银屑病和银屑病关节炎的治疗进展-阿普司特的作用。

IF 5.2 Q1 DERMATOLOGY Psoriasis (Auckland, N.Z.) Pub Date : 2015-09-07 eCollection Date: 2015-01-01 DOI:10.2147/PTT.S69476
Stephan Forchhammer, Kamran Ghoreschi
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引用次数: 6

摘要

银屑病关节炎(PsA)是一种与银屑病(PsO)相关的炎症性关节炎。PsA的治疗可能具有挑战性,包括非甾体抗炎药、合成的抗病性抗风湿病药物和生物制剂。最近建立的一种用于治疗PsO和PsA的新型口服化合物是阿普司特,一种小分子PDE4抑制剂。PDE4的抑制导致细胞内cAMP水平增加,并调节与PsO和PsA发病机制密切相关的炎症介质的表达,如TNF、IL-12、IL-17和IL-23。阿普雷司特于2014年获得美国食品药品监督管理局批准用于治疗精神分裂症和精神分裂症,并于2015年初获得欧洲药品管理局的批准。本文综述了阿普司特的药理学、临床研究的有效性和安全性,以及它在现代精神分裂症/精神分裂症管理中的潜在地位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Update on the treatment of psoriasis and psoriatic arthritis - role of apremilast.

Psoriatic arthritis (PsA) is an inflammatory arthritis associated with psoriasis (PsO). The treatment of PsA can be challenging and includes non-steroidal anti-inflammatory drugs, synthetic disease modifying antirheumatic drugs, and biologicals. One novel oral compound that has been recently established for the treatment of PsO and PsA is apremilast, a small molecule PDE4 inhibitor. The inhibition of PDE4 results in increased intracellular cAMP levels and modulates the expression of inflammatory mediators critically involved in PsO and PsA pathogenesis like TNF, IL-12, IL-17, and IL-23. Apremilast received US Food and Drug Administration approval for the treatment of PsO and PsA in 2014 and received approval from the European Medicines Agency in early 2015. This article summarizes the pharmacology of apremilast, its efficacy and safety in clinical studies, and its potential position in modern PsO/PsA management.

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