Abstract

BackgroundStudies investigating the use of platelet–rich plasma (PRP) in the treatment of intrabony defects have yielded mixed results. The aim of our study was to evaluate the efficacy of PRP by comparing clinical attachment level (CAL) and pocket depth (PD) for patients who received PRP as an adjunct to periodontal intrabony defect therapy with those for patients who did not. We also analyzed the influence of guided tissue regeneration (GTR) and different study designs (parallel and split–mouth studies) on the clinical outcomes of intrabony defects.MethodsWe performed a systematic review of articles published in any language up to June 7, 2015 by searching PubMed, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials. We included only randomized controlled clinical trials (RCTs) that compared clinical outcomes between patients who received PRP as an adjunct to periodontal intrabony defect therapy and patients who did not. We combined data from randomized trials to assess clinical outcomes using a random–effects model.ResultsOf the 307 abstracts that were initially identified, 12 RCTs related to the treatment of periodontal intrabony defects were included in the final analysis. Clinically and significantly greater CAL gains and PD reductions were observed in subjects who received PRP as an adjunct to periodontal intrabony defect therapy than in subjects who did not (CAL: WMD 0.76 mm, 95 % CI = 0.34 to 1.18 mm, P = 0.0004; PD: WMD 0.53 mm, 95 % CI = 0.21 to 0.85 mm, P = 0.001). Subgroup meta-analyses of patients who underwent GTR demonstrated that this approach did not significantly affect treatment outcomes (CAL: WMD 0.08 mm, 95 % CI = −0.30 to 0.46 mm, P = 0.67), as indicated by a comparison with patients who did not undergo GTR (CAL: WMD 1.22 mm, 95 % CI = 0.88 to 1.57 mm, P < 0.00001). Univariate meta-regression analyses revealed that the use of GTR explained the heterogeneity among the included studies (P < 0.05).ConclusionsWithin its limitations, this review suggests that PRP may be beneficial as an adjunct to graft materials for the treatment of periodontal intrabony defects, except in cases involving the use of GTR.

Highlights

  • Studies investigating the use of platelet–rich plasma (PRP) in the treatment of intrabony defects have yielded mixed results

  • Among the polypeptide growth factors (PGFs), platelet-derived growth factor (PDGF) and transforming growth factor-β (TGF-β) have been the most extensively studied in terms of periodontal regeneration

  • PRP is a concentrated source of autologous platelets that is enriched with several growth factors, including PDGF, transforming growth factor-1 (TGF-1), transforming growth factor-2 (TGF-2), vascular endothelial growth factor (VEGF), insulin-like growth factor-1 (IGF-1), insulin-like growth factor-2 (IGF-2), fibroblast growth factor-β (FGF-β) and epithelial growth factor (EGF)

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Summary

Introduction

Studies investigating the use of platelet–rich plasma (PRP) in the treatment of intrabony defects have yielded mixed results. The key to tissue regeneration is to stimulate a cascade of healing events that, if coordinated, can result in the completion of integrated tissue formation Such modulators include the use of growth factors, the application of extracellular matrix proteins and attachment factors, and the use of bone morphogenetic proteins [3]. PRP is a concentrated source of autologous platelets that is enriched with several growth factors, including PDGF, transforming growth factor-1 (TGF-1), transforming growth factor-2 (TGF-2), vascular endothelial growth factor (VEGF), insulin-like growth factor-1 (IGF-1), insulin-like growth factor-2 (IGF-2), fibroblast growth factor-β (FGF-β) and epithelial growth factor (EGF) All of these hormones are secreted by platelets to initiate wound healing [5]. Some studies [6–11] have suggested that following coagulation, the PRP preparation exhibits a “sticky consistency” that may improve the clinical handling properties of the combination of PRP and the graft material, thereby enhancing wound stability

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