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Linagliptin: a novel dipeptidyl peptidase 4 inhibitor with a unique place in therapy

机译:利格列汀:一种新型二肽基肽酶4抑制剂,在治疗中具有独特的地位

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The dipeptidyl peptidase 4 (DPP-4) inhibitors comprise a promising new class of agent for the management of type 2 diabetes. They possess a range of physiological effects associated with improved glycemic control including stimulation of glucose-dependent insulin secretion and suppression of glucagon secretion, and lower blood glucose levels through different, but potentially complementary, mechanisms to standard oral therapies. Linagliptin is the latest DPP-4 inhibitor to complete pivotal phase 3 trials. The data show that linagliptin provides significant, clinically meaningful and sustained improvements in glycemic control, with an incidence of adverse events similar to placebo and an excellent tolerability profile. In addition, linagliptin has been shown to be weight neutral and, importantly, there was no increased risk of hypoglycemia attributed to linagliptin use in monotherapy or combination therapy with metformin or pioglitazone. A unique characteristic of linagliptin that differentiates it from other members of the class is its primarily nonrenal route of excretion. The linagliptin phase 3 program included several hundred patients with type 2 diabetes and different stages of renal disease and the data suggest that the drug would not need dose adjustment, regardless of the degree of renal impairment. There is a particular need for safe and effective therapeutic agents that can be used when renal function declines. Linagliptin has recently been approved by the US Food and Drug Administration and may find a place in therapy as a treatment option for the significant number of patients in whom metformin and the other DPP-4 inhibitors are either contraindicated or require dose adjustment because of moderate to severe renal impairment.
机译:二肽基肽酶4(DPP-4)抑制剂是用于治疗2型糖尿病的新型有前途的药物。它们具有与改善血糖控制相关的一系列生理作用,包括刺激葡萄糖依赖性胰岛素分泌和抑制胰高血糖素分泌,以及通过与标准口服疗法不同但可能互补的机制降低血糖水平。利格列汀是完成关键3期试验的最新DPP-4抑制剂。数据显示,利格列汀在血糖控制方面提供了重要的,临床上有意义的和持续的改善,不良事件的发生率与安慰剂相似,并且耐受性良好。此外,利拉列汀已被证明是体重中性的,而且重要的是,没有因利拉列汀用于二甲双胍或吡格列酮的单药治疗或联合治疗而增加低血糖的风险。利格列汀的一个独特特征是其主要的非肾脏排泄途径,从而使其与该类别的其他成员相区别。利格列汀3期计划包括数百名2型糖尿病和不同阶段肾病的患者,数据表明,无论肾功能不全的程度,该药物都不需要调整剂量。特别需要在肾功能下降时可以使用的安全有效的治疗剂。利格列汀最近已获得美国食品和药物管理局的批准,可能会因大量患者因中度至中等剂量而禁用二甲双胍和其他DPP-4抑制剂或需要调整剂量,因此可能在治疗中占有一席之地严重肾功能不全。

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