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IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal
A number of studies have evaluated the role of IGF1 measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate the accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two child...
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Published in: | Endocrine Connections 2020-11, Vol.9 (11), p.1095-1102 |
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creator | Ibba, Anastasia Corrias, Francesca Guzzetti, Chiara Casula, Letizia Salerno, Mariacarolina di Iorgi, Natascia Tornese, Gianluca Patti, Giuseppa Radetti, Giorgio Maghnie, Mohamad Cappa, Marco Loche, Sandro |
description | A number of studies have evaluated the role of IGF1 measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate the accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two children and adolescents with GHD ((63 organic/genetic (OGHD), 79 idiopathic (IGHD)) and 658 short non-GHD children (median age 10.4 years) were included in the analysis. The two groups were subdivided according to age (G1 |
doi_str_mv | 10.1530/EC-20-0347 |
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This study aimed to evaluate the accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two children and adolescents with GHD ((63 organic/genetic (OGHD), 79 idiopathic (IGHD)) and 658 short non-GHD children (median age 10.4 years) were included in the analysis. The two groups were subdivided according to age (G1 <6, G2 6 <9, G3 9 <12, G4 ≥12) and to pubertal status. Serum IGFI was measured by the same chemiluminescence assay in all samples and expressed as age- and sex-based SDS. Receiver operating characteristic (ROC) analysis was used to evaluate the optimal IGF1 SDS cut-off and the diagnostic accuracy. Median IGF1 SDS was significantly lower in the GHD than in non-GHD patients. The area under the curve (AUC) was 0.69, with the best IGF1 cut-off of −1.5 SDS (sensitivity 67.61%, specificity 62.62%). The AUC was 0.75 for OGHD and 0.63 for IGHD. The accuracy was better in the pubertal (AUC = 0.81) than the prepubertal group (AUC = 0.64). In our cohort, IGF1 measurement has poor accuracy in discriminating GHD from non-GHD. Our findings confirm and reinforce the belief that IGF1 values should not be used alone in the diagnosis of GHD but should be interpreted in combination with other clinical and biochemical parameters.</description><identifier>ISSN: 2049-3614</identifier><identifier>EISSN: 2049-3614</identifier><identifier>DOI: 10.1530/EC-20-0347</identifier><identifier>PMID: 33112822</identifier><language>eng</language><publisher>England: Bioscientifica Ltd</publisher><subject>adolescents ; children ; growth hormone deficiency ; insulin-like growth factor 1 ; short stature</subject><ispartof>Endocrine Connections, 2020-11, Vol.9 (11), p.1095-1102</ispartof><rights>2020 The authors</rights><rights>2020 The authors 2020 The authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b551t-e9e007f9d51f61206c5194c9534116afc12c3951ce1a2cc4e3ae6a3498bc17453</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774770/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7774770/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33112822$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ibba, Anastasia</creatorcontrib><creatorcontrib>Corrias, Francesca</creatorcontrib><creatorcontrib>Guzzetti, Chiara</creatorcontrib><creatorcontrib>Casula, Letizia</creatorcontrib><creatorcontrib>Salerno, Mariacarolina</creatorcontrib><creatorcontrib>di Iorgi, Natascia</creatorcontrib><creatorcontrib>Tornese, Gianluca</creatorcontrib><creatorcontrib>Patti, Giuseppa</creatorcontrib><creatorcontrib>Radetti, Giorgio</creatorcontrib><creatorcontrib>Maghnie, Mohamad</creatorcontrib><creatorcontrib>Cappa, Marco</creatorcontrib><creatorcontrib>Loche, Sandro</creatorcontrib><title>IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal</title><title>Endocrine Connections</title><addtitle>Endocr Connect</addtitle><description>A number of studies have evaluated the role of IGF1 measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate the accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two children and adolescents with GHD ((63 organic/genetic (OGHD), 79 idiopathic (IGHD)) and 658 short non-GHD children (median age 10.4 years) were included in the analysis. The two groups were subdivided according to age (G1 <6, G2 6 <9, G3 9 <12, G4 ≥12) and to pubertal status. Serum IGFI was measured by the same chemiluminescence assay in all samples and expressed as age- and sex-based SDS. Receiver operating characteristic (ROC) analysis was used to evaluate the optimal IGF1 SDS cut-off and the diagnostic accuracy. Median IGF1 SDS was significantly lower in the GHD than in non-GHD patients. The area under the curve (AUC) was 0.69, with the best IGF1 cut-off of −1.5 SDS (sensitivity 67.61%, specificity 62.62%). The AUC was 0.75 for OGHD and 0.63 for IGHD. The accuracy was better in the pubertal (AUC = 0.81) than the prepubertal group (AUC = 0.64). In our cohort, IGF1 measurement has poor accuracy in discriminating GHD from non-GHD. Our findings confirm and reinforce the belief that IGF1 values should not be used alone in the diagnosis of GHD but should be interpreted in combination with other clinical and biochemical parameters.