SGLT2 inhibitors

肾葡萄糖重吸收 医学 低血糖 血糖性 达帕格列嗪 糖尿病 2型糖尿病 胰岛素 人口 泌尿系统 2型糖尿病 内科学 胰岛素抵抗 内分泌学 药理学 环境卫生
作者
I. Dardi,Tasha Kouvatsos,Serge Jabbour
出处
期刊:Biochemical Pharmacology [Elsevier BV]
卷期号:101: 27-39 被引量:31
标识
DOI:10.1016/j.bcp.2015.09.005
摘要

Diabetes mellitus is a serious health issue and an economic burden, rising in epidemic proportions over the last few decades worldwide. Although several treatment options are available, only half of the global diabetic population achieves the recommended or individualized glycemic targets. Sodium-glucose cotransporter 2 (SGLT2) inhibitors are a new class of antidiabetic agents with a novel insulin-independent action. SGLT2 is a transporter found in the proximal renal tubules, responsible for the reabsorption of most of the glucose filtered by the kidney. Inhibition of SGLT2 lowers the blood glucose level by promoting the urinary excretion of excess glucose. Due to their insulin-independent action, SGLT2 inhibitors can be used with any degree of beta-cell dysfunction or insulin resistance, related to a very low risk of hypoglycemia. In addition to improving glycemic control, SGLT2 inhibitors have been associated with a reduction in weight and blood pressure when used as monotherapy or in combination with other antidiabetic agents in patients with type 2 diabetes mellitus (T2DM). Treatment with SGLT2 inhibitors is usually well tolerated; however, they have been associated with an increased incidence of urinary tract and genital infections, although these infections are usually mild and easy to treat. SGLT2 inhibitors are a promising new option in the armamentarium of drugs for patients with T2DM.
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