Correlation of initial autoantibody profile and clinical outcome in primary biliary cirrhosis

被引:167
作者
Wesierska-Gadek, J
Penner, E
Battezzati, PM
Selmi, C
Zuin, M
Hitchman, E
Worman, HJ
Gershwin, ME
Podda, M
Invernizzi, P
机构
[1] Univ Milan, San Paolo Sch Med, Dept Med, Div Internal Med, I-20142 Milan, Italy
[2] Vienna Med Univ, Inst Canc Res, Dept Internal Med 1, Vienna, Austria
[3] Vienna Med Univ, Dept Internal Med, Vienna, Austria
[4] Univ Calif Davis, Div Rheumatol Allergy & Clin Immunol, Davis, CA 95616 USA
[5] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY USA
[6] Columbia Univ, Coll Phys & Surg, Dept Anat & Cell Biol, New York, NY USA
关键词
D O I
10.1002/hep.21172
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Although there have been significant advances in understanding the clinical and biochemical features of primary biliary cirrhosis (PBC), there is still a paucity of data on the usefulness of biomarkers as prognostic indicators. This is particularly important at the time of initial diagnosis. indeed, the widespread use of antimitochondrial antibody testing has led to an earlier diagnosis of asymptomatic PBC and it is difficult to predict which patients will experience a benign versus a rapidly progressive course. To address this issue, we examined a unique population of 127 newly diagnosed patients with PBC during a 15-year period of observation that began in January 1990. Sera from these patients were analyzed for antimitochondrial, antinuclear, and anti-smooth muscle antibodies, and immunoblotting was performed for nuclear pore complex (NPC). The patients were then followed up longitudinally using biochemical liver function tests. No patient was under any medical therapy for PBC at the time of the initial sera collection. Data were analyzed based not only on the clinical features, but also the Mayo score and specific outcome measures, including time to death, need for liver transplantation, and complication free survival. Among patients with early disease, bilirubin increased to > 2 mg/dL in the anti-NPC(+) patients (26% vs. 5%, P = .019). Anti-NPC antibodies remained stable or slightly increased over the period of observation. In conclusion, anti-NPC identifies patients likely to experience an unfavorable clinical course and more rapid disease progression.
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页码:1135 / 1144
页数:10
相关论文
共 39 条
[1]   Development of autoantibodies before the clinical onset of systemic lupus erythematosus [J].
Arbuckle, MR ;
McClain, MT ;
Rubertone, MV ;
Scofield, RH ;
Dennis, GJ ;
James, JA ;
Harley, JB .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 349 (16) :1526-1533
[2]  
Bloch DB, 2005, J RHEUMATOL, V32, P477
[3]  
Bogdanos Dimitrios-Petrou, 2003, Clin Liver Dis, V7, P759, DOI 10.1016/S1089-3261(03)00104-1
[4]   THE 210-KD NUCLEAR-ENVELOPE POLYPEPTIDE RECOGNIZED BY HUMAN AUTOANTIBODIES IN PRIMARY BILIARY-CIRRHOSIS IS THE MAJOR GLYCOPROTEIN OF THE NUCLEAR-PORE [J].
COURVALIN, JC ;
LASSOUED, K ;
BARTNIK, E ;
BLOBEL, G ;
WOZNIAK, RW .
JOURNAL OF CLINICAL INVESTIGATION, 1990, 86 (01) :279-285
[5]   The role of antibodies in myasthenia gravis [J].
De Baets, M ;
Stassen, MHW .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2002, 202 (1-2) :5-11
[6]   PROGNOSIS IN PRIMARY BILIARY-CIRRHOSIS - MODEL FOR DECISION-MAKING [J].
DICKSON, ER ;
GRAMBSCH, PM ;
FLEMING, TR ;
FISHER, LD ;
LANGWORTHY, A .
HEPATOLOGY, 1989, 10 (01) :1-7
[7]   MODIFIED PROCEDURE FOR ISOLATION OF A PORE COMPLEX LAMINA FRACTION FROM RAT-LIVER NUCLEI [J].
DWYER, N ;
BLOBEL, G .
JOURNAL OF CELL BIOLOGY, 1976, 70 (03) :581-591
[8]  
GERSHWIN ME, 1987, J IMMUNOL, V138, P3525
[9]   Antinuclear antibodies in primary biliary cirrhosis [J].
Invernizzi, P ;
Selmi, C ;
Ranftler, C ;
Podda, M ;
Wesierska-Gadek, J .
SEMINARS IN LIVER DISEASE, 2005, 25 (03) :298-310
[10]   Comparison of the clinical features and clinical course of antimitochondrial antibody-positive and -negative primary biliary cirrhosis [J].
Invernizzi, P ;
Crosignani, A ;
Battezzati, PM ;
Covini, G ;
DeValle, G ;
Larghi, A ;
Zuin, M ;
Podda, M .
HEPATOLOGY, 1997, 25 (05) :1090-1095