2025 Volume 37 Issue 2 Pages 76-83
[Objective] To investigate the effectiveness and safety of ipragliflozin in glucocorticoid-induced hyperglycemia in patients with autoimmune diseases. [Methods] We retrospectively examined HbA1c levels and adverse events after initiation of ipragliflozin treatment for glucocorticoid-induced hyperglycemia in patients with autoimmune diseases who were followed up for 24 weeks at our hospital between 2015 and 2021. [Results] Among the 39 patients on ipragliflozin, 8 discontinued it because of insufficient effects and adverse events. The remaining 31 patients(rheumatoid arthritis 22, systemic lupus erythematosus 4, others 6; 21females and 10 males, median age 68.0 years old)were followed up for 24 weeks on ipragliflozin. At 24 weeks, the HbA1c value was significantly reduced(7.6[7.3, 8.3]to 7.2[6.5, 8.0], p=0.008), even though the prednisolone(PSL)dose was significantly reduced(6.0[2.3, 7.9]mg/day to 5.0[2.3, 6.3]mg/day, p<0.001). In 11 patients receiving a fixed or increased dose of PSL and fixed antidiabetic drugs, HbA1c values were also significantly reduced(7.5[7.3, 7.9]to 7.2[6.8, 7.7], p=0.024). No serious adverse effects were observed. [Conclusions] In the short term, ipragliflozin is an effective and safe treatment for glucocorticoid-induced hyperglycemia in patients with autoimmune diseases.