Characterization of oral biomarkers during early healing at augmented dental implant sites

Author:

Tavelli Lorenzo1234ORCID,Barootchi Shayan124ORCID,Rodriguez Maria Vera45,Sugai Jim4,Wu David T.167ORCID,Yu Ning18ORCID,Giannobile William V.1ORCID

Affiliation:

1. Division of Periodontology, Department of Oral Medicine, Infection, and Immunity Harvard School of Dental Medicine Boston Massachusetts USA

2. Center for Clinical Research and Evidence Synthesis in Oral Tissue Regeneration (CRITERION) Boston Massachusetts USA

3. School of Dentistry Universidad Catolica de Santiago de Guayaquil (UCSG) Guayaquil Ecuador

4. Department of Periodontics & Oral Medicine University of Michigan School of Dentistry Ann Arbor Michigan USA

5. Postgraduate Periodontics, Division of Periodontics Columbia University College of Dental Medicine New York City New York USA

6. Harvard John A. Paulson School of Engineering and Applied Sciences Harvard University Cambridge Massachusetts USA

7. Wyss Institute for Biologically Inspired Engineering Harvard University Boston Massachusetts USA

8. ADA Forsyth Institute Cambridge Massachusetts USA

Abstract

AbstractAimThe aim of this study is to assess early wound healing expression of local angiogenic biomarkers following connective tissue graft (CTG) at dental implant sites.MethodsTwenty‐eight subjects with single dental implants exhibiting a soft tissue dehiscence were included and randomly treated with CTG, either with coronally advanced flap (CAF) or with tunnel technique (TUN). Peri‐implant crevicular fluid (PICF) was collected at the midfacial and midlingual aspect of the implant sites at baseline and at 3, 7, 14, 30, and 90 days after the surgical intervention. The expression of angiogenin (ANG), fibroblast growth factor‐2 (FGF‐2), platelet‐derived growth factor (PDGF), tissue inhibitor of metalloproteinases‐2 (TIMP‐2), and vascular endothelial growth factor (VEGF) was investigated over a period of 3 months. Patient‐reported outcomes, clinical measurements, and ultrasonography scans at multiple time points were also evaluated.ResultsThe longitudinal regression revealed a significant difference in the expression of VEGF and TIMP‐2 between CAF‐ and TUN‐treated sites over 3 months (p = .033 and p = .004, respectively), whereas no significant differences were observed for ANG, FGF‐2 and PDGF between the two groups. At 7 days, a direct correlation was observed between ANG levels and ultrasonographic color velocity in the CAF group (p < .001) and between ANG levels and ultrasonographic color power in the TUN group (p = .028). VEGF levels and ultrasonographic mean perfused area of the CTG were significantly correlated at the 7‐day time point (p < .001 for both CAF and TUN). The expression of VEGF at 7 days was directly associated with mucosal thickness gain at 1 year (p < .001 for both groups). Early TIMP‐2 expression showed an inverse correlation with time to recovery (p = .002). TIMP‐2 levels at 3 months exhibited inverse correlations with mean dehiscence coverage (p = .004) and the rate of complete dehiscence coverage (p = .012).ConclusionPICF biomarkers can be used to monitor early wound healing events following soft tissue grafting at implant sites. VEGF and TIMP‐2 showed correlations with the 1‐year clinical and volumetric outcomes, as well as with post‐operative patient‐reported outcomes and Doppler Ultrasonographic tissue perfusion‐related parameters.

Funder

Delta Dental Foundation

Publisher

Wiley

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