Kılıç Gamze, Kılıç Erkan, Tekeoğlu İbrahim, Sargın Betül, Cengiz Gizem, Balta Nihan Cüzdan, Alkan Hakan, Kasman Sevtap Acer, Şahin Nilay, Orhan Kevser, Gezer İlknur Albayrak, Keskin Dilek, Mülkoğlu Cevriye, Reşorlu Hatice, Ataman Şebnem, Bal Ajda, Duruöz Mehmet Tuncay, Kücükakkaş Okan, Şen Nesrin, Toprak Murat, Yurdakul Ozan Volkan, Melikoğlu Meltem Alkan, Ayhan Fikriye Figen, Baykul Merve, Bodur Hatice, Çalış Mustafa, Çapkın Erhan, Devrimsel Gül, Hizmetli Sami, Kamanlı Ayhan, Keskin Yaşar, Ecesoy Hilal, Kutluk Öznur, Şendur Ömer Faruk, Tolu Sena, Tuncer Tiraje, Özgöçmen Salih, Nas Kemal
Department of PMR, Hacettepe University School of Medicine, Ankara, Turkey.
Rheumatology Clinic, Sincan Training and Research Hospital, Ankara, Turkey.
Rheumatol Int. 2025 Sep 9;45(9):225. doi: 10.1007/s00296-025-05984-3.
To identify clinical and demographic predictors associated with the timing of transition from psoriasis (PsO) to psoriatic arthritis (PsA), and to compare the characteristics of patients with concurrent PsO-PsA onset versus those with prolonged transition. A multi-center, observational study was conducted using data from the Turkish League Against Rheumatism (TLAR) network including PsA patients fulfilling CASPAR criteria. Patients were categorized into two groups: Group 1 (concurrent PsO and PsA onset within ± 1 year) and Group 2 (prolonged transition to PsA, > 1 year after PsO). Demographic, clinical, and laboratory characteristics, disease activity, and patient-reported outcomes were compared between groups. Logistic regression was employed to determine independent predictors of prolonged transition. Among 799 patients (mean age 46.8 ± 12.3 years), 237 (29.7%) had concurrent onset and 562 (70.3%) had a prolonged transition, with a mean PsO-to-PsA interval of 12.9 ± 9.6 years. Depression (p = 0.005) and fatigue levels (p = 0.011) were significantly higher in patients with prolonged transition to PsA. Multivariate analysis revealed that scalp psoriasis (OR = 7.162), nail psoriasis (OR = 3.270), family history of PsO (OR = 1.813), and enthesitis ever (OR = 2.187) were associated with prolonged transition. Conversely, family history of PsA (OR = 0.421) and older age at PsO onset (OR = 0.957) predicted shorter transition. Prolonged transition from PsO to PsA is influenced by distinct clinical and demographic factors. Scalp/nail psoriasis, family history of PsO, and enthesitis ever may signal higher risk for prolonged PsA onset. Recognizing these markers can support timely referral and intervention, minimizing diagnostic delay and improving long-term patient outcomes.
为了确定与从银屑病(PsO)转变为银屑病关节炎(PsA)的时间相关的临床和人口统计学预测因素,并比较同时发生PsO-PsA发病的患者与转变时间延长的患者的特征。利用来自土耳其风湿病联盟(TLAR)网络的数据进行了一项多中心观察性研究,该网络包括符合CASPAR标准的PsA患者。患者被分为两组:第1组(PsO和PsA在±1年内同时发病)和第2组(向PsA的转变时间延长,PsO发病后>1年)。比较两组之间的人口统计学、临床和实验室特征、疾病活动度以及患者报告的结局。采用逻辑回归确定转变时间延长的独立预测因素。在799例患者(平均年龄46.8±12.3岁)中,237例(29.7%)同时发病,562例(70.3%)转变时间延长,PsO到PsA的平均间隔为12.9±9.6年。向PsA转变时间延长的患者抑郁(p=0.005)和疲劳水平(p=0.011)显著更高。多变量分析显示,头皮银屑病(OR=7.162)、指甲银屑病(OR=3.270)、PsO家族史(OR=1.813)和曾经有过附着点炎(OR=2.187)与转变时间延长相关。相反,PsA家族史(OR=0.421)和PsO发病时年龄较大(OR=0.957)预示着转变时间较短。从PsO到PsA的转变时间延长受不同的临床和人口统计学因素影响。头皮/指甲银屑病、PsO家族史和曾经有过附着点炎可能预示PsA发病时间延长的风险较高。识别这些标志物有助于及时转诊和干预,最大限度地减少诊断延迟并改善患者长期结局。