Adherence to growth hormone therapy guidelines in a real-world French cohort of adult patients with growth hormone deficiency

Ann Endocrinol (Paris). 2021 Feb;82(1):59-68. doi: 10.1016/j.ando.2020.11.007. Epub 2020 Dec 5.

Abstract

Objective: Using real-world data from patients with growth hormone deficiency (GHD), we evaluated whether clinical practice in France adheres to international guidelines regarding somatropin dose adjustment, and assessed the long-term effectiveness and safety of somatropin.

Methods: Data were obtained from a national prospective systematic longitudinal routine follow-up programme of naive/non-naive adults with childhood-onset (CO) or adult-onset (AO) GHD treated with Norditropin® (Novo Nordisk A/S).

Results: Between 2003 and 2006, 331 treatment-naive and non-naive adults with severe GHD were enrolled and followed for a median duration of approximately 5 years; 328 patients were available for analysis. At baseline, mean patient age was 39.2 years; median standard deviation score (SDS) for insulin-like growth factor-1 (IGF-1) level was -2.2 in naive patients, subsequently fluctuating between -0.1 and +0.3 SDS during the study period. Mean GH doses ranged between 0.25 and 0.51mg/day (naive patients) and 0.39 and 0.46mg/day (non-naive patients). Despite generally receiving a higher somatropin dose, women (naive/non-naive) tended to have lower IGF-1 levels than men. Median somatropin dose was consistently higher in patients with CO-GHD than patients with AO-GHD. Extreme IGF-1 values (<-2 or >+2 SDS) were not systematically accompanied by somatropin dose adjustments. Waist circumference improved in approximately one third of patients, at a mean 3.5 years. Somatropin was well tolerated; there were no cardiovascular or cerebrovascular events during the 5-year analysis period.

Conclusion: Current clinical practice of physicians in France follows international guidelines regarding somatropin dose adjustment in adults with GHD. However, dose adjustments are not always sufficient, notably in women, and treatment effects may have been delayed due to low somatropin dose (Clinical trial registration NCT01580605).

Keywords: AGHD growth hormone registry; Adultes; Adults; Données de vie réelle; Déficit en hormone de croissance; Growth hormone deficiency; Programme français de prescription d’hormone de croissance pour adultes (Registre AGHD); Real-world data; Somatropin; Somatropine.

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Cohort Studies
  • Dose-Response Relationship, Drug
  • Drug Dosage Calculations
  • Female
  • Follow-Up Studies
  • France / epidemiology
  • Guideline Adherence / standards
  • Guideline Adherence / statistics & numerical data*
  • Hormone Replacement Therapy / methods
  • Hormone Replacement Therapy / standards
  • Hormone Replacement Therapy / statistics & numerical data
  • Human Growth Hormone* / administration & dosage
  • Human Growth Hormone* / deficiency
  • Humans
  • Hypopituitarism / drug therapy*
  • Hypopituitarism / epidemiology
  • Male
  • Middle Aged
  • Practice Patterns, Physicians' / standards*
  • Practice Patterns, Physicians' / statistics & numerical data
  • Young Adult

Substances

  • Human Growth Hormone

Associated data

  • ClinicalTrials.gov/NCT01580605