Holstein A, Egberts E-H
1st Department of Medicine, Klinikum Lippe-Detmold, Detmold, Germany.
Exp Clin Endocrinol Diabetes. 2003 Oct;111(7):405-14. doi: 10.1055/s-2003-44287.
In patients with Type 2 diabetes, the appropriate intensity of glucose control is determined by age, life expectancy, and the presence of concomitant disease. Geriatric patients are especially susceptible to hypoglycaemia and therefore particular care should be taken in this group characterized by polypharmacy, renal or hepatic dysfunction, cardiovascular multimorbidity and malnutrition. As hypoglycaemia is a significant cause of morbidity and mortality, treatment regimens for diabetes should minimize the occurrence of hypoglycaemic episodes and be tailored to the patient's individual needs. The pharmacological options for treating Type 2 diabetes have increased considerably and the risk of hypoglycaemia of the currently available drugs varies considerably. Metformin, thiazolidinediones, and acarbose, oral antidiabetic drugs that decrease insulin resistance or postprandial glucose absorption, are associated with a low risk of hypoglycaemia. These drugs can also be used effectively in various combination regimens; however, by improving insulin sensitivity, combinations of metformin and thiolidinediones with sulphonylureas or meglitinides may considerably increase the risk of hypoglycaemia. On account of its complex pharmacoprofile glibenclamide is a problematic substance carrying a high risk of hypoglycaemia. There are limited preliminary data indicating that, under routine conditions, glimepiride may be associated with a lower risk of hypoglycaemia than glibenclamide and is no more likely to cause hypoglycaemia than other shorter-acting agents such as gliclazide and glipizide. Nateglinide and repaglinide as short-acting insulin secretagogues may be associated with a reduced risk of hypoglycaemia compared with glibenclamide, in particular when dosed flexibly. Repaglinide might be beneficial in individuals with renal impairment.
在2型糖尿病患者中,血糖控制的适当强度由年龄、预期寿命和合并疾病的存在情况决定。老年患者尤其易发生低血糖,因此对于这个以多种药物治疗、肾或肝功能不全、心血管多种合并症和营养不良为特征的群体应格外小心。由于低血糖是发病和死亡的重要原因,糖尿病治疗方案应尽量减少低血糖发作的发生,并根据患者的个体需求进行调整。治疗2型糖尿病的药理学选择已大幅增加,目前可用药物的低血糖风险差异很大。二甲双胍、噻唑烷二酮类和阿卡波糖等口服抗糖尿病药物可降低胰岛素抵抗或餐后葡萄糖吸收,低血糖风险较低。这些药物也可有效地用于各种联合治疗方案;然而,二甲双胍和噻唑烷二酮类与磺脲类或格列奈类联合使用通过改善胰岛素敏感性可能会大幅增加低血糖风险。由于其复杂的药理特性,格列本脲是一种有问题的药物,低血糖风险很高。有限的初步数据表明,在常规情况下,格列美脲的低血糖风险可能低于格列本脲,且引起低血糖的可能性并不高于其他短效药物如格列齐特和格列吡嗪。那格列奈和瑞格列奈作为短效胰岛素促泌剂,与格列本脲相比,低血糖风险可能降低,尤其是在灵活给药时。瑞格列奈可能对肾功能损害患者有益。