A review of the efficacy and safety of oral antidiabetic drugs

被引:262
作者
Stein, Stephanie Aleskow [1 ]
Lamos, Elizabeth Mary [1 ]
Davis, Stephen N. [1 ]
机构
[1] Univ Maryland, Med Ctr, Baltimore, MD 21201 USA
关键词
alpha-glucosidase inhibitor; bile-acid sequestrant; bromocriptine; DPP-4; inhibitor; meglitinide; metformin; sulfonylurea; thiazolidinedione; type; 2; diabetes; TYPE-2; DIABETES-MELLITUS; DIPEPTIDYL PEPTIDASE-4 INHIBITOR; INADEQUATE GLYCEMIC CONTROL; GLUCAGON-LIKE PEPTIDE-1; ALPHA-GLUCOSIDASE INHIBITORS; ADD-ON THERAPY; DOUBLE-BLIND; ELDERLY-PATIENTS; CLINICAL PHARMACOKINETICS; COLESEVELAM HYDROCHLORIDE;
D O I
10.1517/14740338.2013.752813
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Introduction: Additional oral antidiabetic agents to metformin, sulfonylureas (SU) and thiazolidinediones (TZD) are approved for the treatment of type 2 diabetes. Areas covered: The efficacy and safety of metformin, SUs, TZDs, dipeptidyl peptidase-IV (DPP-4) inhibitors, meglitinide analogs, alpha-glucosidase inhibitors (AGIs), bile-acid sequestrants (BAS) and bromocriptine will be reviewed. Expert opinion: Several new oral agents have been approved for type 2 diabetes management in recent years. It is important to understand the efficacy and safety of these medications in addition to the older agents to best maximize oral drug therapy for diabetes. Of the recently introduced oral hypoglycemic/antihyperglycemic agents, the DPP-4 inhibitors are moderately efficacious compared with mainstay treatment with metformin with a low side-effect profile and have good efficacy in combination with other oral agents and insulin. They are a recommended alternative when metformin use is limited by gastrointestinal (GI) side effects or when SU treatment results in significant hypoglycemia or weight gain. Meglitinide analogs are limited by their frequent dosing, expense and hypoglycemia (repaglinide > nateglinide), while AGIs are also limited by their dosing schedule and GI side-effect profile. BAS and bromocriptine have the lowest efficacy with regard to HbA(1c) reduction, also are plagued by GI adverse reactions, but have a low risk of hypoglycemia.
引用
收藏
页码:153 / 175
页数:23
相关论文
共 161 条
[1]
Does bromocriptine improve glycemic control of obese type-2 diabetics? [J].
Aminorroaya, A ;
Janghorbani, M ;
Ramezani, M ;
Haghighi, S ;
Amini, M .
HORMONE RESEARCH, 2004, 62 (02) :55-59
[2]
[Anonymous], 2012, CARDIOVASCULAR OUTCO
[3]
[Anonymous], INDIAN J ENDOCRINOL
[4]
[Anonymous], 2008, PREC
[5]
[Anonymous], 2009, CYCL
[6]
[Anonymous], 2012, CARIOVASCULAR OUTCOM
[7]
[Anonymous], 2008, WECH
[8]
[Anonymous], 2012, 0431082 AMI TECOS
[9]
Efficacy and safety of treatment with sitagliptin or glimepiride in patients with type 2 diabetes inadequately controlled on metformin monotherapy: a randomized, double-blind, non-inferiority trial [J].
Arechavaleta, R. ;
Seck, T. ;
Chen, Y. ;
Krobot, K. J. ;
O'Neill, E. A. ;
Duran, L. ;
Kaufman, K. D. ;
Williams-Herman, D. ;
Goldstein, B. J. .
DIABETES OBESITY & METABOLISM, 2011, 13 (02) :160-168
[10]
Efficacy and safety of monotherapy of sitagliptin compared with metformin in patients with type 2 diabetes [J].
Aschner, P. ;
Katzeff, H. L. ;
Guo, H. ;
Sunga, S. ;
Williams-Herman, D. ;
Kaufman, K. D. ;
Goldstein, B. J. .
DIABETES OBESITY & METABOLISM, 2010, 12 (03) :252-261