Porcellati F, Rossetti P, Pampanelli S, Fanelli C G, Torlone E, Scionti L, Perriello G, Bolli G B
Section of Internal Medicine, Endocrinology and Metabolism, University of Perugia, Via E. Dal Pozzo, I-06126 Perugia, Italy.
Diabet Med. 2004 Nov;21(11):1213-20. doi: 10.1111/j.1464-5491.2004.01323.x.
Glargine is a long-acting insulin analogue potentially more suitable than NPH insulin in intensive treatment of Type 1 diabetes mellitus (T1 DM), but no study has proven superiority. The aim of this study was to test superiority of glargine on long-term blood glucose (BG) as well as on responses to hypoglycaemia vs. NPH.
One hundred and twenty-one patients with T1 DM on intensive therapy on four times/day NPH and lispro insulin at each meal, were randomized to either continuation of NPH four times/day (n = 60), or once daily glargine at dinner-time (n = 61) for 1 year. Lispro insulin at meal-time was continued in both groups. In 11 patients from each group, responses to stepped hyperinsulinaemic-hypoglycaemia were measured before and after 1 year's treatment.
Mean daily BG was lower with glargine [7.6 +/- 0.11 mmol/l (137 +/- 2 mg/dl)] vs. NPH [8.1 +/- 0.22 mmol/l (146 +/- 4 mg/dl)] (P < 0.05). HbA(1c) at 4 months did not change with NPH, but decreased with glargine (from 7.1 +/- 0.1 to 6.7 +/- 0.1%), and remained lower than NPH at 12 months (6.6 +/- 0.1%, P < 0.05 vs. NPH). Frequency of mild hypoglycaemia [self-assisted episodes, blood glucose < or = 4.0 mmol/l (72 mg/dl)] was lower with glargine vs. NPH (7.2 +/- 0.5 and 13.2 +/- 0.6 episodes/patient-month, P < 0.05). After 1 year, NPH treatment resulted in no change of responses to hypoglycaemia, whereas with glargine plasma glucose, thresholds and maximal responses of plasma adrenaline and symptoms to hypoglycaemia improved (P < 0.05).
The simpler glargine regimen decreases the percentage of HbA(1c) and frequency of hypoglycaemia and improves responses to hypoglycaemia more than NPH. Thus, glargine appears more suitable than NPH as basal insulin for intensive treatment of T1 DM.
甘精胰岛素是一种长效胰岛素类似物,在1型糖尿病(T1 DM)强化治疗中可能比中性鱼精蛋白锌胰岛素(NPH)更适用,但尚无研究证实其优越性。本研究旨在测试甘精胰岛素在长期血糖(BG)控制以及低血糖反应方面相对于NPH的优越性。
121例接受强化治疗的T1 DM患者,每日四次注射NPH胰岛素且每餐注射赖脯胰岛素,将其随机分为两组,一组继续每日四次注射NPH胰岛素(n = 60),另一组改为晚餐时每日一次注射甘精胰岛素(n = 61),为期1年。两组患者进餐时均继续注射赖脯胰岛素。每组选取11例患者,在治疗1年前和1年后测量其对逐步递增胰岛素低血糖试验的反应。
甘精胰岛素组的平均每日血糖[7.6±0.11 mmol/L(137±2 mg/dl)]低于NPH组[8.1±0.22 mmol/L(146±4 mg/dl)](P < 0.05)。4个月时NPH组的糖化血红蛋白(HbA1c)未变化,而甘精胰岛素组降低(从7.1±0.1降至6.7±0.1%),且在12个月时仍低于NPH组(6.6±0.1%,与NPH组相比P < 0.05)。甘精胰岛素组轻度低血糖[自我辅助发作,血糖≤4.0 mmol/L(72 mg/dl)]的发生频率低于NPH组(分别为7.2±0.5和13.2±0.6次/患者月,P < 0.05)。1年后,NPH治疗对低血糖反应无影响,而甘精胰岛素治疗使血浆葡萄糖、血浆肾上腺素阈值及对低血糖的最大反应和症状均得到改善(P < 0.05)。
与NPH相比,更简便的甘精胰岛素治疗方案可降低HbA1c百分比和低血糖发生频率,并改善对低血糖的反应。因此,甘精胰岛素作为基础胰岛素用于T1 DM强化治疗似乎比NPH更适用。