Dos Santos Pereira Rodrigo, Boos Fernanda Brasil, Gorla Luis Fernado, Garcia Idelmo Rangel, Okamoto Roberta, Hochuli-Vieira Eduardo
Int J Periodontics Restorative Dent. 2017 November/December;37(6):e321–e327. doi: 10.11607/prd.2606. Epub 2017 Aug 23.
The purpose of this study was to evaluate a composite graft of ChronOS, a beta-tricalcium phosphate (β-TCP), mixed 1:1 with an autogenous bone graft in human maxillary sinus augmentation. A total of 12 maxillary sinuses were grafted with an autogenous bone graft (control group), and 9 maxillary sinuses were grafted with ChronOS mixed 1:1 with an autogenous bone graft (test group). After 6 months, biopsy samples were obtained concurrent to the placement of dental implants and were subjected to histomorphometric and immunohistochemical analyses for Runt-related transcription factor 2 (RUNX2), vascular endothelial growth factor (VEGF), tartrate-resistant acid phosphatase, and osteocalcin. Histologic analysis of samples obtained from the test group revealed the presence of immature bone, while samples from the control group indicated lamellar bone formation. However, both types of bone grafts were well vascularized. The new bone formation averaged 25.4% ± 6.4% in the test group and 38.6% ± 10.5% in the control group (P = .001). Immunostaining of samples in the test group showed high cellular turnover. The outcomes of this study demonstrate a delay in bone formation but intense cellular differentiation after 6 months of bone graft healing in the test group. The amount of immature bone and the immunostaining for RUNX2 and VEGF provide evidence of an osteogenic pathway that can improve the bone formation rate.
本研究的目的是评估ChronOS(一种β-磷酸三钙(β-TCP))与自体骨移植以1:1混合的复合移植物在上颌窦提升术中的效果。总共12个上颌窦接受了自体骨移植(对照组),9个上颌窦接受了ChronOS与自体骨移植以1:1混合的移植(试验组)。6个月后,在植入牙种植体的同时获取活检样本,并对其进行组织形态计量学和免疫组织化学分析,检测与Runt相关的转录因子2(RUNX2)、血管内皮生长因子(VEGF)、抗酒石酸酸性磷酸酶和骨钙素。对试验组获取的样本进行组织学分析发现存在未成熟骨,而对照组的样本显示有板层骨形成。然而,两种类型的骨移植物都有良好的血管化。试验组的新骨形成平均为25.4%±6.4%,对照组为38.6%±10.5%(P = .001)。试验组样本的免疫染色显示细胞更新率高。本研究结果表明,试验组在骨移植愈合6个月后骨形成延迟,但细胞分化强烈。未成熟骨的量以及RUNX2和VEGF的免疫染色为一种可提高骨形成率的成骨途径提供了证据。