Garber Alan J
Department of Medicine, Division of Diabetes, Endocrinology and Metabolism, Baylor College of Medicine, One Baylor Plaza-BCM620, Houston, Texas 77030, USA.
Rev Diabet Stud. 2011 Fall;8(3):307-22. doi: 10.1900/RDS.2011.8.307. Epub 2011 Nov 10.
Although newer treatments for type 2 diabetes (T2D) patients have produced continual improvements in outcome, a large and growing population with prediabetes remains under-treated. In the last few years, incretin-based therapies have become an important treatment option for patients with T2D. There are two classes of incretin agents: the dipeptidyl peptidase-4 (DPP-4) inhibitors and the glucagon like peptide 1 (GLP-1) receptor agonists. The ultimate goal of agents within both of these classes is to increase GLP-1 signaling, which results in augmented glucose-induced insulin secretion, inhibition of glucagon secretion, and decreased appetite. This should result in improved regulation of glucose homeostasis. GLP-1 receptor agonists enable patients to achieve significant weight loss. In contrast, DPP-4 inhibitors result in a less dramatic increase in GLP-1 levels; therefore, they are weight neutral. Incretin therapies are currently recommended for use early in the treatment algorithm for T2D patients whose disease is not manageable by diet and exercise alone, but the potential for these agents may be farther reaching. Current studies are evaluating the potential benefits of combining incretin therapies with basal insulin to provide continuous glucose control before and after meals. In addition, these agents may be promising for patients with prediabetes since they effectively reduce glycosylated hemoglobin levels and fasting plasma glucose levels, enable weight control, and have the potential to preserve β-cell function. Clearly, all of these properties are desirable for patients with prediabetes.
尽管针对2型糖尿病(T2D)患者的新型治疗方法已使治疗效果不断改善,但大量且不断增加的糖尿病前期人群仍未得到充分治疗。在过去几年中,肠促胰岛素疗法已成为T2D患者的重要治疗选择。肠促胰岛素药物有两类:二肽基肽酶-4(DPP-4)抑制剂和胰高血糖素样肽1(GLP-1)受体激动剂。这两类药物的最终目标都是增加GLP-1信号传导,从而导致葡萄糖诱导的胰岛素分泌增加、胰高血糖素分泌受到抑制以及食欲下降。这应能改善葡萄糖稳态的调节。GLP-1受体激动剂能使患者实现显著的体重减轻。相比之下,DPP-4抑制剂导致GLP-1水平的升高幅度较小;因此,它们对体重没有影响。目前建议在仅通过饮食和运动无法控制病情的T2D患者的治疗方案早期使用肠促胰岛素疗法,但这些药物的潜力可能更大。目前的研究正在评估将肠促胰岛素疗法与基础胰岛素联合使用以实现餐前后持续血糖控制的潜在益处。此外,这些药物对糖尿病前期患者可能很有前景,因为它们能有效降低糖化血红蛋白水平和空腹血糖水平,有助于控制体重,并且有可能保留β细胞功能。显然,所有这些特性都是糖尿病前期患者所期望的。