Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK
Rheumatology Research, Swedish Medical Center and University of Washington, Seattle, Washington, USA.
RMD Open. 2022 Jul;8(2). doi: 10.1136/rmdopen-2022-002366.
We used the Study of Etanercept And Methotrexate in Combination or as Monotherapy in Subjects with Psoriatic Arthritis (SEAM-PsA) data set to examine the impact of presence of enthesitis, dactylitis, nail disease and/or psoriasis on treatment response in patients with early psoriatic arthritis (PsA).
This post hoc analysis evaluated the effect of baseline Spondyloarthritis Research Consortium of Canada (SPARCC) Enthesitis Index (EI), Leeds Enthesitis Index (LEI), Leeds Dactylitis Index (LDI), modified Nail Psoriasis Severity Index (mNAPSI) scores and body surface area (BSA) on composite outcomes of minimal disease activity (MDA) responses, Psoriatic Arthritis Disease Activity Score (PASDAS) low disease activity (LDA), PASDAS changes and Good Responses and Disease Activity Index for Psoriatic Arthritis (DAPSA) scores at Week 24.
Overall, 851 patients completed the SEAM-PsA trial and were included in the analysis. Baseline enthesitis (SPARCC EI>0 vs SPARCC EI=0 or LEI>0 vs LEI=0) was not associated with improved outcomes. Baseline dactylitis (LDI>0 vs LDI=0) was positively associated with improved MDA (OR: 1.4, p=0.0457), PASDAS LDA (OR: 1.8, p=0.0014) and Good Responses (OR: 1.6, p=0.0101) and greater reductions in PASDAS (estimate: -0.9, p<0.0001) and DAPSA scores (estimate: -3.8, p=0.0155) at Week 24. Similarly, baseline nail disease (mNAPSI >1 vs mNAPSI≤1) was positively associated with improved MDA (OR: 1.8, p=0.0233) and PASDAS LDA (OR: 1.8, p=0.0168) responses and greater reduction in PASDAS (estimate: -0.7, p=0.0005) at Week 24.
Results from our analysis suggest that presence of dactylitis and nail disease, but not enthesitis, are associated with improved outcomes in patients with early PsA who were treated with methotrexate and/or etanercept.
我们使用关节炎研究协会联合治疗中依那西普与甲氨蝶呤疗效研究(SEAM-PsA)的数据,来评估附着点炎、指(趾)炎、甲病和/或银屑病在早期银屑病关节炎(PsA)患者治疗反应中的影响。
本回顾性分析评估了基线时脊柱关节炎研究协会加拿大(SPARCC)附着点炎指数(EI)、利兹附着点炎指数(LEI)、利兹指(趾)炎指数(LDI)、改良甲银屑病严重程度指数(mNAPSI)和体表面积(BSA)对最小疾病活动度(MDA)反应、银屑病关节炎疾病活动评分(PASDAS)低疾病活动度(LDA)、PASDAS 变化和良好反应及银屑病关节炎疾病活动指数(DAPSA)评分的复合终点的影响。
总体而言,851 例患者完成了 SEAM-PsA 试验并纳入分析。基线附着点炎(SPARCC EI>0 与 SPARCC EI=0 或 LEI>0 与 LEI=0)与改善结局无关。基线指(趾)炎(LDI>0 与 LDI=0)与 MDA 改善(OR:1.4,p=0.0457)、PASDAS LDA(OR:1.8,p=0.0014)和良好反应(OR:1.6,p=0.0101)相关,且 PASDAS(估计值:-0.9,p<0.0001)和 DAPSA 评分(估计值:-3.8,p=0.0155)在第 24 周时降幅更大。同样,基线甲病(mNAPSI>1 与 mNAPSI≤1)与 MDA 改善(OR:1.8,p=0.0233)和 PASDAS LDA 反应(OR:1.8,p=0.0168)以及 PASDAS 评分(估计值:-0.7,p=0.0005)在第 24 周时降幅更大相关。
我们分析的结果表明,在接受甲氨蝶呤和/或依那西普治疗的早期 PsA 患者中,附着点炎和甲病的存在与改善结局相关,而不是附着点炎。