比较九个欧洲国家首次使用 TNF 抑制剂的银屑病关节炎患者的 DAPSA、DAPSA28 和 DAS28-CRP。

IF 3.7 2区 医学 Q1 RHEUMATOLOGY
Louise Linde, Stylianos Georgiadis, Lykke M. Ørnbjerg, Simon H. Rasmussen, Brigitte Michelsen, Johan Askling, Daniela Di Giuseppe, Johan K. Wallman, Jakub Závada, Karel Pavelka, Miguel Bernardes, Carolina O. Matos, Bente Glintborg, Anne Gitte Loft, Dan Nordström, Laura Kuusalo, Burkhard Möller, Michael J. Nissen, Catalin Codreanu, Corina Mogosan, Bjorn Gudbjornsson, Thorvardur Jon Love, Cansu Akleylek, Florenzo Iannone, Tore K. Kvien, Ziga Rotar, Isabel Castrejon, Gary J. Macfarlane, Merete L. Hetland, Mikkel Østergaard
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引用次数: 0

摘要

目的:由于在常规治疗中并不总是进行 66/68 个关节计数,因此我们旨在确定在无法使用原始 DAPSA(66/68 个关节)监测银屑病关节炎(PsA)的疾病活动性时,应首选改良的银屑病关节炎 28 个关节疾病活动性指数(DAPSA28)还是带 C 反应蛋白的 28 个关节疾病活动性评分(DAS28-CRP):方法:汇集了前瞻性收集的首次使用肿瘤坏死因子抑制剂的欧洲仿生PsA患者的真实世界数据。通过缓解(DAPSA ≤ 4,DAPSA28 ≤ 4,DAS28-CRP < 2.6)、应答(DAPSA 和 DAPSA28 改善 75%)以及 DAS28-CRP 的 EULAR 良好/中度应答组合,在 6 个月时对缓解和应答状态进行评估。对多重估算数据进行逻辑回归分析,以确定基线预测因素:缓解组和应答组分别包括3159名和1866名患者。6个月缓解/应答比例分别为DAPSA(27%/44%)、DAPSA28(28%/44%)和DAS28-CRP(59%/80%)。在 14 个可能的基线预测因子中,有 11 个可预测 DAPSA 和 DAPSA28 缓解(其中 8 个也可预测其反应,用 "*"表示):病程较长*、男性*和较高的 CRP* 是阳性预测因子,而年龄较大*、体重指数较高*、患者疲劳*、总体评分、医生总体评分、健康评估问卷评分*以及关节触痛和肿胀*计数是阴性预测因子。其中8项和5项分别预测了DAS28-CRP的缓解和反应:结论:在PsA患者中,当无法获得66/68个关节计数时,DAPSA28应优先于DAS28-CRP作为DAPSA的替代指标,因为DAPSA和DAPSA28在缓解和反应状态以及预测指标方面存在大量重叠。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparing DAPSA, DAPSA28, and DAS28-CRP in Patients With Psoriatic Arthritis Initiating a First Tumor Necrosis Factor Inhibitor Across Nine European Countries

Comparing DAPSA, DAPSA28, and DAS28-CRP in Patients With Psoriatic Arthritis Initiating a First Tumor Necrosis Factor Inhibitor Across Nine European Countries

Objective

Because 66/68 joint counts are not always performed in routine care, we aimed to determine which of the modified 28-joint disease activity index for psoriatic arthritis (DAPSA28) or 28-joint disease activity score with C-reactive protein (DAS28-CRP) should be preferred for monitoring disease activity in psoriatic arthritis (PsA) when the original DAPSA (66/68 joints) is not available.

Methods

Prospectively collected real-world data of European bionaive patients with PsA initiating a first tumor necrosis factor inhibitor were pooled. Remission and response status were evaluated at 6 months by remission (DAPSA ≤ 4, DAPSA28 ≤ 4, and DAS28-CRP < 2.6), response (75% improvement for DAPSA and DAPSA28), and combined EULAR good/moderate responses for DAS28-CRP. Logistic regression analyses on multiple imputed data were used to identify baseline predictors.

Results

Remission and response cohorts included 3,159 and 1,866 patients, respectively. The 6-month proportions achieving remission/response were DAPSA (27%/44%), DAPSA28 (28%/44%), and DAS28-CRP (59%/80%). Of 14 possible baseline predictors, 11 predicted both DAPSA and DAPSA28 remission (8 of which also predicted their response, indicated by “*”): longer disease duration*, male sex*, and higher CRP* were positive, whereas older age*, higher body mass index*, patient fatigue*, and global, physician global, health assessment questionnaire score*, and tender and swollen* joint counts were negative predictors. Eight and five of these predicted DAS28-CRP remission and response, respectively.

Conclusion

In patients with PsA, DAPSA28 should be preferred over DAS28-CRP as a substitute for DAPSA when 66/68 joint counts are not available because of the large overlap in remission and response status and in predictors between DAPSA and DAPSA28.

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来源期刊
CiteScore
9.40
自引率
6.40%
发文量
368
审稿时长
3-6 weeks
期刊介绍: Arthritis Care & Research, an official journal of the American College of Rheumatology and the Association of Rheumatology Health Professionals (a division of the College), is a peer-reviewed publication that publishes original research, review articles, and editorials that promote excellence in the clinical practice of rheumatology. Relevant to the care of individuals with rheumatic diseases, major topics are evidence-based practice studies, clinical problems, practice guidelines, educational, social, and public health issues, health economics, health care policy, and future trends in rheumatology practice.
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