Differences in phosphatidylcholine and bile acids in bile from Egyptian and UK patients with and without cholangiocarcinoma

HPB (Oxford). 2011 Jun;13(6):385-90. doi: 10.1111/j.1477-2574.2011.00296.x. Epub 2011 Mar 22.

Abstract

Background: Cholangiocarcinoma (CC) is a fatal malignancy, the incidence of which is increasing worldwide, with substantial regional variation. Current diagnostic techniques to distinguish benign from malignant biliary disease are unsatisfactory. Metabolic profiling of bile may help to differentiate benign from malignant disease. No previous studies have compared the metabolic profiles of bile from two geographically and racially distinct groups of CC patients.

Objectives: This study aimed to compare metabolic profiles of bile, using in vitro proton magnetic resonance spectroscopy, from CC patients from Egypt and the UK, and from patients with CC and patients with non-malignant biliary disease.

Methods: A total of 29 bile samples, collected at cholangiography, were analysed using an 11.7-T system. Samples were from eight CC patients in either Egypt (n = 4) or the UK (n = 4) and 21 patients with benign biliary disease (choledocholithiasis [n = 8], sphincter of Oddi dysfunction [n = 8], primary sclerosing cholangitis [n = 5]).

Results: Bile phosphatidylcholine (PtC) was significantly reduced in CC patients. Egyptian CC patients had significantly lower biliary PtC levels compared with UK patients. Taurine- and glycine-conjugated bile acids (H-26 and H-25 protons, respectively) were significantly elevated in bile from patients with CC compared with bile from patients with benign diseases (P = 0.013 and P < 0.01, respectively).

Conclusions: Biliary PtC levels potentially differentiate CC from benign biliary disease. Reduced biliary PtC in Egyptian compared with UK patients may reflect underlying carcinogenic mechanisms.

Publication types

  • Comparative Study
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Bile / metabolism*
  • Bile Acids and Salts / metabolism*
  • Bile Duct Neoplasms / diagnostic imaging
  • Bile Duct Neoplasms / metabolism*
  • Bile Ducts, Intrahepatic / diagnostic imaging
  • Bile Ducts, Intrahepatic / metabolism*
  • Biomarkers, Tumor / metabolism*
  • Cholangiocarcinoma / diagnostic imaging
  • Cholangiocarcinoma / metabolism*
  • Cholangiopancreatography, Endoscopic Retrograde
  • Cholangitis, Sclerosing / metabolism
  • Choledocholithiasis / metabolism
  • Diagnosis, Differential
  • Egypt
  • Female
  • Humans
  • Magnetic Resonance Spectroscopy
  • Male
  • Metabolomics / methods
  • Middle Aged
  • Phosphatidylcholines / metabolism*
  • Predictive Value of Tests
  • Sphincter of Oddi Dysfunction / metabolism
  • United Kingdom

Substances

  • Bile Acids and Salts
  • Biomarkers, Tumor
  • Phosphatidylcholines