Therapy of psoriatic arthritis

被引:0
|
作者
Maerker-Hermann, E. [1 ]
机构
[1] HSK Dr Horst Schmidt Kliniken GmbH, Klin Innere Med Rheumatol Klin Immunol Nephrol 4, D-65199 Wiesbaden, Germany
来源
ZEITSCHRIFT FUR RHEUMATOLOGIE | 2013年 / 72卷 / 08期
关键词
Disease modifying antirheumatic drugs; TNF alpha inhibitor; Biological therapy; Ustekinumab; Apremilast; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; RHEUMATOID-ARTHRITIS; MONOCLONAL-ANTIBODY; PREDICTORS THEREOF; DANBIO REGISTRY; DRUG SURVIVAL; USTEKINUMAB; EFFICACY; SAFETY;
D O I
10.1007/s00393-013-1190-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In psoriatic arthritis (PsA) the heterogeneous spectrum of the disease with arthritis/synovitis, axial manifestation, enthesitis, dactylitis, psoriatic skin disease and nail psoriasis has to be considered. Moreover, PsA activity and severity as well as comorbidities are of importance for making therapeutic decisions. Measurement instruments developed for therapeutic studies of rheumatoid arthritis or ankylosing spondylitis are often not appropriate for application in PsA investigations. In this paper established therapies with nonsteroidal antirheumatic drugs, disease modifying antirheumatic drugs (DMARDs) and TNF-alpha inhibitors and the current EULAR guidelines from 2012 are reviewed. However, there is a need for new therapeutic agents for those patients who do not respond to or do not tolerate the current therapies. Other biologic agents have also been tested for PsA with moderate effects only. New therapeutic options could result from the anti-IL12 and anti-IL23 receptor monoclonal antibody ustekinumab and from small molecules such as the oral PDE-4 inhibitor apremilast.
引用
收藏
页码:784 / +
页数:6
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