Gastroduodenal and intestinal permeability in primary biliary cirrhosis

Eur J Gastroenterol Hepatol. 2003 Sep;15(9):967-73. doi: 10.1097/00042737-200309000-00005.

Abstract

Objectives: To evaluate gastrointestinal permeability in primary biliary cirrhosis (PBC), using a sensitive method to detect epithelial damage, and to correlate it with the Mayo score, histological stage, ascites, spontaneous bacterial peritonitis, endoscopic signs of portal hypertension and Helicobacter pylori infection.

Methods: Fifty consecutive patients with PBC and 39 patients with cirrhosis of other aetiologies (non-PBC) were enrolled in the study. Coeliac disease was initially ruled out in all participants. Permeability was assessed using sucrose (gastro-duodenum) and lactulose-mannitol (intestine).

Results: Sucrose excretion was above the limit in both PBC and non-PBC patients. Twenty-two per cent of PBC patients had an increased result for the lactulose-mannitol test compared to 12.8% of non-PBC cirrhotic patients. PBC patients had high sucrose excretion levels irrespective of the presence of any oesophageal varices, which significantly increased the gastroduodenal permeability in non-PBC patients only when associated with hypertensive gastropathy. Sucrose excretion was significantly enhanced by hypertensive gastropathy in non-PBC patients (P < 0.001) but not in PBC patients. No significant correlation was found in either group between gastrointestinal permeability and the other parameters.

Conclusions: Gastrointestinal permeability is increased in PBC. Portal hypertension contributes to altered gastric mucosal permeability in non-PBC cirrhosis, whereas different epithelial dysfunction can be hypothesized in PBC.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Digestive System / metabolism*
  • Duodenum / metabolism
  • Female
  • Gastric Mucosa / metabolism
  • Humans
  • Intestinal Absorption
  • Intestinal Mucosa / metabolism
  • Intestine, Small / metabolism
  • Liver Cirrhosis, Alcoholic / metabolism
  • Liver Cirrhosis, Biliary / metabolism*
  • Male
  • Middle Aged
  • Permeability
  • Sucrose

Substances

  • Sucrose