Unconjugated secondary bile acids in the serum of patients with colorectal adenomas

• Published in: Gut Vol. 36; no. 2; pp. 268 - 273
• Main Authors: Bayerdörffer, E, Mannes, G A, Ochsenkühn, T, Dirschedl, P, Wiebecke, B, Paumgartner, G
• Format: Journal Article
• Language: English
• Published: London BMJ Publishing Group Ltd and British Society of Gastroenterology 01-02-1995; BMJ; BMJ Publishing Group LTD
• Subjects: Adenoma - blood; Bile Acids and Salts - blood; Biological and medical sciences; Cocarcinogenesis; Colorectal Neoplasms - blood; Colorectal Neoplasms - etiology; Deoxycholic Acid - blood; Gastroenterology. Liver. Pancreas. Abdomen; Humans; Male; Medical sciences; Middle Aged; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tumors; Colonic disease; Human; Rectal disease; Bile acid; Rectum; Digestive diseases; Benign neoplasm; Adenoma; Colon
• ISSN: 0017-5749; 1468-3288; 1458-3288
• DOI: 10.1136/gut.36.2.268

A positive association between deoxcholic acid (DCA) in the serum and colorectal adenomas, the precursors of colorectal cancer has recently been found, which supported the hypothesis of a pathogenic role of DCA in colonic carcinogenesis. This approach was based on the hypothesis that DCA formed in the colon is absorbed into the portal venous blood and exhibits a constant spillover to the systemic circulation. To further substantiate this hypothesis this study investigated whether in the serum of adenoma patients DCA was higher in the unconjugated fraction, which originates directly from the colon. DCA was found to be 2.8-fold higher in the unconjugated fraction of patients with colorectal adenomas than in controls (0.89 v 0.32 mumol/l, p < 0.0025), 1.9-fold in the total DCA fraction (1.89 v 0.95 mumol/l, p < 0.0001), and 1.4-fold in the conjugated fraction (0.67 v 0.47 mumol/l, p < 0.05). It was further found that the bacterial isomerisation product 3 beta-DCA was twofold higher in the unconjugated fraction of adenoma patients than in controls (0.08 v 0.04 mumol/l, p = 0.27), 1.8-fold in the total iso-DCA fraction (0.11 v 0.06 mumol/l, p < 0.05), and 1.5-fold in the conjugated iso-DCA fraction (0.03 v 0.02 mumol/l, p = 0.68). The data suggest that the positive association between the serum DCA concentration and colorectal adenoma as described previously results from the DCA fraction that is absorbed from the colon. This further supports a pathogenic role of DCA in the carcinogenesis of colorectal cancer.