青少年肥胖中的代谢综合征与胰岛素样生长因子I调节

The metabolic syndrome and insulin-like growth factor I regulation in adolescent obesity.

作者信息

Attia N, Tamborlane W V, Heptulla R, Maggs D, Grozman A, Sherwin R S, Caprio S

机构信息

Department of Pediatrics, Yale University School of Medicine, New Haven, Connecticut 06520, USA.

出版信息

J Clin Endocrinol Metab. 1998 May;83(5):1467-71. doi: 10.1210/jcem.83.5.4827.

Abstract

Although low GH levels are commonly seen in obese adults and children, the effects of obesity on the insulin-like growth factor (IGF)/IGF-binding protein (IGFBP) system have not been established. As GH and IGF-I normally increase during adolescence, we investigated the effects of obesity on circulating total and free IGF-I levels and IGFBP-1, -2, and -3 in 19 obese adolescents [14 +/- 1 yr old; body mass index (BMI), 34 +/- 3], 20 lean adolescents (14 +/- 1 yr old; BMI, 23 +/- 0.5), and 10 lean adults (22 +/- 0.7 yr; BMI, 22 +/- 0.7). Fasting plasma insulin levels were significantly greater in obese adolescents than in either lean group, whereas circulating IGFBP-1 levels were suppressed in an inverse relationship to basal insulin (r = -0.49; P < 0.01). Low IGFBP-1 levels were associated with normal to increased free IGF-I levels in obese adolescents, even though total IGF-I values were lower than those in lean adolescents. Basal GH and IGFBP-3 levels were also lower in obese vs. lean adolescents. Basal IGFBP-1 levels were markedly reduced in obese adolescents (14 +/- 3 ng/mL) vs. those in adolescents and adults. No further suppression of IGFBP-1 levels was observed in the obese group during a two-step 8 and 40 mU/m2 insulin clamp. In contrast, IGFBP-1 levels were promptly lowered in lean adults. Basal IGFBP-2 levels were significantly lower in both groups of adolescents vs. lean adults (P < 0.05), and IGFBP-2 levels did not change during euglycemic hyperinsulinemia. These data suggest that the compensatory hyperinsulinemia that characterizes adolescent obesity chronically suppresses levels of IGFBP-1, and low IGFBP-1 concentrations may serve to increase the bioavailability of free IGF-I, which may, in turn, contribute to lower circulating GH, total IGF-I, and IGFBP-3 concentrations.

摘要

虽然肥胖的成人和儿童中普遍存在生长激素(GH)水平较低的情况,但肥胖对胰岛素样生长因子(IGF)/IGF结合蛋白(IGFBP)系统的影响尚未明确。由于GH和IGF-I通常在青春期升高,我们研究了肥胖对19名肥胖青少年[14±1岁;体重指数(BMI),34±3]、20名瘦青少年(14±1岁;BMI,23±0.5)和10名瘦成年人(22±0.7岁;BMI,22±0.7)循环中总IGF-I和游离IGF-I水平以及IGFBP-1、-2和-3的影响。肥胖青少年的空腹血浆胰岛素水平显著高于两个瘦人群组,而循环中的IGFBP-1水平与基础胰岛素呈负相关,被抑制(r = -0.49;P < 0.01)。肥胖青少年中IGFBP-1水平较低与游离IGF-I水平正常至升高相关,尽管总IGF-I值低于瘦青少年。肥胖青少年与瘦青少年相比,基础GH和IGFBP-3水平也较低。肥胖青少年的基础IGFBP-1水平(14±3 ng/mL)明显低于青少年和成年人。在两步8和40 mU/m²胰岛素钳夹期间,肥胖组未观察到IGFBP-1水平进一步被抑制。相比之下,瘦成年人的IGFBP-1水平迅速降低。两组青少年的基础IGFBP-2水平均显著低于瘦成年人(P < 0.05),且在正常血糖高胰岛素血症期间IGFBP-2水平未发生变化。这些数据表明,青少年肥胖特征性的代偿性高胰岛素血症会长期抑制IGFBP-1水平,而低IGFBP-1浓度可能有助于提高游离IGF-I的生物利用度,这反过来可能导致循环中的GH、总IGF-I和IGFBP-3浓度降低。

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