Matsuoka Naoki, Yajima Nobuyuki, Inoue Eisuke, Sato Shuzo, Ogawa Shotaro, Sumichika Yuya, Saito Kenji, Yoshida Shuhei, Matsumoto Haruki, Temmoku Jumpei, Fujita Yuya, Asano Tomoyuki, Fukita Jumpei, Sada Ken-Ei, Ichinose Kunihiro, Yoshimi Ryusuke, Ohno Shigeru, Kajiyama Hiroshi, Shimojima Yasuhiro, Fujiwara Michio, Kida Takashi, Miyawaki Yoshia, Matsuo Yusuke, Onishi Takahisa, Nishimura Keisuke, Migita Kiyoshi
Department of Rheumatology, Fukushima Medical University School of Medicine, Fukushima, Japan
Department of Internal Medicine, Showa Medical university, Tokyo, Japan.
RMD Open. 2025 Jul 22;11(3):e005558. doi: 10.1136/rmdopen-2025-005558.
We aimed to compare the incidence of severe infections between mycophenolate mofetil (MMF) and other immunosuppressants in patients with systemic lupus erythematosus (SLE) on maintenance therapy using data from the Lupus Registry of Nationwide Institutions in Japan.
This study employed a prospective cohort design, including patients with SLE undergoing maintenance therapy. Exposure was defined as MMF treatment, and the control group included individuals who received other immunosuppressants (non-MMF) treatments. Severe infections requiring hospitalisation were the primary outcomes, whereas secondary outcomes included all-cause hospitalisation, changes in prednisolone dosage, disease activity and organ damage. Statistical analyses employed marginal structural models with stabilised inverse probability of treatment weighting to adjust for confounders.
The analysis included 1004 patients; the incidence of severe infections was 6.5% in the MMF group and 7.5% in the non-MMF group, with no significant difference (OR 0.69, 95% CI 0.34 to 1.39). Similarly, all-cause hospitalisation rates were comparable between the groups (OR 0.72, 95% CI 0.47 to 1.09). Prednisolone dosage was significantly reduced in the MMF group (-0.66 mg/day, 95% CI -1.09 to -0.23). The organ damage score was modestly reduced in the MMF group (-0.19 points, 95% CI -0.37 to -0.01), whereas the change of disease activity score was comparable between the groups (-0.10 points, 95% CI -0.74 to 0.55).
MMF does not significantly increase the risk of severe infections compared with other immunosuppressants in SLE maintenance therapy. MMF may contribute to reducing the dose of prednisolone.
我们旨在利用日本全国性机构狼疮登记处的数据,比较霉酚酸酯(MMF)与其他免疫抑制剂在接受维持治疗的系统性红斑狼疮(SLE)患者中严重感染的发生率。
本研究采用前瞻性队列设计,纳入接受维持治疗的SLE患者。暴露定义为MMF治疗,对照组包括接受其他免疫抑制剂(非MMF)治疗的个体。需要住院治疗的严重感染为主要结局,次要结局包括全因住院、泼尼松龙剂量变化、疾病活动度和器官损伤。统计分析采用具有稳定治疗权重逆概率的边际结构模型来调整混杂因素。
分析纳入1004例患者;MMF组严重感染发生率为6.5%,非MMF组为7.5%,差异无统计学意义(OR 0.69,95%CI 0.34至1.39)。同样,两组间全因住院率相当(OR 0.72,95%CI 0.47至1.09)。MMF组泼尼松龙剂量显著降低(-0.66mg/天,95%CI -1.09至-0.23)。MMF组器官损伤评分略有降低(-0.19分,95%CI -0.37至-0.01),而两组间疾病活动度评分变化相当(-0.10分,95%CI -0.74至0.55)。
在SLE维持治疗中,与其他免疫抑制剂相比,MMF不会显著增加严重感染的风险。MMF可能有助于降低泼尼松龙的剂量。