{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,10]],"date-time":"2026-03-10T05:20:38Z","timestamp":1773120038980,"version":"3.50.1"},"reference-count":37,"publisher":"S. Karger AG","license":[{"start":{"date-parts":[[2026,1,23]],"date-time":"2026-01-23T00:00:00Z","timestamp":1769126400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"},{"start":{"date-parts":[[2026,1,23]],"date-time":"2026-01-23T00:00:00Z","timestamp":1769126400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/karger.com\/pages\/terms-and-conditions"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Horm Res Paediatr"],"abstract":"<jats:p>Introduction: Long-term glucocorticoid (GC) therapy is a leading cause of growth retardation in children with chronic renal and rheumatic diseases. While recombinant human growth hormone (rhGH) is used to counteract these effects, its efficacy relative to spontaneous catch-up growth following GC withdrawal remains inadequately quantified. This study aimed to compare the efficacy of rhGH treatment against spontaneous catch-up growth in children with GC-induced short stature. Methods: This retrospective, non-randomized controlled study was conducted at a single tertiary children\u2019s hospital, including patients treated between 2010 and 2020. We established a treatment group of 34 children (23 with nephrotic syndrome [NS]) with GC-induced short stature who received rhGH therapy (0.15\u20130.2 IU\/kg\/day, approx. 0.05\u20130.067 mg\/kg\/day) for at least 1 year. A historical control group comprised 20 children with NS who exhibited short stature after GC cessation and were monitored for spontaneous catch-up growth for 6\u201312 months. The primary outcome was the annualized growth velocity after 1 year. Secondary outcomes included changes in height standard deviation score (SDS), bone age (BA), IGF-1 SDS, and IGF-binding protein 3 (IGF-BP3) levels. Results: The primary analysis focused on patients with NS. The mean annualized growth velocity in the rhGH-treated NS subgroup (n = 23) was significantly higher than in the control group (n = 20) (10.48 \u00b1 2.58 cm\/year vs. 5.79 \u00b1 0.49 cm\/year, p &lt; 0.001). Within the entire rhGH treatment cohort (n = 34), after 1 year of therapy, the height SDS significantly improved (p &lt; 0.001). The discrepancy between BA and chronological age narrowed from 2.61 \u00b1 1.64 years at baseline to a median of 1.0 year (interquartile range: 0.45, 2.6) post-treatment (p &lt; 0.001). Serum IGF-1 SDS increased significantly from \u22121.45 \u00b1 0.82 to 1.12 \u00b1 0.95 (p &lt; 0.001). rhGH therapy was well-tolerated. Conclusion: In children with NS and GC-induced short stature, rhGH treatment results in a significantly greater improvement in growth velocity compared to spontaneous catch-up growth alone. It effectively enhances linear growth and normalizes the GH-IGF-1 axis with a favorable safety profile.<\/jats:p>","DOI":"10.1159\/000550406","type":"journal-article","created":{"date-parts":[[2026,1,23]],"date-time":"2026-01-23T17:00:49Z","timestamp":1769187649000},"page":"1-9","source":"Crossref","is-referenced-by-count":0,"title":["Efficacy of Recombinant Human Growth Hormone on Glucocorticoid-Induced Short Stature in Children: A Retrospective Controlled 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