Clinical evidence and mechanistic basis for vildagliptin's action when added to metformin

被引:59
作者
Ahren, B. [1 ]
Foley, J. E. [2 ]
Bosi, E. [3 ]
机构
[1] Lund Univ, Dept Clin Sci, SE-22184 Lund, Sweden
[2] Novartis Pharmaceut, E Hanover, NJ USA
[3] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Dept Internal Med, Diabetes & Endocrinol Unit, Milan, Italy
关键词
antidiabetic drug; beta cell; diabetes mellitus; dipeptidyl peptidase-4; DPP-4; inhibitor; GIP; GLP-1; HbA1c; insulin resistance; islet function; type; 2; diabetes; PEPTIDASE-IV INHIBITOR; GLUCAGON-LIKE PEPTIDE-1; DRUG-NAIVE PATIENTS; BETA-CELL FUNCTION; SELECTIVE DPP-4 INHIBITOR; IMPROVES GLYCEMIC CONTROL; ADD-ON THERAPY; DOUBLE-BLIND; TREATED PATIENTS; INSULIN SENSITIVITY;
D O I
10.1111/j.1463-1326.2010.01321.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Several new oral antidiabetic agents, known as 'gliptins' or 'enzyme dipeptidyl peptidase-IV (DPP-4) inhibitors', have been developed for the treatment of type 2 diabetes and a key clinical use of the gliptins is in combination with metformin. There are important differences in the kinetics of the interaction of different gliptins with the catalytic site of DPP-4, which may lead to varying pharmacokinetics, pharmacodynamics and dosing regimens. Therefore, individual gliptins need to be characterized and here we discuss the extensively studied DPP-4 inhibitor vildagliptin, which has binding characteristics that ensure inhibition of the enzyme beyond the presence of detectable drug levels in plasma. As vildagliptin has been used most often at doses of 50 mg once or twice daily, in combination with metformin, this review focuses on these dose regimens. All clinical trials employing vildagliptin (50 mg once or twice daily) as an add-on therapy to metformin (identified by MEDLINE search using keywords vildagliptin and metformin or known by authors to be in press) are reviewed, as is current knowledge of the mechanism of action of vildagliptin. Vildagliptin added to a stable dose of metformin elicits a dose-related decrease in both HbA1c and fasting plasma glucose. The additional efficacy seen with 50 mg twice daily [delta HbA1c similar to- 1.1% (-12.1 mmol/mol)] relative to 50 mg once daily [delta HbA1c similar to- 0.7% (-7.7 mmol/mol)] is attributable to an overnight effect of the evening dose of vildagliptin, with prolonged DPP-4 inhibition and elevated fasting levels of the intact and insulinotropic form of glucagon-like peptide-1 (GLP-1). Vildagliptin's therapeutic actions are primarily mediated by GLP-1 and metformin enhances vildagliptin's effect to raise plasma levels of intact GLP-1. Vildagliptin is weight-neutral and has a very low hypoglycaemic potential, explained by its remarkable ability to enhance both alpha-cell and beta-cell sensitivity to glucose. Therefore, vildagliptin offers a clinically important outcome when added to metformin with a twice daily dose regimen, taking advantage of its tight binding and slow dissociation characteristics that lead to a sustained overnight effect.
引用
收藏
页码:193 / 203
页数:11
相关论文
共 76 条
[1]   Improved meal-related β-cell function and insulin sensitivity by the dipeptidyl peptidase-IV inhibitor vildagliptin in metformin-treated patients with type 2 diabetes over 1 year [J].
Ahrén, B ;
Pacini, G ;
Foley, JE ;
Schweizer, A .
DIABETES CARE, 2005, 28 (08) :1936-1940
[2]   Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes [J].
Ahrén, B ;
Gomis, R ;
Standl, E ;
Mills, D ;
Schweizer, A .
DIABETES CARE, 2004, 27 (12) :2874-2880
[3]   Changes in Prandial Glucagon Levels After a 2-Year Treatment With Vildagliptin or Glimepiride in Patients With Type 2 Diabetes Inadequately Controlled With Metformin Monotherapy [J].
Ahren, Bo ;
Foley, James E. ;
Ferrannini, Ele ;
Matthews, David R. ;
Zinman, Bernard ;
Dejager, Sylvie ;
Fonseca, Vivian A. .
DIABETES CARE, 2010, 33 (04) :730-732
[4]   Vildagliptin Enhances Islet Responsiveness to Both Hyper- and Hypoglycemia in Patients with Type 2 Diabetes [J].
Ahren, Bo ;
Schweizer, Anja ;
Dejager, Sylvie ;
Dunning, Beth E. ;
Nilsson, Peter M. ;
Persson, Margaretha ;
Foley, James E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (04) :1236-1243
[5]  
[Anonymous], THERAPY
[6]  
[Anonymous], INT J CLIN PRACT S
[7]   Measurements of islet function and glucose metabolism with the dipeptidyl peptidase 4 inhibitor vildagliptin in patients with type 2 diabetes [J].
Azuma, Koichiro ;
Radikova, Zofia ;
Mancino, Juliet ;
Toledo, Frederico G. S. ;
Thomas, Ernestine ;
Kangani, Cyrous ;
Man, Chiara Dalla ;
Cobelli, Claudio ;
Holst, Jens J. ;
Deacon, Carolyn F. ;
He, YanLing ;
Ligueros-Saylan, Monica ;
Serra, Denise ;
Foley, James E. ;
Kelley, David E. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2008, 93 (02) :459-464
[8]   The dipeptidyl peptidase IV inhibitor vildagliptin suppresses endogenous glucose production and enhances islet function after single-dose administration in type 2 diabetic patients [J].
Balas, Bogdan ;
Baig, Muhammad R. ;
Watson, Catherine ;
Dunning, Beth E. ;
Ligueros-Saylan, Monica ;
Wang, Yibin ;
He, Yan-Ling ;
Darland, Celia ;
Holst, Jens J. ;
Deacon, Carolyn F. ;
Cusi, Kenneth ;
Mari, Andrea ;
Foley, James E. ;
DeFronzo, Ralph A. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 92 (04) :1249-1255
[9]  
Bergenstal R, 2010, DIABETES, V59, pA16
[10]   Efficacy and safety of exenatide once weekly versus sitagliptin or pioglitazone as an adjunct to metformin for treatment of type 2 diabetes (DURATION-2): a randomised trial [J].
Bergenstal, Richard M. ;
Wysham, Carol ;
MacConell, Leigh ;
Malloy, Jaret ;
Walsh, Brandon ;
Yan, Ping ;
Wilhelm, Ken ;
Malone, Jim ;
Porter, Lisa E. .
LANCET, 2010, 376 (9739) :431-439