Reducing the Risk of Developing Psoriatic Arthritis in Patients with Psoriasis.

IF 5.2 Q1 DERMATOLOGY Psoriasis (Auckland, N.Z.) Pub Date : 2022-08-10 eCollection Date: 2022-01-01 DOI:10.2147/PTT.S323300
Paolo Gisondi, Francesco Bellinato, Martina Maurelli, Davide Geat, Alen Zabotti, Dennis McGonagle, Giampiero Girolomoni
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Abstract

Psoriatic arthritis (PsA) is a heterogeneous chronic inflammatory arthritis associated with psoriasis, which may manifest with different domains such as dactylitis, enthesitis, synovitis and spondylitis. The estimated prevalence of PsA in patients with psoriasis ranges widely between 6% and 42%. In most cases, PsA is preceded by skin involvement by an average time of 7-8 years. In the complex patho-mechanisms involved in the transition from psoriasis to PsA, the gut and skin have been proposed as the sites of immune activation triggering or contributing to the development of PsA. In such a transition, a subclinical phase has been identified, characterized by enthesopathy where soluble biomarkers and imaging findings but no clinical symptoms are detectable. Recent studies have provided some evidence that timely treated psoriasis may reduce the risk of developing PsA.

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降低银屑病患者罹患银屑病关节炎的风险。
银屑病关节炎(PsA)是一种与银屑病相关的异质性慢性炎症性关节炎,可表现为趾关节炎、关节内炎、滑膜炎和脊柱炎等不同部位。据估计,PsA 在银屑病患者中的发病率介于 6% 和 42% 之间。在大多数病例中,PsA 的皮肤受累时间平均为 7-8 年。在从银屑病向 PsA 过渡的复杂病理机制中,肠道和皮肤被认为是引发或导致 PsA 发生的免疫激活部位。在这一转变过程中,亚临床阶段已被确定,其特征是可溶性生物标志物和影像学发现的肌腱病,但没有临床症状。最近的研究提供了一些证据,表明及时治疗银屑病可以降低 PsA 的发病风险。
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