Urinary bile acids in late pregnancy and in recurrent cholestasis of pregnancy
Article first published online: 20 MAR 2008
European Journal of Clinical Investigation
Volume 9, Issue 6, pages 425–432, December 1979
How to Cite
THOMASSEN, P. A. (1979), Urinary bile acids in late pregnancy and in recurrent cholestasis of pregnancy. European Journal of Clinical Investigation, 9: 425–432. doi: 10.1111/j.1365-2362.1979.tb00907.x
- Issue published online: 20 MAR 2008
- Article first published online: 20 MAR 2008
- Received 8 January 1979 and in revised form 16 May 1979
- bile acids;
- gas chromatography-mass spectrometry
Abstract. The metabolic profiles of urinary bile acids in pregnant women in the last trimester and patients with recurrent intrahepatic cholestasis of pregnancy (RCP) were studied. Following separation according to mode of conjugation, about thirty different bile acids were quantitatively analysed by gas chromatography-mass spectrometry. In all patients the sulphate fraction comprised 50–90% of the total bile acids. In RCP a shift from glycine to taurine conjugation was noted together with a slight relative increase in sulphation.
A ten- to hundred-fold increase in cholic and chenodeoxycholic acids was seen in RCP, the increase being mainly in the sulphate fraction. Tetrahydroxylated bile acids, tentatively regarded as 1- and 6-hydroxylated products of cholic acid, were quantitatively important in patients with RCP. The relative amounts of the secondary bile acids, deoxycholic and lithocholic acids, decreased with increasing cholestasis. Metabolites hydroxylated at C-6 were common, and the excretion of hyocholic acid was positively correlated to that of chenodeoxycholic acid. An increase in the excretion of 5α-configurated bile acids in RCP was noted.
A positive correlation between the excretion of 3β-hydroxy-5-cholenoic acid and 3β,12α-dihydroxy-5-cholenoic acid indicates a metabolic relationship between the two compounds. Because of the relatively small amounts of lithocholic and 3β-hydroxy-5-cholenoic acids in patients with RCP, these compounds do not seem to be of pathogenetic importance in this type of cholestasis.