Growth hormone substitution increases gene expression of members of the IGF family in cortical bone from women with adult onset growth hormone deficiency--relationship with bone turn-over

Bone. 2003 Oct;33(4):638-45. doi: 10.1016/s8756-3282(03)00240-0.

Abstract

Objective: To investigate the effects of growth hormone (GH) replacement therapy on bone matrix gene expression of insulin-like growth factors (IGFs) and markers of bone metabolism in women with adult-onset GH deficiency (GHD).

Design and methods: Nineteen women, mean age 45 (range 24-56) years, were included in a double-blind, placebo-controlled parallel group study for 12 months. Biochemical markers were measured at baseline, 6 and 12 months. Bone biopsies were obtained and BMD was measured at baseline and after 12 months.

Results: Maximum responses were observed after 6 and 12 months, for bone resorptive and bone formative markers respectively. GH therapy enhanced gene expression in cortical bone of IGFs, GH-and calcitonin-receptor (CR) and osteoprotegerin (OPG), however with the most pronounced effects on CR and IGF-I. Changes in IGF-I gene expression during longitudinal follow-up were significantly correlated with changes in both circulating IGF-I (r = 0.82, p < 0.05), changes in markers of enhanced osteoclastic activity, measured both locally in bone (CR, r = 0.87, p < 0.01) and in serum (CTX-I, r = 0.86, p < 0.05), as well as serum bone ALP (r = 0.96, p < 0.01).

Conclusions: This study indicates that both liver- and bone-derived IGF-I may be significant in mediating the effects of GH on bone metabolism in humans.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Base Sequence
  • Bone Remodeling / drug effects
  • Bone Remodeling / genetics
  • Bone and Bones / drug effects*
  • Bone and Bones / metabolism*
  • DNA / genetics
  • Female
  • Gene Expression / drug effects
  • Glycoproteins / blood
  • Human Growth Hormone / deficiency*
  • Human Growth Hormone / therapeutic use*
  • Humans
  • Insulin-Like Growth Factor Binding Protein 3 / genetics
  • Insulin-Like Growth Factor I / genetics
  • Middle Aged
  • Osteoprotegerin
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Cytoplasmic and Nuclear / blood
  • Receptors, Tumor Necrosis Factor
  • Recombinant Proteins / therapeutic use
  • Reverse Transcriptase Polymerase Chain Reaction
  • Somatomedins / genetics*

Substances

  • Glycoproteins
  • Insulin-Like Growth Factor Binding Protein 3
  • Osteoprotegerin
  • RNA, Messenger
  • Receptors, Cytoplasmic and Nuclear
  • Receptors, Tumor Necrosis Factor
  • Recombinant Proteins
  • Somatomedins
  • TNFRSF11B protein, human
  • Human Growth Hormone
  • Insulin-Like Growth Factor I
  • DNA