Diabetes Research Institute, Mills-Peninsula Health Services, San Mateo, CA 94401, USA.
Adv Ther. 2010 Dec;27(12):881-94. doi: 10.1007/s12325-010-0077-7. Epub 2010 Oct 20.
In addition to progressive pancreatic β-cell failure resulting in impaired insulin secretion, and increased insulin resistance in muscle and liver, incretin hormone-related abnormalities have been identified as key underlying defects in patients with type 2 diabetes mellitus. Treatment goals for patients with type 2 diabetes should be aligned with the basic defects of the disease. Many of the available antidiabetes agents correct hyperglycemia but do not impact other cardiovascular risk factors, and may actually aggravate some. This paper reviews the role of defects in the incretin system in the pathophysiology of type 2 diabetes, and discusses recent advances in the use of incretinbased agents that target the fundamental disease mechanisms of type 2 diabetes. The incretinbased agents reduce hyperglycemia and provide beneficial effects on surrogate markers of cardiovascular risk, including weight gain, elevated blood pressure, and dyslipidemia.
除了导致胰岛素分泌受损和肌肉及肝脏胰岛素抵抗的进行性胰岛β细胞衰竭之外,肠促胰岛素激素相关异常也已被确定为 2 型糖尿病患者的主要潜在缺陷。2 型糖尿病患者的治疗目标应与疾病的基本缺陷相吻合。许多现有的抗糖尿病药物可纠正高血糖,但不会影响其他心血管危险因素,实际上可能会加重某些因素。本文综述了肠促胰岛素系统缺陷在 2 型糖尿病发病机制中的作用,并讨论了基于肠促胰岛素的药物在针对 2 型糖尿病基本发病机制方面的最新应用进展。这些基于肠促胰岛素的药物可降低高血糖,并对心血管风险的替代标志物产生有益作用,包括体重增加、血压升高和血脂异常。