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在日常生活条件下,亚洲银屑病患者接受甲氨蝶呤治疗的临床应答效果及其相关因素:一项回顾性队列研究。

Effectiveness of and factors associated with clinical response to methotrexate under daily life conditions in Asian patients with psoriasis: A retrospective cohort study.

机构信息

Department of Dermatology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.

出版信息

J Dermatol. 2018 May;45(5):540-545. doi: 10.1111/1346-8138.14270. Epub 2018 Mar 6.

Abstract

Given the relative scarcity of data concerning the efficacy of methotrexate under daily life conditions in psoriasis, this study aimed to investigate the effectiveness of methotrexate in Asian psoriatic patients and to identify factors associated with clinical response. This observational retrospective cohort study included adult psoriatic patients who had been treated with or were going to start methotrexate. Psoriasis Area and Severity Index (PASI) scores at baseline and at 3, 6 and 12 months were recorded. At 3 months, patients achieving 50% or more reduction from baseline PASI score were defined as responders. One hundred, 74 and 61 patients were followed for 3, 6 and 12 months, respectively. Mean follow-up time was 15.3 ± 10.2 months. A reduction in PASI score of at least 75% was achieved in 26%, 32.5% and 45.2% at 3, 6 and 12 months, respectively. At 12 and 24 months, Kaplan-Meier analysis showed 68.7% and 52.1% probability of drug survival, respectively. Male sex, body mass index (BMI) of less than 25 kg/m and absence of abdominal obesity were factors associated with response to treatment in univariate analysis. Male sex was the only significant factor in multivariate analysis. The effectiveness of methotrexate in clinical practise seemed to be lower than in clinical trials, but effectiveness increased with longer duration of treatment. Problems associated with methotrexate use in clinical practise may be due to medication adherence rather than lack of medication effectiveness. Female sex, abdominal obesity and BMI of 25 kg/m or more might decrease response to methotrexate.

摘要

鉴于日常生活中关于甲氨蝶呤治疗银屑病疗效的数据相对较少,本研究旨在探讨甲氨蝶呤在亚洲银屑病患者中的疗效,并确定与临床反应相关的因素。这是一项观察性回顾性队列研究,纳入了接受或即将开始甲氨蝶呤治疗的成年银屑病患者。记录患者基线时和治疗后 3、6 和 12 个月的银屑病面积和严重程度指数(PASI)评分。治疗 3 个月时,PASI 评分较基线降低 50%或更多的患者定义为应答者。分别有 100、74 和 61 例患者随访 3、6 和 12 个月,平均随访时间为 15.3±10.2 个月。治疗 3、6 和 12 个月时,PASI 评分至少降低 75%的患者比例分别为 26%、32.5%和 45.2%。12 和 24 个月时,Kaplan-Meier 分析显示药物存活率分别为 68.7%和 52.1%。单因素分析显示,男性、BMI<25kg/m2 和无腹型肥胖与治疗应答相关。多因素分析显示,男性是唯一有统计学意义的因素。甲氨蝶呤在临床实践中的疗效似乎低于临床试验,但随着治疗时间的延长疗效增加。甲氨蝶呤在临床实践中存在的问题可能与药物依从性有关,而不是药物疗效不足。女性、腹型肥胖和 BMI≥25kg/m2 可能降低对甲氨蝶呤的应答。

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