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Vitamin D in children with growth hormone deficiency due to pituitary stalk interruption syndrome
Cécile Delecroix1, Raja Brauner2, Jean-Claude Souberbielle3
1Fondation Ophtalmologique Adolphe de Rothschild and Université Paris Descartes, Paris, France.
Insights
This study found that vitamin D levels in children with growth hormone (GH) deficiency due to pituitary stalk interruption syndrome (PSIS) are similar to healthy children. A positive correlation exists between GH peak and vitamin D metabolites, suggesting an interplay between the GH/IGF1 axis and vitamin D.
Area of Science:
- Pediatric Endocrinology
- Nutritional Biochemistry
- Endocrine Disorders
Background:
- Emerging evidence links vitamin D status with growth hormone (GH) and insulin-like growth factor 1 (IGF1) levels.
- Pituitary stalk interruption syndrome (PSIS) is a cause of GH deficiency in children.
Purpose of the Study:
- To evaluate vitamin D status in children with PSIS.
- To explore the relationship between 25-hydroxyvitamin D (25OHD) and 1,25-dihydroxyvitamin D (1,25(OH)2D) serum levels and patient characteristics in this cohort.
Main Methods:
- A retrospective single-center study analyzed 25OHD and 1,25(OH)2D serum concentrations.
- Data were collected from 50 children diagnosed with PSIS before initiating treatment.
Main Results:
- Mean 25OHD was 33.2 ± 18.0 ng/mL and mean 1,25(OH)2D was 74.5 ± 40.7 ng/L.
- 25OHD levels were higher in boys and during sunny seasons.
- Significant positive correlations were found between GH peak and 1,25(OH)2D levels (p=0.015) and the 1,25(OH)2D/25OHD ratio (p<0.05).
Conclusions:
- Vitamin D status in children with PSIS is comparable to healthy populations.
- Despite impaired GH secretion and low IGF1, a significant interplay between the GH/IGF1 axis and vitamin D system persists in children with PSIS.
Background:
Recent studies have shown a relationship between vitamin D status and growth hormone (GH) and insulin-like growth factor 1 (IGF1). The objective of this study was to assess vitamin D status in children with GH deficiency due to pituitary stalk interruption syndrome (PSIS) and to investigate the relationship between 25-hydroxyvitamin D (25OHD) and 1,25-dihydroxyvitamin D (1,25 (OH) 2D) serum levels and patient characteristics.
Methods:
A retrospective single-center study of 25OHD and 1,25(OH)2D serum concentrations in 50 children with PSIS at the initial evaluation before treatment.
Results:
Mean concentrations of 33.2 ± 18.0 ng/mL for 25OHD and 74.5 ± 40.7 ng/L for 1,25(OH)2D were measured. Additionally, 25OHD concentrations were significantly higher in boys than in girls (p = 0.04) and lower in the cold season than in the sunny season (p = 0.03). Significant positive correlations were observed between the GH peak and serum 1,25 (OH) 2D concentrations (Rho = 0.35; p = 0.015) and the 1,25(OH)2D/25OHD ratio (Rho = 0.29; p < 0.05). No correlation was found for other characteristics, including IGF1.
Conclusions:
Vitamin D status in children with hypothalamic-pituitary deficiency due to PSIS was similar to that reported in national and European studies in healthy children. The positive significant correlations between the GH peak and the 1,25 (OH)2D concentration as well as with the 1,25 (OH)2D/25OHD ratio suggest that even in these patients who had severely impaired GH secretion and low IGF1 levels, an interplay between the GH/IGF1 axis and the vitamin D system still exists.
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