Harada Yosuke, Hiyama Tomona, Kiuchi Yoshiaki
Department of Ophthalmology and Visual Science, Graduate School of Biomedical Sciences, Hiroshima University, Hiroshima, Japan.
Front Med (Lausanne). 2021 Nov 18;8:732427. doi: 10.3389/fmed.2021.732427. eCollection 2021.
This single-center retrospective study investigated the clinical characteristics and efficacy of methotrexate (MTX) for the treatment of non-infectious uveitis for more than 6 months at Hiroshima University, from February 2016 to May 2021. Outcome variables included changes in systemic immunosuppressive treatment and intraocular inflammation. Out of 448 patients with non-infectious uveitis, 35 patients (14 male patients and 21 female patients; 65 eyes) treated with MTX for more than 6 months were analyzed. There were 15 patients with anterior uveitis and 20 with posterior and panuveitis. The mean dose of systemic corticosteroids decreased from 12.1 mg/day at baseline to 1.3 mg/day at 6 months and 0.6 mg at 12 months after starting MTX, and approximately 90% of patients were corticosteroid-free at 12 months. The percentage of eyes with inactive uveitis at 6, 12, and 24 months was 49.2%, 59.6%, and 90.0%, respectively. Mean relapse rate score also significantly decreased from 2.88 at baseline to 0.85 at 12 months ( < 0.001). Inflammatory control was achieved with MTX doses of 8-16 mg/week, with a median dose of 12 mg/week. Adverse effects of MTX were observed in 34.3% of patients, and 11.4% required discontinuation; most commonly hepatotoxicity (58.3%), followed by fatigue (25.0%), and hair loss (16.7%). No significant differences were found between the survival curves of patients with anterior uveitis and posterior/panuveitis (Wilcoxon rank-sum test). The percentage of eyes without IOP-lowering eye drops was significantly higher in patients with posterior/panuveitis at 24 months ( = 0.001). Our study suggests that MTX is effective in controlling ocular inflammation for Japanese patients with non-infectious uveitis. Relatively high incidence of MTX-related adverse effects in the Japanese population indicates that careful monitoring and dose adjustments are crucial for the long-term use of this therapy.
本单中心回顾性研究调查了2016年2月至2021年5月期间,广岛大学使用甲氨蝶呤(MTX)治疗非感染性葡萄膜炎超过6个月的临床特征和疗效。结果变量包括全身免疫抑制治疗的变化和眼内炎症。在448例非感染性葡萄膜炎患者中,分析了35例(14例男性患者和21例女性患者;65只眼)接受MTX治疗超过6个月的患者。其中前葡萄膜炎患者15例,后葡萄膜炎和全葡萄膜炎患者20例。全身皮质类固醇的平均剂量从基线时的12.1毫克/天降至开始使用MTX后6个月时的1.3毫克/天和12个月时的0.6毫克,约90%的患者在12个月时无需使用皮质类固醇。在6个月、12个月和24个月时,葡萄膜炎无活动的眼的百分比分别为49.2%、59.6%和90.0%。平均复发率评分也从基线时的2.88显著降至12个月时的0.85(<0.001)。MTX剂量为8 - 16毫克/周时可实现炎症控制,中位剂量为12毫克/周。34.3%的患者观察到MTX的不良反应,11.4%的患者需要停药;最常见的是肝毒性(58.3%),其次是疲劳(25.0%)和脱发(16.7%)。前葡萄膜炎患者与后葡萄膜炎/全葡萄膜炎患者的生存曲线之间未发现显著差异(Wilcoxon秩和检验)。在24个月时,后葡萄膜炎/全葡萄膜炎患者中无需使用降眼压滴眼液的眼的百分比显著更高(=0.001)。我们的研究表明,MTX对日本非感染性葡萄膜炎患者控制眼部炎症有效。日本人群中MTX相关不良反应的发生率相对较高,表明长期使用该疗法时仔细监测和调整剂量至关重要。