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吸入型人胰岛素(依克苏肽):用于成年糖尿病患者的综述

Inhaled human insulin (Exubera): a review of its use in adult patients with diabetes mellitus.

作者信息

Dunn Christopher, Curran Monique P

机构信息

Adis International Limited, 51 Centorian Drive, Mairangi Bay, Auckland 1311, New Zealand.

出版信息

Drugs. 2006;66(7):1013-32. doi: 10.2165/00003495-200666070-00019.

Abstract

Inhaled human insulin (Exubera) (insulin human [rDNA origin]) Inhalation Powder) has recently been approved in the European Union and the US for preprandial use in adult patients with diabetes mellitus. This formulation of insulin has a more rapid onset, but similar duration, of glucose-lowering activity compared with subcutaneously administered regular human insulin. Preprandial inhaled human insulin provided glycaemic control that was comparable to preprandial subcutaneous regular insulin when added to long- or intermediate-acting subcutaneous basal insulin in patients with type 1 diabetes mellitus. Inhaled human insulin is also effective when administered alone, when combined with oral antihyperglycaemic therapy, or when combined with basal subcutaneous insulin in patients with type 2 diabetes mellitus. Comparable rates of hypoglycaemia occurred in patients treated with inhaled human insulin and in those treated with subcutaneous regular human insulin. Patients treated with inhaled human insulin demonstrated a greater decline in pulmonary function (forced expiratory volume in 1 second [FEV(1)], carbon monoxide diffusing capacity [DL(CO)]) than patients treated with comparator antihyperglycaemic agents; the mean difference between the treatment groups that favoured the comparators was noted within the first several weeks of treatment, and did not change over a 2-year treatment period. This agent has also been associated with significant improvements in some quality-of-life and treatment satisfaction scores, especially when compared with subcutaneous mealtime insulin regimens. Inhaled human insulin is an effective and well tolerated formulation suitable for preprandial use in combination with basal subcutaneous insulin in patients with type 1 diabetes. It is also well tolerated and effective in patients with type 2 diabetes when administered alone, when combined with oral antihyperglycaemic therapy, or when combined with basal subcutaneous insulin.

摘要

吸入型人胰岛素(优泌乐)(重组人胰岛素吸入粉)最近在欧盟和美国被批准用于糖尿病成年患者的餐前使用。与皮下注射的常规人胰岛素相比,这种胰岛素制剂的降血糖活性起效更快,但持续时间相似。在1型糖尿病患者中,当餐前吸入型人胰岛素与长效或中效皮下基础胰岛素联合使用时,其血糖控制效果与餐前皮下注射常规胰岛素相当。吸入型人胰岛素在单独使用、与口服降糖治疗联合使用或与2型糖尿病患者的皮下基础胰岛素联合使用时也有效。吸入型人胰岛素治疗的患者和皮下注射常规人胰岛素治疗的患者发生低血糖的发生率相当。与使用对照降糖药物治疗的患者相比,吸入型人胰岛素治疗的患者肺功能(一秒用力呼气量[FEV(1)]、一氧化碳弥散量[DL(CO)])下降更大;治疗组之间有利于对照药物的平均差异在治疗的最初几周内就已显现,并且在2年的治疗期内没有变化。这种药物还与一些生活质量和治疗满意度评分的显著改善有关,特别是与皮下餐时胰岛素治疗方案相比。吸入型人胰岛素是一种有效且耐受性良好的制剂,适用于1型糖尿病患者与皮下基础胰岛素联合餐前使用。它在2型糖尿病患者单独使用、与口服降糖治疗联合使用或与皮下基础胰岛素联合使用时也耐受性良好且有效。

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