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非胰岛素依赖型糖尿病中的磺脲类药物。

Sulfonylureas in NIDDM.

作者信息

Groop L C

机构信息

Fourth Department of Medicine, Helsinki University Hospital, Finland.

出版信息

Diabetes Care. 1992 Jun;15(6):737-54. doi: 10.2337/diacare.15.6.737.

Abstract

Sulfonylureas have represented the backbone of oral therapy in non-insulin-dependent diabetes mellitus for greater than 30 yr. Despite this, our knowledge about the mode of actions of these agents is limited, and the use of them is far from rational. Sulfonylureas lower blood glucose concentrations primarily by stimulating insulin secretion. The evidence for clinically significant extrapancreatic effects is scanty. Therefore, the effect of sulfonylurea is limited to patients with preserved beta-cell function, with the best effect observed in the early stages of the disease. Sulfonylurea treatment is often started relatively late and is continued when the agents can no longer achieve the treatment goals. Drug dosages are increased to maximum recommended doses, although there is no evidence for a dose-response relationship between the sulfonylurea dose and its biological effect. To rationalize the use of sulfonylureas, we should ask the questions to whom, how much, and for how long? The decision to stop treatment is as important as the decision to start treatment.

摘要

30多年来,磺脲类药物一直是非胰岛素依赖型糖尿病口服治疗的主要药物。尽管如此,我们对这些药物作用方式的了解仍然有限,其使用也远非合理。磺脲类药物主要通过刺激胰岛素分泌来降低血糖浓度。关于临床上显著的胰腺外效应的证据很少。因此,磺脲类药物的作用仅限于胰岛β细胞功能保留的患者,在疾病早期观察到的效果最佳。磺脲类药物治疗通常开始得相对较晚,并且在药物不再能达到治疗目标时仍继续使用。尽管没有证据表明磺脲类药物剂量与其生物学效应之间存在剂量反应关系,但药物剂量会增加到最大推荐剂量。为了合理使用磺脲类药物,我们应该问这样几个问题:给谁用、用多少以及用多久?停止治疗的决定与开始治疗的决定同样重要。

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