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中轴型银屑病关节炎的靶向治疗

Targeted Therapies in Axial Psoriatic Arthritis.

作者信息

Floris Alberto, Congia Mattia, Chessa Elisabetta, Angioni Maria Maddalena, Piga Matteo, Cauli Alberto

机构信息

Unità Operativa Complessa di Reumatologia, Dipartimento di Scienze Mediche e Sanità Pubblica, Azienda Ospedaliero-Universitaria e Università di Cagliari, Monserrato, Italy.

出版信息

Front Genet. 2021 Jun 28;12:689984. doi: 10.3389/fgene.2021.689984. eCollection 2021.

Abstract

Specific and high-quality evidence on the efficacy of the current targeted therapies for axial disease in psoriatic arthritis (axPsA) is still scarce. Indeed, almost all the cohorts investigated in clinical trials on PsA consisted of patients with peripheral arthritis, where a small number of them also had axial involvement. Only one randomized controlled trial was so far specifically designed to assess the efficacy of a biological disease-modifying antirheumatic drug (DMARD) in axPsA. For other biological and synthetic targeted DMARDs, the most specific evidence for treatment in axPsA is extrapolated from analyses based on PsA patients with concomitant peripheral and axial manifestations. Furthermore, the current trials and analysis on axPsA are affected by major limitations, including the lack of a widely accepted definition of axPsA and the lack of specific and validated outcome measures. Finally, poor data are available on the genetics of axPsA, although alleles differentially expressed in different patterns of axPsA might offer advantages in the prospective of personalized medicine in axPsA patients. Overall, this review suggests that there is an urgent need for more reliable evidence derived from studies specifically designed for axPsA and based on a validated definition of axPsA and on specific outcome measures.

摘要

目前针对银屑病关节炎(axPsA)中轴性疾病的靶向治疗疗效的具体且高质量证据仍然匮乏。实际上,几乎所有银屑病关节炎临床试验所研究的队列均由外周关节炎患者组成,其中仅有少数患者伴有中轴受累。到目前为止,仅有一项随机对照试验专门设计用于评估一种生物改善病情抗风湿药(DMARD)对axPsA的疗效。对于其他生物和合成靶向DMARDs,axPsA治疗的最具体证据是从对伴有外周和中轴表现的银屑病关节炎患者的分析中推断出来的。此外,目前关于axPsA的试验和分析受到主要限制的影响,包括缺乏被广泛接受的axPsA定义以及缺乏具体且经过验证的结局指标。最后,尽管在axPsA不同模式中差异表达的等位基因可能为axPsA患者的个性化医疗提供优势,但关于axPsA遗传学的可用数据较少。总体而言,本综述表明迫切需要来自专门为axPsA设计的研究的更可靠证据,这些研究基于经过验证的axPsA定义和具体结局指标。

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