Affiliation:
1. Discipline of Pediatrics, School of Women's and Children's Health, Faculty of Medicine University of New South Wales Randwick New South Wales Australia
2. Department of Nutrition and Dietetics Sydney Children's Hospital Randwick New South Wales Australia
3. Department of Speech Pathology Sydney Children's Hospital Randwick New South Wales Australia
4. Department of Gastroenterology Sydney Children's Hospital Randwick New South Wales Australia
Abstract
AbstractObjectivesThis study aims to compare the intestinal microbiota and intestinal inflammation of children with esophageal atresia (EA) to matched healthy controls, and to investigate the relationship between these factors and clinical outcomes.MethodsA cross‐sectional study of 35 children with EA and 35 matched healthy controls (HC) from a single tertiary pediatric hospital in Australia was conducted. Demographic and dietary data were collected using surveys. Stool samples were analyzed using 16S rRNA sequencing, and fecal calprotectin measurements were used to measure intestinal inflammation. Comparisons were made between the groups, and correlations between the microbiota and clinical factors were investigated in the EA cohort.ResultsCompared to HC, children with EA had similar alpha diversity, but beta diversity analysis revealed clustering of EA and HC cohorts. Children with EA had a significantly higher relative abundance of the order Lactobacillales, and a lower abundance of the genus uncultured Bacteroidales S24‐7. Fecal calprotectin was significantly higher in children with EA compared to HC. In the EA cohort, children taking proton pump inhibitors (PPI's) had lower alpha diversity and higher calprotectin levels compared to those not taking PPI's. There was a negative correlation between calprotectin and length/height‐for‐age z scores, and children with higher calprotectin levels had a greater burden of gastrointestinal symptoms.ConclusionsChildren with EA have an altered intestinal microbiota compared to HC, which is likely related to PPI use, and may be impacting on growth and quality of life. It is important to rationalize PPI use in this cohort.
Subject
Gastroenterology,Pediatrics, Perinatology and Child Health