Abstract

To evaluate the effect of adjunctive antiseptic irrigation of periodontal pockets on microbial and cytokine profiles. Fifty-nine patients with severe periodontitis were allocated to one of three groups for scaling and root planing facilitated with different adjunctive antiseptics: 1% polyhexamethyleneguanidine phosphate (PHMG-P) (n = 19), 0.2% chlorhexidine (CHX) (n = 21) or distilled water (n = 19). Gingival crevicular fluid and subgingival bacterial samples were collected at baseline, and at 2 weeks, and 1 and 4 months. The levels of interleukin (IL)-1β, IL-8, IL-10, and IL-17A, matrix metalloproteinase (MMP)-8, Porphyromonas gingivalis, Tannerella forsythia, Treponema denticola, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans, and Prevotella intermedia were determined. There were no intergroup differences in cytokine concentrations and bacterial counts at any follow-up, however, varying patterns were observed. In the PHMG-P and water groups IL-1β expression peaked at 2 weeks and then gradually declined. In all three groups, the dynamics of MMP-8 concentration were non-linear, increasing by 2 weeks and then declining to below baseline (p > 0.05). P. gingivalis and T. forsythia declined within the first month and increased thereafter, not regaining the baseline level. Adjunctive antiseptic treatment was associated with changes in biomarkers and bacterial counts in the course of the study. The effects of adjunctive antiseptic irrigation were limited in the applied protocol.

Highlights

  • The permanent presence of microbial flora in the human oral cavity is beneficial and is essential to health [1]

  • The aim of this study is to compare the effects of adjunctive polyhexamethyleneguanidine phosphate (PHMG-P) and CHX irrigation on the microbial and cytokine profiles of periodontal pockets

  • The concentration of total protein in the Polyhexamethylene guanidine (PHMG)-P group was rising from the baseline level, whereas in the CHX and water groups it remained below the initial titer

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Summary

Introduction

The permanent presence of microbial flora in the human oral cavity is beneficial and is essential to health [1]. Bacteria may act as causal agents of oral diseases [2]. Dental biofilm is recognized as a cause and significant risk factor for periodontal diseases [3]. The role of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, and Tannerella forsythia is generally accepted and they are regarded as ‘consensus’ periodontopathogens. Eubacterium nodatum, Fusobacterium nucleatum, Prevotella intermedia, Prevotella nigrescens, and Treponema denticola are strongly associated with chronic periodontitis [4].

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