4.4 Article

Impact of smoking on peri-implant bleeding on probing

Journal

CLINICAL IMPLANT DENTISTRY AND RELATED RESEARCH
Volume 24, Issue 2, Pages 151-165

Publisher

WILEY
DOI: 10.1111/cid.13062

Keywords

biofilm; dental implants; diagnosis; peri-implantitis; smoking

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This study aimed to investigate the impact of smoking on peri-implant bleeding, bone loss, and microbiota. The results showed an inverse correlation between smoking and bleeding, and a positive correlation with gingival inflammation, probing pocket depth, and gender. Moreover, smoking led to changes in the peri-implant microbiota.
Background Studies around natural dentition demonstrated that smoking can reduce the tendency of inflamed tissue to bleed upon probing after controlling for possible confounders. In addition, previous research suggested that smokers may present alterations of the peri-implant microbiome. Aim This study aimed at investigating the impact of smoking on: (1) peri-implant bleeding on probing (BOP; primary objective); (2) the association between BOP/bone loss and BOP/visible gingival inflammation; (3) peri-implant microbiome. Methods Partially edentulous patients with implants restored with a single crowns were included in this study. Subjects were either smokers (>= 1 cigarettes per day) or nonsmokers (never smokers). The primary outcome of this cross-sectional study was BOP and secondary outcomes included: Probing pocket depth (PPD), Modified gingival Index (mGI) and Progressive Marginal Bone Loss. In addition, microbial profiles of the subjects were assessed through sequencing of the 16S rRNA gene. Univariate and multilevel multivariate analyses by means of Generalized Estimating Equations were conducted to analyze the association between smoking and peri-implant BOP. Results Overall, 27 nonsmokers and 27 smokers were included and 96.3% and 77.78% of patients presented peri-implant BOP in the nonsmoker and smoker group, respectively (p = 0.046). Smoking was inversely associated with BOP in the multivariate multilevel analysis (OR = 0.356; 95% CI: 0.193-0.660; p = 0.001) whereas a positive correlation was demonstrated for mGI > 0 (OR = 3.289; 95% CI: 2.014-5.371; p < 0.001); PPD (OR = 1.692; 95% CI: 0.263-0.883; p = 0.039) and gender (OR = 2.323; 95% CI: 1.310-4.120 p = 0.004). A decrease of BOP sensitivity in detecting visible gingival inflammation (mGI > 0) was observed in smokers. Besides, taxonomic and changes in diversity regarding the peri-implant microbiota were detected comparing the two groups. Significantly higher richness of the microbiota was demonstrated in the smoker group when implants affected by peri-implantitis were compared to either healthy implants or implants presenting mucositis. Conclusions Smoking is a potential modifier of BOP and peri-implant microbiota.

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