Elucidating the Benefit of Perforated vs Non-Perforated Membranes in Guided Bone Regeneration: An in Vivo Histologic Evaluation and Histomorphometric Analysis

骨膜 小猎犬 阻隔膜 软组织 体内 医学 再生(生物学) 骨形成 牙科 生物医学工程 解剖 化学 病理 内科学 细胞生物学 生物 生物化学 生物技术
作者
István Urbán,Nicholas A. Mirsky,Matteo Serroni,Nick Tovar,Vasudev Vivekanand Nayak,Lukasz Witek,Charles Marin,Muhammed Saleh,Andrea Ravidà,István Baczkó,László Pa̋rkányi,Katalin Nagy,Paulo G. Coelho
出处
期刊:International Journal of Periodontics & Restorative Dentistry [Quintessence Publishing Company]
卷期号:: 1-27 被引量:3
标识
DOI:10.11607/prd.7110
摘要

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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