Literature DB >> 9249725

Antimitochondrial antibody profiles in primary biliary cirrhosis distinguish at early stages between a benign and a progressive course: a prospective study on 200 patients followed for 10 years.

R Klein1, H Pointner, W Zilly, B Glässner-Bittner, N Breuer, W Garbe, V Fintelmann, J F Kalk, D Müting, R Fischer, W Tittor, J Pausch, K P Maier, P A Berg.   

Abstract

In recent retrospective studies, it was shown that subtypes of antimitochondrial antibodies (AMA) can help to discriminate between a benign [only anti-M9 and/or anti-M2 positive by enzyme-linked immunosorbent assay (ELISA)] and a rather progressive course (anti-M2, -M4 and/or -M8 positive). According to different constellations of these AMA subspecificities in ELISA and complement fixation test (CFT), four AMA profiles (A-D) were defined. In 1984 we started a prospective study based on 200 PBC patients with known AMA profiles in order to correlate the antibody pattern with the clinical outcome. Progression was defined primarily as the necessity of liver transplantation and death due to hepatic failure or variceal bleeding. At entry, 18 (9%) of the 200 patients had AMA profile A (only anti-M9), 57 (29%) profile B (only anti-M2 with or without anti-M9), 74 (37%) profile C (anti-M2 in association with anti-M4/-M8 by ELISA), and 51 (26%) profile D (anti-M2/-M4/-M8 by ELISA and CFT). At the beginning of the study, 177 patients had PBC stage I/II. During the observation period of ten years, ten patients died and in 18 orthotopic liver transplantation (OLT) was performed; all these patients belonged to profile C/D. Furthermore, 44% of the patients with profile C and 31% of the patients with profile D progressed to late stages, as defined by histology and clinical manifestations such as portal hypertension and increase of bilirubin, while only one of the patients with profile B and none of the profile A-patients developed late stage PBC. A significant increase of bilirubin was observed only in C/D-patients. AMA profiles did not change during the follow-up. In conclusion, AMA profiles discriminate between a benign and a progressive course of PBC already at early stages.

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Year:  1997        PMID: 9249725     DOI: 10.1111/j.1600-0676.1997.tb00793.x

Source DB:  PubMed          Journal:  Liver        ISSN: 0106-9543


  9 in total

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

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4.  Catalytic domain of PDC-E2 contains epitopes recognized by antimitochondrial antibodies in primary biliary cirrhosis.

Authors:  Sandra Braun; Christoph Berg; Sandra Buck; Michael Gregor; Reinhild Klein
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5.  Efficacy of ursodeoxycholic acid combined with Tongdan Decoction () on immunological indices and histopathological changes in primary biliary cirrhosis patients.

Authors:  Guang-Dong Tong; Hai-Hong Tang; Chun-Shan Wei; Ying-Jie Chen; Jin-Song He; Xiao-Zhou Zhou; Ying-Jun Zheng; Da-Qiao Zhou
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Review 6.  Autoantigens in primary biliary cirrhosis.

Authors:  D E Jones
Journal:  J Clin Pathol       Date:  2000-11       Impact factor: 3.411

7.  Demonstration of autoantibodies to recombinant human sulphite oxidase in patients with chronic liver disorders and analysis of their clinical relevance.

Authors:  B Preuss; C Berg; F Altenberend; M Gregor; S Stevanovic; R Klein
Journal:  Clin Exp Immunol       Date:  2007-08-17       Impact factor: 4.330

8.  Autoantibodies to muscarinic acetylcholine receptors found in patients with primary biliary cirrhosis.

Authors:  Christoph P Berg; Karin Blume; Kirsten Lauber; Michael Gregor; Peter A Berg; Sebastian Wesselborg; Gerburg M Stein
Journal:  BMC Gastroenterol       Date:  2010-10-16       Impact factor: 3.067

Review 9.  Biomarkers for primary biliary cholangitis: current perspectives.

Authors:  Elias Kouroumalis; Demetrius Samonakis; Argyro Voumvouraki
Journal:  Hepat Med       Date:  2018-06-18
  9 in total

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