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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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. |
doi_str_mv | 10.1210/jc.2003-030126 |
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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 < 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.</description><identifier>ISSN: 0021-972X</identifier><identifier>EISSN: 1945-7197</identifier><identifier>DOI: 10.1210/jc.2003-030126</identifier><identifier>PMID: 12970274</identifier><identifier>CODEN: JCEMAZ</identifier><language>eng</language><publisher>Bethesda, MD: Endocrine Society</publisher><subject>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</subject><ispartof>The journal of clinical endocrinology and metabolism, 2003-09, Vol.88 (9), p.4124-4129</ispartof><rights>Copyright © 2003 by The Endocrine Society</rights><rights>2004 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4836-1c8d77bcb1df1de47a7cbb28daadd112b7ff4e0aefb5b8e2c2d662e334cd3ad33</citedby><cites>FETCH-LOGICAL-c4836-1c8d77bcb1df1de47a7cbb28daadd112b7ff4e0aefb5b8e2c2d662e334cd3ad33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15149185$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12970274$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shalet, Stephen M.</creatorcontrib><creatorcontrib>Shavrikova, Elena</creatorcontrib><creatorcontrib>Cromer, Morris</creatorcontrib><creatorcontrib>Child, Christopher J.</creatorcontrib><creatorcontrib>Keller, Eberhard</creatorcontrib><creatorcontrib>Zapletalová, Jirina</creatorcontrib><creatorcontrib>Moshang, Thomas</creatorcontrib><creatorcontrib>Blum, Werner F.</creatorcontrib><creatorcontrib>Chipman, John J.</creatorcontrib><creatorcontrib>Quigley, Charmian A.</creatorcontrib><creatorcontrib>Attanasio, Andrea F.</creatorcontrib><title>Effect of Growth Hormone (GH) Treatment on Bone in Postpubertal GH-Deficient Patients: A 2-Year Randomized, Controlled, Dose-Ranging Study</title><title>The journal of clinical endocrinology and metabolism</title><addtitle>J Clin Endocrinol Metab</addtitle><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.</description><subject>Absorptiometry, Photon</subject><subject>Adult</subject><subject>Alkaline Phosphatase - metabolism</subject><subject>Body Height - drug effects</subject><subject>Bone and Bones - enzymology</subject><subject>Bone Density - drug effects</subject><subject>Bone Development - drug effects</subject><subject>Calcification, Physiologic - drug effects</subject><subject>Cohort Studies</subject><subject>Collagen Type I - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Double-Blind Method</subject><subject>Female</subject><subject>Growth Hormone - administration & dosage</subject><subject>Growth Hormone - adverse effects</subject><subject>Growth Hormone - therapeutic use</subject><subject>Human Growth Hormone - deficiency</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Male</subject><subject>Prospective Studies</subject><subject>Puberty - physiology</subject><subject>Sex Characteristics</subject><issn>0021-972X</issn><issn>1945-7197</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-L1DAUgIso7rp69Si5KApmTNK0ab2ts-uMsOCiK-gppMnLTsc2GZOUYf0T_KtNmYE9iYHw8uN774V8RfGckgVllLzb6gUjpMSkJJTVD4pT2vIKC9qKh8UpIYziVrDvJ8WTGLeEUM6r8nFxQlkrCBP8tPhzaS3ohLxFq-D3aYPWPozeAXq9Wr9BNwFUGsFlwKEP83Hv0LWPaTd1EJIa0GqNL8D2up-ha5XmGN-jc8TwD1ABfVHO-LH_DeYtWnqXgh-GeX3hI-B8edu7W_Q1TebuafHIqiHCs2M8K759vLxZrvHV59Wn5fkV1rwpa0x1Y4TodEeNpQa4UEJ3HWuMUsZQyjphLQeiwHZV1wDTzNQ1g7Lk2pTKlOVZ8epQdxf8rwlikmMfNQyDcuCnKEVZM9rU_wdp01YVY00GFwdQBx9jACt3oR9VuJOUyFmT3Go5a5IHTTnhxbHy1I1g7vGjlwy8PAIqajXYoJzu4z1XUd7SpsocP3B7PyQI8ecw7SHIDaghbSTJg9eiwXNv0uYdzpPO_atDGmQ5OvQOdgFilFs_BZf__l_v_gusA7w2</recordid><startdate>200309</startdate><enddate>200309</enddate><creator>Shalet, Stephen M.