Loading…

Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)

Growth hormone (GH) therapy has evolved rapidly over the past decade. Ongoing research has demonstrated a clear role for therapeutic GH in a wide spectrum of pediatric disorders involving both poor growth and abnormal body composition. Although guidelines for GH dosing are not fully established, a s...

Full description

Saved in:
Bibliographic Details
Published in:Growth hormone & IGF research 2005-07, Vol.15, p.13-20
Main Authors: Park, Patricia, Cohen, Pinchas
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33
cites cdi_FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33
container_end_page 20
container_issue
container_start_page 13
container_title Growth hormone & IGF research
container_volume 15
creator Park, Patricia
Cohen, Pinchas
description Growth hormone (GH) therapy has evolved rapidly over the past decade. Ongoing research has demonstrated a clear role for therapeutic GH in a wide spectrum of pediatric disorders involving both poor growth and abnormal body composition. Although guidelines for GH dosing are not fully established, a series of key studies has delineated the range of dosages that are useful in the treatment of children with growth disorders. The recent approval of idiopathic short stature (ISS) as an indication for GH therapy presents further challenges in optimizing the care of GH-treated patients. ISS is now recognized as a diverse collection of environmental and molecular abnormalities, some of which involve the GH–IGF axis. Emerging data indicate that serum IGF-I measurements are not only useful in the diagnosis of growth abnormalities but, in conjunction with auxological measurements, are also a powerful tool for assessing GH efficacy. While it is clear that many ISS patients respond to GH, some individuals will not show a satisfactory response. Monitoring IGF-I levels and change in height SDS during treatment can assist the physician in distinguishing those patients in whom GH successfully and safely induces statural growth from those with partial or complete GH insensitivity who might benefit from modified GH treatment protocols or alternate therapies. In addition, serum IGF-I measurements are increasingly used as part of a rational monitoring strategy to ensure safety of GH dosing in light of cumulative data associating high IGF-I levels with potential malignancy risk, and low IGF-I levels with cardiovascular disease risk.
doi_str_mv 10.1016/j.ghir.2005.06.011
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_68091359</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1096637405000638</els_id><sourcerecordid>68091359</sourcerecordid><originalsourceid>FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33</originalsourceid><addsrcrecordid>eNp9kM1u1DAURi0Eoj_wAiyQV6izSLi2M24ssakqOo1UiUVhbXnsm8ZDEg-2A-rb49FMxY6V7-J8R_Ih5AODmgGTn3f10-BjzQHWNcgaGHtFztla8Ipz0b4uNyhZSXHdnJGLlHYAoETbvCVnTIJQrRLnJHZzWkY_V6P_ifQphj95oL2xOUTa0atuc1d1KzqhSUvECeecqJ9fuCHEKcxIrzb3K5oHjGb_TENPvfNhb_LgLU2FyTRlk8u--B4fV-_Im96MCd-f3kvy4-7r99v76uHbpru9eahswyFXXDCrEKCRDTIF2HKGTrlWohFbw5zrRSPgWirD0bVGim0PYDnrmW1VY4W4JJ-O3n0MvxZMWU8-WRxHM2NYkpYtKCbWqoD8CNoYUorY6330k4nPmoE-lNY7fSitD6U1SF1Kl9HHk33ZTuj-TU5pC_DlCGD542-PUSfrcbbofESbtQv-f_6_A9COuw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>68091359</pqid></control><display><type>article</type><title>Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)</title><source>ScienceDirect Journals</source><creator>Park, Patricia ; Cohen, Pinchas</creator><creatorcontrib>Park, Patricia ; Cohen, Pinchas</creatorcontrib><description>Growth hormone (GH) therapy has evolved rapidly over the past decade. Ongoing research has demonstrated a clear role for therapeutic GH in a wide spectrum of pediatric disorders involving both poor growth and abnormal body composition. Although guidelines for GH dosing are not fully established, a series of key studies has delineated the range of dosages that are useful in the treatment of children with growth disorders. The recent approval of idiopathic short stature (ISS) as an indication for GH therapy presents further challenges in optimizing the care of GH-treated patients. ISS is now recognized as a diverse collection of environmental and molecular abnormalities, some of which involve the GH–IGF axis. Emerging data indicate that serum IGF-I measurements are not only useful in the diagnosis of growth abnormalities but, in conjunction with auxological measurements, are also a powerful tool for assessing GH efficacy. While it is clear that many ISS patients respond to GH, some individuals will not show a satisfactory response. Monitoring IGF-I levels and change in height SDS during treatment can assist the physician in distinguishing those patients in whom GH successfully and safely induces statural growth from those with partial or complete GH insensitivity who might benefit from modified GH treatment protocols or alternate therapies. In addition, serum IGF-I measurements are increasingly used as part of a rational monitoring strategy to ensure safety of GH dosing in light of cumulative data associating high IGF-I levels with potential malignancy risk, and low IGF-I levels with cardiovascular disease risk.