Rheumatology, Hospital Universitari Vall d'Hebron, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.
NIHR Leeds BRC, Leeds Teaching Hospitals Trust and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, UK.
RMD Open. 2022 Dec;8(2). doi: 10.1136/rmdopen-2022-002513.
To explore the clinical and radiographical characteristics of axial psoriatic arthritis (PsA) and to compare it with ankylosing spondylitis (AS) with psoriasis.
Cross-sectional study from the national multicentre registry REGISPONSER where participants fulfilled the European Spondyloarthropathy Study Group spondyloarthritis criteria at entry. Clinical, laboratory and radiographical characteristics between patients classified as axial PsA and AS with psoriasis by their rheumatologist are compared according to HLA-B27 status.
Of 2367 patients on REGISPONSER, n=405 had PsA, of whom 27% (n=109) had axial involvement as per the treating rheumatologist. 30% (n=26/86) of axial PsA were HLA-B27 positive. In the AS group, 9% (127/1422) had a history of psoriasis and were more frequently male, with longer diagnostic delay and more anterior uveitis than those with axial PsA who had more peripheral involvement and nail disease. Patients with HLA-B27-negative axial PsA reported less inflammatory pain and structural damage compared with AS with psoriasis. By contrast, HLA-B27-positive axial PsA shared clinical characteristics similar to AS and psoriasis although with a lower BASRI score. In the multivariable analysis, patients with AS and psoriasis were independently associated with HLA-B27 positivity (OR 3.34, 95% CI 1.42 to 7.85) and lumbar structural damage scored by BASRI (OR 2.14, 95% CI 1.4 to 3.19).
The more prevalent axial PsA phenotype is predominantly HLA-B27 negative and presents different clinical and radiological manifestations when compared with AS with psoriasis. There is great heterogeneity in what rheumatologists consider axial PsA from a clinical and imaging perspective, highlighting the need for research into possible genetic drivers and a consensus definition.
探讨轴性银屑病关节炎(PsA)的临床和影像学特征,并将其与伴银屑病的强直性脊柱炎(AS)进行比较。
这是一项来自全国多中心 REGISPONSER 登记研究的横断面研究,入组时患者符合欧洲脊柱关节病研究组(ESSG)的脊柱关节炎标准。根据 HLA-B27 状态,比较风湿病学家分类为轴性 PsA 和伴银屑病的 AS 患者的临床、实验室和影像学特征。
在 REGISPONSER 的 2367 例患者中,n=405 例患有 PsA,其中 27%(n=109)的患者根据治疗风湿病学家的评估存在轴性受累。30%(n=26/86)的轴性 PsA 患者 HLA-B27 阳性。在 AS 组中,9%(127/1422)有银屑病病史,更常见于男性,诊断延迟时间更长,前葡萄膜炎更常见,而轴性 PsA 患者的外周受累和甲病更多。与伴银屑病的 AS 相比,HLA-B27 阴性的轴性 PsA 患者报告的炎症性疼痛和结构损伤较少。相比之下,HLA-B27 阳性的轴性 PsA 与 AS 和银屑病具有相似的临床特征,但 BASRI 评分较低。在多变量分析中,AS 和银屑病与 HLA-B27 阳性(OR 3.34,95%CI 1.42-7.85)和 BASRI 评分的腰椎结构损伤(OR 2.14,95%CI 1.40-3.19)独立相关。
更常见的轴性 PsA 表型主要为 HLA-B27 阴性,与伴银屑病的 AS 相比,其临床表现和影像学表现不同。从临床和影像学角度来看,风湿病学家对轴性 PsA 的认识存在很大差异,这突显了对可能的遗传驱动因素和共识定义进行研究的必要性。