Sodium-glucose co-transporter 2 inhibitors: evidence and place in therapy

被引:2
|
作者
Minze, Molly G. [1 ]
Koffarnus, Robin L. [2 ]
Bailey, Trista A. [1 ]
Diec, Sandy [1 ]
Edwards, Krystal L. [2 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Sch Pharm Pharm Practice, Abilene, TX 79601 USA
[2] Texas Tech Univ, Hlth Sci Ctr, Sch Pharm Pharm Practice, Dallas, TX USA
关键词
canagliflozin; dapagliflozin; empagliflozin; luseogliflozin; SGLT-2; inhibitor; sodium-glucose co-transporter 2 inhibitor; type 2 diabetes mellitus;
D O I
10.1586/17446651.2015.1099431
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Type 2 diabetes effects millions of people yet remains difficult to treat with oral pharmacotherapy. Metformin is the first line recommended therapy, and current guidelines suggest individualized therapy for second line selection. Sodium-glucose co-transporter 2 ( SGLT-2) inhibitors are the newest class of agents in treating type 2 diabetes via an insulin independent mechanism to lower blood glucose. Currently marketed agents, including canagliflozin, dapagliflozin, empagliflozin, and luseogliflozin, reduce hemoglobin A1c (HbA1c) similar to 0.8-1%, reduce fasting and post prandial glucose, and have little hypoglycemia associated with them when added to therapies including metformin, a sulfonylurea, pioglitazone, or insulin. Patients receiving SGLT-2 inhibitors have reduced weight and blood pressure, but are more susceptible to urinary tract infections and genital mycotic infections. This review summarizes current literature regarding the SGLT-2 inhibitors.
引用
收藏
页码:645 / 661
页数:17
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