Rheumatoid arthritis

被引:2903
作者
Scott, David L. [1 ]
Wolfe, Frederick [2 ,3 ]
Huizinga, Torn W. J. [4 ]
机构
[1] Kings Coll London, Sch Med, Weston Educ Ctr, Dept Rheumatol, London SE5 9RJ, England
[2] Natl Data Bank Rheumat Dis, Wichita, KS USA
[3] Univ Kansas, Sch Med, Wichita, KS 67214 USA
[4] Leiden Univ, Med Ctr, Dept Rheumatol, Leiden, Netherlands
关键词
MODIFYING ANTIRHEUMATIC DRUGS; CYCLIC CITRULLINATED PEPTIDE; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; HLA-DRB1 SHARED EPITOPE; DISEASE-ACTIVITY; DOUBLE-BLIND; UNDIFFERENTIATED ARTHRITIS; BIOLOGICS REGISTER; AMERICAN-COLLEGE; BRITISH SOCIETY;
D O I
10.1016/S0140-6736(10)60826-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Rheumatoid arthritis is characterised by persistent synovitis, systemic inflammation, and autoantibodies (particularly to rheumatoid factor and citrullinated peptide). 50% of the risk for development of rheumatoid arthritis is attributable to genetic factors. Smoking is the main environmental risk. In industrialised countries, rheumatoid arthritis affects 0.5-1.0% of adults, with 5-50 per 100 000 new cases annually. The disorder is most typical in women and elderly people. Uncontrolled active rheumatoid arthritis causes joint damage, disability, decreased quality of life, and cardiovascular and other comorbidities. Disease-modifying antirheumatic drugs (DMARDs), the key therapeutic agents, reduce synovitis and systemic inflammation and improve function. The leading DMARD is methotrexate, which can be combined with other drugs of this type. Biological agents are used when arthritis is uncontrolled or toxic effects arise with DMARDs. Tumour necrosis factor inhibitors were the first biological agents, followed by abatacept, rituximab, and tocilizumab. Infections and high costs restrict prescription of biological agents. Long-term remission induced by intensive, short-term treatment selected by biomarker profiles is the ultimate goal.
引用
收藏
页码:1094 / 1108
页数:15
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