Rheumatology Unit, Internal Medicine Service, Hospital Italiano de Buenos Aires and Instituto Universitario Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Dermatology Service, Hospital Italiano de Buenos Aires, Buenos Aires, Argentina.
Ann Rheum Dis. 2022 Jan;81(1):74-79. doi: 10.1136/annrheumdis-2021-220865. Epub 2021 Jul 19.
To compare the incidence of psoriatic arthritis (PsA) in patients with psoriasis (PsO) according to different treatments for their skin: topics/no treatment, conventional disease-modifying antirheumatic drugs (DMARDs) (cDMARDs) or biological DMARDs (bDMARDs).
Patients with PsO without PsA followed at a university hospital were included in this retrospective cohort study. Patients were classified according to their treatment in topics (topics, phototherapy or no treatment), cDMARDs (methotrexate and cyclosporine) and bDMARDs (tumour necrosis factor inhibitors (TNFi), interleukin 17 inhibitors (IL-17i) and IL-12-23i ((interleukin (IL) 12/IL-23 inhibitor))) groups. Incident cases of PsA were attributed to one treatment if developed during the administration of that treatment. A Cox proportional hazards model was used to evaluate the adjusted risk of PsA development by treatment group.
1719 patients with PsO contributed a total of 14 721 patient/years (py). 1387 (81%) patients were in the topics, 229 (13%) in cDMARDs and 103 (6%) in the bDMARDs group. During follow-up, 239 patients (14%) developed PsA (231 under topics, six under cDMARDs and two under bDMARDs). Global incidence was 1.6 per 100 py. The risk of developing PsA in patients with PsO treated with bDMARDs was significantly lower (incidence rate ratio (IRR)=0.26; 95% CI 0.03 to 0.94; p=0.0111), compared with topics, but not compared with cDMARDs (IRR=0.35; 95% CI 0.035 to 1.96; p=0.1007). Adjusted Cox proportional hazards regression analysis showed that male sex, nail involvement and higher body max index were associated with increased risk of developing PsA, while biologics use was protective (HR: 0.19; 95% CI 0.05 to 0.81).
Treatment with biologics in patients with PsO reduced the risk of PsA development.
比较不同皮肤治疗方案(未治疗、传统疾病修正抗风湿药物[DMARDs](cDMARDs)或生物 DMARDs[bDMARDs])下银屑病(PsO)患者发生银屑病关节炎(PsA)的发生率。
本回顾性队列研究纳入在一所大学医院就诊的无 PsA 的银屑病患者。根据治疗方案将患者分为未治疗组(未治疗、光疗或未治疗)、cDMARDs 组(甲氨蝶呤和环孢素)和 bDMARDs 组(肿瘤坏死因子抑制剂[TNFi]、白细胞介素 17 抑制剂[IL-17i]和白细胞介素 12/23 抑制剂[IL-12/IL-23i])。如果在治疗过程中发生 PsA,则将其归因于一种治疗。采用 Cox 比例风险模型评估按治疗组调整的 PsA 发展风险。
1719 例银屑病患者共提供 14721 患者/年(py)。1387 例(81%)患者在未治疗组,229 例(13%)在 cDMARDs 组,103 例(6%)在 bDMARDs 组。在随访期间,239 例(14%)患者发生 PsA(231 例在未治疗组,6 例在 cDMARDs 组,2 例在 bDMARDs 组)。全球发病率为 1.6/100py。与未治疗组相比,接受 bDMARDs 治疗的银屑病患者发生 PsA 的风险显著降低(发病率比[IRR]=0.26;95%CI 0.03 至 0.94;p=0.0111),但与 cDMARDs 组相比则没有(IRR=0.35;95%CI 0.035 至 1.96;p=0.1007)。调整后的 Cox 比例风险回归分析显示,男性、指甲受累和更高的体质量指数与发生 PsA 的风险增加相关,而生物制剂的使用具有保护作用(HR:0.19;95%CI 0.05 至 0.81)。
在银屑病患者中使用生物制剂治疗可降低 PsA 发展的风险。