Division of Endocrinology, Philadelphia College of Osteopathic Medicine, Philadelphia, PA 19131, USA.
Postgrad Med. 2013 May;125(3):214-26. doi: 10.3810/pgm.2013.05.2672.
Diabetes, especially type 2 diabetes mellitus (T2DM), continues to be a global health care problem. Although the beneficial effects of glycemic control are well established, in the United States, > 40% of adults with diabetes fail to achieve target glycated hemoglobin levels. Antidiabetic drug classes vary with respect to their mechanisms of action, glucose-lowering potential, and safety and tolerability profiles. Antidiabetic drug classes include some agents that depend on the presence or action of insulin for their therapeutic effect. As the disease state of T2DM progresses, patient pancreatic β-cell function declines, and therapies that stimulate insulin secretion or improve insulin sensitivity become less effective for this population. Therefore, the development of additional antidiabetic agents with novel mechanisms of action that can be used alone or in combination with currently approved medications may help patients achieve glycemic control. Agents that have comparable glucose-lowering capabilities but different mechanisms of action may fill treatment gaps or meet the needs of patient subpopulations. For example, inhibitors of sodium-glucose co-transporter 2 (SGLT2) represent an emerging class of glucose-lowering agents. The SGLT2 inhibitors reduce glucose reabsorption by the kidney, leading to increased urinary glucose excretion and caloric loss. In clinical trials, these agents have been shown to improve glycemic control and to reduce body weight in patients with T2DM. Additionally, SGLT2 inhibitors pose a low risk for hypoglycemia and are generally well tolerated; however, their use has been associated with an increase in the frequency of genital infections and, in some studies, urinary tract infections. Sodium-glucose co-transporter 2 inhibitors may provide an alternative or an addition to existing therapies for the treatment of patients with T2DM.
糖尿病,尤其是 2 型糖尿病(T2DM),仍然是一个全球性的医疗保健问题。尽管血糖控制的有益效果已得到充分证实,但在美国,超过 40%的糖尿病患者未能达到糖化血红蛋白目标水平。抗糖尿病药物类别在作用机制、降低血糖的潜力以及安全性和耐受性方面存在差异。抗糖尿病药物类别包括一些依赖胰岛素的存在或作用来发挥治疗作用的药物。随着 T2DM 疾病状态的进展,患者的胰腺β细胞功能下降,对于这一人群,刺激胰岛素分泌或改善胰岛素敏感性的治疗方法效果降低。因此,开发具有新作用机制的额外抗糖尿病药物,单独使用或与目前批准的药物联合使用,可能有助于患者实现血糖控制。具有可比降糖能力但作用机制不同的药物可能会填补治疗空白或满足患者亚群的需求。例如,钠-葡萄糖共转运蛋白 2(SGLT2)抑制剂是一类新兴的降糖药物。SGLT2 抑制剂通过肾脏减少葡萄糖重吸收,导致尿糖排泄和热量损失增加。在临床试验中,这些药物已被证明可改善 T2DM 患者的血糖控制并减轻体重。此外,SGLT2 抑制剂低血糖风险低,一般耐受性良好;然而,它们的使用与生殖器感染的频率增加有关,在一些研究中还与尿路感染有关。SGLT2 抑制剂可能为治疗 T2DM 患者提供现有治疗方法的替代或补充。