Katzeff H L, Williams-Herman D, Xu L, Golm G T, Wang H, Dong Q, Johnson J R, O'Neill E A, Kaufman K D, Engel S S, Goldstein B J
Merck & Co. Inc., Kenilworth , NJ , USA.
Curr Med Res Opin. 2015 Jun;31(6):1071-7. doi: 10.1185/03007995.2015.1037259.
To evaluate the efficacy of once daily sitagliptin 100 mg as monotherapy or as add-on to metformin in patients with type 2 diabetes mellitus (T2DM) over 2 years of treatment.
The monotherapy analysis used pooled 104 week data from 64 patients in two randomized, double-blind trials evaluating the safety and efficacy of sitagliptin monotherapy. Data used were from patients who were randomized to sitagliptin 100 mg/day, were not on an antihyperglycemic agent at the screening visit, had baseline A1C of 7.0%-10.0%, and had Week 104 A1C measurements. The add-on to metformin analysis used pooled data from 347 patients in two randomized double-blind trials evaluating the safety and efficacy of sitagliptin + metformin combination therapy. Data used were from patients who were randomized to sitagliptin 100 mg/day + metformin ≥1500 mg/day, had baseline A1C of 7%-10%, and had Week 104 A1C measurements. Excluded from either analysis were patients who discontinued prior to 2 years (e.g., due to lack of efficacy, a need for rescue medications, or adverse experiences). Analysis endpoints were A1C, fasting plasma glucose (FPG), HOMA-β, proinsulin/insulin (P/I) ratio, and for monotherapy, 2 hour post-meal plasma glucose (PMG).
For the pooled monotherapy cohort, after 2 years of treatment, mean A1C, FPG, and 2 hour PMG decreased from baseline values of 7.9%, 156 mg/dL, and 223 mg/dL to 6.9%, 143 mg/dL, and 191 mg/dL, respectively, while HOMA-β increased from 67% to 85% and P/I ratio improved from 0.57 to 0.28. For the pooled add-on to metformin cohort, after 2 years of treatment, mean A1C and FPG decreased from baseline values of 7.7% and 160 mg/dL to 6.9% and 140 mg/dL, respectively, while HOMA-β increased from 50% to 62% and P/I ratio improved from 0.33 to 0.28. These analyses are limited in that only patients who were able to complete 104 weeks of study were included.
In the subset of patients with T2DM who maintained and completed treatment for 2 years with sitagliptin as monotherapy or as add-on to metformin, improvements in glycemic control and measures of β-cell function were observed over the course of treatment.
评估每日一次服用100毫克西格列汀作为单药治疗或联合二甲双胍治疗2型糖尿病(T2DM)患者2年的疗效。
单药治疗分析采用了两项评估西格列汀单药治疗安全性和疗效的随机、双盲试验中64例患者的汇总104周数据。所使用的数据来自随机分配至每日服用100毫克西格列汀、筛查访视时未使用抗高血糖药物、基线糖化血红蛋白(A1C)为7.0%-10.0%且有第104周A1C测量值的患者。联合二甲双胍治疗分析采用了两项评估西格列汀+二甲双胍联合治疗安全性和疗效的随机双盲试验中347例患者的汇总数据。所使用的数据来自随机分配至每日服用100毫克西格列汀+≥1500毫克/日二甲双胍、基线A1C为7%-10%且有第104周A1C测量值的患者。两项分析均排除了在2年之前停药的患者(例如,由于疗效不佳、需要急救药物或出现不良事件)。分析终点为A1C、空腹血糖(FPG)、胰岛素抵抗指数(HOMA-β)、胰岛素原/胰岛素(P/I)比值,单药治疗还包括餐后2小时血糖(PMG)。
对于汇总的单药治疗队列,治疗2年后,平均A1C、FPG和餐后2小时PMG分别从基线值7.9%、156毫克/分升和223毫克/分升降至6.9%、143毫克/分升和191毫克/分升,而HOMA-β从67%增至85%,P/I比值从0.57改善至0.28。对于汇总的联合二甲双胍治疗队列,治疗2年后,平均A1C和FPG分别从基线值7.7%和160毫克/分升降至6.9%和140毫克/分升,而HOMA-β从50%增至62%,P/I比值从0.33改善至0.28。这些分析的局限性在于仅纳入了能够完成104周研究的患者。
在以西格列汀作为单药治疗或联合二甲双胍维持并完成2年治疗的T2DM患者亚组中,在治疗过程中观察到血糖控制和β细胞功能指标有所改善。