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银屑病关节炎的治疗进展。

Advances in the management of psoriatic arthritis.

机构信息

Rheumatology Department of Lucania, San Carlo Hospital of Potenza, Via Potito Petrone Snc, Potenza 85100, Italy.

Rheumatology Department of Lucania, Madonna delle Grazie Hospital of Matera, Contrada Cattedra Ambulante Snc, Matera 75100, Italy.

出版信息

Nat Rev Rheumatol. 2014 Sep;10(9):531-42. doi: 10.1038/nrrheum.2014.106. Epub 2014 Jul 8.

Abstract

Psoriatic arthritis (PsA), which affects musculoskeletal structures, skin and nails, is a heterogeneous chronic inflammatory disease with a wide clinical spectrum and variable course. Patients with PsA are more likely than healthy individuals to have metabolic syndrome or cardiovascular disease. To include these comorbidities, 'psoriatic disease' has been suggested as an umbrella term. The management of PsA has changed tremendously over the past decade owing to early diagnosis and improvement in treatment strategies, including, early referral from dermatologists and primary-care physicians to rheumatologists, early initiation of therapy, treating to the target of remission or low disease activity, and advances in pharmacological therapy. Outcome assessment is also improving, because of validated instruments for clinical disease manifestations. The commercialization of TNF blockers, including adalimumab, etanercept, golimumab and infliximab, is representative of a revolution in the treatment of PsA. A new anti-TNF agent, certolizumab pegol, and a fully human monoclonal antibody against IL-12 and IL-23, ustekinumab, are approved for the treatment of active PsA. The efficacy of ustekinumab suggests that inhibiting the type 17 T helper pathway might be an alternative to blocking TNF. PsA management must now use improved measures to predict patient outcomes and define remission, and develop better-targeted therapies.

摘要

银屑病关节炎(PsA)影响肌肉骨骼结构、皮肤和指甲,是一种具有广泛临床谱和多变病程的异质性慢性炎症性疾病。与健康个体相比,PsA 患者更有可能患有代谢综合征或心血管疾病。为了包括这些合并症,有人提出“银屑病性疾病”作为一个伞式术语。由于早期诊断和治疗策略的改善,包括皮肤科医生和初级保健医生向风湿病医生的早期转诊、早期开始治疗、以缓解或低疾病活动度为目标进行治疗,以及药理学治疗的进步,过去十年中 PsA 的治疗发生了巨大变化。由于针对临床疾病表现的验证性仪器,结局评估也在改善。肿瘤坏死因子(TNF)阻滞剂的商业化,包括阿达木单抗、依那西普、戈利木单抗和英夫利昔单抗,代表了 PsA 治疗的一场革命。一种新型抗 TNF 药物培塞利珠单抗和一种针对 IL-12 和 IL-23 的全人源单克隆抗体乌司奴单抗已获准用于治疗活动性 PsA。乌司奴单抗的疗效表明,抑制 1 型辅助性 T 细胞途径可能是阻断 TNF 的替代方法。现在,PsA 的管理必须使用改进的措施来预测患者结局和定义缓解,并开发更有针对性的治疗方法。

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