Proton Pump Inhibitors Alter Specific Taxa in the Human Gastrointestinal Microbiome: A Crossover Trial

被引:237
作者
Freedberg, Daniel E. [1 ]
Toussaint, Nora C. [2 ]
Chen, Sway P. [3 ]
Ratner, Adam J. [4 ]
Whittier, Susan [5 ]
Wang, Timothy C. [1 ]
Wang, Harris H. [5 ,6 ]
Abrams, Julian A. [1 ]
机构
[1] Columbia Univ, Med Ctr, Div Digest & Liver Dis, Dept Med, New York, NY 10032 USA
[2] Columbia Univ, Med Ctr, New York Genome Ctr, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Coll Phys & Surg, New York, NY 10032 USA
[4] Columbia Univ, Med Ctr, Dept Pediat, Div Infect Dis, New York, NY 10032 USA
[5] Columbia Univ, Dept Pathol & Cell Biol, New York, NY 10032 USA
[6] Columbia Univ, Dept Syst Biol, New York, NY 10032 USA
关键词
Clostridium difficile Infection; Pharmacology; Gastroesophageal Reflux Disease; Acid Suppression; ANTIBIOTIC-TREATMENT; DIVERSITY; THERAPY; RISK;
D O I
10.1053/j.gastro.2015.06.043
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We conducted an open-label crossover trial to test whether proton pump inhibitors (PPIs) affect the gastrointestinal microbiome to facilitate Clostridium difficile infection (CDI). Twelve healthy volunteers each donated 2 baseline fecal samples, 4 weeks apart (at weeks 0 and 4). They then took PPIs for 4 weeks (40 mg omeprazole, twice daily) and fecal samples were collected at week 8. Six individuals took the PPIs for an additional 4 weeks (from week 8 to 12) and fecal samples were collected from all subjects at week 12. Samples were analyzed by 16S ribosomal RNA gene sequencing. We found no significant within-individual difference in microbiome diversity when we compared changes during baseline vs changes on PPIs. There were, however, significant changes during PPI use in taxa associated with CDI (increased Enterococcaceae and Streptococcaceae, decreased Clostridiales) and taxa associated with gastrointestinal bacterial overgrowth (increased Micrococcaceae and Staphylococcaceae). In a functional analysis, there were no changes in bile acids on PPIs, but there was an increase in genes involved in bacterial invasion. These alterations could provide a mechanism by which PPIs predispose to CDI.
引用
收藏
页码:883 / U531
页数:12
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