New Myositis Classification Criteria-What We Have Learned Since Bohan and Peter

被引:64
|
作者
Leclair, Valerie [1 ]
Lundberg, Ingrid E. [2 ,3 ]
机构
[1] Karolinska Univ Hosp, Karolinska Inst, Rheumatol Unit, Dept Med, SE-17176 Stockholm, Sweden
[2] Karolinska Inst, Rheumatol Unit, Dept Med, SE-17176 Solna, Sweden
[3] Karolinska Univ Hosp, Rheumatol Unit, SE-17176 Stockholm, Sweden
基金
瑞典研究理事会;
关键词
Classification criteria; Inflammatory myopathy; Dermatomyositis; Polymyositis; Inclusion body myositis; INCLUSION-BODY MYOSITIS; IDIOPATHIC INFLAMMATORY MYOPATHIES; ANTI-SYNTHETASE SYNDROME; DIAGNOSTIC-CRITERIA; RHEUMATIC-DISEASES; JUVENILE DERMATOMYOSITIS; OVERDIAGNOSED ENTITY; POLYMYOSITIS; AUTOANTIBODIES; ADULT;
D O I
10.1007/s11926-018-0726-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of Review Idiopathic inflammatory myopathy (IIM) classification criteria have been a subject of debate for many decades. Despite several limitations, the Bohan and Peter criteria are still widely used. The aim of this review is to discuss the evolution of IIM classification criteria. Recent Findings New IIM classification criteria are periodically proposed. The discovery of myositis-specific and myositis-associated autoantibodies led to the development of clinico-serological criteria, while in-depth description of IIM morphological features improved histopathology-based criteria. The long-awaited European League Against Rheumatism and American College of Rheumatology (EULAR/ACR) IIM classification criteria were recently published. Summary The Bohan and Peter criteria are outdated and validated classification criteria are necessary to improve research in IIM. The new EULAR/ACR IIM classification criteria are thus a definite improvement and an important step forward in the field.
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页数:8
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