Insulin sensitivity in growth hormone-deficient children: influence of replacement treatment

Summary objective  In adults, excessive GH secretion may lead to secondary diabetes mellitus, while prolonged GH treatment may accelerate the onset of type 2 diabetes mellitus in predisposed children. The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group...

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Veröffentlicht in:Clinical endocrinology (Oxford) 2004-10, Vol.61 (4), p.473-477
Hauptverfasser: Radetti, Giorgio, Pasquino, Bruno, Gottardi, Elena, Contadin, Isabella Boscolo, Rigon, Franco, Aimaretti, Gianluca
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container_end_page 477
container_issue 4
container_start_page 473
container_title Clinical endocrinology (Oxford)
container_volume 61
creator Radetti, Giorgio
Pasquino, Bruno
Gottardi, Elena
Contadin, Isabella Boscolo
Rigon, Franco
Aimaretti, Gianluca
description Summary objective  In adults, excessive GH secretion may lead to secondary diabetes mellitus, while prolonged GH treatment may accelerate the onset of type 2 diabetes mellitus in predisposed children. The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group of GH‐deficient children treated with GH for a period of 6 years. patients and design  One hundred and twenty‐eight children (40 females, 88 males) were included in the study. At the beginning of treatment chronological age was 8·9 ± 3·2 years, height standard deviation score (SDS) −2·43 ± 0·90 and body mass index (BMI) SDS 0·18 ± 1·60. At the end of the study chronological age was 13·0 ± 2·9 years, height SDS −1·24 ± 1·27 and BMI SDS 0·23 ± 1·54. GH was administered at a mean weekly dosage of 0·3 mg/kg, injected subcutaneously over 6–7 days. GT was assessed according to the criteria of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. IS was evaluated with the quantitative insulin sensitivity check index (QUICKI). results  No cases of impaired GT or diabetes were recorded during the follow‐up period. IS, already lower than in controls before starting treatment with GH, decreased significantly during the first year of therapy (QUICKI: 0·346 ± 0·033 vs. 0·355 ± 0·044, P 
doi_str_mv 10.1111/j.1365-2265.2004.02113.x
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The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group of GH‐deficient children treated with GH for a period of 6 years. patients and design  One hundred and twenty‐eight children (40 females, 88 males) were included in the study. At the beginning of treatment chronological age was 8·9 ± 3·2 years, height standard deviation score (SDS) −2·43 ± 0·90 and body mass index (BMI) SDS 0·18 ± 1·60. At the end of the study chronological age was 13·0 ± 2·9 years, height SDS −1·24 ± 1·27 and BMI SDS 0·23 ± 1·54. GH was administered at a mean weekly dosage of 0·3 mg/kg, injected subcutaneously over 6–7 days. GT was assessed according to the criteria of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. IS was evaluated with the quantitative insulin sensitivity check index (QUICKI). results  No cases of impaired GT or diabetes were recorded during the follow‐up period. IS, already lower than in controls before starting treatment with GH, decreased significantly during the first year of therapy (QUICKI: 0·346 ± 0·033 vs. 0·355 ± 0·044, P &lt; 0·05), with no further decrease in the following years. No correlation was found between QUICKI, BMI, years of treatment and onset of puberty. conclusions  GH treatment in GH‐deficient children does not lead to an impaired GT or type 2 diabetes mellitus, although it does significantly decrease IS.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/j.1365-2265.2004.02113.x</identifier><identifier>PMID: 15473880</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Science Ltd</publisher><subject>Biological and medical sciences ; Blood Glucose - analysis ; Case-Control Studies ; Chi-Square Distribution ; Child ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. 