</creator><creator>Shavrikova, Elena</creator><creator>Cromer, Morris</creator><creator>Child, Christopher J.</creator><creator>Keller, Eberhard</creator><creator>Zapletalová, Jirina</creator><creator>Moshang, Thomas</creator><creator>Blum, Werner F.</creator><creator>Chipman, John J.</creator><creator>Quigley, Charmian A.</creator><creator>Attanasio, Andrea F.</creator><general>Endocrine Society</general><general>Copyright by The Endocrine Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7X8</scope></search><sort><creationdate>200309</creationdate><title>Effect of Growth Hormone (GH) Treatment on Bone in Postpubertal GH-Deficient Patients: A 2-Year Randomized, Controlled, Dose-Ranging Study</title><author>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.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4836-1c8d77bcb1df1de47a7cbb28daadd112b7ff4e0aefb5b8e2c2d662e334cd3ad33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Absorptiometry, Photon</topic><topic>Adult</topic><topic>Alkaline Phosphatase - metabolism</topic><topic>Body Height - drug effects</topic><topic>Bone and Bones - enzymology</topic><topic>Bone Density - drug effects</topic><topic>Bone Development - drug effects</topic><topic>Calcification, Physiologic - drug effects</topic><topic>Cohort Studies</topic><topic>Collagen Type I - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Double-Blind Method</topic><topic>Female</topic><topic>Growth Hormone - administration & dosage</topic><topic>Growth Hormone - adverse effects</topic><topic>Growth Hormone - therapeutic use</topic><topic>Human Growth Hormone - deficiency</topic><topic>Humans</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Male</topic><topic>Prospective Studies</topic><topic>Puberty - physiology</topic><topic>Sex Characteristics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shalet, Stephen M.</creatorcontrib><creatorcontrib>Shavrikova, Elena</creatorcontrib><creatorcontrib>Cromer, Morris</creatorcontrib><creatorcontrib>Child, Christopher J.</creatorcontrib><creatorcontrib>Keller, Eberhard</creatorcontrib><creatorcontrib>Zapletalová, Jirina</creatorcontrib><creatorcontrib>Moshang, Thomas</creatorcontrib><creatorcontrib>Blum, Werner F.</creatorcontrib><creatorcontrib>Chipman, John J.</creatorcontrib><creatorcontrib>Quigley, Charmian A.</creatorcontrib><creatorcontrib>Attanasio, Andrea F.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of clinical endocrinology and metabolism</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shalet, Stephen M.</au><au>Shavrikova, Elena</au><au>Cromer, Morris</au><au>Child, Christopher J.</au><au>Keller, Eberhard</au><au>Zapletalová, Jirina</au><au>Moshang, Thomas</au><au>Blum, Werner F.</au><au>Chipman, John J.</au><au>Quigley, Charmian A.</au><au>Attanasio, Andrea F.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Growth Hormone (GH) Treatment on Bone in Postpubertal GH-Deficient Patients: A 2-Year Randomized, Controlled, Dose-Ranging Study</atitle><jtitle>The journal of clinical endocrinology and metabolism</jtitle><addtitle>J Clin Endocrinol Metab</addtitle><date>2003-09</date><risdate>2003</risdate><volume>88</volume><issue>9</issue><spage>4124</spage><epage>4129</epage><pages>4124-4129</pages><issn>0021-972X</issn><eissn>1945-7197</eissn><coden>JCEMAZ</coden><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 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.</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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