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银屑病关节炎的长期甲氨蝶呤治疗:临床和放射学结果

Longterm methotrexate therapy in psoriatic arthritis: clinical and radiological outcome.

作者信息

Abu-Shakra M, Gladman D D, Thorne J C, Long J, Gough J, Farewell V T

机构信息

University of Toronto Rheumatic Disease Unit, ON, Canada.

出版信息

J Rheumatol. 1995 Feb;22(2):241-5.

PMID:7738945
Abstract

OBJECTIVE

To determine whether methotrexate (MTX) therapy for 24 months prevents progression of radiographic damage in psoriatic arthritis (PsA).

METHODS

Patients who were given MTX during their attendance at the psoriatic arthritis clinic were enrolled in the study. Patients who had never had MTX and who were matched by damage, actively inflamed joints, sex, and disease duration were identified from the PsA database as controls. The outcome measure was increase in the number of damaged joints.

RESULTS

The study population comprised 38 patients (16 F, 22 M) with a mean age of 44.6 years and disease duration of 11.4 years. Twenty-three patients continued therapy for 24 months. Clinical evaluation revealed that 45% of the patients had > or = 40% improvement in actively inflamed joint count at 6 and 24 months. Radiographs were available for 19 of the 23 patients who took MTX for 24 months, and they were compared to their respective controls. Radiographic damage scores at 24 months showed an increase in the damage score in 63% of the patients. Compared to the matched controls, there was no statistically significant difference in the progression in damage.

CONCLUSION

Our results suggest that compared to other regimens, MTX conferred no advantage with respect to clinical response or longterm damage even after 24 months of therapy.

摘要

目的

确定甲氨蝶呤(MTX)治疗24个月能否预防银屑病关节炎(PsA)的影像学损害进展。

方法

纳入在银屑病关节炎门诊接受MTX治疗的患者。从PsA数据库中确定从未使用过MTX且在损害程度、关节炎症活动度、性别和病程方面相匹配的患者作为对照。观察指标为受损关节数量的增加。

结果

研究人群包括38例患者(16例女性,22例男性),平均年龄44.6岁,病程11.4年。23例患者持续治疗24个月。临床评估显示,45%的患者在6个月和24个月时炎症活动关节计数改善≥40%。23例接受MTX治疗24个月的患者中有19例有影像学资料,将其与各自的对照进行比较。24个月时的影像学损害评分显示,63%的患者损害评分增加。与匹配的对照相比,损害进展无统计学显著差异。

结论

我们的结果表明,与其他治疗方案相比,即使治疗24个月,MTX在临床反应或长期损害方面也没有优势。

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