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Published on: November 17, 2018
[Proton Pump Inhibitors and their Microbiome-Mediated Side Effects]
Angela Horvath1,2, Vanessa Stadlbauer1
1Klinische Abteilung für Gastroenterologie und Hepatologie, Medizinische Universität Graz, Österreich.
Proton pump inhibitors reduce stomach acid but disrupt the gut microbiome, increasing infection risks. This highlights the need to consider microbiome changes in therapy and explore alternatives.
Area of Science:
- Gastroenterology
- Microbiology
- Immunology
Background:
- Proton pump inhibitors (PPIs) effectively treat acid-related disorders by inhibiting gastric acid secretion.
- Reduced gastric acid compromises the natural defense against ingested pathogens.
- The gastric barrier is crucial for protecting the intestinal microbiome from oral bacteria and food-borne pathogens.
Purpose of the Study:
- To investigate the impact of proton pump inhibitors on the intestinal microbiome.
- To explore the link between PPI-induced microbiome alterations and potential side effects.
- To assess the clinical relevance of these changes, particularly in liver cirrhosis patients.
Main Methods:
- Review of existing literature on PPIs and their effects on gastric acid and the microbiome.
- Analysis of studies linking microbiome changes to PPI therapy side effects.
- Examination of data on oral bacteria in the gut and its association with liver disease severity.
Main Results:
- PPIs reduce gastric acid, impairing a key component of the innate immune system.
- Alterations in the intestinal microbiome, including reduced diversity and bacterial overgrowth, are associated with PPI use.
- Increased oral bacteria in the gut of liver cirrhosis patients correlate with inflammation, permeability, and mortality risk.
Conclusions:
- PPI therapy can lead to microbiome-mediated side effects, such as increased susceptibility to infections like Clostridium difficile.
- PPI-induced changes in gut bacteria may contribute to gastrointestinal discomfort and other adverse events.
- Microbiome-mediated effects should be integrated into the risk-benefit assessment of PPIs and the development of alternative treatments.
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