Myositis-specific and myositis-associated antibodies in overlap myositis in comparison to primary dermatopolymyositis: Relevance for clinical classification: Retrospective study of 169 patients

被引:58
|
作者
Vancsa, Andrea [1 ,2 ]
Gergely, Lajos
Ponyi, Andrea [3 ]
Lakos, Gabriella
Nemeth, Julia [4 ]
Szodoray, Peter
Danko, Katalin
机构
[1] Univ Debrecen, DEOEC, Inst Internal Med,Div Clin Immunol, Med & Hlth Sci Ctr,Dept Internal Med 3, H-4032 Debrecen, Hungary
[2] Univ Debrecen, Med & Hlth Sci Ctr, Div Clin Immunol, Inst Internal Med,Dept Rheumatol, H-4032 Debrecen, Hungary
[3] Semmelweis Univ, Dept Pediat 2, Inst Internal Med, H-1085 Budapest, Hungary
[4] Natl Inst Hlth, Dept Immunodiagnost, Inst Internal Med, Budapest, Hungary
基金
新加坡国家研究基金会;
关键词
Idiopathic inflammatory myopathy (IIM); Overlap syndrome; Myositis-specific antibodies (MSA); Myositis-associated antibodies (MAA); Immunosuppressive therapy; INFLAMMATORY MYOPATHIES; IMMUNOGENETIC FEATURES; PM-SCL; AUTOANTIBODIES; POLYMYOSITIS;
D O I
10.1016/j.jbspin.2009.08.008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: The current study was performed in order to determine the prevalence of different myositis-specific and myositis-associated antibodies, as well as their association with clinical characteristics, disease course and response to therapy in 169 Hungarian patients with idiopathic inflammatory myopathy. Methods: Sera of 130 primary and 39 overlap myositis including systemic sclerosis (13), rheumatoid arthritis (12), systemic lupus erythematosus (5) and Sjogren's syndrome (9) cases were analyzed. Antinuclear antibody, scleroderma-associated antibodies (anti-centromere, anti-topoisomerase I), anti-Jo-1, anti-PL-7, anti-PL-12, anti-Mi-2, anti-SRP and anti-PM-Scl, anti-Ku, anti-SS-A, anti-SS-B, anti-U1snRNP were tested. Autoantibody results were compared with clinical characteristics, disease course of overlap versus primary myositis patients, as well as with response to therapy. Results: Associated connective tissue disease occurred in 23.1% of the patients. Myositis-associated antibodies were found in 8.5% of primary myositis patients, indicating that 11 additional primary myositis patients (23% vs. 29.6%) can be classified as overlap in all cohort according to the newly proposed diagnostic criteria. Polymyositis was found to be the most common myositis form in overlap myositis (87.2%), while scleroderma was the most common disease associated (33.3%). ANA was positive in 25.4% of primary and in 61.5% of overlap myositis cases. Altogether 39.6% of myositis patients (n = 67) had autoantibodies, most commonly anti Jo-1 (18.3%) correlating with a polycyclic disease course. Conclusion: Inclusion of myositis-specific and associated antibodies into the newly proposed diagnostic criteria for inflammatory myopathies is of great importance in order to determine subclasses and to introduce adequate therapy in time. (C) 2010 Societe francaise de rhumatologie. Published by Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:125 / 130
页数:6
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