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生长激素治疗不会改变生长激素缺乏儿童的胰岛素样生长因子-I/胰岛素样生长因子结合蛋白-3摩尔比。

Growth hormone therapy does not alter the insulin-like growth factor-I/insulin-like growth factor binding protein-3 molar ratio in growth hormone-deficient children.

作者信息

Scirè G, Del Bianco C, Spadoni G L, Cianfarani S

机构信息

Rina Balducci Center of Pediatric Endocrinology, Department of Public Health and Cell Biology, Tor Vergata University, IT-00133, Rome, Italy.

出版信息

J Endocrinol Invest. 2008 Feb;31(2):153-8. doi: 10.1007/BF03345582.

Abstract

BACKGROUND

Recent studies have linked raised levels of IGF-I and/or reduced levels of its main binding protein, IGF binding protein (IGFBP)-3, with the risk of developing cancer. A GH dose-dependent increase in IGF-I/IGFBP-3 molar ratio has been reported in subjects treated with GH, raising concern about the long-term safety.

OBJECTIVE

The aim of this study was to evaluate changes in serum IGF-I, IGFBP-3, and IGF-I/IGFBP-3 molar ratio over the first 12 months of replacement GH therapy in GH deficient (GHD) children.

METHODS

The study included 20 GHD children who had not previously received GH treatment, and 40 untreated non-GHD short children closely matched for age, gender, pubertal stage, and body mass index (BMI), as controls. Serum IGF-I, IGFBP-3 levels were measured before and after 12 months of GH treatment. Based on the molecular weight of IGF-I (7500) and IGFBP- 3 (40,000, mean of glycosylated variants), we calculated the molar ratio of IGF-I/IGFBP-3.

RESULTS

IGF-I/IGFBP-3 molar ratio significantly increased during GH therapy (p=0.01). No significant difference in IGF-I/IGFBP-3 ratio was found between GHD children and controls at the different time points. In the multiple regression analysis, BMI (beta=0.33) and age (beta=0.33) proved to be the major predictors of the IGF-I/IGFBP-3 molar ratio (adjusted r2=0.53, p<0.0001).

CONCLUSIONS

Our results suggest that at a conventional replacement dose GH does not alter the IGF-I/IGFBP-3 molar ratio. Potential fears related to long-term cancer risk are likely to be greatest in patients exposed to high-dose GH therapy and with genetic predisposition to high IGF-I and/or low IGFBP-3 concentrations.

摘要

背景

近期研究表明,胰岛素样生长因子-I(IGF-I)水平升高和/或其主要结合蛋白胰岛素样生长因子结合蛋白(IGFBP)-3水平降低与患癌风险相关。据报道,接受生长激素(GH)治疗的患者中,IGF-I/IGFBP-3摩尔比呈GH剂量依赖性增加,这引发了对长期安全性的担忧。

目的

本研究旨在评估生长激素缺乏(GHD)儿童在接受GH替代治疗的前12个月内血清IGF-I、IGFBP-3及IGF-I/IGFBP-3摩尔比的变化。

方法

本研究纳入20例既往未接受过GH治疗的GHD儿童,以及40例未接受治疗、年龄、性别、青春期阶段和体重指数(BMI)与之匹配的非GHD矮小儿童作为对照。在GH治疗12个月前后检测血清IGF-I、IGFBP-3水平。根据IGF-I(7500)和IGFBP-3(40000,糖基化变体的平均值)的分子量,计算IGF-I/IGFBP-3的摩尔比。

结果

GH治疗期间IGF-I/IGFBP-3摩尔比显著升高(p=0.01)。在不同时间点,GHD儿童与对照组之间的IGF-I/IGFBP-3比值无显著差异。在多元回归分析中,BMI(β=0.33)和年龄(β=0.33)被证明是IGF-I/IGFBP-3摩尔比的主要预测因素(调整后r2=0.53,p<0.0001)。

结论

我们的结果表明,在常规替代剂量下,GH不会改变IGF-I/IGFBP-3摩尔比。对于接受高剂量GH治疗且有IGF-I水平高和/或IGFBP-3浓度低的遗传易感性患者,与长期癌症风险相关的潜在担忧可能最大。

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