Update in mortality in GH-treated patients

Eva Marie Erfurth1

  • 1Department of Endocrinology, Skåne University Hospital, SE-221 85 Lund, Sweden. Eva_Marie.Erfurth@med.lu.se.

Insights

Growth hormone (GH) therapy shows improved survival for adult-onset GH deficiency, especially in males. However, underlying conditions remain key mortality predictors, particularly in childhood-onset cases.

Area of Science:

  • Endocrinology
  • Oncology
  • Public Health

Background:

  • Growth hormone deficiency (GHD) affects both adults and children, with varying mortality risks.
  • Previous studies indicated potential mortality risks associated with GHD and its treatments.

Purpose of the Study:

  • To evaluate all-cause mortality in adult-onset GHD patients undergoing GH therapy.
  • To identify predictors of mortality in both adult and childhood-onset GHD cohorts.

Main Methods:

  • Analysis of mortality data in adult-onset GHD patients treated with GH therapy.
  • Review of published cohort studies on GH-treated childhood-onset GHD patients.

Main Results:

  • Adult males with nonfunctioning adenomas showed no increased mortality; adult females had a slightly higher risk.
  • Underlying conditions like craniopharyngioma and malignant hypopituitarism were major mortality predictors.
  • Childhood-onset GHD cohorts showed increased mortality, often linked to underlying severe conditions and CNS tumors.

Conclusions:

  • GH therapy has improved survival in adult-onset GHD, but risk stratification is crucial.
  • The primary disease and its severity are critical determinants of mortality in GHD patients.
  • Further research is needed to fully understand long-term outcomes in diverse GHD populations.