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© The Author(s) 2018. Published by Oxford University Press on behalf of the European Orthodontic Society. All rights reserved.
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Randomized controlled trial
Effect of orthodontic force magnitude on
cytokine networks in gingival crevicular fuid: a
longitudinal randomized split-mouth study
Beral Afacan
1
, Veli Özgen Öztürk
1
, Mine Geçgelen Cesur
2
,
Timur Köse
3
and Nagihan Bostanci
4,5
Departments of
1
Periodontology and
2
Orthodontics, School of Dentistry, Adnan Menderes University, Aydın,
3
Department of Biostatistics and Medical Informatics, Faculty of Medicine, Ege University, İzmir, Turkey
4
Department
of Dental Medicine, Karolinska Institutet, Stockholm, Sweden and
5
Center of Dental Medicine, University of Zurich,
Zurich, Switzerland
Correspondence to: Nagihan Bostanci, Department of Dental Medicine, Karolinska Institutet, Alfred Nobels allè 8, 14104
Huddinge, Stockholm, Sweden. E-mail:nagihan.bostanci@ki.se
Summary
Objective: To compare effect of two different orthodontic forces on maxillary canine distalization
via evaluation of 30 analytes including cytokines, growth factors, and chemokines in gingival
crevicular fuid (GCF) obtained from tension and compression sites.
Design: Longitudinal, split-mouth, randomized controlled trial.
Methods: The upper right and left canines were randomly distalized by a continuous force of either
75 or 150 g, in 15 individuals with Class II division 1 malocclusion. GCF samples were obtained
from the tension and the pressure sides of each canine at appliance placement (baseline) and
after force application at 24 hours and 28 days without reactivation of the coil spring. The protein
content of GCF was analysed by a multiplexed immunoassay. The effects of force, side, and time
on the analyte levels were assessed by the Brunner–Langer method.
Outcome: The changes of GCF analyte levels from baseline to 24 hours and 28 days.
Randomization: Coin fipping was used for allocation of two forces.
Blinding: The participants and periodontist who performed clinical measurements and GCF
sampling were blinded to group assignment and interventions (double-blinded trial).
Results: All patients completed the study. No harm was observed. When compared to baseline,
both forces caused signifcant up-regulation of tumour necrosis factor-α and interleukin (IL)-1RA in
the tension and the pressure sides at 28 days (P < 0.05), but not at 24 hours. Although GCF volume
was similar between the two force groups over time (P > 0.05), IL-8 and MCP-1 levels in GCF were
signifcantly lower at the pressure sites receiving higher force (150 g) at 24 hours (P < 0.05).
Limitations: Although sample size (15 patients, 30 teeth) was adequate according to the initial power
calculation, borderline signifcances may indicate lack of power or large variability among the samples.
Conclusions: Although a higher force of 150 g did not result in increased cumulative canine
movement or GCF production, selective host mediators were differentially regulated by the
magnitude and duration of the force.
Registration and trial protocol: The trial was registered retrospectively in the U.S. National
Institutes of Health Clinical Trials Registry. Full details of trial protocol NCT03555747 are available
on request.
European Journal of Orthodontics, 2018, 214–222
doi:10.1093/ejo/cjy068
Advance Access publication 12 October 2018
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