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Liver damage in human small intestinal bacterial overgrowth
S M Riordan1, C J McIver, R Williams
1Institute of Hepatology, University College London Medical School, England.
The American Journal of Gastroenterology
|February 19, 1998
Summary
Small intestinal bacterial overgrowth (SIBO) is not a significant risk factor for liver damage in humans. Even with obligate anaerobes, SIBO does not necessarily lead to liver damage or increased intestinal permeability.
Area of Science:
- Gastroenterology
- Hepatology
- Microbiology
Background:
- Small intestinal bacterial overgrowth (SIBO) is linked to hepatic damage in rodents, potentially due to increased intestinal permeability.
- Human data on SIBO prevalence and associated liver damage are limited.
- This study investigates the relationship between SIBO and liver damage in adult humans.
Purpose of the Study:
- To determine the prevalence of hepatic damage in human subjects with SIBO.
- To investigate the association between specific types of bacterial overgrowth and liver injury.
- To assess the role of small intestinal permeability in SIBO-related liver damage.
Main Methods:
- Bacteriological analysis of small intestinal aspirates was performed on 70 adult subjects.
- Serum liver enzymes (ALP, GGT, AST, ALT) and nutritional indices were measured.
- Urinary lactulose/mannitol ratio assessed small intestinal permeability in subjects with SIBO and liver damage.
Main Results:
- SIBO was detected in 57.1% of subjects.
- Liver damage was observed in only one of eight subjects with SIBO involving obligate anaerobic colonic bacteria (12.5%).
- Increased small intestinal permeability was noted in some SIBO patients, normalizing after treatment; it did not always correlate with liver damage.
Conclusions:
- SIBO is not a major risk factor for liver damage in humans, irrespective of bacterial type.
- Increased small intestinal permeability associated with SIBO does not invariably result in liver damage.
- The findings suggest a low direct risk of hepatic injury from SIBO in this patient population.