Yata Yusuke, Hosojima Michihiro, Kabasawa Hideyuki, Ishikawa Tomomi, Kaseda Ryohei, Iino Noriaki, Suzuki Yoshiki, Saito Akihiko, Narita Ichiei
Division of Clinical Nephrology and Rheumatology, Niigata University Graduate School of Medical and Dental Sciences, Japan.
Department of Clinical Nutrition Science, Niigata University Graduate School of Medical and Dental Sciences, Japan.
Intern Med. 2017 Oct 1;56(19):2555-2562. doi: 10.2169/internalmedicine.8296-16. Epub 2017 Sep 6.
Objective The administration of glucocorticoids usually causes a mild increase in fasting glucose levels and a greater dose-dependent increase in postprandial values in patients without pre-existing diabetes mellitus. Patients with persistent hyperglycemia due to glucocorticoid therapy sometimes require insulin therapy, which might result in increased weight gain and more episodes of hypoglycemia, some of which are severe. On the other hand, scant evidence is available on the efficacy of oral hypoglycemic agents in treating glucocorticoid-induced diabetes. In this study, we evaluated the efficacy of dipeptidyl peptidase (DPP)-4 inhibitors in patients with glucocorticoid-induced diabetes by continuous glucose monitoring (CGM). Methods We examined the glycemic profiles using CGM at baseline and 1-4 weeks after initiating DPP-4 inhibitor treatment in patients with newly developed glucocorticoid-induced diabetes. Results Eleven patients who had been diagnosed with kidney disease or other diseases with renal involvement were recruited for the present retrospective study. After starting DPP-4 inhibitors, the mean and standard deviation (SD) of the glucose level, and the mean amplitude of glycemic excursion (MAGE) were significantly improved in comparison to baseline. Furthermore, the area over the curve (AOC) for the glucose levels <70 mg/dL was not increased in comparison to baseline after the initiation of DPP-4 inhibitor treatment. The results indicate that the treatment of patients with glucocorticoid-induced diabetes using DPP-4 inhibitors can minimize the risk of hypoglycemia and reduce glucose variability. Conclusion DPP-4 inhibitors are potentially useful for blood glucose control in patients with glucocorticoid-induced diabetes.
在无糖尿病病史的患者中,糖皮质激素的使用通常会导致空腹血糖水平轻度升高,餐后血糖水平则会随剂量增加而有更明显升高。因糖皮质激素治疗导致持续性高血糖的患者有时需要胰岛素治疗,这可能会导致体重增加及更多低血糖发作,其中一些低血糖发作较为严重。另一方面,关于口服降糖药治疗糖皮质激素诱发的糖尿病的疗效,现有证据较少。在本研究中,我们通过持续葡萄糖监测(CGM)评估了二肽基肽酶(DPP)-4抑制剂对糖皮质激素诱发的糖尿病患者的疗效。方法:我们在新诊断为糖皮质激素诱发的糖尿病患者中,于基线及开始DPP-4抑制剂治疗后1至4周,使用CGM检查血糖谱。结果:本回顾性研究招募了11例被诊断患有肾脏疾病或其他累及肾脏疾病的患者。开始使用DPP-4抑制剂后,与基线相比,血糖水平的平均值、标准差(SD)以及血糖波动幅度平均值(MAGE)均有显著改善。此外,开始DPP-4抑制剂治疗后,血糖水平<70 mg/dL的曲线下面积(AUC)与基线相比未增加。结果表明,使用DPP-4抑制剂治疗糖皮质激素诱发的糖尿病患者可将低血糖风险降至最低,并减少血糖变异性。结论:DPP-4抑制剂对糖皮质激素诱发的糖尿病患者的血糖控制可能有用。