Clinical Indications for Growth Hormone Therapy
- PMID: 35985710
- PMCID: PMC9754707
- DOI: 10.1016/j.yapd.2022.03.005
Clinical Indications for Growth Hormone Therapy
Abstract
Growth hormone (GH) is an injectable medication originally used to replace the deficiency of the hormone, but has expanded to treating conditions that may reduce growth and adult height even when the body maintains endogenous GH production. In the United States, there are 8 Food and Drug Administration (FDA)-approved indications for pediatric GH therapy: GH deficiency, Prader-Willi Syndrome, small for gestational age (SGA) without catch-up growth, idiopathic short stature, Turner syndrome, SHOX gene haploinsufficiency, Noonan Syndrome, and chronic renal insufficiency. We characterize the growth patterns and effects of GH treatment in each of these indications. We also review patterns of growth that warrant referral to a pediatric endocrinologist, as well as safety updates. This review is intended to guide practitioners on the initial evaluation and management of patients with short stature, and the indications for GH therapy.
Keywords: Growth; Growth hormone; Growth hormone deficiency; Idiopathic short stature; Prader–Willi syndrome; Short stature; Turner syndrome.
Copyright © 2022 Elsevier Inc. All rights reserved.
Conflict of interest statement
Disclosure A. Grimberg received the 2020 Growth Hormone Research Competitive Grant Program Award from Pfizer. M. Danowitz has nothing to disclose.
References
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- Grimberg A, DiVall SA, Polychronakos C, et al. Guidelines for Growth Hormone and Insulin-like Growth Factor-1 Treatment in Children Children and Adolescents: Growth Hormone Deficiency, Idiopathic Short Stature, and Primary Insulin-like Growth Factor-1 Deficiency. Horm Res Paediatr 2016;86(6):361–397. - PubMed
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- Lanes R, Soros A, Gunczler P, et al. Growth hormone deficiency, low levels of adiponectin, and unfavorable plasma lipid and lipoproteins. Journal Pediatr 2006;149(3): 324–329. - PubMed
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