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Fecal Glucocorticoid Analysis: Non-invasive Adrenal Monitoring in Equids
Published on: April 25, 2016
Children with organic growth hormone deficiency have elevated cortisol responses to stimuli
J W Finkelstein1, D E Rusovici, E Green
1Department of Biobehavioral Health, College of Health and Human Development, The Pennsylvania State University, University Park, Pennsylvania 16802, USA. jwf3@psu.edu
Insights
Children with organic growth hormone (GH) deficiency often show hypothalamic-pituitary-adrenal (HPA) axis dysregulation. Idiopathic GH deficiency or no GH deficiency did not present with significant HPA axis differences.
Area of Science:
- Pediatric Endocrinology
- Neuroendocrinology
- HPA Axis Function
Background:
- Growth hormone (GH) deficiency is a condition affecting childhood development.
- The hypothalamic-pituitary-adrenal (HPA) axis plays a crucial role in stress response and metabolism.
- Understanding HPA axis function in GH-deficient children is essential for comprehensive care.
Purpose of the Study:
- To investigate the function of the hypothalamic-pituitary-adrenal (HPA) axis in children diagnosed with GH deficiency.
- To compare HPA axis function across different categories of GH deficiency: organic, idiopathic, and non-deficient.
Main Methods:
- Evaluated 94 children for GH and cortisol (F) deficiency.
- Utilized clinical criteria and stimulation tests (L-dopa, insulin-induced hypoglycemia).
- Employed time series, cross-sectional, and regression analyses.
Main Results:
- Children with organic GH deficiency (OGHD) exhibited significantly elevated cortisol levels compared to the non-GH-deficient (NGHD) group.
- Cortisol levels in the idiopathic GH deficient (IGHD) group were not significantly different from the NGHD group.
- HPA axis dysregulation was prevalent in OGHD but less common in IGHD and NGHD.
Conclusions:
- HPA axis dysregulation is a common finding in children with organic GH deficiency.
- HPA axis dysfunction is less frequently observed in children with idiopathic GH deficiency or without GH deficiency.
- Anatomical disruption or stress may contribute to HPA axis dysregulation in OGHD.
Abstract:
The aim of this study was to investigate hypothalamic-pituitary-adrenal (HPA) function in children with GH deficiency. Ninety-four patients were evaluated for GH deficiency and cortisol (F) deficiency using clinical criteria and L-dopa and insulin-induced hypoglycemia stimulation tests. They were assigned to three diagnostic groups: organic GH deficient (OGHD), idiopathic GH deficient (IGHD), and not GH-deficient (NGHD). Time series, cross-sectional, regression analysis revealed statistically significantly elevated F [>828 nmol/L (30 microg/dL)] in the OGHD group vs. the NGHD group. The value for F in the IGHD group was not different from the NGHD group. This finding suggests that dysregulation of the HPA axis is present in most children with OGH deficiency and significantly less often in children with IGH deficiency or without GH deficiency. Anatomical disruption of the control pathways for the HPA axis or stress may cause the dysregulation.
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