Lima L L, Gonçalves P F, Sallum E A, Casati M Z, Nociti F H
Division of Periodontics, School of Dentistry at Piracicaba, University of Campinas, Piracicaba, SP, Brazil.
J Periodontal Res. 2008 Aug;43(4):459-64. doi: 10.1111/j.1600-0765.2008.01094.x.
Guided tissue regeneration has been shown to lead to periodontal regeneration, however, the mechanisms involved remain to be clarified. The present study was carried out to assess the expression of genes involved in the healing process of periodontal tissues in membrane-protected vs. nonprotected intrabony defects in humans.
Thirty patients with deep intrabony defects (> or = 5 mm, two or three walls) around teeth that were scheduled for extraction were selected and randomly assigned to receive one of the following treatments: flap surgery alone (control group) or flap surgery plus guided tissue regeneration (expanded polytetrafluorethylene (e-PTFE) membrane) (test group). Twenty-one days later, the newly formed tissue was harvested and quantitatively assessed using the polymerase chain reaction assay for the expression of the following genes: alkaline phosphatase, receptor activator of nuclear factor-kappa B ligand, osteoprotegerin, osteopontin, osteocalcin, bone sialoprotein, basic fibroblast growth factor, interleukin-1, interleukin-4, interleukin-6, matrix metalloproteinase-2 and matrix metalloproteinase-9.
Data analysis demonstrated that mRNA levels for alkaline phosphatase, receptor activator of nuclear factor-kappa B ligand, osteoprotegerin, osteopontin, bone sialoprotein, basic fibroblast growth factor, interleukin-1, interleukin-6, matrix metalloproteinase-2 and matrix metalloproteinase -9 were higher in the sites where guided tissue regeneration was applied compared with the control sites (p < 0.05), whereas osteocalcin mRNA levels were lower (p < 0.05). No difference was observed in interleukin-4 mRNA levels between control and test groups.
Within the limits of this study, it can be concluded that genes are differentially expressed in membrane barrier-led periodontal healing when compared with flap surgery alone, and this may account for the clinical outcome achieved by guided tissue regeneration.
引导组织再生已被证明可导致牙周组织再生,然而,其中涉及的机制仍有待阐明。本研究旨在评估人类膜保护与非保护骨内缺损中牙周组织愈合过程相关基因的表达情况。
选取30例计划拔牙的牙齿周围存在深骨内缺损(≥5mm,两壁或三壁)的患者,随机分为以下治疗组之一:单纯翻瓣手术(对照组)或翻瓣手术加引导组织再生(膨体聚四氟乙烯(e-PTFE)膜)(试验组)。21天后,采集新形成的组织,采用聚合酶链反应分析对以下基因的表达进行定量评估:碱性磷酸酶、核因子κB受体活化因子配体、骨保护素、骨桥蛋白、骨钙素、骨唾液蛋白、碱性成纤维细胞生长因子、白细胞介素-1、白细胞介素-4、白细胞介素-6、基质金属蛋白酶-2和基质金属蛋白酶-9。
数据分析表明,与对照组相比,应用引导组织再生的部位碱性磷酸酶、核因子κB受体活化因子配体、骨保护素、骨桥蛋白、骨唾液蛋白、碱性成纤维细胞生长因子、白细胞介素-1、白细胞介素-6、基质金属蛋白酶-2和基质金属蛋白酶-9的mRNA水平较高(p<0.05),而骨钙素mRNA水平较低(p<0.05)。对照组和试验组之间白细胞介素-4 mRNA水平未观察到差异。
在本研究范围内,可以得出结论,与单纯翻瓣手术相比,基因在膜屏障引导的牙周愈合中存在差异表达,这可能解释了引导组织再生所取得的临床效果。