Metabolic factors influencing the efficacy of recombinant human growth hormone therapy in children with short stature

TL;DR

This study finds that metabolic factors like insulin resistance and thyroid hormone levels affect how well growth hormone therapy works in short children.

Contribution

The study identifies specific metabolic factors that predict the efficacy of rhGH therapy in children with short stature.

Findings

Higher baseline insulin resistance and lower FT3 levels correlate with reduced growth response to rhGH therapy.

Children with better metabolic profiles showed greater improvements in height standard deviation scores.

Metabolic profiling can help optimize rhGH therapy for improved growth outcomes.

Abstract

This study analyzed metabolic indicators and height gain in short-statured children within the first year of recombinant human growth hormone (rhGH) therapy, identifying predictive factors for treatment efficacy.

A retrospective analysis of 72 children with short stature (growth hormone deficiency or idiopathic short stature) receiving rhGH therapy (January 2022 to January 2024) was performed. Data included height, weight, age, skeletal age (SA), and laboratory results (IGF1, fasting glucose, insulin, C-peptide, thyroid function, lipids). Analyses focused on height standard deviation score (HSDS), HSDS for SA, and factors associated with 12-month changes in HSDS for SA (△HSDS for SA).

The mean initial rhGH dose was 0.053 ± 0.010mg/kg/day, with a mean starting age of 8.36 ± 2.24 years. Significant increases in HSDS and HSDS for SA were observed after 12 months. △HSDS for SA negatively correlated with baseline homeostasis model assessment of insulin resistance (HOMA-IR) and fasting insulin, and positively correlated with baseline free triiodothyronine (FT3). Children with △HSDS for SA>0.5 had lower baseline insulin and HOMA-IR, and higher FT3, high-density lipoprotein cholesterol (HDL), and hemoglobin.

Insulin resistance, hyperinsulinemia, FT3, and HDL determine rhGH efficacy in short-statured children. Metabolic profiling optimizes rhGH therapy, and targeting insulin resistance may improve growth outcomes.

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