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Updated: Sep 20, 2026

Comparative Analysis of Human Growth Hormone in Serum Using SPRi, Nano-SPRi and ELISA Assays
Published on: January 7, 2016
Treatment of growth hormone deficiency in very young children
Jean-Claude Carel1, Frédéric Huet, Jean-Louis Chaussain
1Groupe hospitalier Cochin-Saint Vincent de Paul and Faculté Cochin, Université Paris V, Paris, France. carel@cochin.inserm.fr
Insights
Growth hormone (GH) deficiency in children causes rapid height loss. GH therapy promotes catch-up growth, with injection frequency being key, though long-term outcomes require further study.
Area of Science:
- Pediatric Endocrinology
- Hormone Replacement Therapy
- Rare Childhood Diseases
Background:
- Growth hormone (GH) deficiency presents diagnostic and therapeutic challenges in young children.
- Early-onset hypopituitarism leads to significant and rapid height deceleration (loss of standard deviation scores).
Purpose of the Study:
- To review current information on GH and pituitary hormone substitution in pediatric patients with GH deficiency.
- To assess the efficacy and outcomes of growth hormone therapy in children with hypopituitarism.
Main Methods:
- Review of existing literature on growth hormone and pituitary hormone substitution in pediatric hypopituitarism.
- Analysis of auxological data, including height standard deviation scores and treatment parameters.
Main Results:
- Growth hormone therapy effectively induces rapid catch-up growth in children with hypopituitarism.
- The frequency of GH injections appears more critical for growth response than the dosage amount.
- Long-term auxological outcomes are favorable compared to historical data, though available for a limited patient cohort.
Conclusions:
- Significant progress has been made in treating early-onset severe hypopituitarism with GH therapy.
- Further research is needed to fully normalize the condition, focusing on psychological and neurodevelopmental outcomes.
- Comprehensive evaluation of long-term endocrine replacement therapies is essential for assessing final results.
Abstract:
Growth hormone (GH) deficiency is a rare disease in very young children and a challenge to the physician in terms of clinical recognition, diagnosis and treatment. Here, we review the available information regarding substitution of GH and other pituitary hormones in this patient group. Our results confirm the severity of the clinical presentation and the rapid loss of height (measured in standard deviation scores) in hypopituitary patients that occurs early in life. GH therapy induces a rapid catch-up of growth and the frequency of injections appears to be a more important determinant than the size of the dose itself. Long-term results are available in only a small percentage of patients, yet they show a favourable auxological outcome, compared with target height or historical height data from patients with severe hypopituitarism. In conclusion, although tremendous progress has been made in providing for those children with early onset and severe hypopituitarism, there is still a long way to go before we can claim that we have completely normalized their condition. In particular, careful assessments of the psychological and neurodevelopmental outcomes will become necessary in order to evaluate the 'final results' of endocrine replacement therapies.
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