Matrix metalloproteinase-8 level in the peri-implant sulcular fluid around dental implant abutments with different geometries and manufacturing strategies: A randomized controlled trial
Résumé
Abstract Background. The purpose of this clinical trial was to assess soft tissue reaction around custom dental implant abutments by evaluation of Matrix Metalloproteinase-8 (MMP-8) level in peri-implant sulcular fluid (PISF) and clinical parameters. Methods. Thirty participants with missing mandibular first molar were enrolled in this randomized controlled trial. Each participant underwent implant placement following the standard 2-stage surgical protocol. All participants were randomly allocated to one of the two groups; Control Group (n=15): Pre-machined stock titanium abutment, and Study Group (n=15): Custom titanium CAD-CAM abutment. Combined screw- and cement-retained zirconia crowns were used to restore implants. The PISF samples were collected at 1, 3, 6 and 12 months after placement of restorations. MMP-8 level was assessed by Enzyme-Linked ImmunoSorbent Assay. Peri-implant probing depth (PPD), simplified mucosal index (SMI) and modified plaque index (mPI) scores were assessed at all time-points. Crestal bone loss (CBL) was assessed by using bitewing radiographs made at baseline and 12-month time points. Two-way repeated-measures ANOVA and Friedman test were used to analyze data. Results. There was a significant effect of the interaction of time and abutment type where the change in MMP-8 and PPD in CA was higher than in SA. SMI, mPI and CBL recorded no statistical differences between the two groups after one year (P > 0.05). Conclusions. The change in the level of MMP-8 and in PPD after one year is significantly higher in custom abutments. However, this change was of low clinical impact. Trial Registery: the trial was registered in the Pan African Clinical Trial Registry under identification number PACTR201809736563842 (25/ 09/ 2018)
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