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Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency

PURPOSE: Growth hormone (GH) plays a key role in the regulation of body composition, lipid metabolism, and quality of life in adults with GH deficiency (GHD). This study investigated changes in laboratory findings and body composition after GH recommencement for adult GHD and analyzed correlation be...

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Autores principales: Kim, Ja Hye, Cho, Ja Hyang, Yoo, Han-Wook, Choi, Jin-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Endocrinology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049546/
https://www.ncbi.nlm.nih.gov/pubmed/24926461
http://dx.doi.org/10.6065/apem.2014.19.1.32
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author Kim, Ja Hye
Cho, Ja Hyang
Yoo, Han-Wook
Choi, Jin-Ho
author_facet Kim, Ja Hye
Cho, Ja Hyang
Yoo, Han-Wook
Choi, Jin-Ho
author_sort Kim, Ja Hye
collection PubMed
description PURPOSE: Growth hormone (GH) plays a key role in the regulation of body composition, lipid metabolism, and quality of life in adults with GH deficiency (GHD). This study investigated changes in laboratory findings and body composition after GH recommencement for adult GHD and analyzed correlation between GH interruption period and endocrine or anthropometric parameters. METHODS: A total of 45 patients (17 females and 28 males) diagnosed with childhood-onset GHD (CO-GHD) were investigated and all patients had organic brain lesions. Patients diagnosed CO-GHD were retested to confirm adult GHD at age 20.4±5.0 years (18.0-32.1 years). Recombinant human GH was administered at a dose of 0.44 mg/day. Clinical and laboratory parameters such as weight, height, body mass index (BMI), serum insulin-like growth factor 1 (IGF-1), serum total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, and triglyceride levels, were compared between baseline and 12 months after treatment using paired t-test. In addition, correlation between GH interruption period and clinical parameters including BMI, lipid profile, IGF-1, and IGFBP-3, was analyzed. RESULTS: Of 45 patients, 33 patients had GH interruption period of 4.3±3.6 years (0.7-12.5 years). Serum HDL-cholesterol level increased significantly, whereas LDL-cholesterol decreased after 1 year of GH replacement therapy. However, body weight and BMI showed no significant changes after 1 year of GH replacement therapy. There were no significant correlations between GH interruption period and lipid profile or anthropometric parameters. CONCLUSION: BMI and body weight were not affected by GH replacement. However, GH replacement in adults with GHD offers benefits in lipid metabolism.
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spelling pubmed-40495462014-06-12 Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency Kim, Ja Hye Cho, Ja Hyang Yoo, Han-Wook Choi, Jin-Ho Ann Pediatr Endocrinol Metab Original Article PURPOSE: Growth hormone (GH) plays a key role in the regulation of body composition, lipid metabolism, and quality of life in adults with GH deficiency (GHD). This study investigated changes in laboratory findings and body composition after GH recommencement for adult GHD and analyzed correlation between GH interruption period and endocrine or anthropometric parameters. METHODS: A total of 45 patients (17 females and 28 males) diagnosed with childhood-onset GHD (CO-GHD) were investigated and all patients had organic brain lesions. Patients diagnosed CO-GHD were retested to confirm adult GHD at age 20.4±5.0 years (18.0-32.1 years). Recombinant human GH was administered at a dose of 0.44 mg/day. Clinical and laboratory parameters such as weight, height, body mass index (BMI), serum insulin-like growth factor 1 (IGF-1), serum total cholesterol, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, and triglyceride levels, were compared between baseline and 12 months after treatment using paired t-test. In addition, correlation between GH interruption period and clinical parameters including BMI, lipid profile, IGF-1, and IGFBP-3, was analyzed. RESULTS: Of 45 patients, 33 patients had GH interruption period of 4.3±3.6 years (0.7-12.5 years). Serum HDL-cholesterol level increased significantly, whereas LDL-cholesterol decreased after 1 year of GH replacement therapy. However, body weight and BMI showed no significant changes after 1 year of GH replacement therapy. There were no significant correlations between GH interruption period and lipid profile or anthropometric parameters. CONCLUSION: BMI and body weight were not affected by GH replacement. However, GH replacement in adults with GHD offers benefits in lipid metabolism. The Korean Society of Pediatric Endocrinology 2014-03 2014-03-31 /pmc/articles/PMC4049546/ /pubmed/24926461 http://dx.doi.org/10.6065/apem.2014.19.1.32 Text en © 2014 Annals of Pediatric Endocrinology & Metabolism http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Ja Hye
Cho, Ja Hyang
Yoo, Han-Wook
Choi, Jin-Ho
Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title_full Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title_fullStr Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title_full_unstemmed Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title_short Efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
title_sort efficacy of growth hormone therapy in adults with childhood-onset growth hormone deficiency
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4049546/
https://www.ncbi.nlm.nih.gov/pubmed/24926461
http://dx.doi.org/10.6065/apem.2014.19.1.32
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