Copenhagen Center for Arthritis Research, Center for Rheumatology and Spine Diseases, Rigshospitalet, Glostrup.
Department of Clinical Medicine, University of Copenhagen.
Rheumatology (Oxford). 2022 Jul 6;61(7):2835-2847. doi: 10.1093/rheumatology/keab865.
To investigate and compare clinical features and US signs of inflammation in joints and entheses in patients with psoriasis with and without musculoskeletal pain, and the additional value of US in classification of PsA. Furthermore, to explore the association between such findings and patient-reported outcomes (PROs) and the performance of screening-questionnaires for identifying patients with PsA.
Patients with psoriasis (n = 126) recruited from a nationwide survey were evaluated at one of four rheumatology departments. The evaluation included clinical examination, laboratory tests, radiography, greyscale and colour Doppler US of 48 joints and 12 entheses, PROs, and four screening questionnaires for PsA. Patients were classified with Classification for PsA (CASPAR), US-modified CASPAR, and US-only criteria.
When subgroups of self-reported pain (63%), no pain (29%) and diagnosed PsA (9%) were compared, patients with pain had higher tenderness-related clinical scores (tender joints, entheses and FM points) and US greyscale sum-scores, compared with 'no pain' patients. PROs were negligibly moderately correlated with pain-related clinical scores (Spearman's rho = 0.11-0.59, all patients), and negligibly weakly with US sum-scores (rho = 0.01-0.34). More patients could be classified as PsA when US synovitis/enthesitis was included as an entry criterion (US-modified CASPAR, 66% of all patients) compared with conventional CASPAR (35%) or US-only criteria (52%). Sensitivities of screening questionnaires were low for fulfilment of CASPAR (0.23-0.66), US-modified CASPAR (0.17-0.57), and US-only (0.20-0.57) criteria.
Self-reported pain in psoriasis is related to US inflammation. US-modified CASPAR criteria identified almost twice as many patients as conventional CASPAR criteria. Screening questionnaires showed limited value.
探讨和比较有和无肌肉骨骼疼痛的银屑病患者关节和附着点炎症的临床特征和超声表现,以及超声在银屑病关节炎(PsA)分类中的附加价值。此外,还探讨这些发现与患者报告的结局(PROs)的关系,以及用于识别患有 PsA 患者的筛查问卷的性能。
从一项全国性调查中招募了 126 名银屑病患者,在四个风湿病科中的一个科室进行评估。评估包括临床检查、实验室检查、影像学检查、48 个关节和 12 个附着点的灰阶和彩色多普勒超声检查、PROs 和四种用于筛查 PsA 的问卷。患者根据分类的银屑病关节炎(CASPAR)、超声改良的 CASPAR 和超声仅有的标准进行分类。
当比较自我报告的疼痛(63%)、无疼痛(29%)和诊断为 PsA(9%)的亚组时,与“无疼痛”患者相比,有疼痛的患者有更高的触痛相关的临床评分(触痛关节、附着点和 FM 点)和超声灰阶总评分。PROs 与疼痛相关的临床评分有轻微到中度的相关性(Spearman's rho=0.11-0.59,所有患者),与超声总评分有轻微到弱的相关性(rho=0.01-0.34)。当将超声滑膜炎/附着点炎作为纳入标准时,更多的患者可以被分类为 PsA(超声改良的 CASPAR,所有患者的 66%),而不是传统的 CASPAR(35%)或超声仅有的标准(52%)。筛查问卷对满足 CASPAR(0.23-0.66)、超声改良的 CASPAR(0.17-0.57)和超声仅有的(0.20-0.57)标准的患者的敏感性较低。
银屑病患者的自我报告疼痛与超声炎症有关。超声改良的 CASPAR 标准比传统的 CASPAR 标准识别出近两倍的患者。筛查问卷的价值有限。