Literature DB >> 8742915

Sequential changes in serum levels of individual bile acids in patients with chronic cholestatic liver disease.

S A Azer1, S A Coverdale, K Byth, G C Farrell, N H Stacey.   

Abstract

In order to determine the value of serum bile acids in predicting the course of chronic cholestatic liver diseases, we measured individual serum bile acids serially, using high-performance liquid chromatography, over a 4 year observation period in 12 patients with primary biliary cirrhosis and six patients with primary sclerosing cholangitis. The changes in individual serum bile acids and the ratios thereof, conventional liver tests and Child-Turcotte and Mayo scores were compared between survivors (n = 10) and patients who underwent liver transplantation for (n = 3) or died of the liver disease (n = 5). Patients with a serum total chenodeoxycholic acid concentration at study entry that exceded 15 mumol/L were 10 times more likely to die or need a liver transplant in the following 4 years than those with chenodeoxycholic acid levels < 15 mumol/L (P < 0.05). None of the other biochemical parameters or clinicopathological scores could similarly discriminate between the two groups at entry. Time-dependent analyses for the cholic acid/chenodeoxycholic acid ratio, serum total bilirubin and albumin concentrations and Child-Turcotte and Mayo scores were able to differentiate between primary sclerosing cholangitis patients who died or were transplanted and those who were not, whereas age of the patients and other parameters did not. The taurocholic acid/taurochenodeoxycholic acid ratio fell during progression of primary biliary cirrhosis but rose in temporal relationship with primary sclerosing cholangitis. This differential pattern of change was unique compared with other clinical and laboratory indices. In conclusion, serum chenodeoxycholic acid levels and the cholic acid/chenodeoxycholic acid ratio in both diseases were independent indices that allowed for the prediction of survival or the need for liver transplantation. These indices are worthy of further examination in a larger group of patients as prognostic criteria for chronic cholestatic liver disease and in the assessment of the efficacy of therapeutic interventions, including liver transplantations.

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Year:  1996        PMID: 8742915     DOI: 10.1111/j.1440-1746.1996.tb00064.x

Source DB:  PubMed          Journal:  J Gastroenterol Hepatol        ISSN: 0815-9319            Impact factor:   4.029


  9 in total

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Authors:  H Arndt; F Kullmann; J Schölmerich; K D Palitzsch
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2.  Visualization of bile homeostasis using (1)H-NMR spectroscopy as a route for assessing liver cancer.

Authors:  G A Nagana Gowda; Narasimhamurthy Shanaiah; Amanda Cooper; Mary Maluccio; Daniel Raftery
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3.  Bile acids conjugation in human bile is not random: new insights from (1)H-NMR spectroscopy at 800 MHz.

Authors:  G A Nagana Gowda; Narasimhamurthy Shanaiah; Amanda Cooper; Mary Maluccio; Daniel Raftery
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4.  Chenodeoxycholic and deoxycholic acids induced positive inotropic and negative chronotropic effects on rat heart.

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7.  Differential Feedback Regulation of Δ4-3-Oxosteroid 5β-Reductase Expression by Bile Acids.

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Authors:  Monika Rau; Johannes Schmitt; Thomas Berg; Andreas E Kremer; Bruno Stieger; Katharina Spanaus; Bertram Bengsch; Marta R Romero; Jose J Marin; Verena Keitel; Hartwig Klinker; Hans-Peter Tony; Beat Müllhaupt; Andreas Geier
Journal:  PLoS One       Date:  2018-12-03       Impact factor: 3.240

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Authors:  Juliet Emamaullee; Sara Khan; Carly Weaver; Cameron Goldbeck; George Yanni; Rohit Kohli; Yuri Genyk; Shengmei Zhou; Nick Shillingford; Patrick M Sullivan; Cheryl Takao; Jon Detterich; Paul F Kantor; John D Cleveland; Cynthia Herrington; S Ram Kumar; Vaughn Starnes; Sarah Badran; Neil D Patel
Journal:  JHEP Rep       Date:  2021-09-14
  9 in total

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