Biesenbach Georg, Grafinger Peter, Raml Andreas
2nd Department of Internal Medicine, Hospital Linz, Linz, Austria.
Wien Klin Wochenschr. 2006 Sep;118(17-18):543-8. doi: 10.1007/s00508-006-0656-4.
Insulin resistance is a common problem in obese patients with type 2 diabetes. In a prospective randomized study, we investigated the improvement of metabolic control after a 3-5 day period of intravenous insulin infusion in poorly insulin-treated, overweight type 2-diabetic patients with and without additional glitazone therapy.
Twenty-eight overweight patients (BMI > 28) with poorly insulin-treated type 2 diabetes (HbA1c > 8%) requiring > 80 IU insulin/day received a continuous insulin infusion for 3-5 days (initially 4-6 IU insulin/hour). Thereafter, 14 of the patients also received pioglitazone (15 mg/day). The two groups were compared for HbA1c, mean blood glucose (MBG), body weight, cholesterol, triglycerides and insulin requirement (IU/day) three months before insulin infusion, during infusion, and at three and six months after the infusion.
Glycemic control was immediately improved under insulin infusion in both groups: MBG was reduced from 188 +/- 32 mg/dl at baseline to 142 +/- 28 mg/dl at the end of insulin infusion (p < 0.05). In the group receiving pioglitazone, the mean HbA1c three months after the insulin infusion was 16% lower and after six months 17% lower than baseline values (p < 0.02). Concomitantly, the required insulin dose decreased significantly by 15% after three months and 18% after six months (p < 0.02). Two patients (14%) were non-responders (< 10% reduction of required insulin dose). In the group without pioglitazone the mean HbA1c level three months after insulin infusion was 10% lower (p < 0.05) than at baseline; at six months the HbA1c value was the same as that before the infusion. The required insulin dose was 10% lower after three months and only 3% lower after six months (NS). Four patients (28%) were non-responders.
Short-term insulin infusion therapy is effective in improving metabolic control and, concomitantly, in reducing insulin requirement in poorly insulin-treated type 2-diabetic patients; however, these effects are mostly limited to three months. With additional glitazone treatment after the insulin infusion, the improvement in metabolic control and the reduced insulin requirement can be maintained for more than six months.
胰岛素抵抗是肥胖的2型糖尿病患者常见的问题。在一项前瞻性随机研究中,我们调查了在接受胰岛素治疗效果不佳的超重2型糖尿病患者中,在进行3 - 5天静脉输注胰岛素治疗期间,无论是否联合使用格列酮类药物,代谢控制情况的改善。
28名超重患者(BMI>28),胰岛素治疗效果不佳的2型糖尿病(糖化血红蛋白>8%),每日胰岛素需求量>80 IU,接受持续胰岛素输注3 - 5天(初始剂量为4 - 6 IU/小时)。此后,其中14名患者还接受了吡格列酮治疗(15 mg/天)。比较两组患者在胰岛素输注前3个月、输注期间以及输注后3个月和6个月时的糖化血红蛋白、平均血糖(MBG)、体重、胆固醇、甘油三酯和胰岛素需求量(IU/天)。
两组患者在胰岛素输注期间血糖控制立即得到改善:平均血糖从基线时的188±32 mg/dl降至胰岛素输注结束时的142±28 mg/dl(p<0.05)。在接受吡格列酮治疗的组中,胰岛素输注后3个月平均糖化血红蛋白比基线值低16%,6个月后低17%(p<0.02)。同时,3个月后所需胰岛素剂量显著降低15%,6个月后降低18%(p<0.02)。两名患者(14%)无反应(所需胰岛素剂量降低<10%)。在未接受吡格列酮治疗的组中,胰岛素输注后3个月平均糖化血红蛋白水平比基线时低10%(p<0.05);6个月时糖化血红蛋白值与输注前相同。3个月后所需胰岛素剂量降低10%,6个月后仅降低3%(无统计学意义)。四名患者(28%)无反应。
短期胰岛素输注治疗对于改善胰岛素治疗效果不佳的2型糖尿病患者的代谢控制以及同时降低胰岛素需求量是有效的;然而,这些效果大多仅限于3个月。在胰岛素输注后加用格列酮类药物治疗,代谢控制的改善和胰岛素需求量的降低可以维持超过6个月。