Engel Andrew, Xie Christopher, Summer Ross, Loizidis Giorgos
Division of Pulmonary, Allergy and Critical Care and the Center for Translational Medicine, Department of Medicine, The Jane & Leonard Korman Respiratory Institute, Thomas Jefferson University, Philadelphia, PA, USA.
Department of Medicine, Thomas Jefferson University, Philadelphia, PA, USA.
Rheumatol Adv Pract. 2025 May 27;9(3):rkaf059. doi: 10.1093/rap/rkaf059. eCollection 2025.
Psoriasis (PsO) is a systemic autoimmune disease primarily characterized by erythematous plaques on the skin. While extra-dermal manifestations like psoriatic arthritis (PsA) are well recognized, data linking PsO to interstitial lung disease (ILD) remain limited. This study aimed to evaluate whether patients with PsA have a higher risk of developing ILD compared with patients with PsO.
A retrospective analysis of the TriNetX US database (2014-24) was performed. Adult patients with PsO or PsA treated with systemic immunosuppressive medications were included, excluding those with other autoimmune diseases. ILD risk in PsO and PsA cohorts was compared with a reference population without autoimmune disease. Propensity score matching (PSM) adjusted for age, sex, race, BMI, smoking status and medications known to cause ILD was performed. Baseline immunosuppressive therapies were included in the PSM when comparing PsO and PsA. Statistical significance was determined using the χ test of independence.
After PSM, PsA patients ( = 13 168) had a significantly higher ILD risk compared with the general population ( = 13 168) (risk ratio [RR] 1.94; 95% CI 1.29-2.92; = 0.0011). PsO patients ( = 24 039) showed no significant difference in ILD risk compared with controls ( = 23 786) (RR 0.79; 95% CI 0.57-1.08; = 0.14). PsA ( = 13 838) exhibited an over 1.5 times increase in ILD risk compared with PsO ( = 13 842) (RR 1.52; 95% CI 1.06-2.20; = 0.0226).
PsA was associated with a significantly higher likelihood of developing ILD compared with PsO without inflammatory arthritis. These findings underscore the importance of respiratory monitoring in PsA and highlight the need for further studies.
银屑病(PsO)是一种全身性自身免疫性疾病,主要特征为皮肤上出现红斑鳞屑性斑块。虽然银屑病关节炎(PsA)等皮肤外表现已得到充分认识,但将PsO与间质性肺病(ILD)联系起来的数据仍然有限。本研究旨在评估与PsO患者相比,PsA患者发生ILD的风险是否更高。
对TriNetX美国数据库(2014 - 2024年)进行回顾性分析。纳入接受全身免疫抑制药物治疗的成年PsO或PsA患者,排除患有其他自身免疫性疾病的患者。将PsO和PsA队列中的ILD风险与无自身免疫性疾病的参考人群进行比较。进行倾向评分匹配(PSM)以调整年龄、性别、种族、体重指数、吸烟状况和已知可导致ILD的药物。比较PsO和PsA时,基线免疫抑制治疗纳入PSM。使用独立性χ检验确定统计学显著性。
PSM后,PsA患者(n = 13168)发生ILD的风险显著高于普通人群(n = 13168)(风险比[RR] 1.94;95%可信区间1.29 - 2.92;P = 0.0011)。PsO患者(n = 24039)与对照组(n = 23786)相比,ILD风险无显著差异(RR 0.79;95%可信区间0.57 - 1.08;P = 0.14)。与PsO(n = 13842)相比,PsA(n = 13838)发生ILD的风险增加超过1.5倍(RR 1.52;95%可信区间1.06 - 2.20;P = 0.0226)。
与无炎性关节炎的PsO相比,PsA发生ILD的可能性显著更高。这些发现强调了PsA患者进行呼吸监测的重要性,并突出了进一步研究的必要性。