Godbout Ariane, Chiasson Jean-Louis
Division of Endocrinology-Nutrition and Metabolism, Centre hospitalier de l'Université de Montréal, Montréal, Québec, Canada.
Curr Diab Rep. 2007 Oct;7(5):333-9. doi: 10.1007/s11892-007-0055-x.
Although most commonly used drugs such as biguanides, sulfonylureas, and more recently, thiazolidinediones, are effective in controlling fasting hyperglycemia, a high percentage of patients have sustained elevated hemoglobin A(1c) because of persistent elevation of postprandial plasma glucose (PPPG). alpha-Glucosidase inhibitors (AGIs) specifically target PPPG. AGIs have been shown in several randomized controlled trials to be effective in controlling blood glucose, whether they are used as monotherapy or in combination with other antidiabetic medications. Among the AGIs, acarbose has also been shown to decrease the risk of progressing to diabetes in subjects with impaired glucose tolerance (IGT). Studies have also suggested that acarbose could decrease the risk of cardiovascular disease, both in IGT and in diabetes. Furthermore, AGIs are very safe and are nontoxic drugs. Their only side effects are gastrointestinal, such as flatulence and diarrhea; however, these can be minimized by the "start low, go slow" approach. AGIs should be considered whenever postprandial hyperglycemia is the dominant metabolic abnormality.
尽管大多数常用药物,如双胍类、磺脲类,以及最近的噻唑烷二酮类,在控制空腹血糖方面有效,但由于餐后血浆葡萄糖(PPPG)持续升高,仍有很大比例的患者血红蛋白A(1c)持续升高。α-葡萄糖苷酶抑制剂(AGIs)专门针对PPPG。在多项随机对照试验中已表明,AGIs无论是作为单一疗法还是与其他抗糖尿病药物联合使用,在控制血糖方面均有效。在AGIs中,阿卡波糖还被证明可降低糖耐量受损(IGT)患者进展为糖尿病的风险。研究还表明,阿卡波糖在IGT和糖尿病患者中均可降低心血管疾病风险。此外,AGIs非常安全,是无毒药物。其唯一的副作用是胃肠道反应,如肠胃胀气和腹泻;然而,通过“起始剂量低,增量速度慢”的方法可将这些副作用降至最低。只要餐后高血糖是主要的代谢异常,就应考虑使用AGIs。