da Silva Giordana Maluf, Nogueira Katia Camarano, Fukui Rosa Tsuneshiro, Correia Marcia Regina Soares, Dos Santos Rosa Ferreira, da Silva Maria Elizabeth Rossi
Faculdade de Medicina da Universidade de São Paulo, Av Dr Arnaldo, 455 sala 3324. Sao Paulo/SP - 01246-903, Brazil.
Curr Pharm Des. 2016;22(44):6716-6721. doi: 10.2174/1381612822666161208144411.
We conducted a comparison between the dipeptidyl-peptidase-4(DPP-4) inhibitor sitagliptin versus NPH insulin as an add-on therapies in patients with type 2 diabetes mellitus (T2D) failing oral medications. The objective was to ascertain the better indication in long-duration diabetes.
thirty-five T2D patients inadequately controlled with metformin plus glyburide were randomized to receive sitagliptin (n=18) or bedtime NPH insulin (n=17) for 12 months. HbA1c levels and a metabolic and hormonal profile at fasting and post-meal (every 30 minutes for 4 hours) were evaluated before and after 6 months (short-term) and 12 months (long-term) after adding sitagliptin or bedtime NPH insulin to their drug regime.
Sitagliptin and NPH insulin decreased HbA1c levels equally after 6 months (p<0.001) with no further improvement after 12 months: sitagliptin (8.1±0.7% vs. 7.3±0.8% vs. 7.4±1.9%) and insulin (8.1±0.6% vs. 7.3±0.7% vs. 7.2±1.0%). Fasting glucose, fasting and postprandial triglyceride and C-peptide levels were also reduced by NPH insulin whereas postprandial insulin was decreased by sitagliptin. Body weight and postchallenge free fatty acid levels increased with insulin treatment. The transitory suppression (at 6 months) of postprandial proinsulin levels with both therapies, and of glucagon with sitagliptin, was followed by values similar or worse to those at pre-treatment.
The use of either NPH insulin or a DPP-4 inhibitor as add-on treatments improves glucose control in patients with T2D failing on metformin plus glyburide therapy. The results were not attributed to a permanent improvement in alpha or beta cell function in patients with long-duration diabetes.
我们对二肽基肽酶-4(DPP-4)抑制剂西他列汀与中性鱼精蛋白锌胰岛素(NPH胰岛素)作为口服药物治疗失败的2型糖尿病(T2D)患者的附加疗法进行了比较。目的是确定在病程较长的糖尿病患者中哪种疗法更具优势。
35例使用二甲双胍加格列本脲血糖控制不佳的T2D患者被随机分为两组,分别接受西他列汀治疗(n = 18)或睡前NPH胰岛素治疗(n = 17),为期12个月。在将西他列汀或睡前NPH胰岛素添加到其药物治疗方案后的6个月(短期)和12个月(长期)前后,评估糖化血红蛋白(HbA1c)水平以及空腹和餐后(每30分钟一次,共4小时)的代谢和激素指标。
6个月后,西他列汀和NPH胰岛素降低HbA1c水平的效果相当(p<0.001),12个月后无进一步改善:西他列汀组(8.1±0.7%对7.3±0.8%对7.4±1.9%)和胰岛素组(8.1±0.6%对7.3±0.7%对7.2±1.0%)。NPH胰岛素还降低了空腹血糖、空腹和餐后甘油三酯以及C肽水平,而西他列汀降低了餐后胰岛素水平。胰岛素治疗使体重和餐后游离脂肪酸水平升高。两种疗法在6个月时均短暂抑制了餐后胰岛素原水平,西他列汀抑制了胰高血糖素水平,随后这些指标的值与治疗前相似或更差。
使用NPH胰岛素或DPP-4抑制剂作为附加治疗可改善二甲双胍加格列本脲治疗失败的T2D患者的血糖控制。结果并非归因于病程较长的糖尿病患者α或β细胞功能的永久性改善。