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Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV
Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day)...
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Published in: | Bone (New York, N.Y.) N.Y.), 1999-10, Vol.25 (4), p.501-505 |
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creator | Vieira, N.E Marini, J.C Hopkins, E Abrams, S.A Yergey, A.L |
description | Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day) treatment period of 1–1.5 years. Subjects were given
42Ca intravenously and
44Ca orally. The sera and urine
42Ca and
44Ca isotopic enrichments were followed over 7 days using thermal ionization mass spectrometry. The S
aam program was used to fit a three-compartment model to the tracer data. No significant differences were observed between: (1) children with type III and IV disease; or (2) baseline studies of boys and girls within each disease type. However, GH treatment significantly increased: (1) the exchangeable calcium pool (EP) in type III patients (2086 vs. 4422 mg/day,
p = 0.02); and (2) the parameter associated with bone calcium accretion in type IV patients (Vo
+: 973 vs. 1560 mg/day,
p = 0.03) with boys responding with a significantly greater increase than girls
(p = 0.008). Although not statistically significant, a trend toward an increase in Vo
+ in type III patients and in EP in type IV was observed following treatment. Our observations imply that more Ca was available for bone mineralization following GH treatment in these subjects. |
doi_str_mv | 10.1016/S8756-3282(99)00186-6 |
format | article |
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42Ca intravenously and
44Ca orally. The sera and urine
42Ca and
44Ca isotopic enrichments were followed over 7 days using thermal ionization mass spectrometry. The S
aam program was used to fit a three-compartment model to the tracer data. No significant differences were observed between: (1) children with type III and IV disease; or (2) baseline studies of boys and girls within each disease type. However, GH treatment significantly increased: (1) the exchangeable calcium pool (EP) in type III patients (2086 vs. 4422 mg/day,
p = 0.02); and (2) the parameter associated with bone calcium accretion in type IV patients (Vo
+: 973 vs. 1560 mg/day,
p = 0.03) with boys responding with a significantly greater increase than girls
(p = 0.008). Although not statistically significant, a trend toward an increase in Vo
+ in type III patients and in EP in type IV was observed following treatment. Our observations imply that more Ca was available for bone mineralization following GH treatment in these subjects.</description><identifier>ISSN: 8756-3282</identifier><identifier>EISSN: 1873-2763</identifier><identifier>DOI: 10.1016/S8756-3282(99)00186-6</identifier><identifier>PMID: 10511119</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Adolescent ; Biological and medical sciences ; Bone ; Calcification, Physiologic - drug effects ; Calcium ; Calcium - blood ; Calcium - urine ; Child ; Child, Preschool ; Children ; Female ; Growth Hormone - pharmacology ; Growth Hormone - therapeutic use ; Hormones. Endocrine system ; Humans ; Male ; Medical sciences ; Metabolism ; Osteogenesis imperfecta (OI) ; Osteogenesis Imperfecta - drug therapy ; Osteogenesis Imperfecta - metabolism ; Osteogenesis Imperfecta - physiopathology ; Pharmacology. Drug treatments ; Stable isotopes</subject><ispartof>Bone (New York, N.Y.), 1999-10, Vol.25 (4), p.501-505</ispartof><rights>1999 Elsevier Science Inc.</rights><rights>1999 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-1a0ebf8dfc2193182631278d827dca3dfbaa50c8639df4afd567690cd5d590103</citedby><cites>FETCH-LOGICAL-c442t-1a0ebf8dfc2193182631278d827dca3dfbaa50c8639df4afd567690cd5d590103</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1961201$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10511119$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Vieira, N.E</creatorcontrib><creatorcontrib>Marini, J.C</creatorcontrib><creatorcontrib>Hopkins, E</creatorcontrib><creatorcontrib>Abrams, S.A</creatorcontrib><creatorcontrib>Yergey, A.L</creatorcontrib><title>Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV</title><title>Bone (New York, N.Y.)</title><addtitle>Bone</addtitle><description>Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day) treatment period of 1–1.5 years. Subjects were given
42Ca intravenously and
44Ca orally. The sera and urine
42Ca and
44Ca isotopic enrichments were followed over 7 days using thermal ionization mass spectrometry. The S
aam program was used to fit a three-compartment model to the tracer data. No significant differences were observed between: (1) children with type III and IV disease; or (2) baseline studies of boys and girls within each disease type. However, GH treatment significantly increased: (1) the exchangeable calcium pool (EP) in type III patients (2086 vs. 4422 mg/day,
p = 0.02); and (2) the parameter associated with bone calcium accretion in type IV patients (Vo
+: 973 vs. 1560 mg/day,
p = 0.03) with boys responding with a significantly greater increase than girls
(p = 0.008). Although not statistically significant, a trend toward an increase in Vo
