Tsurutani Yuya, Omura Masao, Matsuzawa Yoko, Saito Jun, Higa Mariko, Taniyama Matsuo, Nishikawa Tetsuo
Endocrinology and Diabetes Center, Yokohama Rosai Hospital, Yokohama, Japan.
Division of Diabetology and Endocrinology, Department of Internal Medicine, Saiseikai Yokohama-shi Tobu Hospital, Yokohama, Japan.
Curr Ther Res Clin Exp. 2017 Mar 10;84:26-31. doi: 10.1016/j.curtheres.2016.12.002. eCollection 2017.
Sitagliptin, a dipeptidyl peptidase-4 inhibitor, is widely used in patients with type 2 diabetes. However, the pleiotropic effects of sitagliptin is not well understood.
To assess the clinical efficacy and safety of sitagliptin on atherosclerosis, β-cell function, and glycemic control in Japanese patients with type 2 diabetes.
A prospective observational study of 270 patients with type 2 diabetes mellitus was carried out. Patients (aged 64.3 [12.4] years, body mas index 25.2 [4.3]) with glycated hemoglobin >6.9% (52 mmol/mol) or fasting plasma glucose >130 mg/dL were treated with sitagliptin for 12 months. The primary end point was glycated hemoglobin level changes from baseline to 3 months. The secondary end points included changes in several biomarkers related to inflammation and β-cell function from baseline to 3 months, as well as changes in glycated hemoglobin level from baseline to 12 months.
Glycated hemoglobin levels were significantly lower in patients treated with sitagliptin for 3 months than at baseline (8.1% [1.4%]-7.3% [1.2%]) (65 [16.9]-56 [13.1] mmol/mol]) ( < 0.0001), which continued after 12 months (7.4% [1.3%]) (56 [15.2] mmol/mol) ( < 0.0001). In addition, a marker of vascular-specific inflammation, pentraxin-3, and a marker of β-cell function (proinsulin/insulin ratio), respectively, were lower after treatment with sitagliptin for 3 months than at baseline (1.88 [0.78]-1.65 [0.63] ng/mL [ = 0.0038] and 0.20 [0.14]-0.17 [0.11] [ = 0.01], respectively). On the other hand, a biomarker reflecting whole body inflammation; that is, high-sensitivity C-reactive protein level, was unchanged. Adverse events occurred in 14 patients (5.18%).
Sitagliptin may have beneficial effects on vascular inflammation and β-cell function in Japanese patients with type 2 diabetes. Pentraxin-3 may be an early predictive marker for detecting the antiatherosclerotic effects of dipeptidyl peptidase-4.
西他列汀是一种二肽基肽酶-4抑制剂,广泛应用于2型糖尿病患者。然而,西他列汀的多效性作用尚未完全明确。
评估西他列汀对日本2型糖尿病患者动脉粥样硬化、β细胞功能及血糖控制的临床疗效和安全性。
对270例2型糖尿病患者进行前瞻性观察研究。糖化血红蛋白>6.9%(52 mmol/mol)或空腹血糖>130 mg/dL的患者(年龄64.3[12.4]岁,体重指数25.2[4.3])接受西他列汀治疗12个月。主要终点是从基线到3个月糖化血红蛋白水平的变化。次要终点包括从基线到3个月与炎症和β细胞功能相关的几种生物标志物的变化,以及从基线到12个月糖化血红蛋白水平的变化。
接受西他列汀治疗3个月的患者糖化血红蛋白水平显著低于基线水平(8.1%[1.4%]-7.3%[1.2%])(65[16.9]-56[13.1] mmol/mol)(P<0.0001),12个月后仍持续降低(7.4%[1.3%])(56[15.2] mmol/mol)(P<0.0001)。此外,血管特异性炎症标志物五聚素-3和β细胞功能标志物(胰岛素原/胰岛素比值)在接受西他列汀治疗3个月后分别低于基线水平(1.88[0.78]-1.65[0.63] ng/mL[P=0.0038]和0.20[0.14]-0.17[0.11][P=0.01])。另一方面,反映全身炎症的生物标志物,即高敏C反应蛋白水平未发生变化。14例患者(5.18%)发生不良事件。
西他列汀可能对日本2型糖尿病患者的血管炎症和β细胞功能有有益作用。五聚素-3可能是检测二肽基肽酶-4抗动脉粥样硬化作用的早期预测标志物。