BACKGROUND: Clinically significant primary biliary cirrhosis occurs in 2.5% of patients with systemic sclerosis. Primary biliary cirrhosis-specific autoantibodies include anti-mitochondrial, anti-glycoprotein 210, and anti-sp100 antibodies. The majority of asymptomatic anti-mitochondrial-positive subjects express histological features of primary biliary cirrhosis. Early detection of primary biliary cirrhosis is important, as timely introduction of ursodeoxycholic acid may improve prognosis. The aim was to assess the prevalence of MIT3 IgG-anti-mitochondrial, gp210, sp100 and other autoantibodies in patients with systemic sclerosis and compare the clinical and biochemical parameters in those who are primary biliary cirrhosis-specific autoantibodies positive and negative. MATERIALS/ METHODS: Fifty-two consecutive patients with systemic sclerosis were included. Thirty-three suffered from limited skin SS and 19 from diffuse SS. RESULTS: Eight (15%) patients with systemic sclerosis tested positive for primary biliary cirrhosis-specific autoantibodies. No significant differences were observed between primary biliary cirrhosis-specific autoantibodies positive and negative subjects in terms of various demographic, clinical or biochemical features. A trend towards increased prevalence of chronic fatigue in primary biliary cirrhosis-specific autoantibodies positive patients was observed. CONCLUSIONS: Primary biliary cirrhosis-specific autoantibodies were detected in 15% of the systemic sclerosis patients. Since patients with primary biliary cirrhosis-specific antibodies are at high-risk or do suffer from primary biliary cirrhosis, screening for primary biliary cirrhosis-specific autoantibodies may be considered during routine assessment of systemic sclerosis.
BACKGROUND: Clinically significant primary biliary cirrhosis occurs in 2.5% of patients with systemic sclerosis. Primary biliary cirrhosis-specific autoantibodies include anti-mitochondrial, anti-glycoprotein 210, and anti-sp100 antibodies. The majority of asymptomatic anti-mitochondrial-positive subjects express histological features of primary biliary cirrhosis. Early detection of primary biliary cirrhosis is important, as timely introduction of ursodeoxycholic acid may improve prognosis. The aim was to assess the prevalence of MIT3 IgG-anti-mitochondrial, gp210, sp100 and other autoantibodies in patients with systemic sclerosis and compare the clinical and biochemical parameters in those who are primary biliary cirrhosis-specific autoantibodies positive and negative. MATERIALS/ METHODS: Fifty-two consecutive patients with systemic sclerosis were included. Thirty-three suffered from limited skin SS and 19 from diffuse SS. RESULTS: Eight (15%) patients with systemic sclerosis tested positive for primary biliary cirrhosis-specific autoantibodies. No significant differences were observed between primary biliary cirrhosis-specific autoantibodies positive and negative subjects in terms of various demographic, clinical or biochemical features. A trend towards increased prevalence of chronic fatigue in primary biliary cirrhosis-specific autoantibodies positive patients was observed. CONCLUSIONS:Primary biliary cirrhosis-specific autoantibodies were detected in 15% of the systemic sclerosispatients. Since patients with primary biliary cirrhosis-specific antibodies are at high-risk or do suffer from primary biliary cirrhosis, screening for primary biliary cirrhosis-specific autoantibodies may be considered during routine assessment of systemic sclerosis.
Authors: Cristina Rigamonti; Dimitrios P Bogdanos; Maria G Mytilinaiou; Daniel S Smyk; Eirini I Rigopoulou; Andrew K Burroughs Journal: Int J Rheumatol Date: 2011-12-06
Authors: Rudi Alberts; Elisabeth M G de Vries; Elizabeth C Goode; Xiaojun Jiang; Fotis Sampaziotis; Krista Rombouts; Katrin Böttcher; Trine Folseraas; Tobias J Weismüller; Andrew L Mason; Weiwei Wang; Graeme Alexander; Domenico Alvaro; Annika Bergquist; Niklas K Björkström; Ulrich Beuers; Einar Björnsson; Kirsten Muri Boberg; Christopher L Bowlus; Maria C Bragazzi; Marco Carbone; Olivier Chazouillères; Angela Cheung; Georgios Dalekos; John Eaton; Bertus Eksteen; David Ellinghaus; Martti Färkkilä; Eleonora A M Festen; Annarosa Floreani; Irene Franceschet; Daniel Nils Gotthardt; Gideon M Hirschfield; B van Hoek; Kristian Holm; Simon Hohenester; Johannes Roksund Hov; Floris Imhann; Pietro Invernizzi; Brian D Juran; Henrike Lenzen; Wolfgang Lieb; Jimmy Z Liu; Hanns-Ulrich Marschall; Marco Marzioni; Espen Melum; Piotr Milkiewicz; Tobias Müller; Albert Pares; Christian Rupp; Christian Rust; Richard N Sandford; Christoph Schramm; Stefan Schreiber; Erik Schrumpf; Mark S Silverberg; Brijesh Srivastava; Martina Sterneck; Andreas Teufel; Ludovic Vallier; Joanne Verheij; Arnau Vich Vila; Boudewijn de Vries; Kalliopi Zachou; Roger W Chapman; Michael P Manns; Massimo Pinzani; Simon M Rushbrook; Konstantinos N Lazaridis; Andre Franke; Carl A Anderson; Tom H Karlsen; Cyriel Y Ponsioen; Rinse K Weersma Journal: Gut Date: 2017-08-04 Impact factor: 23.059