+ in type III patients and in EP in type IV was observed following treatment. Our observations imply that more Ca was available for bone mineralization following GH treatment in these subjects.</description><subject>Adolescent</subject><subject>Biological and medical sciences</subject><subject>Bone</subject><subject>Calcification, Physiologic - drug effects</subject><subject>Calcium</subject><subject>Calcium - blood</subject><subject>Calcium - urine</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Female</subject><subject>Growth Hormone - pharmacology</subject><subject>Growth Hormone - therapeutic use</subject><subject>Hormones. Endocrine system</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metabolism</subject><subject>Osteogenesis imperfecta (OI)</subject><subject>Osteogenesis Imperfecta - drug therapy</subject><subject>Osteogenesis Imperfecta - metabolism</subject><subject>Osteogenesis Imperfecta - physiopathology</subject><subject>Pharmacology. Drug treatments</subject><subject>Stable isotopes</subject><issn>8756-3282</issn><issn>1873-2763</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><recordid>eNqFkD1vFDEQhq0IlByBnxDkAkVQLPjj1mtXURQFWCkSBYHW8tnjxOTW3tg-ovx7fLlToGOaKeZ5Z0YPQieUfKSEik_f5dCLjjPJ3iv1gRAqRScO0ILKgXdsEPwFWjwjR-hVKb8IIVwN9BAdUdLTVmqB0qX3YCtOHt_k9FBv8W3KU4qAawZTJ4htFrE1axs2E74LEWqwBYeIZ1NDGxf8EFoslQrpBiKUUPA4zZC3ew2-fpwBj-OITXR4_PkavfRmXeDNvh-jH58vry--dlffvowX51edXS5Z7aghsPLSecuo4lQywSkbpJNscNZw51fG9MRKwZXzS-NdLwahiHW96xWhhB-j093eOaf7DZSqp1AsrNcmQtoUPRBJ-mapgf0OtDmVksHrOYfJ5EdNid6a1k-m9VajVko_mdai5d7uD2xWE7h_Uju1DXi3B0xp-nw20Ybyl1OCMkIbdrbDoNn4HSDrYptWCy7kJlC7FP7zyR8Uiptf</recordid><startdate>19991001</startdate><enddate>19991001</enddate><creator>Vieira, N.E</creator><creator>Marini, J.C</creator><creator>Hopkins, E</creator><creator>Abrams, S.A</creator><creator>Yergey, A.L</creator><general>Elsevier Inc</general><general>Elsevier Science</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>7X8</scope></search><sort><creationdate>19991001</creationdate><title>Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV</title><author>Vieira, N.E ; Marini, J.C ; Hopkins, E ; Abrams, S.A ; Yergey, A.L</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-1a0ebf8dfc2193182631278d827dca3dfbaa50c8639df4afd567690cd5d590103</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Adolescent</topic><topic>Biological and medical sciences</topic><topic>Bone</topic><topic>Calcification, Physiologic - drug effects</topic><topic>Calcium</topic><topic>Calcium - blood</topic><topic>Calcium - urine</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Female</topic><topic>Growth Hormone - pharmacology</topic><topic>Growth Hormone - therapeutic use</topic><topic>Hormones. Endocrine system</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Metabolism</topic><topic>Osteogenesis imperfecta (OI)</topic><topic>Osteogenesis Imperfecta - drug therapy</topic><topic>Osteogenesis Imperfecta - metabolism</topic><topic>Osteogenesis Imperfecta - physiopathology</topic><topic>Pharmacology. Drug treatments</topic><topic>Stable isotopes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Vieira, N.E</creatorcontrib><creatorcontrib>Marini, J.C</creatorcontrib><creatorcontrib>Hopkins, E</creatorcontrib><creatorcontrib>Abrams, S.A</creatorcontrib><creatorcontrib>Yergey, A.L</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>MEDLINE - Academic</collection><jtitle>Bone (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Vieira, N.E</au><au>Marini, J.C</au><au>Hopkins, E</au><au>Abrams, S.A</au><au>Yergey, A.L</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV</atitle><jtitle>Bone (New York, N.Y.)</jtitle><addtitle>Bone</addtitle><date>1999-10-01</date><risdate>1999</risdate><volume>25</volume><issue>4</issue><spage>501</spage><epage>505</epage><pages>501-505</pages><issn>8756-3282</issn><eissn>1873-2763</eissn><abstract>Using a dual stable isotope technique, the effect of growth hormone (GH) on whole body calcium (Ca) metabolism was studied in children (ages 5–14 years) with type III (n = 9) and IV (n = 8) osteogenesis imperfecta. Each subject was studied twice: at baseline and following a GH (0.1–0.2 U/kg per day) treatment period of 1–1.5 years. Subjects were given
42Ca intravenously and
44Ca orally. The sera and urine
42Ca and
44Ca isotopic enrichments were followed over 7 days using thermal ionization mass spectrometry. The S
aam program was used to fit a three-compartment model to the tracer data. No significant differences were observed between: (1) children with type III and IV disease; or (2) baseline studies of boys and girls within each disease type. However, GH treatment significantly increased: (1) the exchangeable calcium pool (EP) in type III patients (2086 vs. 4422 mg/day,
p = 0.02); and (2) the parameter associated with bone calcium accretion in type IV patients (Vo
+: 973 vs. 1560 mg/day,
p = 0.03) with boys responding with a significantly greater increase than girls
(p = 0.008). Although not statistically significant, a trend toward an increase in Vo
+ in type III patients and in EP in type IV was observed following treatment. Our observations imply that more Ca was available for bone mineralization following GH treatment in these subjects.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>10511119</pmid><doi>10.1016/S8756-3282(99)00186-6</doi><tpages>5</tpages></addata></record> |
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subjects | Adolescent Biological and medical sciences Bone Calcification, Physiologic - drug effects Calcium Calcium - blood Calcium - urine Child Child, Preschool Children Female Growth Hormone - pharmacology Growth Hormone - therapeutic use Hormones. Endocrine system Humans Male Medical sciences Metabolism Osteogenesis imperfecta (OI) Osteogenesis Imperfecta - drug therapy Osteogenesis Imperfecta - metabolism Osteogenesis Imperfecta - physiopathology Pharmacology. Drug treatments Stable isotopes |
title | Effect of growth hormone treatment on calcium kinetics in patients with osteogenesis Imperfecta Type III and IV |
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