Influence of Potassium-Competitive Acid Blockers and Proton Pump Inhibitors on the Gut Microbiome of Helicobactor Pylori -Negative Healthy Individuals

2017 ◽  
Vol 152 (5) ◽  
pp. S631-S632
Author(s):  
Taketo Otsuka ◽  
Mitsushige Sugimoto ◽  
Ryo Inoue ◽  
Masashi Ohno ◽  
Hiromitsu Ban ◽  
...  
Author(s):  
Tae Jun Kim ◽  
Hyuk Lee

Proton pump inhibitors (PPIs) are commonly used for the treatment of gastric acid-related disorders, and are generally well tolerated. However, by reducing the secretion of gastric acid in the long term, PPI can increase the risk of inducing an imbalance in the gut microbiome composition. Moreover, gastric hypochlorhydria that is caused by PPIs favors the survival and migration of oral bacteria in the lower part of the gastrointestinal tract, with a possible induction of pro-inflammatory microenvironment. Therefore, gut dysbiosis that is associated with the use of PPI has been found to cause adverse infectious and inflammatory diseases. In this regard, adverse effects of the PPI-related gut dysbiosis have been reported in different observational studies, but their clinical relevance remains unclear. Therefore, the aim of this review was to explore the available data on the PPI-related gut dysbiosis in order to better understand its clinical significance.


2016 ◽  
Vol 72 (4) ◽  
pp. 498-500 ◽  
Author(s):  
Caoilfhionn O'Donoghue ◽  
Katie Solomon ◽  
Lynda Fenelon ◽  
Fidelma Fitzpatrick ◽  
Lorraine Kyne

Gut ◽  
2015 ◽  
Vol 65 (5) ◽  
pp. 740-748 ◽  
Author(s):  
Floris Imhann ◽  
Marc Jan Bonder ◽  
Arnau Vich Vila ◽  
Jingyuan Fu ◽  
Zlatan Mujagic ◽  
...  

2016 ◽  
Vol 43 (9) ◽  
pp. 974-984 ◽  
Author(s):  
A. G. Clooney ◽  
C. N Bernstein ◽  
W. D. Leslie ◽  
K. Vagianos ◽  
M. Sargent ◽  
...  

2021 ◽  
Vol 14 ◽  
pp. 175628482199473
Author(s):  
Kanika Sehgal ◽  
Sahil Khanna

The pathogenesis of Clostridioides difficile infection (CDI) was recognized with its link to the use of antimicrobials. Antimicrobials significantly alter gut microbiota structure and composition, which led to the discovery of the association of this gut perturbation with the development of CDI. A number of factors implicated in its pathogenesis, such as advancing age, proton-pump inhibitors, and gastrointestinal diseases, are linked to gut microbiota perturbations. In an effort to better understand CDI, a multitude of studies have tried to ascertain protective and predictive microbial footprints linked with CDI. It has further been realized that CDI in itself can alter the gut microbiome. Its spore-forming capability poses as an impediment in the management of the infection and contributes to its recurrence. Antibiotic therapies used for its management have also been linked to gut microbiota changes, making its treatment a little more challenging. In an effort to exploit and utilize this association, gut microbial restoration therapies, particularly in the form of fecal microbial transplant, are increasingly being put to use and are proving to be beneficial. In this review, we summarize the association of the gut microbiome and microbial perturbation with initial and recurrent CDI.


2018 ◽  
Vol 36 (5_suppl) ◽  
pp. 208-208
Author(s):  
Sarbajit Mukherjee ◽  
Bilal Khalid ◽  
Sami Ibrahimi ◽  
Jordan Malie Morton ◽  
Darwin Roman ◽  
...  

208 Background: Recent studies have shown that manipulating the gut microbiome modulates the efficacy of anti-PD1/PD-L1 directed therapy leading to increase in the activity of CD8+ T-cells. Proton Pump inhibitors (PPIs) affect the gut microbiome. The objective of this study was to investigate the effects of PPIs use on agents that target the PD-1/PD-L1 pathway in patients treated with these agents. Methods: We looked at the outcomes of 158 patients aged 18 years or older, treated at the University of Oklahoma Health Sciences Center between 2014 and 2016. The primary aim of this study was to investigate whether survival of patients treated with agents that target PD-1/PD-L1 pathway was affected by PPI use. The secondary objective was to identify if there is any difference in the immune related side effect profile between PPI users and non-users. The overall survival (OS) and progression free survival (PFS) were compared between PPI users and nonusers using the log-rank tests. Survival curves were generated using the Kaplan-Meyer method. The proportions of Grade 3 or 4 colitis or pneumonitis were compared between PPI users and nonusers using the Fisher’s exact test. SAS 9.4 was used for the statistical analysis and a 0.05 significance level was used. Results: The majority of patients were females (57%). The median age was 63 years. Lung cancer was the most common diagnosis (20%) followed by melanoma (20%) and ovarian cancer (12%). Nivolumab was the most commonly used agent (47%) followed by Pembrolizumab (22%), other investigational agents (22%) and Atezolizumab (7%). The median follow-up time from the date of first PPI dose was 7 months. There was no statistically significant difference in OS or PFS between PPI users and nonusers (p = 0.77). There were no significant differences in proportions of Grade 3 or 4 colitis between PPI users and nonusers (5% vs. 5.26%, p > .99). Similarly, there were no significant differences in proportions of Grade 3 or 4 pneumonitis between PPI users and nonusers (6.25% vs. 1.75%, p = 0.40). Conclusions: Use of PPI does not affect the outcome of patients receiving agents that target PD1/PD-L1 pathway. The incidence of important immune related side effects was similar between PPI users and non-users.


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