Bambino Gesù Children's Hospital-Istituto di Ricovero e Cura a Carattere Scientifico, 00165 Rome, Italy.
J Clin Endocrinol Metab. 2009 Nov;94(11):4448-52. doi: 10.1210/jc.2009-1079. Epub 2009 Oct 9.
Epidemiological studies have shown an association between birth weight and future risk of type 2 diabetes, with individuals born either small or large for gestational age at increased risk. We sought to investigate the influence of birth weight on the relation between insulin sensitivity and beta-cell function in obese children.
A total of 257 obese/overweight children (mean body mass index-sd score, 2.2 +/- 0.3), aged 11.6 +/- 2.3 yr were divided into three groups according to birth weight percentile: 44 were small for gestational age (SGA), 161 were appropriate for gestational age (AGA), and 52 were large for gestational age (LGA). Participants underwent a 3-h oral glucose tolerance test with glucose, insulin, and C-peptide measurements. Homeostasis model of assessment for insulin resistance, insulinogenic index, and disposition index were calculated to evaluate insulin sensitivity and beta-cell function. Glucose and insulin area under the curve (AUC) were also considered. One-way ANOVA was used to compare the three groups.
SGA and LGA subjects had higher homeostasis model of assessment for insulin resistance than AGA subjects, but they diverged when oral glucose tolerance test response was considered. Indeed, SGA subjects showed higher glucose AUC and lower insulinogenic and disposition indexes. Insulin AUC was not different between groups, but when singular time points were considered, SGA subjects had lower insulin levels at 30 min and higher insulin levels at 180 min.
SGA obese children fail to adequately compensate for their reduced insulin sensitivity, manifesting deficit in early insulin response and reduced disposition index that results in higher glucose AUC. Thus, SGA obese children show adverse metabolic outcomes compared to AGAs and LGAs.
流行病学研究表明,出生体重与 2 型糖尿病的未来风险之间存在关联,出生时为小于胎龄儿或大于胎龄儿的个体患病风险增加。我们试图研究出生体重对肥胖儿童胰岛素敏感性与β细胞功能之间关系的影响。
共纳入 257 名肥胖/超重儿童(平均体重指数标准差为 2.2±0.3),根据出生体重百分位数分为三组:44 名为小于胎龄儿(SGA),161 名为适于胎龄儿(AGA),52 名为大于胎龄儿(LGA)。参与者接受了 3 小时口服葡萄糖耐量试验,检测血糖、胰岛素和 C 肽。计算稳态模型评估的胰岛素抵抗指数、胰岛素生成指数和胰岛β细胞功能指数,以评估胰岛素敏感性和β细胞功能。还考虑了血糖和胰岛素曲线下面积(AUC)。采用单因素方差分析比较三组。
SGA 和 LGA 受试者的稳态模型评估的胰岛素抵抗指数高于 AGA 受试者,但当考虑口服葡萄糖耐量试验的反应时,两组间出现了差异。事实上,SGA 受试者的血糖 AUC 更高,胰岛素生成指数和胰岛β细胞功能指数更低。三组间胰岛素 AUC 无差异,但当考虑单一时间点时,SGA 受试者在 30 分钟时的胰岛素水平较低,在 180 分钟时的胰岛素水平较高。
SGA 肥胖儿童不能充分代偿其胰岛素敏感性降低,表现为早期胰岛素反应缺陷和胰岛β细胞功能指数降低,导致血糖 AUC 升高。因此,与 AGA 和 LGA 相比,SGA 肥胖儿童表现出不良的代谢结局。