The impact of proton pump inhibitors on the intestinal microbiota in chronic hepatitis C patients.
Freya WellhönerNico DöscherTammo Lambert TergastMarius VitalIris PlumeierSilke KahlAndrej PotthoffMichael Peter MannsBenjamin MaasoumyHeiner WedemeyerMarkus CornbergDietmar Helmut PieperBenjamin HeidrichPublished in: Scandinavian journal of gastroenterology (2019)
Objectives: Proton pump inhibitors (PPI), a class of drugs commonly used, are known to be associated with changes in the intestinal microbiota. Published studies were done in heterogeneous cohorts which could hamper conclusions drawn as effects of diseases were not taken into consideration. We aimed to elucidate differences in the intestinal microbiota being associated to the use of PPI in a cohort study of patients with chronic hepatitis C. Material and Methods: The 16S rDNA gene was analyzed in stool samples of patients with and without PPI use. Patients with concomitant medication influencing the microbiota were excluded. Results were compared with the clinical course of hepatitis C patients with decompensated liver cirrhosis. Results: No differences in alpha diversity could be observed, while the microbial community structure differed significantly, especially in patients with liver cirrhosis. The relative abundance of Streptococcus spp., Enterobacter spp. and Haemophilus spp. was significantly increased in patients with PPI use irrespectively of the stage of liver disease. Finally, in patients with decompensated liver cirrhosis due to chronic HCV infection only in these using PPI bacterial phylotypes were isolated. Conclusions: PPI use was associated with significant alterations in the microbial community in patients with chronic hepatitis C, which were even pronounced in patients with liver cirrhosis. In patients with decompensated liver cirrhosis due to chronic HCV infection, the use of PPI may promote infections either directly or indirectly through changes in the microbial community structure. Future studies should further investigate long-term impact on the microbiota and the clinical outcome.
Keyphrases
- microbial community
- protein protein
- heart failure
- ejection fraction
- small molecule
- hepatitis c virus
- antibiotic resistance genes
- end stage renal disease
- liver fibrosis
- healthcare
- emergency department
- peritoneal dialysis
- escherichia coli
- prognostic factors
- copy number
- staphylococcus aureus
- genome wide
- liver failure
- cystic fibrosis
- candida albicans
- adverse drug