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Updated: May 2, 2026

Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Measuring growth hormone and insulin-like growth factor-I in infants: what is normal?
Colin Patrick Hawkes1, Adda Grimberg1
1Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Insights
Growth hormone (GH) and insulin-like growth factor-I (IGF-I) are crucial for infant growth. Understanding normal GH/IGF-I axis physiology in infants under 18 months is essential for interpreting growth patterns.
Area of Science:
- Pediatric Endocrinology
- Growth Hormone Physiology
- Neonatal Development
Background:
- Growth hormone (GH) and insulin-like growth factor-I (IGF-I) play vital roles in fetal and infant development.
- Isolated GH deficiency in infancy may present with hypoglycemia, despite normal birth measurements.
- The GH/IGF-I axis undergoes significant changes during early childhood.
Purpose of the Study:
- To review the normal physiology of the GH/IGF-I axis in infants.
- To provide context for interpreting GH and IGF-I measurements in this age group.
- To highlight variations in assay-specific measurements and their limitations.
Main Methods:
- Literature review of studies on GH and IGF-I secretion in children under 18 months.
- Analysis of normal physiological patterns of GH and IGF-I.
- Examination of assay methodologies and their impact on results.
Main Results:
- GH and IGF-I roles evolve significantly from fetal to postnatal life.
- Hypoglycemia can be an early sign of GH deficiency in infants.
- Assay variations necessitate careful interpretation of GH and IGF-I levels.
Conclusions:
- Understanding infant GH/IGF-I axis physiology is critical for accurate diagnosis.
- Interpreting GH and IGF-I measurements requires consideration of assay limitations.
- This review synthesizes current knowledge on normal GH/IGF-I secretion in early infancy.
Abstract:
The role of growth hormone (GH) and insulinlike growth factor-I (IGF-I) change through early childhood. Whereas poor growth is a later presenting feature, infants with isolated GH deficiency have a normal birth weight and length, and often present with hypoglycemia. IGF-I plays an important role antenatally and post-natally in somatic and brain growth. In order to evaluate the GH/IGF-I axis in infancy, an understanding of the normal physiology is required. Measurements of GH and IGF-I in this population should be interpreted in the context of the assays used, as well as their limitations. In this review, we summarize our current understanding of normal GH and IGF-I secretion in children under 18 months of age, and describe variations in the reported assay-specific measurements.
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