</description><identifier>ISSN: 1096-6374</identifier><identifier>EISSN: 1532-2238</identifier><identifier>DOI: 10.1016/j.ghir.2005.06.011</identifier><identifier>PMID: 16039893</identifier><language>eng</language><publisher>Scotland: Elsevier Ltd</publisher><subject>Body Height - drug effects ; Growth Disorders - blood ; Growth Disorders - drug therapy ; Growth hormone ; Human Growth Hormone - therapeutic use ; Humans ; Idiopathic short stature ; Insulin-like growth factor binding protein 3 ; Insulin-like growth factor I ; Insulin-Like Growth Factor I - metabolism ; Monitoring ; Optimization ; Safety</subject><ispartof>Growth hormone &amp; IGF research, 2005-07, Vol.15, p.13-20</ispartof><rights>2005 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33</citedby><cites>FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16039893$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Patricia</creatorcontrib><creatorcontrib>Cohen, Pinchas</creatorcontrib><title>Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)</title><title>Growth hormone &amp; IGF research</title><addtitle>Growth Horm IGF Res</addtitle><description>Growth hormone (GH) therapy has evolved rapidly over the past decade. Ongoing research has demonstrated a clear role for therapeutic GH in a wide spectrum of pediatric disorders involving both poor growth and abnormal body composition. Although guidelines for GH dosing are not fully established, a series of key studies has delineated the range of dosages that are useful in the treatment of children with growth disorders. The recent approval of idiopathic short stature (ISS) as an indication for GH therapy presents further challenges in optimizing the care of GH-treated patients. ISS is now recognized as a diverse collection of environmental and molecular abnormalities, some of which involve the GH–IGF axis. Emerging data indicate that serum IGF-I measurements are not only useful in the diagnosis of growth abnormalities but, in conjunction with auxological measurements, are also a powerful tool for assessing GH efficacy. While it is clear that many ISS patients respond to GH, some individuals will not show a satisfactory response. Monitoring IGF-I levels and change in height SDS during treatment can assist the physician in distinguishing those patients in whom GH successfully and safely induces statural growth from those with partial or complete GH insensitivity who might benefit from modified GH treatment protocols or alternate therapies. In addition, serum IGF-I measurements are increasingly used as part of a rational monitoring strategy to ensure safety of GH dosing in light of cumulative data associating high IGF-I levels with potential malignancy risk, and low IGF-I levels with cardiovascular disease risk.</description><subject>Body Height - drug effects</subject><subject>Growth Disorders - blood</subject><subject>Growth Disorders - drug therapy</subject><subject>Growth hormone</subject><subject>Human Growth Hormone - therapeutic use</subject><subject>Humans</subject><subject>Idiopathic short stature</subject><subject>Insulin-like growth factor binding protein 3</subject><subject>Insulin-like growth factor I</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Monitoring</subject><subject>Optimization</subject><subject>Safety</subject><issn>1096-6374</issn><issn>1532-2238</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp9kM1u1DAURi0Eoj_wAiyQV6izSLi2M24ssakqOo1UiUVhbXnsm8ZDEg-2A-rb49FMxY6V7-J8R_Ih5AODmgGTn3f10-BjzQHWNcgaGHtFztla8Ipz0b4uNyhZSXHdnJGLlHYAoETbvCVnTIJQrRLnJHZzWkY_V6P_ifQphj95oL2xOUTa0atuc1d1KzqhSUvECeecqJ9fuCHEKcxIrzb3K5oHjGb_TENPvfNhb_LgLU2FyTRlk8u--B4fV-_Im96MCd-f3kvy4-7r99v76uHbpru9eahswyFXXDCrEKCRDTIF2HKGTrlWohFbw5zrRSPgWirD0bVGim0PYDnrmW1VY4W4JJ-O3n0MvxZMWU8-WRxHM2NYkpYtKCbWqoD8CNoYUorY6330k4nPmoE-lNY7fSitD6U1SF1Kl9HHk33ZTuj-TU5pC_DlCGD542-PUSfrcbbofESbtQv-f_6_A9COuw</recordid><startdate>20050701</startdate><enddate>20050701</enddate><creator>Park, Patricia</creator><creator>Cohen, Pinchas</creator><general>Elsevier