The value of antinuclear antibodies in primary biliary cirrhosis

被引:58
作者
Gao, Lixia [1 ]
Tian, Xinping [1 ]
Liu, Bin [1 ]
Zhang, Fengchun [1 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll Hosp, Dept Rheumatol & Immunol, Beijing 100730, Peoples R China
关键词
primary biliary cirrhosis; anti-gp210; antibody; anti-centromere antibodies; hepatic failure; portal hypertension; Sjogren's syndrome;
D O I
10.1007/s10238-008-0150-6
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
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 Sjogren'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.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 39 条
[1]
Long-term ursodeoxycholic acid delays histological progression in primary biliary cirrhosis [J].
Angulo, P ;
Batts, KP ;
Therneau, TM ;
Jorgensen, RA ;
Dickson, ER ;
Lindor, KD .
HEPATOLOGY, 1999, 29 (03) :644-647
[2]
ANTICENTROMERE ANTIBODY IN PRIMARY BILIARY-CIRRHOSIS [J].
BERNSTEIN, RM ;
CALLENDER, ME ;
NEUBERGER, JM ;
HUGHES, GRV ;
WILLIAMS, R .
ANNALS OF THE RHEUMATIC DISEASES, 1982, 41 (06) :612-614
[3]
CHRISTENSEN E, 1980, GASTROENTEROLOGY, V78, P236
[4]
PREVALENCE OF SJOGRENS-SYNDROME IN AUTOIMMUNE-DISEASES [J].
COLL, J ;
RIVES, A ;
GRINO, MC ;
SETOAIN, J ;
VIVANCOS, J ;
BALCELLS, A .
ANNALS OF THE RHEUMATIC DISEASES, 1987, 46 (04) :286-289
[5]
Histopathological study of primary biliary cirrhosis and the effect of ursodeoxycholic acid treatment on histology progression [J].
Degott, C ;
Zafrani, ES ;
Callard, P ;
Balkau, B ;
Poupon, RE ;
Poupon, R .
HEPATOLOGY, 1999, 29 (04) :1007-1012
[6]
PRIMARY BILIARY-CIRRHOSIS - PARADIGM OR PARADOX FOR AUTOIMMUNITY [J].
GERSHWIN, ME ;
MACKAY, IR .
GASTROENTEROLOGY, 1991, 100 (03) :822-833
[7]
Management of primary biliary cirrhosis [J].
Heathcote, EJ .
HEPATOLOGY, 2000, 31 (04) :1005-1013
[8]
HTLV-I associated Sjogren's syndrome is aetiologically distinct from anti-centromere antibodies positive Sjogren's syndrome [J].
Hida, A ;
Kawabe, Y ;
Kawakami, A ;
Migita, K ;
Tominaga, M ;
Nakamura, H ;
Eguchi, K .
ANNALS OF THE RHEUMATIC DISEASES, 1999, 58 (05) :320-322
[9]
Anti-centromere antibodies as a marker of Raynaud's phenomenon in pediatric rheumatologic diseases [J].
Hossny, E ;
Hady, HA ;
Mabrouk, R .
PEDIATRIC ALLERGY AND IMMUNOLOGY, 2000, 11 (04) :250-255
[10]
Anti-CENP-H antibodies in patients with Sjogren's syndrome [J].
Hsu, TC ;
Chang, CH ;
Lin, MC ;
Liu, ST ;
Yen, TJ ;
Tsay, GJ .
RHEUMATOLOGY INTERNATIONAL, 2006, 26 (04) :298-303