</description><subject>adolescents</subject><subject>children</subject><subject>growth hormone deficiency</subject><subject>insulin-like growth factor 1</subject><subject>short stature</subject><issn>2049-3614</issn><issn>2049-3614</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNp9kc9rFDEUx4MotrS9-AdIjiKM5uXHJONBkGVbFwq92GvD20yykzI7WZNZpf-9WbeW9mIueeR9-LwkX0LeAfsESrDPy0XDWcOE1K_IKWeya0QL8vWz-oRclHLP6jLQGsHekhMhALjh_JTcra4ugYaU6Tx42kfcTKnEQlOgm5x-zwMdUt6mqfZ8iC76yT3QOFE3xLHPfqI49RT7NPri_DSXLxRp9rjbZYwFx3PyJuBY_MXjfkZuL5c_Ft-b65ur1eLbdbNWCubGd54xHbpeQWiBs9Yp6KTrlJAALQYH3IlOgfOA3DnpBfoWhezM2oGWSpyR1dHbJ7y3uxy3mB9swmj_HqS8sZjn6EZv0SnTtdK4XjpZK-yhFUGb6qyjA1bX16Nrt19vfX94VsbxhfRlZ4qD3aRfVmsttWZV8OFRkNPPvS-z3cb6O-OIk0_7YrlUykhpjKzoxyPqciol-_A0Bpg95GuXC8uZPeRb4ffPL_aE_kuzAuwIrGMqh6zmWDPD_zn_AD33r6M</recordid><startdate>20201101</startdate><enddate>20201101</enddate><creator>Ibba, Anastasia</creator><creator>Corrias, Francesca</creator><creator>Guzzetti, Chiara</creator><creator>Casula, Letizia</creator><creator>Salerno, Mariacarolina</creator><creator>di Iorgi, Natascia</creator><creator>Tornese, Gianluca</creator><creator>Patti, Giuseppa</creator><creator>Radetti, Giorgio</creator><creator>Maghnie, Mohamad</creator><creator>Cappa, Marco</creator><creator>Loche, Sandro</creator><general>Bioscientifica Ltd</general><general>Bioscientifica</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20201101</creationdate><title>IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal</title><author>Ibba, Anastasia ; Corrias, Francesca ; Guzzetti, Chiara ; Casula, Letizia ; Salerno, Mariacarolina ; di Iorgi, Natascia ; Tornese, Gianluca ; Patti, Giuseppa ; Radetti, Giorgio ; Maghnie, Mohamad ; Cappa, Marco ; Loche, Sandro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b551t-e9e007f9d51f61206c5194c9534116afc12c3951ce1a2cc4e3ae6a3498bc17453</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>adolescents</topic><topic>children</topic><topic>growth hormone deficiency</topic><topic>insulin-like growth factor 1</topic><topic>short stature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ibba, Anastasia</creatorcontrib><creatorcontrib>Corrias, Francesca</creatorcontrib><creatorcontrib>Guzzetti, Chiara</creatorcontrib><creatorcontrib>Casula, Letizia</creatorcontrib><creatorcontrib>Salerno, Mariacarolina</creatorcontrib><creatorcontrib>di Iorgi, Natascia</creatorcontrib><creatorcontrib>Tornese, Gianluca</creatorcontrib><creatorcontrib>Patti, Giuseppa</creatorcontrib><creatorcontrib>Radetti, Giorgio</creatorcontrib><creatorcontrib>Maghnie, Mohamad</creatorcontrib><creatorcontrib>Cappa, Marco</creatorcontrib><creatorcontrib>Loche, Sandro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Endocrine Connections</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ibba, Anastasia</au><au>Corrias, Francesca</au><au>Guzzetti, Chiara</au><au>Casula, Letizia</au><au>Salerno, Mariacarolina</au><au>di Iorgi, Natascia</au><au>Tornese, Gianluca</au><au>Patti, Giuseppa</au><au>Radetti, Giorgio</au><au>Maghnie, Mohamad</au><au>Cappa, Marco</au><au>Loche, Sandro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal</atitle><jtitle>Endocrine Connections</jtitle><addtitle>Endocr Connect</addtitle><date>2020-11-01</date><risdate>2020</risdate><volume>9</volume><issue>11</issue><spage>1095</spage><epage>1102</epage><pages>1095-1102</pages><issn>2049-3614</issn><eissn>2049-3614</eissn><abstract>A number of studies have evaluated the role of IGF1 measurement in the diagnosis of growth hormone deficiency (GHD). This study aimed to evaluate the accuracy and the best cut-off of IGF1 SDS in the diagnosis of GHD in a large cohort of short children and adolescents. One-hundred and forty-two children and adolescents with GHD ((63 organic/genetic (OGHD), 79 idiopathic (IGHD)) and 658 short non-GHD children (median age 10.4 years) were included in the analysis. The two groups were subdivided according to age (G1 <6, G2 6 <9, G3 9 <12, G4 ≥12) and to pubertal status. Serum IGFI was measured by the same chemiluminescence assay in all samples and expressed as age- and sex-based SDS. Receiver operating characteristic (ROC) analysis was used to evaluate the optimal IGF1 SDS cut-off and the diagnostic accuracy. Median IGF1 SDS was significantly lower in the GHD than in non-GHD patients. The area under the curve (AUC) was 0.69, with the best IGF1 cut-off of −1.5 SDS (sensitivity 67.61%, specificity 62.62%). The AUC was 0.75 for OGHD and 0.63 for IGHD. The accuracy was better in the pubertal (AUC = 0.81) than the prepubertal group (AUC = 0.64). In our cohort, IGF1 measurement has poor accuracy in discriminating GHD from non-GHD. Our findings confirm and reinforce the belief that IGF1 values should not be used alone in the diagnosis of GHD but should be interpreted in combination with other clinical and biochemical parameters.</abstract><cop>England</cop><pub>Bioscientifica Ltd</pub><pmid>33112822</pmid><doi>10.1530/EC-20-0347</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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title | IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal |
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