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Proton Pump Inhibitors Modulate Gene Expression Profile in Esophageal Mucosa and Microbiome.

Authors :
Rajagopala SV
Shilts MH
Correa H
Das SR
Choksi YA
Jacobse J
Goettel JA
Hiremath G
Source :
The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG [J Pediatr Pharmacol Ther] 2023; Vol. 28 (6), pp. 504-508. Date of Electronic Publication: 2023 Oct 28.
Publication Year :
2023

Abstract

Objective: Proton pump inhibitors (PPIs) are commonly used to manage children with upper gastrointestinal symptoms and without a formal diagnosis. We investigated the effect of PPIs on esophageal mucosal transcriptome and active microbiota in children with normal esophagi. Furthermore, we examined whether the differences in host esophageal mucosal gene expression were driven by an underlying esophageal epithelial cell type composition.<br />Methods: Using metatranscriptomics, the host transcriptional and active microbial profiles were captured from 17 esophageal biopsy samples (PPI naïve [PPI-], n = 7; PPI exposed [PPI+], n = 10) collected from children without any endoscopic and histologic abnormalities in their esophagus (normal esophagus). Deconvolution computational analysis was performed with xCell to assess if the observed epithelial gene expression changes were related to the cell type composition in the esophageal samples.<br />Results: The median (IQR) age of our cohort was 14 years (12-16) with female (63%) preponderance. Both groups were similar in terms of their demographics and clinical features. Compared with PPI-, the PPI+ had upregulation of 27 genes including the MUC genes. The cell type composition was similar between the PPI- and PPI+ groups. Prevotella sp and Streptococcus sp were abundant in PPI+ group.<br />Conclusions: In children with normal esophagus, PPI exposure can be associated with upregulation of esophageal mucosal homeostasis and epithelial cell function genes in a cell-type independent manner, and an altered esophageal microbiome. Additional studies are warranted to validate our findings and to investigate the causal effect of PPIs on the normal esophageal epithelium and microbial communities.<br />Competing Interests: Disclosures. SRD is one of the advisory board members of Premas Biotech, and consultant to Jansen and Jansen. GH serves as a consultant to Allakos, Bristol Myer Squibb, Regeneron, and Sanofi. He has received speaker fees from Bristol Myer Squibb. All other authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright. Pediatric Pharmacy Association. All rights reserved. For permissions, email: membership@pediatricpharmacy.org.)

Details

Language :
English
ISSN :
1551-6776
Volume :
28
Issue :
6
Database :
MEDLINE
Journal :
The journal of pediatric pharmacology and therapeutics : JPPT : the official journal of PPAG
Publication Type :
Academic Journal
Accession number :
38130344
Full Text :
https://doi.org/10.5863/1551-6776-28.6.504