Bioactive IGF-I Concentrations in Children on GH Therapy
Authors:
- Lea VilmannLVLea Vilmann
- Jakob AlbrethsenJAJakob Albrethsen
- Jørgen Holm PetersenJPJørgen Holm Petersen
- Stine Agergaard HolmboeSHStine Agergaard Holmboe
- Katharina Maria MainKMKatharina Maria Main
- Line CleemannLCLine Cleemann
- Kristian Horsman HansenKHKristian Horsman Hansen
- Jan FrystykJFJan Frystyk
- Casper P HagenCHCasper P Hagen
- Anders JuulAJAnders Juul
Open Access
- 14 October 2025
- journal article
- Published by The Endocrine Society in The Journal of Clinical Endocrinology & Metabolism
- Vol. 111 (4) , 1021-1030
Abstract
Background: Monitoring IGF-I concentration is recommended during GH therapy in children. Supranormal levels of total IGF-I have raised concerns of long-term risks. Aim: To evaluate bioactive and total IGF-I in healthy and in GH-treated children and adolescents. Materials and methods: A reference population of 570 children (59% girls) from the Copenhagen Puberty Study III and 126 short children (36% girls) with GH deficiency (GHD) and other non-GHD conditions. We established pediatric, sex-specific reference ranges of serum concentrations of bioactive IGF-I (KIRA) and compared with total IGF-I and IGF-I/IGFBP-3 molar ratio (iSYS) and total IGF-I, -II, IGFBP-3, and acid labile subunit (liquid chromatography-tandem mass spectrometry) in a subgroup. Further, we compared IGF-I bioactivity with total IGF-I, IGFBP-3 (iSYS) and IGF-I/IGFBP-3 molar ratio during GH therapy. Results: Bioactive IGF-I increased with age in healthy children and correlated positively with total IGF-I and IGF-I/IGFBP-3 in healthy males (r = 0.61 and r = 0.57; P < .001) and females (r = 0.58 and r = 0.59; P < .001) and with IGF-I, BP-3, and acid labile subunit (liquid chromatography-tandem mass spectrometry) (r = 0.56, r = 0.29, and r = 0.38; P < .001). Bioactive IGF-I and IGF-II (r = -0.29; P < .001) correlated negatively. In 13% (17/126) of the patients, bioactive IGF-I was above +2SD, whereas total IGF-I was above +2SD in 25% (32/126) patients. Nine patients had both total and bioactive IGF-I above +2SD. In the non-GHD groups, bioactive IGF-I SDS were lower than IGF-I SDS (P = .015). Conclusion: Bioactive IGF-I was within reference ranges in the majority of GH-treated children. Monitoring bioactive IGF-I may help optimize GH dosing in specific patient subgroups.Keywords
Funding Information
- Kirsten og Freddy Johansens Fond (F-22717-55)
- Novo Nordisk Foundation Center for Protein Research, University of Copenhagen (F-22717-51)
- Centre on Endocrine Disruptors
- Miljøstyrelsen (MST-611-00012)
- OPEN Lab
- Department of Endocrinology
- Odense Universitetshospital
- Forschungsrat des Kantonsspitals Aarau
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