Literature DB >> 3181666

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

Y Adachi1, T Nanno, T Itoh, Y Kurumi, K Yamazaki, Y Sawada, T Yamamoto.   

Abstract

Fifteen bile acids in serum of 5 normal subjects and 21 patients with chronic liver diseases were fractionated by high performance liquid chromatography. Fasting total bile acids (TBA), glycocholic acid, taurocholic acid, glycochenodeoxycholic acid (GCDCA), and taurochenodeoxycholic acid (TCDCA) were significantly increased in patients with liver cirrhosis as compared with normal subjects. The cholic acid (CA) level and the ratio of the sum of free and conjugated CA to the sum of free and conjugated chenodeoxycholic acid (CDCA) were significantly elevated in patients with compensated as compared with decompensated liver cirrhosis, and were useful for differentiation of the two conditions. Serum bile acid levels were determined after oral administration of 500 mg of CDCA in the 5 normal subjects and 11 patients with liver disease. The TBA level reached a peak 90 min after CDCA administration in patients with chronic hepatitis and after 120 min in those with liver cirrhosis. The increase in the TBA level was significantly greater in patients with liver disease than in normal subjects. CDCA, GCDCA, and TCDCA showed changes similar to those in TBA. In patients with decompensated liver cirrhosis, the reduction in the TBA and CDCA levels after the peaks was slow, and GCDCA and TCDCA levels continued to increase until 180 min after the administration of CDCA. The TBA and CDCA levels 180 min after CDCA administration were significantly different among normal subjects, patients with chronic hepatitis, those with compensated liver cirrhosis, and those with decompensated liver cirrhosis, suggesting the usefulness of CDCA administration in differentiation of these conditions.

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Year:  1988        PMID: 3181666     DOI: 10.1007/bf02779208

Source DB:  PubMed          Journal:  Gastroenterol Jpn        ISSN: 0435-1339


  17 in total

Review 1.  Bile acid metabolism: its relation to clinical disease.

Authors:  W Berry; J Reichen
Journal:  Semin Liver Dis       Date:  1983-11       Impact factor: 6.115

2.  Fasting serum bile acid level in cirrhosis. A semi-quantitative index of hepatic function.

Authors:  S Islam; R E Poupon; J C Barbare; Y Chrétien; F Darnis; R Poupon
Journal:  J Hepatol       Date:  1985       Impact factor: 25.083

3.  [Analysis of free, glycine-and taurine-conjugated individual bile acids using high performance liquid chromatography and immobilized 3 alpha-hydroxysteroid dehydrogenase in column form (author's transl)].

Authors:  S Okuyama
Journal:  Rinsho Byori       Date:  1981-05

4.  [Clinical significance of the determination of serum bile acid and oral bile acid loading test in gastrointestinal diseases].

Authors:  Y Matsuzaki; T Osuga; M Imawari; J Shoda; K Mitamura; K Kozawa
Journal:  Nihon Shokakibyo Gakkai Zasshi       Date:  1985-05

5.  Diagnostic value of serum bile acids.

Authors:  S Matern; W Gerok
Journal:  Acta Hepatogastroenterol (Stuttg)       Date:  1979-06

6.  Clinical significance of serum bile acid measurement in liver diseases.

Authors:  T Morita; Y Matsuyama; T Fujimoto; M Higuchi; T Tsujii; Y Matsuoka
Journal:  Gastroenterol Jpn       Date:  1978

7.  Endogenous bile acid tolerance test for liver function.

Authors:  M van Blankenstein; M Frenkel; J W van den Berg; F J ten Kate; E P Bosman-Jacobs; A C Touw-Blommesteyn
Journal:  Dig Dis Sci       Date:  1983-02       Impact factor: 3.199

8.  Cholic acid synthesis as an index of the severity of liver disease in man.

Authors:  W C McCormick; C C Bell; L Swell; Z R Vlahcevic
Journal:  Gut       Date:  1973-11       Impact factor: 23.059

9.  [Evaluation of the serum bile acid measurement for the diagnosis of liver diseases, with special reference to individual serum bile acids in hepatobiliary diseases (author's transl)].

Authors:  R Uenoyama
Journal:  Rinsho Byori       Date:  1981-05

10.  Quantification of individual serum bile acids in patients with liver diseases using high-performance liquid chromatography.

Authors:  H Okuda; H Obata; T Nakanishi; T Hisamitsu; K Matsubara; H Watanabe
Journal:  Hepatogastroenterology       Date:  1984-08
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  4 in total

1.  Immunosuppressive effect of chenodeoxycholic acid on natural killer cell activity in patients with biliary atresia and hepatitis C virus-related liver cirrhosis.

Authors:  Masaru Hirata; Yasushi Harihara; Yoshiaki Kita; Shoichi Saito; Motoko Nishimuraj; Hiroyuki Yoshino; Keiji Sano; Mitsuhiro Ito; Koji Kusaka; Hideo Kawarasaki; Kohei Hashizume; Masatoshi Makuuchi
Journal:  Dig Dis Sci       Date:  2002-05       Impact factor: 3.199

Review 2.  Predictive value of serum bile acids as metabolite biomarkers for liver cirrhosis: a systematic review and meta-analysis.

Authors:  Xu Han; Juan Wang; Hao Gu; Hongtao Guo; Yili Cai; Xing Liao; Miao Jiang
Journal:  Metabolomics       Date:  2022-06-27       Impact factor: 4.747

3.  Glycochenodeoxycholic Acid Does Not Increase Transforming Growth Factor-Beta Expression in Bile Duct Epithelial Cells or Collagen Synthesis in Myofibroblasts.

Authors:  Anna Wang; Dorothy Yu; Yuewen Gong; Jessie Garber; Gerald Y Minuk
Journal:  J Clin Exp Hepatol       Date:  2017-05-13

4.  Integrated Plasma and Bile Metabolomics Based on an UHPLC-Q/TOF-MS and Network Pharmacology Approach to Explore the Potential Mechanism of Schisandra chinensis-Protection From Acute Alcoholic Liver Injury.

Authors:  Lianlin Su; Jing Mao; Min Hao; Tulin Lu; Chunqin Mao; Huangjin Tong; Chenghao Fei
Journal:  Front Pharmacol       Date:  2020-01-16       Impact factor: 5.810

  4 in total

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