Vildagliptin: the evidence for its place in the treatment of type 2 diabetes mellitus

被引:3
作者
Profit, Louise [1 ]
Chrisp, Paul [1 ]
Nadin, Carole [1 ]
机构
[1] Core Med Publishing, Mere House,Brook St, Knutsford WA16 8GP, Cheshire, England
关键词
dipeptidyl peptidase IV (dipeptidyl peptidase 4) inhibition; glycemic control; LAF; 237; type; 2; diabetes; vildagliptin;
D O I
10.3355/ce.2008.009
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Type 2 diabetes is increasing in prevalence worldwide and is a leading cause of morbidity and mortality, mainly due to the development of complications. Vildagliptin is an inhibitor of dipeptidyl peptidase 4 (DPP-4), a new class of oral antidiabetic agents. Aims: To evaluate the role of vildagliptin in the management of type 2 diabetes. Evidence review: Clear evidence shows that vildagliptin improves glycemic control (measured by glycosylated hemoglobin and blood glucose levels) more than placebo in adults with type 2 diabetes, either as monotherapy or in combination with metformin. Vildagliptin is as effective as pioglitazone and rosiglitazone, and slightly less effective than metformin, although better tolerated. Further glycemic control is achieved when adding vildagliptin to metformin, pioglitazone, or glimepride. There is evidence that vildagliptin improves beta-cell function and insulin sensitivity. Vildagliptin does not appear to be associated with weight gain or with a higher risk of hypoglycemia than placebo or other commonly used oral antidiabetic agents. Economic evidence is currently lacking. Place in therapy: Vildagliptin improves glycemic control with little if any weight gain or hypoglycemia in adult patients with type 2 diabetes when given alone or in combination with metformin, thiazolidinediones, or sulfonylureas. Since many diabetic patients require combination therapy, the complementary mechanism of action of vildagliptin and other commonly prescribed antidiabetic drugs represents an important new therapeutic option in diabetes management.
引用
收藏
页码:13 / 30
页数:18
相关论文
共 92 条
[51]  
Kikuchi M, 2006, EUR ASS STUD DIAB AN
[52]  
Kimmel B, 2005, CLIN DIABETES, V23, P64, DOI [DOI 10.2337/DIACLIN.23.2.64, 10.2337/diaclin.23.2.64]
[53]  
Knowler WC, 2002, NEW ENGL J MED, V346, P393, DOI 10.1056/NEJMoa012512
[54]   Glycemic control from 1988 to 2000 among U.S adults diagnosed with type 2 diabetes - A preliminary report [J].
Koro, CE ;
Boialin, SJ ;
Bourgeois, N ;
Fedder, DO .
DIABETES CARE, 2004, 27 (01) :17-20
[55]   Vildagliptin, a dipeptidyl peptidase-IV inhibitor, improves model-assessed β-cell function in patients with type 2 diabetes [J].
Mari, A ;
Sallas, WM ;
He, YL ;
Watson, C ;
Ligueros-Saylan, M ;
Dunning, BE ;
Deacon, CF ;
Holst, JJ ;
Foley, JE .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (08) :4888-4894
[56]  
Mika A, 2003, AM DIABETS ASS SCI S
[57]  
Mimori N, 2006, AM DIAB ASS ANN M
[58]   REDUCED INCRETIN EFFECT IN TYPE-2 (NON-INSULIN-DEPENDENT) DIABETES [J].
NAUCK, M ;
STOCKMANN, F ;
EBERT, R ;
CREUTZFELDT, W .
DIABETOLOGIA, 1986, 29 (01) :46-52
[59]   The therapeutic actions of DPP-IV inhibition are not mediated by glucagon-like peptide-1 [J].
Nauck, MA ;
El-Ouaghlidi, A .
DIABETOLOGIA, 2005, 48 (04) :608-611
[60]   Effects of subcutaneous glucagon-like peptide 1 (GLP-1 [7-36 amide]) in patients with NIDDM [J].
Nauck, MA ;
Wollschlager, D ;
Werner, J ;
Holst, JJ ;
Orskov, C ;
Creutzfeldt, W ;
Willms, B .
DIABETOLOGIA, 1996, 39 (12) :1546-1553