Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Clin Endocrinol (Oxf). 2012 Aug;77(2):215-23. doi: 10.1111/j.1365-2265.2011.04240.x.
We assessed the predictive parameters for therapeutic efficacy of initial combination therapy with sitagliptin and metformin in drug-naïve type 2 diabetic patients. DeSIGN, PATIENTS, AND MEASUREMENTS: In this 52-week treatment study, 150 patients (mean age, 54·9 ± 12·5 years) with type 2 diabetes and HbA1c of 7·0-10% were treated with sitagliptin 100 mg once and metformin 500 mg twice daily. To assess the predictive parameters for therapeutic efficacy, a multivariate regression analysis was performed with baseline fasting glucose, insulin, C-peptide, and glucagon levels, homoeostasis model assessment-insulin resistance (HOMA-IR) and β-cell function (HOMA-B), insulinogenic index (IGI, defined as 30-0 min insulin/30-0 min glucose), and area under the curve for glucose, insulin, and C-peptide obtained after 75-g oral glucose tolerance test.
After 52 weeks, mean HbA1c levels and fasting and postload 2-h glucose were significantly decreased from 8·7 ± 1·4% to 7·2 ± 1·3%, 9·2 ± 3·0 to 7·2 ± 1·8 mm, and 17·5 ± 5·1 to 10·9 ± 3·6 mm, respectively (P < 0·01). HOMA-B and IGI increased significantly from 50·3 ± 33·5 to 75·1 ± 32·8 and from 11·3 ± 1·3 to 35·0 ± 6·3 at 52 weeks, respectively (P < 0·01). Multivariate regression analysis indicated that the reduction in HbA1c was significantly associated with high baseline HbA1c, low IGI, and short duration of diabetes after adjusting for age, sex, body mass index, blood pressure, triglycerides, creatinine, high-sensitivity CRP, glucagon, C-peptide, HOMA-B, and HOMA-IR. No severe adverse events were observed.
These results suggest that drug-naïve type 2 diabetic patients with low β-cell function would benefit the most from early initial combination therapy of sitagliptin and metformin.
我们评估了西格列汀联合二甲双胍初始治疗在初治 2 型糖尿病患者中的疗效预测参数。
设计、患者和方法:在这项为期 52 周的治疗研究中,150 名(平均年龄 54.9 ± 12.5 岁)初治的 2 型糖尿病且糖化血红蛋白(HbA1c)为 7.0-10%的患者接受西格列汀 100mg 每日一次和二甲双胍 500mg 每日两次治疗。为了评估疗效的预测参数,我们对空腹血糖、胰岛素、C 肽和胰高血糖素水平、稳态模型评估胰岛素抵抗(HOMA-IR)和β细胞功能(HOMA-B)、胰岛素原指数(IGI,定义为 30-0 分钟胰岛素/30-0 分钟血糖)以及 75g 口服葡萄糖耐量试验后葡萄糖、胰岛素和 C 肽的曲线下面积进行了多变量回归分析。
52 周后,平均 HbA1c 水平以及空腹和餐后 2 小时血糖分别从 8.7 ± 1.4%显著下降至 7.2 ± 1.3%、9.2 ± 3.0 至 7.2 ± 1.8 mm 和 17.5 ± 5.1 至 10.9 ± 3.6 mm(P < 0.01)。HOMA-B 和 IGI 分别从 50.3 ± 33.5 显著增加至 75.1 ± 32.8 和 11.3 ± 1.3 至 35.0 ± 6.3(P < 0.01)。多变量回归分析表明,在调整年龄、性别、体重指数、血压、甘油三酯、肌酐、高敏 C 反应蛋白、胰高血糖素、C 肽、HOMA-B 和 HOMA-IR 后,HbA1c 的降低与高基线 HbA1c、低 IGI 和糖尿病病程短显著相关。未观察到严重不良事件。
这些结果表明,β细胞功能较低的初治 2 型糖尿病患者将从西格列汀联合二甲双胍的早期初始联合治疗中获益最大。