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The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group of GH‐deficient children treated with GH for a period of 6 years. patients and design  One hundred and twenty‐eight children (40 females, 88 males) were included in the study. At the beginning of treatment chronological age was 8·9 ± 3·2 years, height standard deviation score (SDS) −2·43 ± 0·90 and body mass index (BMI) SDS 0·18 ± 1·60. At the end of the study chronological age was 13·0 ± 2·9 years, height SDS −1·24 ± 1·27 and BMI SDS 0·23 ± 1·54. GH was administered at a mean weekly dosage of 0·3 mg/kg, injected subcutaneously over 6–7 days. GT was assessed according to the criteria of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. IS was evaluated with the quantitative insulin sensitivity check index (QUICKI). results  No cases of impaired GT or diabetes were recorded during the follow‐up period. IS, already lower than in controls before starting treatment with GH, decreased significantly during the first year of therapy (QUICKI: 0·346 ± 0·033 vs. 0·355 ± 0·044, P &lt; 0·05), with no further decrease in the following years. No correlation was found between QUICKI, BMI, years of treatment and onset of puberty. conclusions  GH treatment in GH‐deficient children does not lead to an impaired GT or type 2 diabetes mellitus, although it does significantly decrease IS.</description><subject>Biological and medical sciences</subject><subject>Blood Glucose - analysis</subject><subject>Case-Control Studies</subject><subject>Chi-Square Distribution</subject><subject>Child</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. 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Psychology</topic><topic>Glucose Tolerance Test</topic><topic>Growth Hormone - deficiency</topic><topic>Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>Insulin - blood</topic><topic>Insulin Resistance</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Radetti, Giorgio</creatorcontrib><creatorcontrib>Pasquino, Bruno</creatorcontrib><creatorcontrib>Gottardi, Elena</creatorcontrib><creatorcontrib>Contadin, Isabella Boscolo</creatorcontrib><creatorcontrib>Rigon, Franco</creatorcontrib><creatorcontrib>Aimaretti, Gianluca</creatorcontrib><collection>Istex</collection><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 &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Radetti, Giorgio</au><au>Pasquino, Bruno</au><au>Gottardi, Elena</au><au>Contadin, Isabella Boscolo</au><au>Rigon, Franco</au><au>Aimaretti, Gianluca</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin sensitivity in growth hormone-deficient children: influence of replacement treatment</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol (Oxf)</addtitle><date>2004-10</date><risdate>2004</risdate><volume>61</volume><issue>4</issue><spage>473</spage><epage>477</epage><pages>473-477</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>Summary objective  In adults, excessive GH secretion may lead to secondary diabetes mellitus, while prolonged GH treatment may accelerate the onset of type 2 diabetes mellitus in predisposed children. The aim of the study was to evaluate insulin sensitivity (IS) and glucose tolerance (GT) in a group of GH‐deficient children treated with GH for a period of 6 years. patients and design  One hundred and twenty‐eight children (40 females, 88 males) were included in the study. At the beginning of treatment chronological age was 8·9 ± 3·2 years, height standard deviation score (SDS) −2·43 ± 0·90 and body mass index (BMI) SDS 0·18 ± 1·60. At the end of the study chronological age was 13·0 ± 2·9 years, height SDS −1·24 ± 1·27 and BMI SDS 0·23 ± 1·54. GH was administered at a mean weekly dosage of 0·3 mg/kg, injected subcutaneously over 6–7 days. GT was assessed according to the criteria of the Expert Committee on the Diagnosis and Classification of Diabetes Mellitus. IS was evaluated with the quantitative insulin sensitivity check index (QUICKI). results  No cases of impaired GT or diabetes were recorded during the follow‐up period. IS, already lower than in controls before starting treatment with GH, decreased significantly during the first year of therapy (QUICKI: 0·346 ± 0·033 vs. 0·355 ± 0·044, P &lt; 0·05), with no further decrease in the following years. No correlation was found between QUICKI, BMI, years of treatment and onset of puberty. conclusions  GH treatment in GH‐deficient children does not lead to an impaired GT or type 2 diabetes mellitus, although it does significantly decrease IS.</abstract><cop>Oxford, UK</cop><pub>Blackwell Science Ltd</pub><pmid>15473880</pmid><doi>10.1111/j.1365-2265.2004.02113.x</doi><tpages>5</tpages></addata></record>
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subjects Biological and medical sciences
Blood Glucose - analysis
Case-Control Studies
Chi-Square Distribution
Child
Endocrinopathies
Female
Fundamental and applied biological sciences. Psychology
Glucose Tolerance Test
Growth Hormone - deficiency
Growth Hormone - therapeutic use
Humans
Insulin - blood
Insulin Resistance
Male
Medical sciences
Vertebrates: endocrinology
title Insulin sensitivity in growth hormone-deficient children: influence of replacement treatment
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