Long-term efficacy of sitagliptin as either monotherapy or add-on therapy to metformin: improvement in glycemic control over 2 years in patients with type 2 diabetes

被引:6
作者
Katzeff, H. L. [1 ]
Williams-Herman, D. [1 ]
Xu, L. [1 ]
Golm, G. T. [1 ]
Wang, H. [2 ]
Dong, Q. [3 ]
Johnson, J. R. [1 ]
O'Neill, E. A. [1 ]
Kaufman, K. D. [1 ]
Engel, S. S. [1 ]
Goldstein, B. J. [4 ]
机构
[1] Merck & Co Inc, Kenilworth, NJ USA
[2] Sanofi, Bridgewater, NJ USA
[3] Celgene, Summit, NJ USA
[4] Covance Inc, Princeton, NJ USA
关键词
DPP-4; Beta-cell function; HOMA-beta; Incretins; P/l ratio; Type 2 diabetes disease progression; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; INITIAL COMBINATION THERAPY; BETA-CELL FUNCTION; INTENSIVE INSULIN THERAPY; POOLED ANALYSIS; DOUBLE-BLIND; SAFETY; TOLERABILITY; SULFONYLUREA; GLIPIZIDE;
D O I
10.1185/03007995.2015.1037259
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: 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. Research design and methods: 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 mettormin >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-beta, proinsulin/insulin (P/I) ratio, and for monotherapy, 2 hour post-meal plasma glucose (PMG). Results: 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-beta 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-beta 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. Conclusion: In the subset of patients with T2DM who maintained and completed treatment for 2 years with sitagliptin as monotherapy or as add-on to mefformin, improvements in glycemic control and measures of beta-cell function were observed over the course of treatment.
引用
收藏
页码:1071 / 1077
页数:7
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