Saitoh H, Kamoda T, Nakahara S, Hirano T, Nakamura N
Department of Paediatrics, University of Tsukuba, Japan.
Clin Endocrinol (Oxf). 1998 Apr;48(4):487-92. doi: 10.1046/j.1365-2265.1998.00476.x.
Simple obesity is characterized by normal or accelerated growth in the presence of reduced serum levels of GH, whereas its detailed mechanism remains unknown. We, therefore, evaluated interrelationships among serum levels of insulin, IFG-I, IGF binding protein (IGFBP)-1 and -3 and growth hormone binding protein (GHBP) in prepubertal obese children.
Prepubertal 20 obese children and 20 age-matched control children were included in the study.
Serum levels of insulin, IGF-I and IGFBP-3 in obese children did not differ from those in controls. The serum level of IGFBP-1 was significantly lower in obese children (22.1 +/- 18.4 micrograms/l, P < 0.001) than in control children (76.0 +/- 62.9 micrograms/l). No relationship was found between the serum levels of insulin and IGF-I, IGFBP-1, or IGFBP-3 in obese subjects. The serum level of GHBP in obese children was significantly elevated as compared with that in controls and was positively correlated with body mass index (BMI). No relationship was found between the serum levels of GHBP and IGF-I in obese subjects.
The present study showed for the first time that the fasting IGFBP-1 level was suppressed in prepubertal obese children with fasting normoinsulinaemia. We speculate that the hyperinsulinaemia which cannot be detected in the fasting state may have suppressed hepatic production of IGFBP-1. Alternatively, the reduced IGFBP-1 is likely to be a compensatory response to impaired insulin sensitivity. Thus, the IGFBP-1 level may be a useful predictor for the early identification in the development of insulin resistance in prepubertal obese children.
单纯性肥胖的特征是在血清生长激素(GH)水平降低的情况下生长正常或加速,但其详细机制仍不清楚。因此,我们评估了青春期前肥胖儿童血清胰岛素、胰岛素样生长因子-I(IGF-I)、IGF结合蛋白(IGFBP)-1和-3以及生长激素结合蛋白(GHBP)之间的相互关系。
本研究纳入了20名青春期前肥胖儿童和20名年龄匹配的对照儿童。
肥胖儿童的血清胰岛素、IGF-I和IGFBP-3水平与对照组无差异。肥胖儿童的血清IGFBP-1水平(22.1±18.4微克/升,P<0.001)显著低于对照儿童(76.0±62.9微克/升)。在肥胖受试者中,未发现血清胰岛素水平与IGF-I、IGFBP-1或IGFBP-3之间存在相关性。与对照组相比,肥胖儿童的血清GHBP水平显著升高,且与体重指数(BMI)呈正相关。在肥胖受试者中,未发现血清GHBP水平与IGF-I之间存在相关性。
本研究首次表明,空腹血糖正常的青春期前肥胖儿童空腹IGFBP-1水平受到抑制。我们推测,在空腹状态下无法检测到的高胰岛素血症可能抑制了肝脏IGFBP-1的产生。或者,IGFBP-1降低可能是对胰岛素敏感性受损的一种代偿反应。因此,IGFBP-1水平可能是青春期前肥胖儿童胰岛素抵抗早期识别的一个有用预测指标。