Distraction osteogenesis is a good model for evaluation of fracture healing
with intramembranous bone formation. The purpose of the present study was
to investigate whether homologous GH has a stimulating effect on bone heali
ng in distraction osteogenesis. The left tibiae of 30 micropigs were osteom
ized and distracted with an external fixator 2 mm daily over a period of 10
days. Animals were killed after an additional healing time of 10 days. The
treatment group received 100 mu g r-pGH per kg bodyweight per day. A newly
developed device allowed non-destructive torsional biomechanical evaluatio
n of the regenerate strength as in vivo measurements. After killing, destru
ctive torsional strength testing of the sites of distraction was performed.
To determine the endocrine response to the administration of r-pGH, serum
levels of IGF-I were determined. The non-destructive in vivo testing showed
that torsional stiffness of the regenerate was significantly higher in the
treatment group than in the control group. Final regenerate torsional fail
ure load was 131 % higher and ultimate torsional stiffness was 231 % higher
in the treatment group than in the control group. The mean serum level of
IGF-I increased to 440 % of the preoperative base level in the treatment gr
oup and remained unchanged in the control group. Our data indicate that sys
temic administration of recombinant homologous growth hormone significantly
accelerates ossification of bone regenerate in distraction osteogenesis.