Spotlight on ertugliflozin and its potential in the treatment of type 2 diabetes: evidence to date

被引:71
作者
Cinti, Francesca [1 ]
Moffa, Simona [1 ]
Impronta, Flavia [1 ]
Cefalo, Chiara M. A. [1 ]
Sun, Vinsin A. [1 ]
Sorice, Gian Pio [1 ]
Mezza, Teresa [1 ]
Giaccari, Andrea [1 ]
机构
[1] Univ Cattolica Sacro Cuore, Ctr Endocrine & Metab Dis, Fdn Policlin Univ A Gemelli, Largo A Gemelli 8, I-00168 Rome, Italy
来源
DRUG DESIGN DEVELOPMENT AND THERAPY | 2017年 / 11卷
关键词
antidiabetic drugs; glycosylated hemoglobin; glycemic control; sodium-glucose cotransporter 2 inhibitors; precision medicine; type 1 diabetes mellitus; type 2 diabetes mellitus; weight reduction; GLUCOSE COTRANSPORTER 2; SGLT2; INHIBITORS; CLINICAL CANDIDATE; GLYCEMIC CONTROL; BLOOD-PRESSURE; OUTCOME TRIAL; EFFICACY; SAFETY; DAPAGLIFLOZIN; EMPAGLIFLOZIN;
D O I
10.2147/DDDT.S114932
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Sodium-glucose cotransporter 2 (SGLT2) inhibitors are the latest therapeutic strategy in the treatment of type 2 diabetes mellitus (T2DM). Using an insulin-independent mechanism (glycosuria), they reduce glucose toxicity and improve insulin sensitivity and beta-cell function. The promising results obtained in clinical trials show that SGLT2 significantly improves glycemic control and provides greater cardiovascular protection, combined with a reduction in body weight and blood pressure (BP). This review focuses on ertugliflozin, a new, highly selective, and reversible SGLT2 inhibitor. Clinical trials published to date show that ertugliflozin, both as a monotherapy and as an add-on to oral antidiabetic agents, is safe and effective in reducing glycosylated hemoglobin (HbA1c), body weight, and BP in T2DM patients.
引用
收藏
页码:2905 / 2919
页数:15
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