Division of Dermatology, Department of Medicine, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Drug Des Devel Ther. 2021 May 28;15:2299-2307. doi: 10.2147/DDDT.S304168. eCollection 2021.
The use of methotrexate-acitretin (MTX-ACI) combination therapy in treating psoriasis has been limited due to concerns related to hepatic fibrosis. However, in vitro evidence revealed a protective effect of acitretin in methotrexate (MTX)-induced liver fibrosis.
This study aimed to compare the real-life incidence of hepatic fibrosis in patients with psoriasis receiving MTX-ACI and MTX monotherapy and to investigate factors associated with hepatic fibrosis in MTX-exposed patients.
A retrospective cohort study was conducted based on a real-life registry containing data on patients with psoriasis who were administered MTX-ACI or MTX between 2008 and 2019 and underwent transient elastography according to cumulative MTX dose of 1.0-1.5 g and/or 3.5-4.0 g. Time-to-event analysis was performed to determine the cumulative incidence, incidence rate, and factors potentially affecting the occurrence of hepatic fibrosis.
Of the 160 patients, 32 (20%) were treated with MTX-ACI, and 128 (80%) with MTX alone. Four patients (12.5%) in MTX-ACI group and 21 (16.4%) in MTX group developed hepatic fibrosis ( = 0.59). There was no statistically significant difference in cumulative incidence (16% in MTX-ACI vs 17% in MTX, = 0.89) and incidence rate (37 cases per 1000 person-year in MTX-ACI vs 23 cases per 1000 person-year in MTX; hazard ratio [HR] = 1.07; = 0.90) of hepatic fibrosis between the two groups. Diabetes and obesity were identified as significant factors associated with hepatic fibrosis (adjusted HR = 2.40, 95% confidence interval [CI]: 1.05-5.51; = 0.04 and adjusted HR = 3.28, 95% CI: 1.18-9.16; = 0.02, respectively) regardless of the cumulative MTX dose.
The incidence of hepatic fibrosis in a real-life clinical situation, determined by transient elastography in patients with psoriasis receiving MTX-ACI, was not increased compared to those receiving MTX monotherapy. Type 2 diabetes mellitus and obesity were identified as risk factors of hepatic fibrosis; hence, patients with these factors receiving long-term MTX therapy should be regularly monitored for this particular event.
由于担心肝纤维化,甲氨蝶呤-阿维 A(MTX-ACI)联合疗法在治疗银屑病中的应用受到限制。然而,体外证据显示阿维 A 可保护甲氨蝶呤(MTX)诱导的肝纤维化。
本研究旨在比较接受 MTX-ACI 和 MTX 单药治疗的银屑病患者肝纤维化的真实发生率,并探讨 MTX 暴露患者肝纤维化相关因素。
对 2008 年至 2019 年间接受 MTX-ACI 或 MTX 治疗且根据累积 MTX 剂量(1.0-1.5 g 和/或 3.5-4.0 g)行瞬时弹性成像的银屑病患者进行回顾性队列研究。采用时间事件分析确定肝纤维化的累积发生率、发生率和潜在影响肝纤维化发生的因素。
160 例患者中,32 例(20%)接受 MTX-ACI 治疗,128 例(80%)接受 MTX 单药治疗。MTX-ACI 组有 4 例(12.5%)和 MTX 组有 21 例(16.4%)发生肝纤维化( = 0.59)。两组累积发生率(MTX-ACI 组 16%,MTX 组 17%, = 0.89)和发生率(MTX-ACI 组每 1000 人年 37 例,MTX 组每 1000 人年 23 例;HR=1.07; = 0.90)无统计学差异。无论累积 MTX 剂量如何,糖尿病和肥胖均被确定为肝纤维化的显著相关因素(校正 HR=2.40,95%CI:1.05-5.51; = 0.04 和校正 HR=3.28,95%CI:1.18-9.16; = 0.02)。
通过接受 MTX-ACI 和 MTX 单药治疗的银屑病患者的瞬时弹性成像在真实临床情况下确定的肝纤维化发生率与接受 MTX 单药治疗的患者相比并未增加。2 型糖尿病和肥胖被确定为肝纤维化的危险因素;因此,接受长期 MTX 治疗且具有这些因素的患者应定期监测该特定事件。