From the Dipartimento di Medicina e Scienze della Salute Vincenzo Tiberio, Università degli Studi del Molise, Campobasso, Italy.
E. Lubrano, MD, PhD, Dipartimento di Medicina e Scienze della Salute Vincenzo Tiberio, Università degli Studi del Molise; A. De Socio, MD, Dipartimento di Medicina e Scienze della Salute Vincenzo Tiberio, Università degli Studi del Molise; F.M. Perrotta, MD, Dipartimento di Medicina e Scienze della Salute Vincenzo Tiberio, Università degli Studi del Molise.
J Rheumatol. 2017 Aug;44(8):1159-1164. doi: 10.3899/jrheum.170112. Epub 2017 Jun 1.
In a complex disease such as psoriatic arthritis (PsA), several methods are available to define remission or low disease activity (LDA), including the assessment of different clinical features. The aim of this study was to compare the composite indices tailored for PsA in patients treated with conventional synthetic disease-modifying antirheumatic drugs (csDMARD) and biological DMARD (bDMARD).
Patients with PsA classified with the ClASsification criteria for Psoriatic ARthritis criteria and with > 6 months followup treated with first csDMARD and bDMARD were consecutively enrolled. To assess disease activity, composite indices tailored for PsA were used, such as the Disease Activity Index for Psoriatic Arthritis (DAPSA), clinical DAPSA (cDAPSA), Psoriatic Arthritis Disease Activity Score (PASDAS), minimal disease activity (MDA) 5/7, and MDA 7/7. DAPSA and cDAPSA score ≤ 4, MDA 7/7, and PASDAS ≤ 1.9 identified remission. MDA 5/7, DAPSA score ≤ 14, cDAPSA score ≤ 13, and PASDAS < 3.2 identified the MDA and LDA criteria.
One hundred nine patients with PsA were enrolled: 79 patients were receiving stable treatment with bDMARD and 30 with csDMARD. Overall, 28 (25.6%), 23 (21.1%), 19 (17.4%), and 13 patients (11.9%) were in cDAPSA remission, DAPSA remission, MDA 7/7, and PASDAS ≤ 1.9, respectively. Moreover, 54 (49.5%), 80 (73.3%), 79 (72.3%), and 38 patients (34.8%) were in MDA 5/7, DAPSA LDA, cDAPSA LDA, and PASDAS LDA. Patients treated with bDMARD had significantly lower median DAPSA, cDAPSA, and PASDAS score than patients treated with csDMARD.
Patients with PsA receiving bDMARD are more likely to achieve a status of MDA and remission when compared with csDMARD. PASDAS ≤ 1.9 and MDA 7/7 seem to be stringent remission criteria.
在像银屑病关节炎(PsA)这样的复杂疾病中,有几种方法可用于定义缓解或低疾病活动度(LDA),包括评估不同的临床特征。本研究的目的是比较接受传统合成改善病情抗风湿药物(csDMARD)和生物 DMARD(bDMARD)治疗的 PsA 患者的个体化疾病活动度评估指标。
连续纳入符合银屑病关节炎分类标准的 PsA 患者,并接受至少 6 个月的随访,治疗方案为首次 csDMARD 和 bDMARD。采用个体化疾病活动度评估指标,如银屑病关节炎疾病活动度指数(DAPSA)、临床 DAPSA(cDAPSA)、银屑病关节炎疾病活动评分(PASDAS)、最小疾病活动度(MDA)5/7 和 MDA 7/7,评估疾病活动度。DAPSA 和 cDAPSA 评分≤4、MDA 7/7 和 PASDAS≤1.9 定义为缓解。MDA 5/7、DAPSA 评分≤14、cDAPSA 评分≤13 和 PASDAS<3.2 定义为 MDA 和 LDA 标准。
共纳入 109 例 PsA 患者:79 例患者接受 bDMARD 稳定治疗,30 例患者接受 csDMARD 治疗。总体而言,28(25.6%)、23(21.1%)、19(17.4%)和 13 例(11.9%)患者分别处于 cDAPSA 缓解、DAPSA 缓解、MDA 7/7 和 PASDAS≤1.9 状态。此外,54(49.5%)、80(73.3%)、79(72.3%)和 38 例(34.8%)患者分别处于 MDA 5/7、DAPSA LDA、cDAPSA LDA 和 PASDAS LDA 状态。与接受 csDMARD 治疗的患者相比,接受 bDMARD 治疗的患者 DAPSA、cDAPSA 和 PASDAS 评分中位数显著更低。
与 csDMARD 相比,接受 bDMARD 治疗的 PsA 患者更有可能达到 MDA 和缓解状态。PASDAS≤1.9 和 MDA 7/7 似乎是严格的缓解标准。