Oral antidiabetic agents in type 2 diabetes

被引:87
作者
Levetan, Claresa [1 ]
机构
[1] Lankenau Hosp, Dept Endocrinol, Wynnewood, PA 19096 USA
关键词
dipeptidyl peptidase-4 inhibitors; glucagon-like peptide 1; type; 2; diabetes;
D O I
10.1185/030079907X178766
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Oral antidiabetic agents differ with regard to mechanisms of action, hemoglobin A(1c)-lowering efficacy, safety, and tolerability. Traditional agents consist of those that enhance insulin secretion (i.e., sulfonylureas and glinides), those that enhance insulin sensitivity (i.e., metformin and the thiazolidinediones), and those that inhibit intestinal carbohydrate absorption (i.e., the (x-glucosidase inhibitors). New oral agents include the dipeptidyl peptidase-4 (DPP-4) inhibitors, which potentiate the activity of the incretin glucagon-like peptide 1 and enhance glucose-dependent insulin secretion. Scope: We review the characteristics of the traditional oral agents and these newer additions to the pharmaceutical armamentarium. Abstracts and original clinical and preclinical reports in the English language were identified for review based on MEDLINE literature searches (19702006) and abstract collections from major diabetes meetings. Conclusions: Traditional oral agents provide significant treatment benefits for diabetic patients, including reduction in risk of microvascular complications. However, most patients with type 2 diabetes do not achieve target glycemic levels with traditional therapies, and these agents are also associated with hypoglycemia, weight gain, and poor tolerability. Oral DPP-4 inhibitors offer the potential for significant improvement in glycemic control without hypoglycemia or weight gain, although long-term durability of glycemic control (> 52 weeks) has not been established.
引用
收藏
页码:945 / 952
页数:8
相关论文
共 67 条
[31]   Role of incretin hormones in the regulation of insulin secretion in diabetic and nondiabetic humans [J].
Holst, JJ ;
Gromada, J .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 287 (02) :E199-E206
[32]   Oral antihyperglycemic therapy for type 2 diabetes - Scientific review [J].
Inzucchi, SE .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2002, 287 (03) :360-372
[33]   Glycemic durability of rosiglitazone, metformin, or glyburide monotherapy [J].
Kahn, Steven E. ;
Haffner, Steven M. ;
Heise, Mark A. ;
Herman, William H. ;
Holman, Rury R. ;
Jones, Nigel P. ;
Kravitz, Barbara G. ;
Lachin, John M. ;
O'Neill, M. Colleen ;
Zinman, Bernard ;
Viberti, Giancarlo .
NEW ENGLAND JOURNAL OF MEDICINE, 2006, 355 (23) :2427-2443
[34]   Incretin mimetics and dipeptidyl peptidase-IV inhibitors: A review of emerging therapies for type 2 diabetes [J].
Kendall, David M. ;
Kim, Dennis ;
Maggs, David .
DIABETES TECHNOLOGY & THERAPEUTICS, 2006, 8 (03) :385-396
[35]   Effects of exenatide (exendin-4) on glycemic control over 30 weeks in patients with type 2 diabetes treated with metformin and a sulfonylurea [J].
Kendall, DM ;
Riddle, MC ;
Rosenstock, J ;
Zhuang, DL ;
Kim, DD ;
Fineman, MS ;
Baron, AD .
DIABETES CARE, 2005, 28 (05) :1083-1091
[36]  
KLIMT CR, 1970, DIABETES, V19, P747
[37]  
Knowler WC, 2002, NEW ENGL J MED, V346, P393, DOI 10.1056/NEJMoa012512
[38]   Oral antidiabetic agents - Current role in type 2 diabetes mellitus [J].
Krentz, AJ ;
Bailey, CJ .
DRUGS, 2005, 65 (03) :385-411
[39]   Oral therapies for diabetic hyperglycemia [J].
Lebovitz, HE .
ENDOCRINOLOGY AND METABOLISM CLINICS OF NORTH AMERICA, 2001, 30 (04) :909-+
[40]   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