Effect of adding bone marrow to ceramic graft materials with different interconnectivities in lumbar arthrodesis : quantification of bone formation.

INTRODUCTION: Combining bone marrow (BM) with graft materials can stimulate bone healing. However, bone growth is not quantified in most studies, and the influence of the rate of interconnectivity of ceramics loaded with bone marrow has not yet been quantified. Here, a rabbit model of posterolateral intertransverse arthrodesis was used to quantify the effect of adding BM to partially (PIC) or totally (TIC) interconnected ceramics. MATERIALS AND METHODS: A single lumbar level was grafted on two sides with TIC (n = 12) or PIC (n = 18). The ceramic was loaded with 1.5 ml of BM on one side (chosen at random). The fusion rate was assessed by manual palpation test. Bone formation was quantified on scanning electron microscopy images and by dual-energy X-ray absorptiometry. RESULTS: At week 6, bone formation with TIC was twice as high as that with PIC. When BM was added, 35.1 and 87.8 % more bone formation was observed in the TIC and PIC, respectively. In ceramics loaded with BM, the bone mineral density was significantly higher than that in ceramics alone. CONCLUSIONS: Differences in interconnectivity within the family of biphasic ceramics should be taken into account when applying them clinically. BM increased bone formation regardless of the type of ceramic employed.

The vertebral interbody grafting site's low concentration in osteogenic progenitors can greatly benefit from addition of iliac crest bone marrow.

The ability of bone substitutes to promote bone fusion is contingent upon the presence of osteoinductive factors in the bone environment at the fusion site. Osteoblast progenitor cells are among these environmental osteoinductive factors, and one of the most abundant and available sources of osteoblastic cells is the bone marrow. As far as biological conditions are concerned, the vertebral interbody space appears as a favorable site for fusion, as it is surrounded by spongy bone, theoretically rich in osteogenic cells. This site may, however, not be as rich in osteogenic precursor cells especially at the time of grafting, because decortication of the vertebral end plates during the grafting process may modify cell content of the surrounding spongy bone. We tested this hypothesis by comparing the abundance of human osteogenic precursor cells in bone marrow derived from the iliac crest, the vertebral body, and the decorticated intervertebral body space. The number of potential osteoblast progenitors in each site was estimated by counting the alkaline phosphatase-expressing colony-forming units (CFU-AP). The results, however, demonstrate that the vertebral interbody space is actually poorer in osteoprogenitor cells than the iliac crest (P<0.001) and vertebral body (P<0.01), especially at the time of graft implantation. In light of our results, we advocate addition of iliac crest bone marrow aspirate to increase the success rate of vertebral interbody fusion.