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二肽基肽酶-4抑制剂作为胰岛素的附加治疗:理论依据与证据

Dipeptidyl peptidase-4 inhibitors as add-on therapy to insulin: rationale and evidences.

作者信息

Singh Awadhesh Kumar, Singh Ritu

机构信息

a G.D Hospital & Diabetes Institute , Kolkata , India.

出版信息

Expert Rev Clin Pharmacol. 2016 Apr;9(4):605-616. doi: 10.1586/17512433.2016.1130621. Epub 2016 Jan 8.

Abstract

Type 2 diabetes mellitus being a progressive disease will eventually require insulin therapy. While insulin therapy is the ultimate option, many patients still fall short of target glycemic goals. This could, perhaps be due to the fear, unwillingness and practical barriers to insulin intensification. Hypoglycemia, oedema and weight gain is another limitation. Newer therapies with dipeptidyl peptidase-4 (DPP-4) inhibitors and sodium-glucose co-transporter-2 (SGLT-2) inhibitors are exciting options as both classes do not cause hypoglycemia and are either weight neutral or cause weight loss. DPP-4 inhibitors are an appealing option as an add-on therapy to insulin especially in elderly and patients with renal impairment. Moreover, glucose-dependent insulinotropic polypeptide (GIP) mediated augmentation of glucagon by DPP-4 inhibitors could also protect against hypoglycemia. These collective properties make these class a potential add-on candidate to insulin therapy. This article will review the efficacy and safety of DPP-4 inhibitors as an add-on to insulin therapy.

摘要

2型糖尿病作为一种进行性疾病最终将需要胰岛素治疗。虽然胰岛素治疗是最终选择,但许多患者仍未达到血糖目标。这可能是由于对强化胰岛素治疗的恐惧、不愿意以及实际障碍。低血糖、水肿和体重增加是另一个限制因素。二肽基肽酶-4(DPP-4)抑制剂和钠-葡萄糖协同转运蛋白-2(SGLT-2)抑制剂等新型疗法是令人兴奋的选择,因为这两类药物都不会导致低血糖,而且要么对体重无影响,要么导致体重减轻。DPP-4抑制剂作为胰岛素的附加治疗是一个有吸引力的选择,特别是在老年人和肾功能不全患者中。此外,DPP-4抑制剂通过葡萄糖依赖性促胰岛素多肽(GIP)介导的胰高血糖素增加也可以预防低血糖。这些共同特性使这类药物成为胰岛素治疗潜在的附加候选药物。本文将综述DPP-4抑制剂作为胰岛素治疗附加药物的疗效和安全性。

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