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Troglitazone: a review of its use in the management of type 2 diabetes mellitus.

机译:曲格列酮:综述其在2型糖尿病治疗中的应用。

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摘要

Troglitazone is the first of a new group of oral antidiabetic drugs, the thiazolidinediones, and is indicated for the treatment of patients with type 2 (non-insulin-dependent) diabetes mellitus. Troglitazone acts by enhancing the effects of insulin at peripheral target sites and, unlike the sulphonylurea drugs, is not associated with hypoglycaemia when administered as monotherapy. Clinical trials with troglitazone (usually 200 to 600 mg/day) in patients with type 2 diabetes mellitus consistently showed marked improvement in glycaemic control, as well as reductions in fasting serum insulin, C-peptide and triglyceride levels. Comparative studies with either glibenclamide (glyburide) or metformin indicated similar glycaemic control with troglitazone or these agents. Serum insulin levels were lower with troglitazone than with glibenclamide. Clinical trials of up to approximately 2 years' duration showed that glycaemic control is maintained with troglitazone on a long term basis. In general, troglitazone is well tolerated by the majority of patients. However, discontinuation of troglitazone because of elevated liver enzyme levels occurs in approximately 2% of patients receiving the drug, and frequent monitoring of liver enzymes is required (e.g. at least 11 times during the first year of therapy). Among patients who started troglitazone therapy in 1998 (after the incorporation of a boxed warning and increased monitoring requirements in the product labelling), the estimated risk of liver-related death is approximately 1 in 100,000. CONCLUSIONS: Troglitazone improves the ability of target cells to respond to insulin. The drug has been shown to improve glycaemic control in patients with type 2 diabetes mellitus when used as monotherapy or in combination with other oral antidiabetic drugs or insulin, and its efficacy is similar to that of glibenclamide or metformin. Although troglitazone is generally well tolerated, close monitoring of liver enzyme function is required to minimise the rare occurrence of serious hepatic dysfunction. Drug acquisition and liver function monitoring costs, as well as potential adverse effects, are important factors that may ultimately determine the precise place of troglitazone in the management of type 2 diabetes mellitus. Nevertheless, as the first member of a new class of oral antidiabetic agents, the thiazolidinediones, troglitazone offers an effective treatment option in patients with type 2 diabetes mellitus through its action of improving insulin sensitivity.
机译:曲格列酮是新的口服抗糖尿病药物噻唑烷二酮类药物中的第一种,并被指定用于治疗2型(非胰岛素依赖型)糖尿病患者。曲格列酮通过增强外周靶位点的胰岛素作用而起作用,与磺酰脲类药物不同,单药治疗时与曲格列酮不伴有低血糖。曲格列酮(通常为200至600毫克/天)在2型糖尿病患者中的临床试验始终显示,血糖控制显着改善,空腹血清胰岛素,C肽和甘油三酸酯水平降低。与格列本脲(格列本脲)或二甲双胍的比较研究表明,曲格列酮或这些药物对血糖的控制相似。曲格列酮的血清胰岛素水平低于格列本脲。长达约2年的临床试验表明,曲格列酮可长期维持血糖控制。通常,大多数患者对曲格列酮的耐受性良好。然而,由于约2%的接受该药物的患者会因肝酶水平升高而停用曲格列酮,因此需要频繁监测肝酶(例如,在治疗的第一年中至少进行11次)。在1998年开始使用曲格列酮治疗的患者(在产品包装中加入盒装警告并增加了监测要求之后),估计与肝有关的死亡风险约为100,000分之一。结论:曲格列酮可提高靶细胞对胰岛素的反应能力。当该药物作为单一疗法或与其他口服降糖药或胰岛素组合使用时,已显示可改善2型糖尿病患者的血糖控制,其疗效与格列本脲或二甲双胍相似。尽管曲格列酮通常具有良好的耐受性,但仍需严密监测肝酶功能,以最大程度地减少罕见的严重肝功能障碍的发生。药物获取和肝功能监测成本以及潜在的不良反应,是可能最终决定曲格列酮在2型糖尿病治疗中的确切位置的重要因素。尽管如此,曲格列酮作为新型口服抗糖尿病药噻唑烷二酮类的首个成员,通过改善胰岛素敏感性的作用,为2型糖尿病患者提供了有效的治疗选择。

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