GRAPPA Debate: Be it Resolved That Clinical Enthesitis Indices Do Not Reflect True Enthesitis and Hence Should Be Discontinued.

Betul Macit,Sibel Zehra Aydin,Atul Deodhar
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Abstract

Enthesitis is increasingly recognized as a key manifestation of psoriatic disease (PsD). However, how best to assess enthesitis remains a point of discussion due to limitations of the existing assessment tools, including their inability to differentiate between inflammatory and noninflammatory enthesitis as well as a high placebo response in clinical trials. At the Group for Research and Assessment of Psoriasis and Psoriatic Arthritis (GRAPPA) 2024 annual meeting, a debate was held to address whether traditional clinical enthesitis indices should be discontinued for PsD. Dr. Sibel Aydin advocated for their discontinuation, emphasizing that clinical indices often capture "enthesalgia" (pain at the entheseal sites overlapping with pain disorders like fibromyalgia) rather than true inflammatory enthesitis. These clinical indices may lack specificity for detecting inflammation, which can lead to inaccurate assessments. Further, studies show high reports of placebo response when using clinical indices, suggesting their limitations in discriminating active disease from noninflammatory pain mechanisms. Aydin advocated for prioritizing emerging imaging tools over traditional clinical indices. Dr. Atul Deodhar argued against discontinuation of traditional clinical enthesitis indices, highlighting that despite limitations, these indices have been used successfully in multiple randomized controlled trials, leading to approval of numerous treatment options for psoriatic arthritis. Although promising, alternative imaging modalities like ultrasound to evaluate inflammation come with their own challenges, including operator dependency, variability in interpretation, and lack of regulatory approval as a standardized outcome measure. This report presents both perspectives, analyzing the evidence and implications for the future of enthesitis assessment in clinical practice.
GRAPPA争论:临床炎症指数不能反映真实的炎症,因此应该停止使用。
银屑病越来越被认为是银屑病(PsD)的一个重要表现。然而,由于现有评估工具的局限性,包括无法区分炎症性和非炎症性阑尾炎以及临床试验中较高的安慰剂反应,如何最好地评估阑尾炎仍然是一个值得讨论的问题。在银屑病和银屑病关节炎研究和评估小组(GRAPPA) 2024年年会上,就是否应该停止使用传统的临床炎症指标进行了辩论。Sibel Aydin博士主张停止使用这种药物,强调临床指标通常是“神经痛”(神经痛部位的疼痛与纤维肌痛等疼痛障碍重叠),而不是真正的炎症性神经痛。这些临床指标可能缺乏检测炎症的特异性,这可能导致不准确的评估。此外,研究显示,当使用临床指标时,安慰剂反应的报告很高,这表明它们在区分活动性疾病和非炎症性疼痛机制方面存在局限性。Aydin主张优先考虑新兴的成像工具,而不是传统的临床指标。Atul Deodhar博士反对停止使用传统的临床炎症指数,他强调,尽管有局限性,这些指数已经在多个随机对照试验中成功使用,导致银屑病关节炎的许多治疗方案获得批准。虽然超声等替代成像方式很有前景,但它们也面临着挑战,包括对操作人员的依赖性、解释的可变性以及缺乏监管部门批准作为标准化的结果衡量标准。本报告提出了两种观点,分析了临床实践中对炎症评估的证据和影响。
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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