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早期使用甲氨蝶呤预防银屑病患者发生银屑病关节炎——一项回顾性队列研究。

Early methotrexate treatment for psoriatic arthritis prevention in psoriasis patients - A retrospective cohort study.

作者信息

Bar Danielle, Lidar Merav, Baum Sharon, Barzilai Aviv, Pavlotsky Felix, Druyan Amit

机构信息

Faculty of Medical and Health Sciences, Tel-Aviv University, P.O.B 39040, Ramat Aviv, 69978 Tel Aviv, Israel.

Faculty of Medical and Health Sciences, Tel-Aviv University, P.O.B 39040, Ramat Aviv, 69978 Tel Aviv, Israel; Rheumatology Unit, Sheba Medical Center, Tel Hashomer, 52621 Ramat Gan, Israel.

出版信息

Joint Bone Spine. 2025 Mar;92(2):105833. doi: 10.1016/j.jbspin.2024.105833. Epub 2024 Dec 21.

Abstract

OBJECTIVES

Early initiation of biologic therapies for psoriasis has been explored to prevent or delay the onset of psoriatic arthritis (PsA). This has renewed interest in the potential role of methotrexate (MTX) in mitigating PsA risk in newly diagnosed psoriasis patients. The aim of this study was to evaluate the impact of early MTX initiation on PsA incidence in individuals with psoriasis.

METHODS

A retrospective, longitudinal cohort study of psoriasis patients treated at a tertiary center from 2014 to 2024 was conducted. Patients were categorized into early MTX (MTX initiation within 2 years of psoriasis onset), late MTX (> 2 years after onset), and a control group (non-DMARD treatment). PsA incidence was calculated as events per 100 patient years, and a time-dependent Cox proportional hazard model was used to compare PsA risk across groups. Sensitivity analyses were performed to validate results.

RESULTS

A total of 629 patients were followed for a mean of 13.03 years, accumulating 8498.5 person-years. The overall PsA risk was 3.51 events per 100 patient years. The early MTX group had a significantly lower PsA incidence (1.07 events/100 patient years) compared to both the control (4.45 events/100 patient years, adjusted HR: 0.24, P<0.001) and late MTX groups (2.66 events/100 patient years, adjusted HR: 0.36, P<0.01). This effect persisted in patients naïve to biologics and with a minimum follow-up of 10 years.

CONCLUSIONS

Early initiation of methotrexate in patients with moderate to severe psoriasis may reduce the risk of developing PsA.

摘要

目的

已探讨早期启动银屑病生物治疗以预防或延迟银屑病关节炎(PsA)的发病。这重新引发了对甲氨蝶呤(MTX)在降低新诊断银屑病患者患PsA风险中潜在作用的关注。本研究的目的是评估早期启动MTX对银屑病患者PsA发病率的影响。

方法

对2014年至2024年在一家三级中心接受治疗的银屑病患者进行了一项回顾性纵向队列研究。患者被分为早期MTX组(银屑病发病后2年内启动MTX)、晚期MTX组(发病后>2年)和对照组(非DMARD治疗)。PsA发病率按每100患者年的事件数计算,并使用时间依赖性Cox比例风险模型比较各组的PsA风险。进行敏感性分析以验证结果。

结果

共对629例患者进行了平均13.03年的随访,累计8498.5人年。总体PsA风险为每100患者年3.51例事件。与对照组(4.45例事件/100患者年,调整后HR:0.24,P<0.001)和晚期MTX组(2.66例事件/100患者年,调整后HR:0.36,P<0.01)相比,早期MTX组的PsA发病率显著更低(1.07例事件/100患者年)。这种效应在未使用过生物制剂且最短随访10年的患者中持续存在。

结论

中度至重度银屑病患者早期启动甲氨蝶呤可能降低发生PsA的风险。

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