Platelet‐rich fibrin combined with a particulate bone substitute versus guided bone regeneration in the damaged extraction socket: An in vivo study

富血小板纤维蛋白 纤维蛋白 骨钙素 牙槽 小猎犬 牙科 体内 牙槽嵴 成骨细胞 生物医学工程 病理 医学 化学 外科 内科学 碱性磷酸酶 植入 生物 免疫学 体外 生物化学 生物技术
作者
Jin‐Young Park,Kyu‐Jin Hong,Kyung‐A Ko,Jae‐Kook Cha,Reinhard Gruber,Jung‐Seok Lee
出处
期刊:Journal of Clinical Periodontology [Wiley]
卷期号:50 (3): 358-367 被引量:12
标识
DOI:10.1111/jcpe.13742
摘要

Abstract Aim It has been proposed that platelet‐rich fibrin (PRF) can be used to support bone regeneration during alveolar ridge augmentation. The aim of this study was to determine whether an approach utilizing PRF provides similar performance to the established guided bone regeneration (GBR) procedure. Materials and Methods Two‐wall defects were surgically created in beagle dogs and treated in three experimental groups: (i) a sticky bone (SB) substitute prepared using liquid PRF and deproteinized porcine bone mineral (DPBM); (ii) SB covered with solid PRF compressed into a membrane; and (iii) GBR performed using DPBM covered by a collagen membrane. Quantitative reverse‐transcription polymerase chain reaction was applied to the specimen after 1 week of healing, and microcomputed tomography (micro‐CT) and histological outcomes were analysed after 8 weeks of healing. Results Compared with GBR, PRF resulted in a moderate increase in the expression levels of osteoblast and osteoclast markers, osteocalcin, and calcitonin receptor. Moreover, PRF modestly increased angiogenesis and the inflammation markers vascular endothelial growth factor (VEGF) and IL‐6. Micro‐CT and histological analyses confirmed the expected increased alveolar ridge area, with no significant differences between the three groups. Consistently, graft consolidation, as indicated by new bone formation at the defect site, did not differ significantly between groups. Conclusions The present results demonstrate that PRF‐based approaches perform comparably to the established GBR procedure in terms of the consolidation of DPBM in two‐wall alveolar defects.
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