Goykhman Stanislav, Drincic Andjela, Desmangles Jean Claude, Rendell Marc
Creighton University School of Medicine, Children's Hospital, Diabetes Center, Divisions of Adult and Pediatric Endocrinology, Omaha, NE 68131, USA.
Expert Opin Pharmacother. 2009 Mar;10(4):705-18. doi: 10.1517/14656560902775677.
Insulin Glargine was the first long-acting insulin analog produced by recombinant DNA technology, approved for use by the US FDA in April 2000 and by the European Agency for the Evaluation of Medicinal Products in June, 2000. It has become the most widely used insulin in the USA owing to its long duration of action without a pronounced peak. The principal advantage of insulin Glargine over neutral protamine Hagedorn (NPH) insulin is in a lower frequency of hypoglycemic reactions, thus affording improved safety. It is used in both type 1 and type 2 diabetes, usually as a single daily dose. In type 2 patients, it is often the first insulin introduced as a single daily dose. Although insulin Glargine is typically administered as a single nighttime dose, it can be given in the morning or at any other time convenient for the patient. In labile type 1 diabetes, it is often most effective given as two daily injections. In obese, insulin-resistant patients, it may be best to administer insulin Glargine in two separate doses, owing to the high volumes of injected insulin required. Insulin Glargine does not treat postprandial hyperglycemia. It is necessary to supplement with short-acting insulin at mealtimes to control glucose surges after meals. Insulin Glargine is effective in hospitalized and postsurgical patients on account of its lack of pronounced insulin peaks and long duration of action. Although there is considerable use of Glargine in pregnant diabetic women, there is no definitive study to confirm its benefits. Insulin Glargine is thought to coprecipitate supplementary short-acting insulins when co-administered in the same syringe. Therefore, more injections are typically needed in the usual treatment regimen for insulin requiring diabetes. In many cases, constant basal insulin levels may be achieved with multiple overlapping doses of NPH insulin given together with short-acting insulin at mealtimes. Such a therapy may be less costly, but the major advantage of insulin Glargine remains the greater safety of a lower frequency of hypoglycemic reactions.
甘精胰岛素是首个通过重组DNA技术生产的长效胰岛素类似物,于2000年4月获美国食品药品监督管理局(FDA)批准使用,并于2000年6月获欧洲药品评估局批准。由于其作用持续时间长且无明显峰值,它已成为美国使用最广泛的胰岛素。甘精胰岛素相对于中性鱼精蛋白锌(NPH)胰岛素的主要优势在于低血糖反应的发生率较低,从而提高了安全性。它用于1型和2型糖尿病,通常每日一次给药。在2型患者中,它通常是首次引入的每日一次给药的胰岛素。尽管甘精胰岛素通常在夜间单次给药,但也可在早晨或患者方便的任何其他时间给药。在不稳定的1型糖尿病中,通常每日注射两次最为有效。在肥胖、胰岛素抵抗的患者中,由于所需注射的胰岛素量较大,最好分两次注射甘精胰岛素。甘精胰岛素不能治疗餐后高血糖。有必要在进餐时补充短效胰岛素以控制餐后血糖飙升。甘精胰岛素因其无明显的胰岛素峰值和作用持续时间长,在住院患者和术后患者中有效。尽管甘精胰岛素在妊娠糖尿病女性中使用广泛,但尚无确定性研究证实其益处。当甘精胰岛素与短效胰岛素在同一注射器中混合使用时,被认为会与短效胰岛素共沉淀。因此,在胰岛素依赖型糖尿病的常规治疗方案中通常需要更多次注射。在许多情况下,通过在进餐时将多次重叠剂量的NPH胰岛素与短效胰岛素一起使用,可以实现恒定的基础胰岛素水平。这种治疗方法可能成本较低,但甘精胰岛素的主要优势仍然是低血糖反应发生率较低带来的更高安全性。