Ltd</general><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>20050701</creationdate><title>Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)</title><author>Park, Patricia ; Cohen, Pinchas</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Body Height - drug effects</topic><topic>Growth Disorders - blood</topic><topic>Growth Disorders - drug therapy</topic><topic>Growth hormone</topic><topic>Human Growth Hormone - therapeutic use</topic><topic>Humans</topic><topic>Idiopathic short stature</topic><topic>Insulin-like growth factor binding protein 3</topic><topic>Insulin-like growth factor I</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Monitoring</topic><topic>Optimization</topic><topic>Safety</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Patricia</creatorcontrib><creatorcontrib>Cohen, Pinchas</creatorcontrib><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>Growth hormone &amp; IGF research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Patricia</au><au>Cohen, Pinchas</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)</atitle><jtitle>Growth hormone &amp; IGF research</jtitle><addtitle>Growth Horm IGF Res</addtitle><date>2005-07-01</date><risdate>2005</risdate><volume>15</volume><spage>13</spage><epage>20</epage><pages>13-20</pages><issn>1096-6374</issn><eissn>1532-2238</eissn><abstract>Growth hormone (GH) therapy has evolved rapidly over the past decade. Ongoing research has demonstrated a clear role for therapeutic GH in a wide spectrum of pediatric disorders involving both poor growth and abnormal body composition. Although guidelines for GH dosing are not fully established, a series of key studies has delineated the range of dosages that are useful in the treatment of children with growth disorders. The recent approval of idiopathic short stature (ISS) as an indication for GH therapy presents further challenges in optimizing the care of GH-treated patients. ISS is now recognized as a diverse collection of environmental and molecular abnormalities, some of which involve the GH–IGF axis. Emerging data indicate that serum IGF-I measurements are not only useful in the diagnosis of growth abnormalities but, in conjunction with auxological measurements, are also a powerful tool for assessing GH efficacy. While it is clear that many ISS patients respond to GH, some individuals will not show a satisfactory response. Monitoring IGF-I levels and change in height SDS during treatment can assist the physician in distinguishing those patients in whom GH successfully and safely induces statural growth from those with partial or complete GH insensitivity who might benefit from modified GH treatment protocols or alternate therapies. In addition, serum IGF-I measurements are increasingly used as part of a rational monitoring strategy to ensure safety of GH dosing in light of cumulative data associating high IGF-I levels with potential malignancy risk, and low IGF-I levels with cardiovascular disease risk.</abstract><cop>Scotland</cop><pub>Elsevier Ltd</pub><pmid>16039893</pmid><doi>10.1016/j.ghir.2005.06.011</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1096-6374
ispartof Growth hormone & IGF research, 2005-07, Vol.15, p.13-20
issn 1096-6374
1532-2238
language eng
recordid cdi_proquest_miscellaneous_68091359
source ScienceDirect Journals
subjects Body Height - drug effects
Growth Disorders - blood
Growth Disorders - drug therapy
Growth hormone
Human Growth Hormone - therapeutic use
Humans
Idiopathic short stature
Insulin-like growth factor binding protein 3
Insulin-like growth factor I
Insulin-Like Growth Factor I - metabolism
Monitoring
Optimization
Safety
title Insulin-like growth factor I (IGF-I) measurements in growth hormone (GH) therapy of idiopathic short stature (ISS)
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T05%3A22%3A55IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Insulin-like%20growth%20factor%20I%20(IGF-I)%20measurements%20in%20growth%20hormone%20(GH)%20therapy%20of%20idiopathic%20short%20stature%20(ISS)&rft.jtitle=Growth%20hormone%20&%20IGF%20research&rft.au=Park,%20Patricia&rft.date=2005-07-01&rft.volume=15&rft.spage=13&rft.epage=20&rft.pages=13-20&rft.issn=1096-6374&rft.eissn=1532-2238&rft_id=info:doi/10.1016/j.ghir.2005.06.011&rft_dat=%3Cproquest_cross%3E68091359%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c420t-231c9e00464e190e821ed9d86ea3ba1ddf3430769a2ed8a63bf00c21f1c894c33%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=68091359&rft_id=info:pmid/16039893&rfr_iscdi=true