Evidence map›Paper›PMID 40369331›Full record

ArticleEuropean journal of pediatrics2025

Histopathological differences in pediatric duodenogastric reflux: a comparative study.

Sevde Nur Türker, Zeren Barış, Nazlı Sena Şeker, Yusuf Aydemir

Abstract readComparative Study
In one paragraph

Article in European journal of pediatrics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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. 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

4 authors.

Sevde Nur TürkerFaculty of Medicine, Department of Pediatrics, Eskişehir Osmangazi University, Eskişehir, Turkey.
Zeren BarışFaculty of Medicine, Department of Pediatric Gastroenterology, Eskişehir Osmangazi University, Eskişehir, Turkey. zeren_baris@yahoo.com.ORCID http://orcid.org/0000-0002-4976-9924
Nazlı Sena ŞekerFaculty of Medicine, Department of Pathology, Eskişehir Osmangazi University, Eskişehir, Turkey.
Yusuf AydemirFaculty of Medicine, Department of Pediatric Gastroenterology, Eskişehir Osmangazi University, Eskişehir, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The histopathological effects of duodenogastric reflux (DGR) in children remain poorly described. This study aimed to evaluate and compare the gastric histopathological findings of pediatric patients with endoscopically confirmed DGR gastritis and those without, to identify potential morphological changes associated with bile reflux in childhood. This retrospective study compared children with endoscopically confirmed DGR to age- and sex-matched controls without DGR. Gastric biopsy samples were re-evaluated by a single pathologist blinded to clinical data. Histopathological features, including inflammation severity, activity, fibrosis, vascular congestion, edema, foveolar hyperplasia, the presence of Helicobacter pylori, lymphoid aggregates, reactive gastropathy, intestinal metaplasia, and glandular atrophy were compared. Logistic regression was used to identify significant predictors of DGR. A total of 73 patients with DGR and 65 controls were included. Fibrosis (60.2% vs. 9.2%, p < 0.001), congestion (63.0% vs. 27.7%, p < 0.001), foveolar hyperplasia (32.9% vs. 6.2%, p < 0.001), and edema (24.7% vs. 6.2%, p = 0.003) were significantly more common in the DGR group. Logistic regression identified foveolar hyperplasia (OR 10.67), edema (OR 9.01), fibrosis (OR 6.98), and congestion (OR 5.85) as independent predictors of DGR.

conclusionFibrosis, congestion, foveolar hyperplasia, and edema are significantly associated with DGR in pediatric patients and may serve as supportive histological markers for diagnosis. WHAT IS KNOWN: • DGR in children lacks a standardized diagnostic method, with endoscopy and histopathology being commonly used. • Histopathological features such as foveolar hyperplasia and fibrosis are known in adults but less studied in children. WHAT IS NEW: • This study identifies fibrosis, congestion, foveolar hyperplasia, and edema as significant histopathological markers in pediatric DGR. • It suggests that endoscopic findings, combined with histopathology, can aid in the diagnosis of DGR in children.

Indexed as

Duodenogastric RefluxGastric MucosaGastritisStomachAdolescentBiopsyCase-Control StudiesChildChild, PreschoolFemaleFibrosisHumansHyperplasiaInfantLogistic ModelsMaleBile refluxDuodenogastric refluxFibrosisFoveolar hyperplasiaHistopathologyPediatric

Identifiers

PMID40369331
PMCPMC12078397

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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.