D Cucinotta, F De Luca, T Arrigo, A Di Benedetto, C Sferlazzas, A Gigante, L Rigoli, G Magazzù
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引用次数: 26
摘要
我们研究的目的是确定静脉注射(i.v.)葡萄糖的一期胰岛素反应是否可以作为一种简单快速的检测方法来识别有发展为糖尿病风险的囊性纤维化(CF)患者。40例连续空腹血糖正常,但标准口服糖耐量试验中糖耐量不同程度的CF患者(22例糖耐量正常,16例糖耐量受损,2例糖尿病)和12例年龄和体重指数相匹配的正常人,进行了葡萄糖静脉注射,以评估早期胰岛素释放。与正常受试者相比,CF患者的基础胰岛素水平(76 +/- 50 vs 108 +/- 30 pM/l, 2 p < 0.02)和葡萄糖刺激胰岛素水平(1 + 3分钟胰岛素= 456 +/- 275 vs 951 +/- 170 pM/l, 2 p < 0.01)显著降低。然而,早期胰岛素释放并不能区分正常和糖耐量受损的CF患者;此外,这两名糖尿病患者的胰岛素水平与其他组CF受试者的胰岛素水平没有明显差异。总之,一期胰岛素反应可以识别CF患者的b细胞功能受损;然而,它不能区分不同程度的糖耐量,正如口服糖耐量试验所确定的那样,因此,它不能可靠地识别最终会发展为显性糖尿病的患者。
First-phase insulin response to intravenous glucose in cystic fibrosis patients with different degrees of glucose tolerance.
The aim of our study was to determine whether first-phase insulin response to intravenous (i.v.) glucose could be used as a simple and rapid test to identify cystic fibrosis (CF) patients at risk to develop diabetes mellitus. Forty consecutive CF patients with normal fasting blood glucose values but with different degrees of glucose tolerance on the standard oral glucose tolerance test (22 with normal glucose tolerance, 16 with impaired glucose tolerance, 2 with diabetes mellitus) and 12 normal subjects, matched for age and body mass index, underwent an i.v. glucose bolus to evaluate early phase insulin release. When compared to the normal subjects, CF patients had significantly reduced basal (76 +/- 50 vs 108 +/- 30 pM/l, 2 p < 0.02) and glucose stimulated insulin levels (1 + 3 min insulin = 456 +/- 275 vs 951 +/- 170 pM/l, 2 p < 0.01). Early phase insulin release, however, did not differentiate between CF patients with normal and impaired glucose tolerance; also in the two diabetic patients insulin levels did not clearly differ from those observed in the other groups of CF subjects. In conclusion, first-phase insulin response may identify an impairment of B-cell function in CF subjects; however, it does not discriminate between different degrees of glucose tolerance, as determined by the oral glucose tolerance test and, therefore, it does not reliably identify those patients who will eventually develop overt diabetes mellitus.