Department of Medical and Biological Sciences, Rheumatology Clinic, University Hospital Santa Maria della Misericordia, Udine, Italy
Department of Internal Medicine, Rheumatology and Immunology, University of Erlangen, Erlangen, Germany.
RMD Open. 2024 Apr 10;10(2):e004314. doi: 10.1136/rmdopen-2024-004314.
Subjects with subclinical psoriatic arthritis (PsA), defined as the presence of arthralgia in psoriasis (PsO), are at higher risk of PsA but scant real-world data exist. Our aims were to (1) estimate the probability of PsA development in subclinical PsA, (2) characterise subclinical PsA symptoms and (3) determine the clinical patterns at PsA diagnosis.
Patients with PsO, mainly subclinical PsA, were evaluated longitudinally in two European cohorts. The key outcome was new-onset PsA. Musculoskeletal symptoms including inflammatory and non-inflammatory symptoms before PsA diagnosis were collected. Occurrence of PsA was analysed with survival analysis and cumulative incidence functions (CIFs).
384 patients with PsO were included with a mean follow-up of 33.0 (±20.9) months. 311 of 384 (80.9%) had subclinical PsA with a PsA incidence rate of 7.7 per 100 patient-years. Subclinical PsA displayed a higher risk of PsA development compared with PsO (HR=11.7 (95% CI 1.57 to 86.7), p=0.016). The probability of new-onset PsA estimated by the CIF was 9.4% (95% CI 4.7% to 10.6%) at month 12 and 22.7% (95% CI 17.2% to 28.6%) at month 36. 58.9% of cases reported inflammatory symptoms in the months immediately prior to PsA diagnosis but prior non-inflammatory symptoms were evident in 83.9% prior to PsA diagnosis. Peripheral joint swelling was the predominant PsA presentation pattern (82.1%).
The probability of PsA development among subclinical PsA was relatively high, emphasising the importance of emergent musculoskeletal symptoms when aiming for PsA prevention. Joint swelling was the dominant feature in new-onset PsA, likely reflecting clinical confidence in recognising joint swelling.
定义为银屑病(PsO)中存在关节痛的亚临床银屑病关节炎(PsA)患者患 PsA 的风险较高,但现实世界的数据很少。我们的目的是:(1)估计亚临床 PsA 发展为 PsA 的概率,(2)描述亚临床 PsA 症状,(3)确定 PsA 诊断时的临床模式。
在两个欧洲队列中对患有 PsO 的患者(主要为亚临床 PsA)进行了纵向评估。主要结局是新诊断的 PsA。在 PsA 诊断之前收集了包括炎症性和非炎症性症状在内的肌肉骨骼症状。使用生存分析和累积发生率函数(CIF)分析 PsA 的发生。
纳入 384 例 PsO 患者,平均随访 33.0(±20.9)个月。384 例患者中有 311 例(80.9%)患有亚临床 PsA,PsA 发病率为每 100 例患者年 7.7 例。与 PsO 相比,亚临床 PsA 显示出更高的 PsA 发展风险(HR=11.7(95%CI 1.57 至 86.7),p=0.016)。通过 CIF 估计的新发病例概率在第 12 个月时为 9.4%(95%CI 4.7%至 10.6%),在第 36 个月时为 22.7%(95%CI 17.2%至 28.6%)。58.9%的病例在 PsA 诊断前的几个月报告有炎症性症状,但在 PsA 诊断前 83.9%的病例有先前的非炎症性症状。外周关节肿胀是最主要的 PsA 表现形式(82.1%)。
亚临床 PsA 发展为 PsA 的概率相对较高,这强调了在预防 PsA 时,应注意出现的肌肉骨骼症状。关节肿胀是新发病例的主要特征,这可能反映了临床对识别关节肿胀的信心。