Study Design. An established rabbit posterolateral lumbar fusion model was
used to evaluate the ability of osteogenic protein-1 to overcome the inhibi
tory effect of nicotine.
Objective. To determine whether osteogenic protein-1 should be considered a
s a bone graft alternative for the patient who smokes.
Summary of Background Data. Smoking interferes with the success of posterol
ateral lumbar fusion. This inhibitory effect has been attributed to nicotin
e and confirmed in a New Zealand white rabbit model. Osteoinductive protein
-1 has been shown to induce posterolateral spine fusion reliably in the rab
bit model. The effectiveness with which osteogenic protein-1 induces fusion
in the presence of nicotine has not been studied previously.
Methods. Single-level posterolateral intertransverse process fusions were p
erformed at L5-L6 in 18 New Zealand white rabbits. Either autograft or oste
ogenic protein-1 was used as grafting material. Nicotine was administered v
ia subcutaneous mini-osmotic pumps. The animals were killed 5 weeks after s
urgery, and the resulting fusion masses were studied.
Results. Three rabbits (17%) were excluded because of complications. By man
ual palpation, two of the eight nicotine-exposed autograft rabbits (25%) an
d all of the nicotine-exposed osteogenic protein-1 rabbits (100%) were foun
d to be fused. These results correlated well with those obtained from biome
chanical testing. Histologically, the fusion zones of the nicotine-exposed
autograft rabbits were distinctly less mature than the fusion masses of the
nicotine-exposed osteogenic protein-1 rabbits.
Conclusion. Osteoinductive protein-1 was able to overcome the inhibitory ef
fects of nicotine in a rabbit posterolateral spine fusion model, and to ind
uce bony fusion reliably at 5 weeks.