Clinical characteristics and growth hormone treatment response in children with borderline versus lower peak growth hormone stimulation test responses.
The findings of this retrospective cohort study support interpreting GHST results within the broader clinical, auxological, biochemical, and body-composition context rather than relying on peak GH thresholds alone.
Abstract
Objective
Peak GH responses of 7-<10 ng/mL on growth hormone stimulation testing (GHST) represent a diagnostic grey zone in pediatric GH deficiency (GHD). Whether children in this borderline range differ clinically from those with peak GH <7 ng/mL and whether their growth response to rhGH therapy is comparable remain poorly characterized.
Methods
This retrospective cohort study included treated children with confirmed GHD who had available first-year growth velocity data and were categorized as Group 1 (peak GH <7 ng/mL, n = 121) and Group 2 (peak GH 7-<10 ng/mL, n = 74) at King Abdulaziz University Hospital between 2014 and 2022. Baseline characteristics, first- and second-year growth velocities, and Spearman correlations between peak GH, BMI SDS, and growth velocity were analyzed.
Results
Group 1 had higher BMI (median 16.1 vs 15.0 kg/m2, P < 0.001) and lower IGF-1 SDS (median - 1.4 vs -1.0, P = 0.047). First-year growth velocity did not differ significantly between groups (7.5 vs 7.3 cm/year, P = 0.417), nor did second-year growth velocity (7.0 vs 6.5 cm/year, P = 0.534). Peak GH did not correlate with first-year growth velocity (Spearman's ρ = -0.027, P = 0.746) and was not an independent predictor on multivariable regression (adjusted β = -0.59, P = 0.174).
Conclusion
Peak GH level was not associated with first-year rhGH treatment response in children with confirmed GHD. These findings support interpreting GHST results within the broader clinical, auxological, biochemical, and body-composition context rather than relying on peak GH thresholds alone.
Growth hormone deficiency (GHD) is an important endocrine cause of short stature in childhood, occurring in approximately 1 in 4,000–10,000 live births. Early diagnosis and treatment are critical for achieving optimal height growth. This study was designed to identify factors influencing early growth response to recomb...
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OBJECTIVE
To evaluate real-world auxological and biochemical outcomes in children and adolescents with isolated growth hormone deficiency (GHD) who transitioned from daily recombinant human growth hormone to once-weekly somatrogon.
DESIGN
Single-centre retrospective observational study.
METHODS
Seventy-three paedia...
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OBJECTIVE
Growth hormone neurosecretory dysfunction (NSD) is a clinical condition characterized by impaired spontaneous, particularly nocturnal, growth hormone (GH) secretion despite a normal response to pharmacological GH stimulation tests. This study aimed to compare overnight GH secretion patterns between children w...
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