Meglitinide analogues for type 2 diabetes mellitus (Review)

被引:76
作者
Black, C. [1 ]
Donnelly, P. [1 ]
McIntyre, L. [1 ]
Royle, P. L. [1 ]
Shepard, J. P. [1 ]
Thomas, S. [1 ]
机构
[1] Univ Aberdeen, Aberdeen AB25 2ZD, Scotland
来源
COCHRANE DATABASE OF SYSTEMATIC REVIEWS | 2007年 / 02期
关键词
D O I
10.1002/14651858.CD004654.pub2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background In type 2 diabetes mellitus, impairment of insulin secretion is an important component of the disease. Meglitinide analogues are a class of oral hypoglycaemic agents that increase insulin secretion, in particular, during the early phase of insulin release. Objectives The aim of this review was to assess the effects of meglitinide analogues in patients with type 2 diabetes mellitus. Search strategy We searched several databases including The Cochrane Library, MEDLINE and EMBASE. We also contacted manufacturers and searched ongoing trials databases, and the American Diabetes Association (ADA) and European Association for the Study of Diabetes (EASD) websites. Selection criteria We included randomised controlled, parallel or cross-over trials comparing at least 10 weeks of treatment with meglitinide analogues to placebo, head-to-head, metformin or in combination with insulin. Data collection and analysis Two authors independently extracted data and assessed trial quality. Main results Fifteen trials involving 3781 participants were included. No studies reported the effect of meglitinides on mortality or morbidity. In the eleven studies comparing meglitinides to placebo, both repaglinide and nateglinide resulted in a reductions in glycosylated haemoglobin (0.1% to 2.1% reduction in HbA1c for repaglinide; 0.2% to 0.6% for nateglinide). Only two trials compared repaglinide to nateglinide ( 342 participants), with greater reduction in glycosylated haemoglobin in those receiving repaglinide. Repaglinide ( 248 participants in three trials) had a similar degree of effect in reducing glycosylated haemoglobin as metformin. Nateglinide had a similar or slightly less marked effect on glycosylated haemoglobin than metformin ( one study, 355 participants). Weight gain was generally greater in those treated with meglitinides compared with metformin ( up to three kg in three months). Diarrhoea occurred less frequently and hypoglycaemia occurred more frequently but rarely severely enough as to require assistance. Authors' conclusions Meglitinides may offer an alternative oral hypoglycaemic agent of similar potency to metformin, and may be indicated where side effects of metformin are intolerable or where metformin is contraindicated. However, there is no evidence available to indicate what effect meglitinides will have on important long-term outcomes, particularly mortality.
引用
收藏
页数:44
相关论文
共 94 条
[1]  
[Anonymous], 1995, Diabetes, V44, P1249
[2]  
Baron MA, 2002, DIABETES, V51, pA93
[3]  
Barone M, 2004, DIABETOLOGIA, V47, pA15
[4]   Therapy focused on lowering postprandial glucose, not fasting glucose, may be superior for lowering HbA1c [J].
Bastyr, EJ ;
Stuart, CA ;
Brodows, RG ;
Schwartz, S ;
Graf, CJ ;
Zagar, A ;
Robertson, KE .
DIABETES CARE, 2000, 23 (09) :1236-1241
[5]   The effect of prandial glucose regulation with repaglinide on treatment satisfaction, wellbeing and health status in patients with pharmacotherapy-naive Type 2 diabetes: A placebo-controlled, multicentre study [J].
Bech, P ;
Moses, R ;
Gomis, R .
QUALITY OF LIFE RESEARCH, 2003, 12 (04) :413-425
[6]   Effects of nateglinide on myocardial microvascular reactivity in Type 2 diabetes mellitus - a randomized study using positron emission tomography [J].
Bengel, FM ;
Abletshauser, C ;
Neverve, J ;
Schnell, O ;
Nekolla, SG ;
Standl, E ;
Schwaiger, M .
DIABETIC MEDICINE, 2005, 22 (02) :158-163
[7]   Plasma glucose levels throughout the day and HbA1c interrelationships in type 2 diabetes -: Implications for treatment and monitoring of metabolic control [J].
Bonora, E ;
Calcaterra, F ;
Lombardi, S ;
Bonfante, N ;
Formentini, G ;
Bonadonna, RC ;
Muggeo, M .
DIABETES CARE, 2001, 24 (12) :2023-2029
[8]  
Borch-Johnsen K, 1999, LANCET, V354, P617
[9]  
Breuer HWM, 2000, EUR HEART J SUPPL, V2, pD36
[10]  
Brogard JM, 2000, DIABETOLOGIA, V43, pA186