Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Clinical Research and Medical Innovation Center, Hokkaido University Hospital, Sapporo, Japan.
J Diabetes Investig. 2021 Nov;12(11):1978-1982. doi: 10.1111/jdi.13578. Epub 2021 Jun 16.
Dipeptidyl peptidase-4 (DPP-4), namely CD26, is expressed on the surface of immune cells, suggesting that inhibition of DPP-4 might affect the immune system. The current multicenter observational case-control study was carried out to investigate the effects of DPP-4 inhibitor (DPP-4i) administration on Graves' disease (GD) activity. This study comprised patients with GD and type 2 diabetes, who were administered an oral hypoglycemic agent including DPP-4i. Exacerbation of GD was defined as an increase of antithyroid drug dose by 6 months after oral hypoglycemic agent administration. A total of 80 patients were enrolled and divided into an exacerbation group or a non-exacerbation group. The frequency of DPP-4i administration was significantly higher in the exacerbation group (88%) than that in the non-exacerbation group (31%). In multivariate logistic regression analysis, there was a significant association between DPP-4i administration and GD exacerbation (odds ratio 7.39). The current study suggests that DPP-4i administration is associated with GD exacerbation.
二肽基肽酶-4(DPP-4),也称为 CD26,表达于免疫细胞表面,提示抑制 DPP-4 可能会影响免疫系统。本多中心观察性病例对照研究旨在探讨二肽基肽酶-4 抑制剂(DPP-4i)给药对 Graves 病(GD)活动的影响。该研究纳入了 GD 合并 2 型糖尿病患者,他们接受了包括 DPP-4i 在内的口服降糖药治疗。GD 恶化定义为口服降糖药治疗 6 个月后抗甲状腺药物剂量增加。共纳入 80 例患者,分为恶化组和非恶化组。恶化组(88%)DPP-4i 给药频率明显高于非恶化组(31%)。多变量逻辑回归分析显示,DPP-4i 给药与 GD 恶化之间存在显著关联(比值比 7.39)。本研究提示 DPP-4i 给药与 GD 恶化相关。