Effect of Growth Hormone (GH) Treatment on Bone in Postpubertal GH-Deficient Patients: A 2-Year Randomized, Controlled, Dose-Ranging Study

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 multinat...

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Veröffentlicht in:The journal of clinical endocrinology and metabolism 2003-09, Vol.88 (9), p.4124-4129
Hauptverfasser: 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.
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container_end_page 4129
container_issue 9
container_start_page 4124
container_title The journal of clinical endocrinology and metabolism
container_volume 88
creator 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.
description 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 μg/kg·day (pediatric dose, n = 58) or 12.5 μg/kg·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 μg/liter; pediatric dose: 178.5 ± 143.7 μg/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.
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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 μg/kg·day (pediatric dose, n = 58) or 12.5 μg/kg·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 &lt; 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 μg/liter; pediatric dose: 178.5 ± 143.7 μg/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 &lt; 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. 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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 μg/kg·day (pediatric dose, n = 58) or 12.5 μg/kg·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 &lt; 0.001), but there were no significant dose effects. 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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 μg/kg·day (pediatric dose, n = 58) or 12.5 μg/kg·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 &lt; 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 μg/liter; pediatric dose: 178.5 ± 143.7 μg/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 &lt; 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.</abstract><cop>Bethesda, MD</cop><pub>Endocrine Society</pub><pmid>12970274</pmid><doi>10.1210/jc.2003-030126</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Absorptiometry, Photon
Adult
Alkaline Phosphatase - metabolism
Body Height - drug effects
Bone and Bones - enzymology
Bone Density - drug effects
Bone Development - drug effects
Calcification, Physiologic - drug effects
Cohort Studies
Collagen Type I - metabolism
Dose-Response Relationship, Drug
Double-Blind Method
Female
Growth Hormone - administration & dosage
Growth Hormone - adverse effects
Growth Hormone - therapeutic use
Human Growth Hormone - deficiency
Humans
Insulin-Like Growth Factor I - metabolism
Male
Prospective Studies
Puberty - physiology
Sex Characteristics
title Effect of Growth Hormone (GH) Treatment on Bone in Postpubertal GH-Deficient Patients: A 2-Year Randomized, Controlled, Dose-Ranging Study
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