Schweizer Anja, Foley James E, Kothny Wolfgang, Ahrén Bo
Novartis Pharma AG, Basel, Switzerland.
Vasc Health Risk Manag. 2013;9:57-64. doi: 10.2147/VHRM.S40972. Epub 2013 Feb 15.
Due to the progressive nature of type 2 diabetes, many patients need insulin as add-on to oral antidiabetic drugs (OADs) in order to maintain adequate glycemic control. Insulin therapy primarily targets elevated fasting glycemia but is less effective to reduce postprandial hyperglycemia. In addition, the risk of hypoglycemia limits its effectiveness and there is a concern of weight gain. These drawbacks may be overcome by combining insulin with incretin-based therapies as these increase glucose sensitivity of both the α- and β-cells, resulting in improved postprandial glycemia without the hypoglycemia and weight gain associated with increasing the dose of insulin. The dipeptidyl peptidase-IV (DPP-4) inhibitor vildagliptin has also been shown to protect from hypoglycemia by enhancing glucagon counterregulation. The effectiveness of combining vildagliptin with insulin was demonstrated in three different studies in which vildagliptin decreased A1C levels when added to insulin therapy without increasing hypoglycemia. This was established with and without concomitant metformin therapy. Furthermore, the effectiveness of vildagliptin appears to be greater when insulin is used as a basal regimen as opposed to being used to reduce postprandial hyperglycemia, since improvement in insulin secretion likely plays a minor role when relatively high doses of insulin are administered before meals. This article reviews the clinical experience with the combination of vildagliptin and insulin and discusses the mechanistic basis for the beneficial effects of the combination. The data support the use of vildagliptin in combination with insulin in general and, in line with emerging clinical practice, suggest that treating patients with vildagliptin, metformin, and basal insulin could be an attractive therapeutic option.
由于2型糖尿病的渐进性,许多患者需要在口服抗糖尿病药物(OADs)基础上加用胰岛素,以维持血糖的充分控制。胰岛素治疗主要针对空腹血糖升高,但对降低餐后高血糖的效果较差。此外,低血糖风险限制了其有效性,且存在体重增加的问题。将胰岛素与基于肠促胰岛素的疗法联合使用可能克服这些缺点,因为这些疗法可提高α细胞和β细胞的葡萄糖敏感性,从而改善餐后血糖,且不会出现与增加胰岛素剂量相关的低血糖和体重增加。二肽基肽酶-IV(DPP-4)抑制剂维格列汀也已被证明可通过增强胰高血糖素的代偿调节作用来预防低血糖。在三项不同的研究中证实了维格列汀与胰岛素联合使用的有效性,在这些研究中,维格列汀添加到胰岛素治疗中时可降低糖化血红蛋白(A1C)水平,且不会增加低血糖风险。无论是否同时使用二甲双胍治疗均是如此。此外,与用于降低餐后高血糖相比,当胰岛素作为基础治疗方案使用时,维格列汀的有效性似乎更高,因为在餐前给予相对高剂量胰岛素时,胰岛素分泌的改善可能起较小作用。本文综述了维格列汀与胰岛素联合使用的临床经验,并讨论了联合使用产生有益效果的机制基础。总体而言,数据支持维格列汀与胰岛素联合使用,并且与新出现的临床实践一致,提示用维格列汀、二甲双胍和基础胰岛素治疗患者可能是一种有吸引力的治疗选择。