Full-mouth disinfection effects on gingival fluid calprotectin, osteocalcin, and N-telopeptide of Type I collagen in severe periodontitis.

Autor: Afacan B; Department of Periodontology, Faculty of Dentistry, Adnan Menderes University, Aydın, Turkey., Çınarcık S; Department of Periodontology, Faculty of Dentistry, Ege University, İzmir, Turkey., Gürkan A; Department of Periodontology, Faculty of Dentistry, Ege University, İzmir, Turkey., Özdemir G; Department of Biology, Basic and Industrial Microbiology Section, Faculty of Science, Ege University, Izmir, Turkey., İlhan HA; Department of Biology, Section of Molecular Biology, Faculty of Science and Letters, Celal Bayar University, Manisa, Turkey., Vural C; Department of Biology, Basic and Industrial Microbiology Section, Faculty of Science, Ege University, Izmir, Turkey., Köse T; Department of Biostatistics and Medical Informatics, Faculty of Medicine, Ege University, Izmir, Turkey., Emingil G; Department of Periodontology, Faculty of Dentistry, Ege University, İzmir, Turkey.
Jazyk: angličtina
Zdroj: Journal of periodontology [J Periodontol] 2020 May; Vol. 91 (5), pp. 638-650. Date of Electronic Publication: 2020 Mar 14.
DOI: 10.1002/JPER.19-0445
Abstrakt: Background: To compare the effects of full-mouth disinfection (FMD) and full-mouth ultrasonic debridement (FMUD) on clinical, microbiological and biochemical parameters with conventional quadrant-wise scaling and root planning (Q-SRP) in severe chronic periodontitis.
Methods: In the present prospective randomized controlled clinical trial with three parallel arms (#NCT04038801), 60 chronic periodontitis patients were randomly assigned to three study groups by a consecutive number in ascending order: FMD (n = 20), FMUD (n = 20), and Q-SRP (n = 20). All measurements and treatments were performed by the same investigator. At baseline, gingival crevicular fluid (GCF) and subgingival plaque were collected and clinical periodontal parameters were recorded. Ultrasonic debridement was completed within 24 hours in FMD and FMUD groups. Chlorhexidine gluconate was used for FMD. Q-SRP was performed by hand instruments per quadrant at 1-week-intervals. Clinical measurements and sampling were repeated at 1, 3, and 6 months after treatment. Real-time PCR was used for quantitative analysis of Aggregatibacter actinomycetemcomitans, Porphyromonas gingivalis, Prevotella intermedia, Tannerella forsythia, Fusobacterium nucleatum, and total bacteria count. GCF Calprotectin, osteocalcin, and N-telopeptide of type I collagen (NTx) levels were analyzed by ELISA. The changes of GCF biomarker levels after treatment between groups were the primary outcomes.
Results: No harm was observed. All treatment strategies resulted in significant improvements in all clinical parameters (P < 0.05), with no significant differences between study groups at all time-points (P ˃ 0.05). Aggregatibacter actinomycetemcomitans was significantly decreased in FMD compared to FMUD and Q-SRP at 6 months (P < 0.05). Although GCF NTx total amounts increased in all groups during the study period, this increase was less prominent in full-mouth groups at three time points after treatment (P < 0.05).
Conclusions: Present results represent the short-term effects. Full-mouth treatment approaches offered limited beneficial effects on microbiological and biochemical parameters over quadrant-wise approach. All three treatment strategies can be recommended in the management of severe chronic periodontitis.
(© 2020 American Academy of Periodontology.)
Databáze: MEDLINE
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