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Author Spotlight: Investigating the Pathophysiology of Eosinophilic Esophagitis
Published on: May 10, 2024
Functional dyspepsia is associated with duodenal eosinophilia in an Australian paediatric cohort
L Wauters1, S Nightingale2,3, N J Talley4
1Department of Gastroenterology and Hepatology, University Hospitals Leuven, Leuven, Belgium.
Insights
Functional dyspepsia (FD) in children is linked to increased duodenal eosinophils, even with normal endoscopy. This finding suggests a potential new diagnostic marker for pediatric FD.
Area of Science:
- Pediatric Gastroenterology
- Gastrointestinal Pathology
- Immunology
Background:
- The exact cause of functional dyspepsia (FD) is unknown.
- Duodenal eosinophil infiltration is a potential factor in FD pathophysiology.
Purpose of the Study:
- To investigate the association between dyspeptic symptoms and duodenal eosinophilia in children.
- To determine if duodenal eosinophilia is a marker for functional dyspepsia in pediatric patients.
Main Methods:
- Retrospective cohort study of children undergoing upper gastrointestinal endoscopy.
- Comparison of intramucosal eosinophil counts between FD cases and controls.
- Univariate and multivariate regression analyses to identify predictors of FD.
Main Results:
- Children with FD showed significantly higher duodenal eosinophil counts compared to controls.
- Duodenal eosinophilia (>112 eosinophils/mm²) was highly predictive of FD in children (OR: 33.6).
- Duodenal eosinophilia was also associated with weight loss in pediatric patients.
Conclusions:
- Functional dyspepsia in children is strongly associated with duodenal eosinophilia.
- This association exists even without abnormal endoscopic or routine histological findings.
- The presence of atopic and psychological comorbidities suggests multifactorial mechanisms in pediatric FD.
Background:
The pathophysiology of functional dyspepsia (FD) remains unknown. Duodenal eosinophil infiltration has been reported.
Aim:
To assess the association between dyspeptic symptoms and duodenal eosinophilia in children undergoing upper gastrointestinal endoscopy.
Methods:
In this retrospective cohort study, children with normal upper endoscopy and routine histology at a single tertiary paediatric centre between 2010 and 2014 were included. FD was defined as epigastric pain or discomfort >2 months without response to acid suppression. Controls presented with nonerosive reflux disease, dysphagia or rumination syndrome. Intramucosal eosinophil counts were compared between the groups using uni- and multivariate regression analyses.
Results:
Thirty-six cases and 36 nonmatched controls were identified. Atopic history (39% vs. 25%) and psychological comorbidity (53% vs. 39%; both P = 0.2) were frequent in cases and controls. Self-reported nausea (64% vs. 17%; P < 0.0001), lethargy (19% vs. 0%; P = 0.005) and family functional gastrointestinal disorder(FGID) (28% vs. 3%; P = 0.003) were more common in cases than controls. Duodenal eosinophil counts [median (IQR): 151 (118-207) vs. 76 (60-106) per mm2 ; P < 0.001] were significantly higher in cases than controls with >112 eosinophils per mm2 predictive for FD (OR: 33.6, 95% CI: 7.1-159.0; P < 0.001). Duodenal eosinophilia was associated with weight loss (OR: 7.1, 95% CI: 1.1-45.5; P = 0.04).
Conclusions:
Functional dyspepsia in children is strongly associated with duodenal eosinophilia, in the absence of endoscopic or routine histological findings. Frequent atopic and psychological comorbidity illustrate likely multifactorial mechanisms.
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