阐明穿孔膜与非穿孔膜在引导骨再生中的优势:体内组织学评估和组织形态计量分析。

Istvan A Urban, Nicholas Mirsky, Matteo Serroni, Nick Tovar, Vasudev Vivekanand Nayak, Lukasz Witek, Charles Marin, Muhammad H A Saleh, Andrea Ravida, Istvan Baczko, Laszlo Parkanyi, Katalin Nagy, Paulo G Coelho
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引用次数: 0

摘要

背景:无孔聚四氟乙烯(PTFE)膜可有效用于引导骨再生(GBR),但由于与骨膜的相互作用有限,可能会阻碍细胞迁移。本研究在犬下颌骨模型中比较了使用闭塞膜或穿孔膜结合无细胞胶原海绵(ACS)和重组人骨形态发生蛋白-2(rhBMP-2)进行骨再生的效果。材料与方法:雄性小猎犬(n=3)各接受两个下颌骨缺损,将 ACS/rhBMP-2 与实验组(穿孔组)和对照组(无穿孔组)的膜(n=3 个缺损/组)进行比较。通过组织形态学、组织形态计量学以及使用微计算机断层扫描进行容积重建,对组织愈合情况进行评估。结果显示与未穿孔组相比,穿孔组的骨形成增加,软组织形成减少。在主要结果方面,组织形态学分析显示,穿孔组的再生骨总量(67.08 ± 6.86%)明显高于未穿孔组(25.18 ± 22.44%)(p = 0.036)。与未穿孔膜(74.82 ± 22.44%)相比,穿孔膜的软组织浸润较少(32.91 ± 6.86%)(p = 0.036)。结论:穿孔组膜的通透性增加可能使骨膜前体细胞更容易获得 rhBMP-2。与未穿孔组相比,这种可获得性可能加速了骨膜前体细胞向成熟骨形成细胞的分化,从而刺激了新骨的生成。
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Elucidating the Benefit of Perforated vs Non-Perforated Membranes in Guided Bone Regeneration: An in Vivo Histologic Evaluation and Histomorphometric Analysis.

Background: Non-perforated Polytetrafluoroethylene (PTFE) membranes are effectively utilized in guided bone regeneration (GBR) but may hinder cell migration due to limited interaction with the periosteum. This study compared bone regeneration using occlusive or perforated membranes combined with acellular collagen sponge (ACS) and recombinant human bone morphogenic protein-2 (rhBMP-2) in a canine mandibular model.

Material and methods: Male beagle dogs (n=3) received two mandibular defects each to compare ACS/rhBMP-2 with experimental (perforated group) and control (non-perforated group) membranes (n=3 defects/group). Tissue healing was assessed histomorphologically, histomorphometrically and through volumetric reconstruction using microcomputed tomography.

Results: The perforated group showed increased bone formation and reduced soft tissue formation compared to the non-perforated group. For the primary outcome, histomorphometric analysis revealed significantly greater total regenerated bone in the perforated group (67.08 ± 6.86%) relative to the nonperforated group (25.18 ± 22.44%) (p = 0.036). Perforated membranes had less soft tissue infiltration (32.91 ± 6.86%) compared to non-perforated membranes (74.82 ± 22.44%) (p = 0.036).

Conclusion: The increased permeability of membranes in the perforated group potentially enabled periosteal precursor cells greater accessibility to rhBMP-2. The availability may have accelerated their differentiation into mature bone-forming cells, contributing to the stimulation of new bone production, relative to the non-perforated group.

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