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Growth Hormone Withdrawal in Mid-Puberty: No Impact on Near Adult Height in Adolescents with Transient Idiopathic GHD

  • Joeri Vliegenthart
  • , Jan M Wit
  • , Boudewijn Bakker
  • , Annemieke M Boot
  • , Christiaan de Bruin
  • , Martijn J J Finken
  • , Josine C van der Heyden
  • , Anita C S Hokken-Koelega
  • , Hetty J van der Kamp
  • , Edgar G van Mil
  • , Theo C J Sas
  • , Dina A Schott
  • , Petra van Setten
  • , Saartje Straetemans
  • , Vera van Tellingen
  • , Robbert N H Touwslager
  • , A S Paul van Trotsenburg
  • , Paul G Voorhoeve
  • , Edmond H H M Rings
  • , Erica L T van den Akker
  • Danielle C M van der Kaay
  • Erasmus University Medical Centre, 3000, Netherlands
  • Leiden University Medical Centre
  • Division of Pediatric Endocrinology, Nijmegen, Netherlands
  • University Medical Centre Groningen
  • Dutch Growth Research Foundation
  • University Medical Center Utrecht
  • Jeroen Bosch Hospital
  • Zuyderland Hospital
  • Radboud University Medical Centre
  • Maastricht University Medical Centre
  • St. Antonius Hospital
  • AMsterdam University Medical Center
  • Canisius Wilhelmina Hospital

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

CONTEXT: In children with idiopathic isolated growth hormone deficiency (IIGHD), GH secretion often normalizes by near adult height (NAH). Whether rhGH treatment can be safely discontinued earlier remains unclear.

OBJECTIVE: To investigate if withdrawing rhGH treatment from mid-puberty onwards had no negative effect on attained NAH in adolescents who, after retesting, were no longer GH deficient.

DESIGN: Prospective multicenter patient preference study (2017-2024) with follow-up until NAH (SEENEZ GH Study).

SETTING: Pediatric endocrinology departments in multiple centers.

PATIENTS OR OTHER PARTICIPANTS: 127 adolescents (95 male, 75%) with childhood IIGHD (GH peak 1.7-10 µg/L) who tested GH sufficient (GH peak >6.7 µg/L) at mid-puberty. 44 continued rhGH (GHcont), 83 discontinued (GHstop). 99% of patients completed the study.

INTERVENTIONS: RhGH treatment continuation vs discontinuation from mid-puberty until NAH.

MAIN OUTCOME MEASURES: Primary: NAH-SDS minus target height (TH)-SDS. Secondary: NAH-SDS, total pubertal growth (TPG), and predicted vs attained height gain.

RESULTS: Mean (SD) NAH-SDS minus TH-SDS was -0.17 (0.60) in the GHcont and -0.18 (0.62) in the GHstop group (P=.96). Mean NAH-SDS was -0.91 (0.76) (GHcont) vs -0.78 (0.76) (GHstop) (P=.35). Mean (SD) TPG (from start of puberty) in males was 27.5 cm (7.0; GHcont) vs 25.9 cm (6.2; GHstop) (P =.25) and in females 20.5 cm (5.7; GHcont) vs 20.9 cm (7.6; GHstop) (P = .90). Predicted vs attained height gain based on the prediction model did not differ between groups.

CONCLUSIONS: In adolescents with transient IIGHD, rhGH treatment can be stopped at mid-puberty. These findings support reducing rhGH treatment duration, lowering patient burden and healthcare costs.

Original languageEnglish
JournalJournal of clinical endocrinology and metabolism
DOIs
Publication statusPublished - 15 Nov 2025

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