Lixia Gao1, Xinping Tian, Bin Liu, Fengchun Zhang. 1. Department of Rheumatology and Immunology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing 100730, China.
Abstract
OBJECTIVE: Although autoantibodies have been used for the diagnosis of primary biliary cirrhosis (PBC), their role has not been clarified. In this study, we try to explore the value of gp210 antibody and anti-centromere antibodies (ACA) in PBC. METHODS: Anti-gp210 and ACA were tested in 140 PBC patients by ELISA and indirect immunofluorescence respectively. Their association with clinical, pathological data and prognosis was analysed. RESULTS: 30.5% of PBC patients had positive anti-gp210 antibody and 29.2% had ACA. The anti-gp210 antibody positive group had higher Mayo risk scores and lower serum albumin levels compared to the negative one. Patients with positive anti-gp210 antibody were more likely to develop hepatic failure (p<0.05, OR=9.8460, 95% CI: 1.067-90.901) than patients with negative anti-gp210 antibody. More patients with positive ACA developed portal hypertension than patients with negative ACA (p<0.05, OR=9.259; 95% CI: 1.027-88.410). Furthermore, concurrent Sjögren's syndrome (SjS) and PBC was significantly more likely in the ACA positive group than in the negative ones (68.4% in ACA positive group, 20.7% in ACA negative group p<0.001). CONCLUSIONS: Both anti-gp210 antibody and ACA are related to severe disease course and poor prognosis. For PBC patients with positive ACA, further examinations should be made to detect underlying SjS.
OBJECTIVE: Although autoantibodies have been used for the diagnosis of primary biliary cirrhosis (PBC), their role has not been clarified. In this study, we try to explore the value of gp210 antibody and anti-centromere antibodies (ACA) in PBC. METHODS: Anti-gp210 and ACA were tested in 140 PBCpatients by ELISA and indirect immunofluorescence respectively. Their association with clinical, pathological data and prognosis was analysed. RESULTS: 30.5% of PBCpatients had positive anti-gp210 antibody and 29.2% had ACA. The anti-gp210 antibody positive group had higher Mayo risk scores and lower serum albumin levels compared to the negative one. Patients with positive anti-gp210 antibody were more likely to develop hepatic failure (p<0.05, OR=9.8460, 95% CI: 1.067-90.901) than patients with negative anti-gp210 antibody. More patients with positive ACA developed portal hypertension than patients with negative ACA (p<0.05, OR=9.259; 95% CI: 1.027-88.410). Furthermore, concurrent Sjögren's syndrome (SjS) and PBC was significantly more likely in the ACA positive group than in the negative ones (68.4% in ACA positive group, 20.7% in ACA negative group p<0.001). CONCLUSIONS: Both anti-gp210 antibody and ACA are related to severe disease course and poor prognosis. For PBCpatients with positive ACA, further examinations should be made to detect underlying SjS.
Authors: C Vitali; S Bombardieri; R Jonsson; H M Moutsopoulos; E L Alexander; S E Carsons; T E Daniels; P C Fox; R I Fox; S S Kassan; S R Pillemer; N Talal; M H Weisman Journal: Ann Rheum Dis Date: 2002-06 Impact factor: 19.103
Authors: E V Tsianos; J H Hoofnagle; P C Fox; M Alspaugh; E A Jones; D F Schafer; H M Moutsopoulos Journal: Hepatology Date: 1990-05 Impact factor: 17.425
Authors: Elena Tsangaridou; Hara Polioudaki; Rania Sfakianaki; Martina Samiotaki; Maria Tzardi; Meri Koulentaki; George Panayotou; Elias Kouroumalis; Elias Castanas; Panayiotis A Theodoropoulos Journal: BMC Gastroenterol Date: 2010-03-08 Impact factor: 3.067