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Incretin-based therapy: how do incretin mimetics and DPP-4 inhibitors fit into treatment algorithms for type 2 diabetic patients?

机译:基于肠促胰岛素的疗法:肠降血糖素模拟物和DPP-4抑制剂如何适合2型糖尿病患者的治疗方案?

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Incretin-based antidiabetic medications have been approved for clinical use for approximately two to three years. While their major clinical characteristics have been known from clinical trials, the discussion now focuses on the best clinical use of GLP-1 receptor agonists (incretin mimetics) and inhibitors of the protease dipeptidyl peptidase-4 (DPP-4). Any novel drug will not fully disclose its spectrum of beneficial and adverse activity before long-term trials with clinical endpoints are available. This, typically, will last 5-8 years. Nevertheless, there are convincing reasons to use incretin mimetics and DPP-4 inhibitors even in the absence of such results. This decision should be based on specific patient characteristics and (expected) treatment results, in comparison to other available treatment options. The present manuscript tries to describe the current state-of-the-art of using incretin mimetics and DPP-4 inhibitors in clinical practice, including an attempt to suggest their place in treatment algorithms for type 2-diabetic patients.
机译:基于肠抑素的抗糖尿病药物已被批准用于临床约2至3年。尽管从临床试验中已经知道了它们的主要临床特征,但现在的讨论集中在GLP-1受体激动剂(肠降血糖素模拟物)和蛋白酶二肽基肽酶4(DPP-4)抑制剂的最佳临床应用上。在可以进行具有临床终点的长期试验之前,任何新药都不会完全公开其有益和不利活性的范围。通常,这将持续5-8年。然而,即使在没有此类结果的情况下,也仍然有令人信服的理由使用肠降血糖素模拟物和DPP-4抑制剂。与其他可用的治疗方案相比,该决定应基于特定的患者特征和(预期的)治疗结果。本手稿试图描述在临床实践中使用肠降血糖素模拟物和DPP-4抑制剂的最新技术,包括试图表明它们在2型糖尿病患者的治疗算法中的地位。

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