Levien Terri L, Baker Danial E, White John R, Campbell R Keith
College of Pharmacy, Washington State University Spokane, 99202-1675, USA.
Ann Pharmacother. 2002 Jun;36(6):1019-27. doi: 10.1345/aph.1A301.
To review the pharmacology, pharmacokinetics, dosing guidelines, adverse effects, drug interactions, and clinical efficacy of insulin glargine.
Primary and review articles regarding insulin glargine were identified by MEDLINE search (1966-July 2001); abstracts were identified through Institute for Scientific Information Web of Science (1995-July 2001) and the American Diabetes Association. Additional information was obtained from the insulin glargine product information.
All of the articles and meeting abstracts identified from the data sources were evaluated, and all information deemed relevant was included in this review. Priority was placed on data from the primary medical literature.
Insulin glargine is a long-acting, recombinant human insulin analog that is given once daily as a basal source of insulin in patients with type 1 or type 2 diabetes mellitus. Modification of the basic insulin structure has produced a new insulin that is soluble at an acidic pH, but precipitates in the subcutaneous tissue and is slowly released from a depot. Insulin glargine has a slower onset of action than NPH insulin and a longer duration of action with no peak activity. Once-daily administration of insulin glargine has comparable efficacy to that of NPH insulin administered once or twice daily in basal-bolus regimens when used in combination with intermittent doses of regular insulin or insulin lispro in patients with type 1 and type 2 diabetes, and in conjunction with oral antidiabetic agents in patients with type 2 diabetes. Overall, insulin glargine has an incidence of hypoglycemia comparable to or less than that of NPH insulin, with a reduced incidence of nocturnal hypoglycemia compared with NPH insulin seen in some studies.
Insulin glargine is a long-acting insulin analog capable of providing 24-hour basal insulin coverage when administered once daily at bedtime. Its activity profile, which lacks a pronounced peak, more closely resembles that of endogenous basal insulin than that of other intermediate- or long-acting insulins and appears more likely to be associated with a reduced incidence of hypoglycemia, particularly nocturnal hypoglycemia. Insulin glargine physiologically provides basal insulin but, for most patients, the addition of a rapid-acting insulin, like insulin lispro, before or with meals will need to be included in the treatment regimen to achieve optimal management of blood glucose concentrations.
综述甘精胰岛素的药理学、药代动力学、给药指南、不良反应、药物相互作用及临床疗效。
通过MEDLINE检索(1966年 - 2001年7月)确定了关于甘精胰岛素的原始文献和综述文章;通过科学信息研究所的科学网(1995年 - 2001年7月)及美国糖尿病协会获取了摘要。另外还从甘精胰岛素的产品说明书中获取了信息。
对从资料来源中确定的所有文章和会议摘要进行了评估,所有被认为相关的信息均纳入本综述。重点关注原始医学文献中的数据。
甘精胰岛素是一种长效重组人胰岛素类似物,在1型或2型糖尿病患者中作为基础胰岛素每日给药一次。对基本胰岛素结构的修饰产生了一种新的胰岛素,它在酸性pH下可溶,但在皮下组织中沉淀并从储存库中缓慢释放。甘精胰岛素的起效比中性鱼精蛋白锌胰岛素(NPH胰岛素)慢,作用持续时间更长且无峰值活性。在1型和2型糖尿病患者中,当与常规胰岛素或赖脯胰岛素的间歇剂量联合使用,以及在2型糖尿病患者中与口服抗糖尿病药物联合使用时,每日一次给予甘精胰岛素与每日一次或两次给予NPH胰岛素的基础 - 餐时胰岛素方案具有相当的疗效。总体而言,甘精胰岛素的低血糖发生率与NPH胰岛素相当或更低,在一些研究中与NPH胰岛素相比夜间低血糖发生率降低。
甘精胰岛素是一种长效胰岛素类似物,当在睡前每日给药一次时能够提供24小时基础胰岛素覆盖。其活性曲线无明显峰值,与内源性基础胰岛素的活性曲线比其他中效或长效胰岛素更相似,且似乎更有可能与低血糖发生率降低相关,尤其是夜间低血糖。甘精胰岛素在生理上提供基础胰岛素,但对于大多数患者,在治疗方案中需要在餐前或用餐时加用一种速效胰岛素,如赖脯胰岛素,以实现血糖浓度的最佳管理。