The effect of initial therapy with the fixed-dose combination of sitagliptin and metformin compared with metformin monotherapy in patients with type 2 diabetes mellitus

被引:73
作者
Reasner, C. [1 ]
Olansky, L. [2 ]
Seck, T. L. [3 ]
Williams-Herman, D. E. [3 ]
Chen, M. [3 ]
Terranella, L. [3 ]
Johnson-Levonas, A. O. [3 ]
Kaufman, K. D. [3 ]
Goldstein, B. J. [3 ]
机构
[1] Univ Texas San Antonio, Texas Diabet Unit, San Antonio, TX 78260 USA
[2] Cleveland Clin Fdn, Cleveland, OH 44195 USA
[3] Merck Res Labs, Rahway, NJ USA
关键词
diabetes; GLP-1; GIP; metformin; sitagliptin; type; 2; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; GLYCEMIC CONTROL; DOUBLE-BLIND; IV INHIBITOR; RISK-FACTORS; EFFICACY; SAFETY; INSULIN; COMPLICATIONS; HYPERGLYCEMIA;
D O I
10.1111/j.1463-1326.2011.01390.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims: This study was conducted to compare the glycaemic efficacy and safety of initial combination therapy with the fixed-dose combination of sitagliptin and metformin versus metformin monotherapy in drug-naive patients with type 2 diabetes. Methods: This double-blind study (18-week Phase A and 26-week Phase B) randomized 1250 drug-naive patients with type 2 diabetes [mean baseline haemoglobin A1c (HbA1c) 9.9%] to sitagliptin/metformin 50/500 mg bid or metformin 500 mg bid (uptitrated over 4 weeks to achieve maximum doses of sitagliptin/metformin 50/1000 mg bid or metformin 1000 bid). Results of the primary efficacy endpoint (mean HbA1c reductions from baseline at the end of Phase A) are reported herein. Results: At week 18, mean change from baseline HbA1c was -2.4% for sitagliptin/metformin FDC and -1.8% for metformin monotherapy (p < 0.001); more patients treated with sitagliptin/metformin FDC had an HbA1c value <7% (p < 0.001) versus metformin monotherapy. Changes in fasting plasma glucose were significantly greater with sitagliptin/metformin FDC (-3.8 mmol/l) versus metformin monotherapy (-3.0 mmol/l; p < 0.001). Homeostasis model assessment of beta-cell function (HOMA-beta) and fasting proinsulin/insulin ratio were significantly improved with sitagliptin/metformin FDC versus metformin monotherapy. Baseline body weight was reduced by 1.6 kg in each group. Both treatments were generally well tolerated with a low and similar incidence of hypoglycaemia. Abdominal pain (1.1 and 3.9%; p = 0.002) and diarrhoea (12.0 and 16.6%; p = 0.021) occurred significantly less with sitagliptin/metformin FDC versus metformin monotherapy; the incidence of nausea and vomiting was similar in both groups. Conclusion: Compared with metformin monotherapy, initial treatment with sitagliptin/metformin FDC provided superior glycaemic improvement with a similar degree of weight loss and lower incidences of abdominal pain and diarrhoea.
引用
收藏
页码:644 / 652
页数:9
相关论文
共 34 条
[1]  
[Anonymous], PROD INF JAN SIT MET
[2]  
[Anonymous], FORMUL J
[3]   Effect of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2 diabetes [J].
Aschner, Pablo ;
Kipnes, Mark S. ;
Lunceford, Jared K. ;
Sanchez, Matilde ;
Mickel, Carolyn ;
Williams-Herman, Debora E. .
DIABETES CARE, 2006, 29 (12) :2632-2637
[4]   Pharmacokinetic and pharmacodynamic properties of multiple oral doses of sitagliptin, a dipeptidyl peptidase-IV inhibitor: A double-blind, randomized, placebo-controlled study in healthy male volunteers [J].
Bergman, AJ ;
Stevens, C ;
Zhou, YY ;
Yi, BM ;
Laethem, M ;
De Smet, M ;
Snyder, K ;
Hilliard, D ;
Tanaka, W ;
Zeng, W ;
Tanen, M ;
Wang, AQ ;
Chen, L ;
Winchell, G ;
Davies, MJ ;
Ramael, S ;
Wagner, JA ;
Herman, GA .
CLINICAL THERAPEUTICS, 2006, 28 (01) :55-72
[5]   The evolution of β-cell dysfunction and insulin resistance in type 2 diabetes [J].
Bergman, RN ;
Finegood, DT ;
Kahn, SE .
EUROPEAN JOURNAL OF CLINICAL INVESTIGATION, 2002, 32 :35-45
[6]   Vildagliptin plus metformin combination therapy provides superior glycaemic control to individual monotherapy in treatment-naive patients with type 2 diabetes mellitus [J].
Bosi, E. ;
Dotta, F. ;
Jia, Y. ;
Goodman, M. .
DIABETES OBESITY & METABOLISM, 2009, 11 (05) :506-515
[7]   Inhibitors of dipeptidyl peptidase IV:: a novel approach for the prevention and treatment of Type 2 diabetes? [J].
Deacon, CF ;
Ahrén, B ;
Holst, JJ .
EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2004, 13 (09) :1091-1102
[8]   THE TRIUMVIRATE - BETA-CELL, MUSCLE, LIVER - A COLLUSION RESPONSIBLE FOR NIDDM [J].
DEFRONZO, RA .
DIABETES, 1988, 37 (06) :667-687
[9]   Effect of initial combination therapy with sitagliptin, a dipeptidyl peptidase-4 inhibitor, and metformin on glycemic control in patients with type 2 diabetes [J].
Goldstein, Barry J. ;
Feinglos, Mark N. ;
Lunceford, Jared K. ;
Johnson, Jeremy ;
Williams-Herman, Debora E. .
DIABETES CARE, 2007, 30 (08) :1979-1987
[10]   Pharmacokinetics and pharmacodynamics of sitagliptin, an inhibitor of dipeptidyl peptidase IV, in healthy subjects: Results from two randomized, double-blind, placebo-controlled studies with single oral doses [J].
Herman, GA ;
Stevens, C ;
Van Dyck, K ;
Bergman, A ;
Yi, BM ;
De Smet, M ;
Snyder, E ;
Hilliard, D ;
Tanen, M ;
Tanaka, W ;
Wang, AQ ;
Zeng, W ;
Musson, D ;
Winchell, G ;
Davies, MJ ;
Ramael, S ;
Gottesdiener, KM ;
Wagner, JA .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2005, 78 (06) :675-688