Literature DB >> 7615288

Characterisation of patients with a complete biochemical response to ursodeoxycholic acid.

R A Jorgensen1, E R Dickson, A F Hofmann, S S Rossi, K D Lindor.   

Abstract

Ursodeoxycholic acid (UDCA) leads to biochemical and clinical improvement in many patients with primary biliary cirrhosis (PBC); although, the response is variable. This study compared UDCA treated patients with complete normalisation of biochemical functions to those without such improvement. Of the 65 patients receiving UDCA, 12 (19%) showed normalisation of liver biochemical functions at two years. The remaining 53 patients showed a less complete response. Mean (SD) alkaline phosphatase and total serum bilirubin values were significantly lower at entry in the patients whose liver biochemistry tests normalised (912 (732) U/l v 1417 (1021) U/l, p = 0.003, and 0.7 (12.1 (5.2) mumol/l v 38.9 (48.5) mumol/l, p = 0.0002, respectively), and percentage of UDCA in biliary bile acid was higher (56.3 (9.5)% v 38.3 (21.1)%, p = 0.03). Patients with biochemically and histologically less severe disease, and greater enrichment of biliary bile with UDCA, are more likely to respond favourably to the drug. The main objective of continued study will be to find out if normal liver biochemical functions can retard disease progression. The association of greater UDCA enrichment with complete biochemical responses suggests that higher doses of UDCA should be evaluated.

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Year:  1995        PMID: 7615288      PMCID: PMC1382637          DOI: 10.1136/gut.36.6.935

Source DB:  PubMed          Journal:  Gut        ISSN: 0017-5749            Impact factor:   23.059


  20 in total

1.  Ursodeoxycholic acid-induced changes of plasma and urinary bile acids in patients with primary biliary cirrhosis.

Authors:  A Stiehl; G Rudolph; R Raedsch; B Möller; U Hopf; E Lotterer; J Bircher; U Fölsch; J Klaus; R Endele
Journal:  Hepatology       Date:  1990-09       Impact factor: 17.425

2.  Ursodeoxycholate reduces hepatotoxicity of bile salts in primary human hepatocytes.

Authors:  P R Galle; L Theilmann; R Raedsch; G Otto; A Stiehl
Journal:  Hepatology       Date:  1990-09       Impact factor: 17.425

3.  A multicenter, controlled trial of ursodiol for the treatment of primary biliary cirrhosis. UDCA-PBC Study Group.

Authors:  R E Poupon; B Balkau; E Eschwège; R Poupon
Journal:  N Engl J Med       Date:  1991-05-30       Impact factor: 91.245

4.  Prognosis in primary biliary cirrhosis: model for decision making.

Authors:  E R Dickson; P M Grambsch; T R Fleming; L D Fisher; A Langworthy
Journal:  Hepatology       Date:  1989-07       Impact factor: 17.425

5.  Immunomodulatory effects of ursodeoxycholic acid on immune responses.

Authors:  M Yoshikawa; T Tsujii; K Matsumura; J Yamao; Y Matsumura; R Kubo; H Fukui; S Ishizaka
Journal:  Hepatology       Date:  1992-08       Impact factor: 17.425

6.  A controlled trial of cyclosporine in the treatment of primary biliary cirrhosis.

Authors:  R H Wiesner; J Ludwig; K D Lindor; R A Jorgensen; W P Baldus; H A Homburger; E R Dickson
Journal:  N Engl J Med       Date:  1990-05-17       Impact factor: 91.245

7.  Ursodeoxycholic acid in primary biliary cirrhosis: results of a controlled double-blind trial.

Authors:  U Leuschner; H Fischer; W Kurtz; S Güldütuna; K Hübner; A Hellstern; M Gatzen; M Leuschner
Journal:  Gastroenterology       Date:  1989-11       Impact factor: 22.682

8.  High pressure liquid chromatographic analysis of conjugated bile acids in human bile: simultaneous resolution of sulfated and unsulfated lithocholyl amidates and the common conjugated bile acids.

Authors:  S S Rossi; J L Converse; A F Hofmann
Journal:  J Lipid Res       Date:  1987-05       Impact factor: 5.922

9.  Physicochemical and physiological properties of cholylsarcosine. A potential replacement detergent for bile acid deficiency states in the small intestine.

Authors:  J Lillienau; C D Schteingart; A F Hofmann
Journal:  J Clin Invest       Date:  1992-02       Impact factor: 14.808

10.  Evaluation of colchicine therapy in primary biliary cirrhosis.

Authors:  H Bodenheimer; F Schaffner; J Pezzullo
Journal:  Gastroenterology       Date:  1988-07       Impact factor: 22.682

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  9 in total

1.  Characterisation of patients with primary biliary cirrhosis responding to long term ursodeoxycholic acid treatment.

Authors:  M Leuschner; C F Dietrich; T You; C Seidl; J Raedle; G Herrmann; H Ackermann; U Leuschner
Journal:  Gut       Date:  2000-01       Impact factor: 23.059

Review 2.  Primary biliary cirrhosis: new perspectives in diagnosis and treatment.

Authors:  M I Prince; D E Jones
Journal:  Postgrad Med J       Date:  2000-04       Impact factor: 2.401

Review 3.  Primary biliary cirrhosis: From bench to bedside.

Authors:  Elias Kouroumalis; George Notas
Journal:  World J Gastrointest Pharmacol Ther       Date:  2015-08-06

Review 4.  Latest and emerging therapies for primary biliary cirrhosis and primary sclerosing cholangitis.

Authors:  Claudia O Zein; Keith D Lindor
Journal:  Curr Gastroenterol Rep       Date:  2010-02

Review 5.  Ursodeoxycholic acid for primary biliary cirrhosis.

Authors:  Jelena S Rudic; Goran Poropat; Miodrag N Krstic; Goran Bjelakovic; Christian Gluud
Journal:  Cochrane Database Syst Rev       Date:  2012-12-12

6.  Effect of long term simvastatin administration as an adjunct to ursodeoxycholic acid: evidence for a synergistic effect on biliary bile acid composition but not on serum lipids in humans.

Authors:  F Lanzarotto; B Panarotto; R Sorbara; M Panteghini; F Pagani; S Sosta; A Lanzini
Journal:  Gut       Date:  1999-04       Impact factor: 23.059

7.  Fenofibrate for patients with asymptomatic primary biliary cirrhosis.

Authors:  Kazufumi Dohmen; Toshihiko Mizuta; Makoto Nakamuta; Naoya Shimohashi; Hiromi Ishibashi; Kyosuke Yamamoto
Journal:  World J Gastroenterol       Date:  2004-03-15       Impact factor: 5.742

Review 8.  Pharmacological interventions for primary biliary cholangitis: an attempted network meta-analysis.

Authors:  Francesca Saffioti; Kurinchi Selvan Gurusamy; Leonardo Henry Eusebi; Emmanuel Tsochatzis; Brian R Davidson; Douglas Thorburn
Journal:  Cochrane Database Syst Rev       Date:  2017-03-28

Review 9.  The diagnosis and treatment of primary biliary cirrhosis.

Authors:  Kyung-Ah Kim; Sook-Hyang Jeong
Journal:  Korean J Hepatol       Date:  2011-09
  9 in total

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