Scott R, Loeys T, Davies M J, Engel S S
Lipid and Diabetes Research Group, Christchurch School of Medicine, Christchurch, New Zealand.
Diabetes Obes Metab. 2008 Sep;10(10):959-69. doi: 10.1111/j.1463-1326.2007.00839.x. Epub 2008 Jan 14.
To assess the addition of sitagliptin to ongoing metformin therapy in patients with type 2 diabetes who were inadequately controlled [haemoglobin A(1c) (HbA(1c)) 7-11%] on metformin monotherapy.
Patients (n = 273) on metformin (>/=1500 mg/day) were randomized to receive the addition of once-daily placebo, sitagliptin 100 mg or rosiglitazone 8 mg in a 1 : 1 : 1 ratio for 18 weeks. The efficacy analysis was based on the all-patients-treated population using an analysis of co-variance with change in HbA(1c) from baseline as the primary endpoint.
The mean baseline HbA(1c) was 7.7% for the entire cohort. After 18 weeks, both active add-on therapies led to greater improvements in HbA(1c) from baseline: -0.73% for sitagliptin (p < 0.001 vs. placebo) and -0.79% for rosiglitazone compared with -0.22% for placebo. No difference was observed between the sitagliptin and rosiglitazone treatments (0.06% [95% confidence interval (CI): -0.14 to 0.25]). The proportion of patients achieving an HbA(1c) < 7% was greater with sitagliptin (55%) and rosiglitazone (63%) compared with placebo (38%). Body weight increased from baseline with rosiglitazone (1.5 kg) compared with body weight reduction with sitagliptin (-0.4 kg) and placebo (-0.8 kg). The difference in body weight between the sitagliptin and rosiglitazone groups was 1.9 kg (95% CI: 1.3-2.5). In a prespecified analysis, the proportion of patients experiencing a greater than 3-kg increase in body weight was 21% in the rosiglitazone group compared with 2% in both the sitagliptin and placebo groups. Both active treatments were generally well tolerated, with no increased risk of hypoglycaemia or gastrointestinal adverse events compared with placebo.
In this 18-week study, the addition of sitagliptin was effective and well tolerated in patients with type 2 diabetes inadequately controlled with metformin monotherapy. Treatment with sitagliptin produced similar reductions in HbA(1c) compared with the addition of rosiglitazone.
评估在接受二甲双胍单药治疗但控制不佳(糖化血红蛋白[HbA(1c)]为7 - 11%)的2型糖尿病患者中,加用西他列汀至正在进行的二甲双胍治疗方案中的效果。
正在服用二甲双胍(≥1500毫克/天)的患者(n = 273)按1 : 1 : 1比例随机分组,分别接受每日一次的安慰剂、100毫克西他列汀或8毫克罗格列酮,治疗18周。疗效分析基于所有接受治疗的患者群体,采用协方差分析,以HbA(1c)自基线的变化作为主要终点。
整个队列的平均基线HbA(1c)为7.7%。18周后,两种活性附加治疗均使HbA(1c)自基线有更大改善:西他列汀组为 - 0.73%(与安慰剂相比,p < 0.001),罗格列酮组为 - 0.79%,而安慰剂组为 - 0.22%。西他列汀与罗格列酮治疗之间未观察到差异(0.06%[95%置信区间(CI): - 0.14至0.25])。达到HbA(1c) < 7%的患者比例,西他列汀组(55%)和罗格列酮组(63%)高于安慰剂组(38%)。与西他列汀组体重减轻( - 0.4千克)和安慰剂组体重减轻( - 0.8千克)相比,罗格列酮组体重自基线增加(1.5千克)。西他列汀组与罗格列酮组之间的体重差异为1.9千克(95%CI:1.