in The American journal of tropical medicine and hygiene, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
3.9field-weighted citation impact, top 7% 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

2 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. 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

22 authors at 3 institutions in 2 countries.

Marium KhanDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Zehra JamilDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Lubaina EhsanDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Fatima ZulqarnainDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Sanjana SrivastavaDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Saman SiddiquiDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Philip FernandesDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Muhammad RaghibDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Saurav SenguptaSchool of Data Science, University of Virginia, Charlottesville, Virginia.
Zia MujahidDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Zubair AhmedDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Romana IdreesDepartment of Pathology and Laboratory Medicine, Aga Khan University, Karachi, Pakistan.
Sheraz AhmedDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Fayaz UmraniDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Najeeha IqbalDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Christopher MoskalukDepartment of Pathology, University of Virginia, Charlottesville, Virginia.
Shyam RaghavanDepartment of Pathology, University of Virginia, Charlottesville, Virginia.
Lin ChengDepartment of Pathology, Rush University, Chicago, Illinois.
Sean MooreDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
Syed Asad AliDepartment of Pediatrics and Child Health, Aga Khan University, Karachi, Pakistan.
Junaid IqbalDepartment of Biological and Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Sana SyedDepartment of Pediatrics, School of Medicine, University of Virginia, Charlottesville, Virginia.
University of Virginia · USAga Khan University · PKRush University · US

Funding

Vanderbilt-Emory-Cornell-Duke Global Health Fellowship Consortium-Expanding Diversity for Global Equity (EDGE)D43TW009337 · FIC · VANDERBILT UNIVERSITY MEDICAL CENTER · PI ALIYU, MUKTAR HASSAN, HEIMBURGER, DOUGLAS CORBETT · 2017 to 2021
$6.3M
FIC NIH HHS D43 TW009337
6 · The paper itself

Abstract

Environmental enteric dysfunction (EED) is a subclinical enteropathy prevalent in resource-limited settings, hypothesized to be a consequence of chronic exposure to environmental enteropathogens, resulting in malnutrition, growth failure, neurocognitive delays, and oral vaccine failure. This study explored the duodenal and colonic tissues of children with EED, celiac disease, and other enteropathies using quantitative mucosal morphometry, histopathologic scoring indices, and machine learning-based image analysis from archival and prospective cohorts of children from Pakistan and the United States. We observed villus blunting as being more prominent in celiac disease than in EED, as shorter lengths of villi were observed in patients with celiac disease from Pakistan than in those from the United States, with median (interquartile range) lengths of 81 (73, 127) µm and 209 (188, 266) µm, respectively. Additionally, per the Marsh scoring method, celiac disease histologic severity was increased in the cohorts from Pakistan. Goblet cell depletion and increased intraepithelial lymphocytes were features of EED and celiac disease. Interestingly, the rectal tissue from cases with EED showed increased mononuclear inflammatory cells and intraepithelial lymphocytes in the crypts compared with controls. Increased neutrophils in the rectal crypt epithelium were also significantly associated with increased EED histologic severity scores in duodenal tissue. We observed an overlap between diseased and healthy duodenal tissue upon leveraging machine learning image analysis. We conclude that EED comprises a spectrum of inflammation in the duodenum, as previously described, and the rectal mucosa, warranting the examination of both anatomic regions in our efforts to understand and manage EED.

Indexed as

Celiac DiseaseIntestinal DiseasesChildDuodenumHumansIntestinal MucosaMachine LearningProspective Studies

Identifiers

PMID36913924
PMCPMC10077000
OpenAlexW4324056910

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.