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生长激素(GH)治疗对青春期后生长激素缺乏患者骨骼的影响:一项为期2年的随机、对照、剂量范围研究。

Effect of growth hormone (GH) treatment on bone in postpubertal GH-deficient patients: a 2-year randomized, controlled, dose-ranging study.

作者信息

Shalet Stephen M, Shavrikova Elena, Cromer Morris, Child Christopher J, Keller Eberhard, Zapletalová Jirina, Moshang Thomas, Blum Werner F, Chipman John J, Quigley Charmian A, Attanasio Andrea F

机构信息

Department of Endocrinology, Christie Hospital NHS Trust, Manchester M20 4BX, United Kingdom.

出版信息

J Clin Endocrinol Metab. 2003 Sep;88(9):4124-9. doi: 10.1210/jc.2003-030126.

Abstract

GH treatment in children with GH deficiency is frequently terminated at final height. However, in healthy individuals bone mass continues to accrue until peak bone mass is achieved. Because no prospective data specifically prove the role of GH in attainment of peak bone mass, we performed a multinational, controlled, 2-yr study in patients who had terminated pediatric GH at final height. Patients were randomized to: GH at 25.0 microg/kg x day (pediatric dose, n = 58) or 12.5 microg/kg x day (adult dose, n = 59), or no GH treatment (control, n = 32). Bone mineral content (BMC) and density were measured by dual-energy x-ray absorptiometry and evaluated centrally. Laboratory measurements were also performed centrally. After 2 yr, significant increases were seen with both GH treatments, compared with control in bone-specific alkaline phosphatase (P = 0.004) and type I collagen C-terminal telopeptide:creatinine ratio (P < 0.001), but there were no significant dose effects. Total BMC increased by 9.5 +/- 8.4% in the adult dose group, 8.1 +/- 7.6% in the pediatric dose group, and 5.6 +/- 8.4% in controls (analysis of covariance, P = 0.008), with no significant GH dose effect. BMC increased predominantly at the lumbar spine (11.0 +/- 10.6%, P = 0.015) rather than at the femoral neck or hip. In contrast, a significant dose-dependent increase was seen in IGF-I concentrations (adult dose: 114.5 +/- 119.4 microg/liter; pediatric dose: 178.5 +/- 143.7 microg/liter; P = 0.023). There were no gender-related differences in BMC changes with either dose, whereas the IGF-I increase was significantly higher with the pediatric than with the adult dose in females (P < 0.001) but not males (P = 0.606). In summary, reinstitution of GH replacement after final height in severely GH-deficient patients induced significant progression toward peak bone mass. Although there was a by-gender dose effect on IGF-I concentration, the treatment effect on bone was obtained in both males and females with the adult GH dose regimen.

摘要

生长激素缺乏症患儿的生长激素治疗通常在达到最终身高时终止。然而,在健康个体中,骨量会持续增加直至达到峰值骨量。由于尚无前瞻性数据明确证明生长激素在达到峰值骨量中的作用,我们对已在最终身高时终止儿童生长激素治疗的患者进行了一项为期2年的多国对照研究。患者被随机分为:25.0微克/千克·天的生长激素(儿童剂量,n = 58)或12.5微克/千克·天(成人剂量,n = 59),或不进行生长激素治疗(对照组,n = 32)。通过双能X线吸收法测量骨矿物质含量(BMC)和骨密度,并进行集中评估。实验室检测也进行集中操作。2年后,与对照组相比,两种生长激素治疗组的骨特异性碱性磷酸酶(P = 0.004)和I型胶原C末端肽:肌酐比值(P < 0.001)均显著升高,但无显著剂量效应。成人剂量组的总BMC增加了9.5±8.4%,儿童剂量组增加了8.1±7.6%,对照组增加了5.6±8.4%(协方差分析,P = 0.008),生长激素剂量无显著效应。BMC主要在腰椎处增加(11.0±10.6%,P = 0.015),而非在股骨颈或髋部。相比之下,胰岛素样生长因子-I(IGF-I)浓度出现显著的剂量依赖性增加(成人剂量:114.5±119.4微克/升;儿童剂量:

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