Wedrychowicz Anna, Dziatkowiak Hanna, Nazim Joanna, Sztefko Krystyna
Department of Pediatric Endocrinology, Polish-American Children's Hospital, Jagiellonian University, Kraków, Poland.
Horm Res. 2005;63(5):245-51. doi: 10.1159/000085941. Epub 2005 May 24.
BACKGROUND/AIMS: Numerous clinical and experimental studies suggest that growth factors may contribute to the development of diabetic microvascular complications. The aim of the study was to test the hypothesis that in adolescents with type-1 diabetes mellitus and microalbuminuria (MA) there are specific disorders of serum insulin-like growth factor-1 (IGF-1) and concentrations of its binding proteins, IGFBP-1 and IGFBP-3, that could be of importance in the pathogenesis of microvascular diabetic complications.
25 adolescents with MA, 24 adolescents with diabetes without complications, and 17 controls were examined. There were no differences with regard to age, puberty stage, HbA1c and body mass index between the groups examined. Two of the patients in the first group also had diabetic retinopathy. Serum fasting concentrations of IGF-1 and overnight urine albumin concentrations were measured by radioimmunoassay, IGFBP-1 and IGFBP-3 concentrations by immunoradiometric assay and HbA1c by high-performance liquid chromatography methods. Diabetic patients were examined by an experienced ophthalmologist and neurologist. The data were analyzed using Kruskal-Wallis ANOVA and multiple regression analysis.
Significantly lower IGF-1 concentrations were found in adolescents with diabetes and MA compared to diabetic patients without complications and healthy contemporaries. IGFBP-1 concentrations were significantly higher and IGFBP-3 concentrations were statistically lower in diabetic patients with MA than in patients without complications.
The IGF-IGFBP system is deranged in adolescents with type-1 diabetes mellitus and MA. Our results suggest the participation of circulating IGFBP-1 in the origin of diabetic complications. It could be also possible that IGFBP-3 takes part in the protection from them.
背景/目的:大量临床和实验研究表明,生长因子可能促使糖尿病微血管并发症的发生。本研究旨在验证以下假设:在患有1型糖尿病和微量白蛋白尿(MA)的青少年中,血清胰岛素样生长因子-1(IGF-1)及其结合蛋白IGFBP-1和IGFBP-3的浓度存在特定紊乱,这可能在糖尿病微血管并发症的发病机制中具有重要意义。
对25名患有MA的青少年、24名无并发症的糖尿病青少年和17名对照者进行了检查。所检查的各组在年龄、青春期阶段、糖化血红蛋白(HbA1c)和体重指数方面无差异。第一组中有两名患者还患有糖尿病视网膜病变。采用放射免疫分析法测定血清空腹IGF-1浓度和过夜尿白蛋白浓度,采用免疫放射分析法测定IGFBP-1和IGFBP-3浓度,采用高效液相色谱法测定HbA1c。由经验丰富的眼科医生和神经科医生对糖尿病患者进行检查。使用Kruskal-Wallis方差分析和多元回归分析对数据进行分析。
与无并发症的糖尿病患者和健康同龄人相比,患有糖尿病和MA的青少年中IGF-1浓度显著降低。患有MA的糖尿病患者中IGFBP-1浓度显著升高,IGFBP-3浓度在统计学上低于无并发症的患者。
IGF-IGFBP系统在患有1型糖尿病和MA的青少年中紊乱。我们的结果表明循环IGFBP-1参与糖尿病并发症的发生。IGFBP-3也可能参与对并发症的预防。