Veening Margreet A, van Weissenbruch Mirjam M, Heine Robert J, Delemarre-van de Waal Henriette A
Department of pediatrics, Research institute for Endocrinology, Reproduction and Metabolism Vrÿe Universiteit University Medical Center, Amsterdam, The Netherlands.
Diabetes. 2003 Jul;52(7):1756-60. doi: 10.2337/diabetes.52.7.1756.
Insulin secretion and sensitivity was studied in 28 prepubertal children born small for gestational age (SGA) and in 22 prepubertal children born appropriate for gestational age (AGA). The effect of body size during childhood was also assessed. Insulin sensitivity was measured using the hyperinsulinemic-euglycemic clamp (M value), and beta-cell function was studied with the hyperglycemic clamp plus arginine. First-phase insulin response (FIR) was used to calculate the disposition index (FIR x M value). Arginine-stimulated second-phase insulin response was used as a measure of beta-cell capacity. DeltaBMI(0-1 year), DeltaBMI(0-2 years), and DeltaBMI(2-9 years) were classified in tertiles. SGA children were less insulin sensitive than AGA children (P = 0.009). beta-Cell capacity and disposition indexes were similar in the two groups. In SGA children, M values were lower in the tertile with the highest DeltaBMI(2-9 years) than in the tertile with the lowest DeltaBMI(2-9 years) (P = 0.01). No association between DeltaBMI(0-2 years) and decreased insulin sensitivity was found. In conclusion, prepubertal SGA children show decreased insulin sensitivity rather than decreased beta-cell capacity. Interventions to improve fetal growth and prevent overweight after the second year of life appear to be important factors in the prevention of type 2 diabetes in children born SGA.
对28名小于胎龄(SGA)的青春期前儿童和22名适于胎龄(AGA)的青春期前儿童的胰岛素分泌和敏感性进行了研究。还评估了儿童期体型的影响。使用高胰岛素正葡萄糖钳夹技术(M值)测量胰岛素敏感性,并用高血糖钳夹加精氨酸研究β细胞功能。用第一相胰岛素反应(FIR)计算处置指数(FIR×M值)。精氨酸刺激的第二相胰岛素反应用作β细胞功能的指标。将ΔBMI(0至1岁)、ΔBMI(0至2岁)和ΔBMI(2至9岁)分为三分位数。SGA儿童的胰岛素敏感性低于AGA儿童(P = 0.009)。两组的β细胞功能和处置指数相似。在SGA儿童中,ΔBMI(2至9岁)最高三分位数的M值低于ΔBMI(2至9岁)最低三分位数的M值(P = 0.01)。未发现ΔBMI(0至2岁)与胰岛素敏感性降低之间存在关联。总之,青春期前SGA儿童表现出胰岛素敏感性降低而非β细胞功能降低。改善胎儿生长和预防生命第二年以后超重似乎是预防SGA出生儿童患2型糖尿病的重要因素。