Proton pump inhibitor use and the risk of small intestinal bacterial overgrowth: a meta-analysis

Wai-Kit Lo1, Walter W Chan

  • 1Division of Gastroenterology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.

Abstract

Insights

Proton pump inhibitor (PPI) use is linked to small intestinal bacterial overgrowth (SIBO). This association is significant only when SIBO is diagnosed using accurate methods like duodenal aspirate cultures.

Area of Science:

  • Gastroenterology
  • Microbiology
  • Pharmacology

Background:

  • Proton pump inhibitors (PPIs) may increase the risk of small intestinal bacterial overgrowth (SIBO) by altering the gut environment.
  • Conflicting study results exist regarding the association between PPI use and SIBO.
  • Objective clinical outcome measures are needed to clarify this relationship.

Purpose of the Study:

  • To systematically review and meta-analyze the association between PPI use and SIBO.
  • To evaluate the impact of diagnostic methods on the observed association.
  • To provide a clearer understanding of SIBO risk in PPI users.

Main Methods:

  • A systematic review and meta-analysis of clinical studies comparing PPI users and non-users.
  • Searched major databases (MEDLINE/PubMed, EMBASE, Cochrane, NIH) through July 2012.
  • Extracted data on study characteristics and outcomes, calculating the pooled odds ratio (OR) for SIBO.

Main Results:

  • Eleven studies (3134 participants) were included.
  • The overall pooled OR for SIBO in PPI users was 2.282 (95% CI, 1.238-4.205).
  • A significant association was found in studies using duodenal/jejunal aspirate cultures (OR, 7.587), but not with the glucose hydrogen breath test (OR, 1.93).
  • Publication bias was suggested by funnel plot analysis.

Conclusions:

  • PPI use is statistically associated with an increased risk of SIBO.
  • This association is dependent on the diagnostic accuracy of the test used.
  • Differences in diagnostic modalities may explain conflicting results in previous studies.

Related Concept Videos

Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents01:20

Drugs for Peptic Ulcer Disease: Prostaglandin Analogs as Mucosal Protective Agents

The gastric mucosa produces prostaglandins E2 (PGE2) and prostacyclin (PGI2), crucial in maintaining gastric health. They exert cytoprotective effects, including increasing bicarbonate secretion, releasing protective mucin, reducing gastric acid output, and preventing harmful vasoconstriction. These effects are mediated through various receptors, such as EP1, EP2, EP3, and EP4.
Non-steroidal anti-inflammatory drugs (NSAIDs) can induce peptic ulcers by inhibiting cyclooxygenase, decreasing...
Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors01:13

Acid Suppressive Drugs for Peptic Ulcer Disease: Proton Pump Inhibitors

Peptic ulcers, often induced by H. pylori infections or NSAID usage, arise from disruptions in the delicate balance of gastric acid production. Peptic ulcers stem from heightened gastric acid levels due to H. pylori infections or NSAID use. The protective mucus layer diminishes in the presence of these factors, allowing gastric acid to erode the stomach lining and form ulcers.
Gastric acid, a potent cocktail of hydrogen and chloride ions, is produced in specialized parietal cells within the...
Microbiota of the Stomach and Small Intestine01:27

Microbiota of the Stomach and Small Intestine

The human gastrointestinal (GI) tract is characterized by distinct physicochemical conditions that shape its microbial communities. Among these, the stomach presents a particularly challenging environment for microbial colonization due to its highly acidic pH, ranging from 1 to 3. This extreme acidity effectively limits microbial density. However, certain acid-tolerant microorganisms are capable of surviving in this niche. Notably, Helicobacter pylori can colonize the gastric mucosa,...
Drugs for Treatment of Constipation-Predominant IBS01:21

Drugs for Treatment of Constipation-Predominant IBS

Pharmacological therapies for IBS-C are designed to alleviate abdominal discomfort and enhance bowel function. In patients with IBS-C, fiber supplements may help soften stools and decrease straining, but may also lead to increased gas production and bloating. Osmotic laxatives like milk of magnesia are frequently used to soften stools and increase stool frequency in IBS-C patients. In addition, two drugs approved for use in severe IBS-C adult cases are linaclotide (Linzess) and lubiprostone...
Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors01:24

Pathophysiology of Peptic Ulcer Disease: Mucosal Defense Factors

Peptic ulcer disease, commonly called PUD, represents a multifaceted condition characterized by disruptions in the lining of the gastrointestinal (GI)  tract. Central to the protection of the gastrointestinal lining is the mucosal-bicarbonate barrier. This physiological defense mechanism is a formidable shield against the corrosive effects of gastric acid and pepsin secretion in the stomach. Its role is pivotal in maintaining the structural integrity of the stomach's inner lining. Bicarbonate,...
Peptic Ulcer Disease IV: Management01:26

Peptic Ulcer Disease IV: Management

Medical treatment strategies for peptic ulcers encompass various methods. The primary goal of treatment is to diminish gastric acidity and strengthen mucosal defense mechanisms.
The therapeutic approach involves ensuring adequate rest, implementing drug therapy, promoting smoking cessation, making dietary modifications, and emphasizing long-term follow-up care.
Pharmacological management
The prevailing therapy for peptic ulcers involves a combination of managing the patient's current medication...