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A polyarticular onset predicts erosive and deforming disease in psoriatic arthritis

机译:多关节发作可预测银屑病关节炎的糜烂和变形疾病

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摘要

>Methods: A prospective cohort study was undertaken with 71 patients diagnosed as having PsA (44 men and 27 women, mean age 47 (SD 12) years). At the recruitment period patients had disease without evidence of radiological damage. Patients were studied and followed up according to a standard protocol from January 1991 to June 2001. Erosive and deforming disease was defined by the presence of erosions, joint space narrowing, subluxation, and/or ankylosis of peripheral joints. Univariate and multivariate analyses were performed to evaluate factors predicting erosive and deforming disease. >Results: At the end of the study 32 of 71 (45%) patients had developed erosive and deforming disease. Among them, 18 of 32 (56%) had a polyarticular onset, two of 32 (6%) showed a distal interphalangeal joint disease onset, six of 32 (19%) presented with oligoarthritis, and six of 32 (19%) presented with axial disease as the form of disease onset (p=0.001). Mean time to detect erosions or joint space narrowing was 20 (SD 4) months. Men showed fewer erosions than women (p=0.05). Patients who carried the HLA-B27 antigen showed less erosive disease than patients who lacked it (p=0.05). Patients with erosive and deforming disease had poorer functional performance than those without it as measured with the Health Assessment Questionnaire (HAQ) and the American College of Rheumatology (ACR) criteria (p<0.05 with both measurements). In multivariate analysis, only a polyarticular onset remained as an indicator of erosive and deforming disease (odds ratio (OR) 37, 95% confidence interval (95% CI) 3.6 to 88, p=0.025). >Conclusions: A polyarticular onset (five or more swollen joints) of PsA was the unique independent risk factor which predicted the appearance of erosive and deforming disease over time. These data may be useful for clinicians treating patients with PsA, as it may guide treatment towards a more aggressive and earlier intervention.
机译:>方法:前瞻性队列研究对71名被诊断患有PsA的患者(44名男性和27名女性,平均年龄47(SD 12)岁)进行了研究。在招募期间,患者患有无放射损伤证据的疾病。从1991年1月至2001年6月,根据标准方案对患者进行了研究和随访。糜烂和变形性疾病的定义是出现糜烂,关节间隙变窄,半脱位和/或周围关节强直。进行单因素和多因素分析以评估预测糜烂和变形疾病的因素。 >结果:研究结束时,在71名患者中,有32名(45%)患有糜烂和畸形疾病。其中,32例中有18例(56%)出现多关节发作,32例中有2例(6%)表现为远端指间关节病,32例中有6例(19%)表现为少关节炎,32例中有6例(19%)表现为多关节炎。以轴向疾病为疾病发作形式(p = 0.001)。检测侵蚀或关节间隙变窄的平均时间为20(SD 4)个月。男性表现出的侵蚀少于女性(p = 0.05)。携带HLA-B27抗原的患者比没有HLA-B27抗原的患者表现出更少的糜烂性疾病(p = 0.05)。根据健康评估问卷(HAQ)和美国风湿病学会(ACR)的标准,患有糜烂和畸形疾病的患者的功能表现较不患有糜烂和畸形的患者要差(两种测量均p <0.05)。在多变量分析中,仅保留多关节发作作为糜烂和变形疾病的指标(优势比(OR)37,95%置信区间(95%CI)3.6至88,p = 0.025)。 >结论:PsA的多关节发作(五个或五个以上关节肿胀)是唯一的独立危险因素,可预测随着时间的流逝侵蚀性和变形性疾病的出现。这些数据对于临床医生治疗PsA可能有用,因为它可以指导治疗朝着更积极,更早的方向发展。

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