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首页> 外文期刊>Diabetes, obesity & metabolism >Mid- and high-ratio premix insulin analogues: potential treatment options for patients with type 2 diabetes in need of greater postprandial blood glucose control.
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Mid- and high-ratio premix insulin analogues: potential treatment options for patients with type 2 diabetes in need of greater postprandial blood glucose control.

机译:中高比例的预混胰岛素类似物:需要进一步餐后血糖控制的2型糖尿病患者的潜在治疗选择。

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摘要

Some patients with type 2 diabetes continue to have high postprandial blood glucose levels on twice-daily regimens of 'low-ratio' premix insulin formulations (up to 30% rapid-acting, with 70% protracted insulin). These patients require intensified insulin therapy, which can be provided by a twice- or thrice-daily regimen of mid-ratio (50% rapid-acting and 50% protaminated intermediate-acting insulin - human or analogue) or high-ratio (70% rapid-acting and 30% protaminated insulin - analogue only) premix insulin. Alternatively, a third daily injection of low-ratio premix insulin can be added to the regimen, with the option of incorporating one or more injections of mid- or high-ratio premix as required, and as an alternative to basal-bolus therapy. How these mid- and high-ratio formulations differ from the low-ratio premix insulins is reviewed here, with the aim of identifying the role of these formulations in diabetes management. Glucose clamp studies have shown that premix analogues give serum insulin levels proportional to their percentage of rapid-acting uncomplexed insulin: the higher the proportion, the greater the maximum level reached. Other pharmacokinetic parameters were not always significantly different between the mid- and high-ratio formulations. In clinical trials, postprandial plasma glucose and glycated haemoglobin A1c (HbA(1c)) levels were significantly reduced with thrice-daily mid- /high-ratio premix analogue when compared with twice-daily low-ratio biphasic human insulin (BHI) 30/70 or once-daily insulin glargine. Moreover, glycaemic control with mid-/high-ratio premix analogue was found to be similar to that with a basal-bolus therapy. Mid- and high-ratio premix regimens are generally well tolerated. The frequency of minor hypoglycaemia was reportedly higher with mid- /high-ratio premix analogues than with BHI 30, but nocturnal hypoglycaemia was less frequent. Although there is little evidence that clinical outcomes with mid-ratio premix analogues are different from those with high-ratio, they are useful additions to the low-ratio formulations for the management of diabetes, and addressing postprandial hyperglycaemia in particular.
机译:一些2型糖尿病患者在每天两次的“低比例”预混胰岛素制剂中仍具有较高的餐后血糖水平(速效达30%,长期胰岛素达70%)。这些患者需要强化胰岛素治疗,这可以通过中比例(50%速效和50%污染的中效胰岛素-人或类似药物)或高比例(70%)的每日两次或三次方案提供速效胰岛素和30%污染的胰岛素-仅适用于类似物)预混胰岛素。或者,可以将低比例预混合胰岛素的第三次每日注射添加到方案中,可以选择根据需要并入一次或多次中等或高比例预混合注射,并作为基础推注疗法的替代方法。本文对这些中高比例制剂与低比例预混胰岛素的区别进行了综述,目的是确定这些制剂在糖尿病管理中的作用。葡萄糖钳夹研究表明,预混物类似物的血清胰岛素水平与其速效未复合胰岛素的百分比成正比:比例越高,达到的最大水平就越大。在中高比例制剂之间,其他药代动力学参数并不总是显着不同。在临床试验中,与每日两次低比例双相人胰岛素(BHI)30 /天相比,每日三次/高比例预混物类似物可显着降低餐后血浆葡萄糖和糖化血红蛋白A1c(HbA(1c))的水平。 70或每日一次甘精胰岛素。此外,发现中/高比例预混物类似物的血糖控制与基础推注疗法相似。中高比例的预混方案通常耐受性良好。据报道,中/高比例预混物类似物的轻度低血糖发生率高于BHI 30,但夜间低血糖的发生率较低。尽管几乎没有证据表明中比例预混物类似物的临床结局与高比例预混物类似,但它们是低比例制剂在糖尿病治疗中的有用补充,尤其是解决餐后高血糖症。

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