Literature DB >> 6825535

Endogenous bile acid tolerance test for liver function.

M van Blankenstein, M Frenkel, J W van den Berg, F J ten Kate, E P Bosman-Jacobs, A C Touw-Blommesteyn.   

Abstract

Fasting and postprandial (stimulated) serum conjugated bile acids (CBA) were measured by a solid-phase radioimmunoassay in 329 patients undergoing liver biopsy, and the results were analyzed for 231 who fitted into 10 diagnostic categories. In healthy volunteers the mean fasting CBA of 1.8 +/- 0.7 mumol/liter rose to 3.0 +/- 0.8 mumol/liter postprandially. In patients mean fasting and stimulated CBA were only significantly raised in moderate to severe chronic and acute liver disease. Diagnostic sensitivity was poor in mild liver disease. Individuals with normal results were found in 8 of 11 disease categories. The ratio of stimulated to fasting CBA expressed in a stimulation quotient did not rise in more advanced liver disease. These findings are best explained by a constant fractional clearance of bile acids by the liver. We conclude that the serum conjugated bile acid determination as a test of liver cell function is not sensitive enough to identify all cases of biopsy-proven liver disease.

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Year:  1983        PMID: 6825535     DOI: 10.1007/bf01315143

Source DB:  PubMed          Journal:  Dig Dis Sci        ISSN: 0163-2116            Impact factor:   3.199


  42 in total

1.  A fluorimetric and enzymatic method for the estimation of serum total bile acids.

Authors:  G M Murphy; B H Billing; D N Baron
Journal:  J Clin Pathol       Date:  1970-10       Impact factor: 3.411

2.  Assessment of activity in chronic active liver disease. Serum bile acids compared with conventional tests and histology.

Authors:  M G Korman; A F Hofmann; W H Summerskill
Journal:  N Engl J Med       Date:  1974-06-20       Impact factor: 91.245

3.  Postprandial changes in serum concentrations of individual bile salts in normal subjects and patients with acute viral hepatitis.

Authors:  C B Campbell; C McGuffie; L W Powell; R K Roberts; A W Stewart
Journal:  Am J Dig Dis       Date:  1978-07

4.  [Application of the enzymatic microassay of serum bile acids: value of the post-prandial test and of the clearance of cholic acid (author's transl)].

Authors:  O Duhamel; J Chaintereuil; F Blanc; A C de Paulet; L Bertrand
Journal:  Gastroenterol Clin Biol       Date:  1981

5.  Response of total and individual serum bile acids to endogenous and exogenous bile acid input to the enterohepatic circulation.

Authors:  S G De Barros; W F Balistreri; R D Soloway; S G Weiss; P C Miller; K Soper
Journal:  Gastroenterology       Date:  1982-04       Impact factor: 22.682

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Authors:  O Fausa
Journal:  Scand J Gastroenterol       Date:  1976       Impact factor: 2.423

7.  Bile acid clearance in liver disease.

Authors:  L K Luey; K W Heaton
Journal:  Gut       Date:  1979-12       Impact factor: 23.059

8.  Evaluation of fasting serum bile acid concentration in patients with liver and gastrointestinal disorders.

Authors:  K Samuelson; A Aly; C Johansson; A Norman
Journal:  Scand J Gastroenterol       Date:  1981       Impact factor: 2.423

9.  Serum cholic and chenodeoxycholic acid conjugates and standard liver function tests in various morphological stages of alcoholic liver disease.

Authors:  P Tobiasson; B Boeryd
Journal:  Scand J Gastroenterol       Date:  1980       Impact factor: 2.423

10.  Fasting serum bile acids in liver disease. A comparison with histological features.

Authors:  R Alm; J Carlson; S Eriksson
Journal:  Scand J Gastroenterol       Date:  1982-03       Impact factor: 2.423

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  2 in total

1.  Determination of individual serum bile acids in chronic liver diseases: fasting levels and results of oral chenodeoxycholic acid tolerance test.

Authors:  Y Adachi; T Nanno; T Itoh; Y Kurumi; K Yamazaki; Y Sawada; T Yamamoto
Journal:  Gastroenterol Jpn       Date:  1988-08

2.  Diagnostic value of serum immunoreactive conjugated cholic or chenodeoxycholic acids in detecting hepatobiliary diseases. Comparison with levels of 3 alpha-hydroxy bile acids determined enzymatically and with routine liver tests.

Authors:  R Ferraris; M T Fiorentini; G Galatola; P Rolfo; M De la Pierre
Journal:  Dig Dis Sci       Date:  1987-08       Impact factor: 3.199

  2 in total

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