Update on type 2 diabetes mellitus: understanding changes in the diabetes treatment paradigm

被引:16
作者
Green, J. [1 ]
Feinglos, M. [1 ]
机构
[1] Duke Univ, Med Ctr, Div Metab Endocrinol & Nutr, Durham, NC 27710 USA
关键词
D O I
10.1111/j.1742-1241.2007.01438.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes mellitus, which is increasingly prevalent in the United States and responsible for the bulk of diabetes-related healthcare costs, has not been adequately managed over the long term with the most commonly prescribed oral hypoglycaemic medications. Although there is evidence that successful management of type 2 diabetes must address both beta-cell deficiency and insulin resistance, most oral agents now prescribed do not prevent the progressive loss of beta-cell function that has traditionally continued during treatment. Increasingly aggressive management guidelines have led to the recommendation that metformin therapy be initiated along with lifestyle modification at the time of diagnosis. It seems unlikely, however, that this strategy will impede the progression of beta-cell dysfunction. Treatment paradigms are emerging that combine routinely used drug categories with newer agents based on the incretin pathway to achieve long-term glycaemic control. The current review discusses the clinical implications of these newer therapeutic alternatives, which enhance insulin secretion through glucose-dependent and physiologic mechanisms.
引用
收藏
页码:3 / 11
页数:9
相关论文
共 57 条
[1]   Inhibition of dipeptidyl peptidase-4 reduces glycemia, sustains insulin levels, and reduces glucagon levels in type 2 diabetes [J].
Ahrén, B ;
Landin-Olsson, M ;
Jansson, PA ;
Svensson, M ;
Holmes, D ;
Schweizer, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2004, 89 (05) :2078-2084
[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]  
*AM DIAB ASS, 2006, DIABETES CARE S1, V29, pS34
[4]  
[Anonymous], 1995, Diabetes, V44, P1249
[5]  
Aronoff SL., 2004, Diabetes Spectrum, V17, P183, DOI [10.2337/diaspect.17.3.183, DOI 10.2337/DIASPECT.17.3.183]
[6]   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
[7]   Treating to goal: challenges of current management [J].
Barnett, AH .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2004, 151 :T3-T7
[8]  
Barnett AH, 2004, EUR J ENDOCRINOL, V151, pT29
[9]   Effects of vildagliptin on glucose control over 24 weeks in patients with type 2 diabetes inadequately controlled with metformin [J].
Bosi, Emanuele ;
Camisasca, Riccardo Paolo ;
Collober, Carole ;
Rochotte, Erika ;
Garber, Alan J. .
DIABETES CARE, 2007, 30 (04) :890-895
[10]   Effects of exenatide (exendin-4) on glycemic control over 30 weeks in sulfonylurea-treated patients with type 2 diabetes [J].
Buse, JB ;
Henry, RR ;
Han, J ;
Kim, DD ;
Fineman, MS ;
Baron, AD .
DIABETES CARE, 2004, 27 (11) :2628-2635