Evidence map›Paper›PMID 37184455›Full record

ArticleJournal of pediatric gastroenterology and nutrition2023

The Spectrum of Duodenal Histologic Findings in Patients With Trisomy 21: A Multicenter Study.

Erin Alexander, Marisa Stahl, Amy Weaver, Janaki Devara, Lisa M Fahey, Arunjot Singh, Maureen M Leonard, Vanessa Weisbrod, Mary Shull, Jocelyn Silvester and 4 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Journal of pediatric gastroenterology and nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 21% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. A systematic review of celiac disease recommendations for children with Down syndrome.Journal of pediatric gastroenterology and nutrition · 2026
    Pooled it
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

14 authors at 7 institutions in 1 country.

Erin AlexanderFrom the Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children's Center, Rochester, MN.
Marisa Stahlthe Digestive Health Institute, Department of Pediatrics, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO.
Amy Weaverthe Division of Clinical Trials and Biostatistics, Mayo Clinic, Rochester, MN.
Janaki DevaraFrom the Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children's Center, Rochester, MN.
Lisa M Faheythe Division of Gastroenterology, Hepatology, & Nutrition, The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Arunjot Singhthe Division of Gastroenterology, Hepatology, & Nutrition, The Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA.
Maureen M Leonardthe Center for Celiac Research and Treatment, Division of Pediatric Gastroenterology and Nutrition, Mass General Hospital for Children, Harvard Medical School, Boston, MA.
Vanessa WeisbrodHarvard Celiac Research Program, Boston Children's Hospital, Boston, MA.
Mary Shullthe Digestive Health Institute, Department of Pediatrics, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO.
Jocelyn SilvesterHarvard Celiac Research Program, Boston Children's Hospital, Boston, MA.
Zachary Kramerthe Celiac Disease Program, Division of Gastroenterology, Hepatology, and Nutrition, Children's National Hospital, Washington, DC.
Benny Kerznerthe Celiac Disease Program, Division of Gastroenterology, Hepatology, and Nutrition, Children's National Hospital, Washington, DC.
Edwin Liuthe Digestive Health Institute, Department of Pediatrics, Children's Hospital Colorado, University of Colorado Anschutz Medical Campus, Aurora, CO.
Imad AbsahFrom the Division of Pediatric Gastroenterology and Hepatology, Mayo Clinic Children's Center, Rochester, MN.
Children's Center · USUniversity of Colorado Anschutz Medical Campus · USBoston Children's Hospital · USChildren's National · USUniversity of Pennsylvania · USHarvard University · USMayo Clinic · US

Funding

Institutional Career Development CoreKL2TR002534 · NCATS · UNIVERSITY OF COLORADO DENVER · PI BURNHAM, ELLEN L · 2018 to 2022
$4.6M
Mechanisms and Markers of Small Intestinal Epithelial Injury and Villous AtrophyK23DK119584 · NIDDK · BOSTON CHILDREN'S HOSPITAL · PI SILVESTER, JOCELYN ANNE · 2019 to 2023
$971k
NCATS NIH HHS KL2 TR002534NIDDK NIH HHS K23 DK119584
6 · The paper itself

Abstract

objectivesPatients with Trisomy 21 (T21) commonly have gastrointestinal symptoms and diseases that prompt evaluation with esophagogastroduodenoscopy (EGD). Our objective is to characterize duodenal histological abnormalities in these patients when undergoing EGD. A secondary aim is to explore associations of histologic findings with different therapies.

methodsPatients 30 years old or younger with T21 who underwent EGD from 2000 to 2020 at 6 hospitals were included in this retrospective cohort study. Duodenal biopsies were categorized based on reported histopathology findings as normal or abnormal. Abnormal pathology reports were reviewed and categorized into villous atrophy (VA) and duodenitis without VA. The VA group was further categorized based on the presence or absence of celiac disease (CD).

resultsWe identified 836 patients with T21 who underwent EGD, 419 (50.1%) of whom had duodenal histologic abnormalities. At the time of the first (index) abnormal duodenal biopsy, 290 of 419 had VA and of those, 172 of 290 met CD diagnostic criteria, while 118 of 290 did not meet CD criteria (nonspecific VA). Among the patients with an abnormal biopsy, acid suppression at the time of the index biopsy was less common in patients with VA-CD compared to patients without VA or patients with nonspecific VA (12.2% vs 45.7% vs 44.9%).

conclusionsHalf of the T21 patients in this cohort had abnormal duodenal biopsies including a subgroup with nonspecific VA. In this cohort, acid suppression use was more prevalent in patients with abnormalities other than CD.

Indexed as

Celiac DiseaseDown SyndromeAdultBiopsyDuodenumHumansIntestinal MucosaRetrospective Studies

Identifiers

PMID37184455
PMCPMC12923078
OpenAlexW4376618360

What OpenQuestion holds

Textmetadata
LicenceTDM
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.