Circadian Clock Proteins in Gingival Crevicular Fluid of Individuals With and Without Circadian Rhythm Disruption

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-50
SponsorInonu University

About this trial

This prospective cross-sectional clinical study aims to investigate the relationship between circadian rhythm disruption and periodontal inflammation by evaluating circadian clock protein levels, inflammatory (IL-1beta) and anti-inflammatory (IL-10) cytokine levels in gingival crevicular fluid (GCF) of individuals with and without circadian rhythm disruption.

Participants aged 20-50 years will be classified into four groups based on their circadian rhythm status (disrupted/normal) and gingival health status (gingivitis/healthy). Clinical periodontal parameters including plaque index, gingival index, bleeding on probing, and probing depth will be assessed. Circadian rhythm status will be determined using validated questionnaires (Morningness-Eveningness Questionnaire and Munich Chronotype Questionnaire). Night-shift workers will represent the circadian rhythm disruption group.

GCF samples will be analyzed for circadian clock proteins (BMAL-1, CLOCK, PER-1, PER-2, PER-3, CRY-1, CRY-2, REV-ERB-beta, MTNR1B) and cytokines (IL-1beta, IL-10) using ELISA. Serum cortisol and melatonin levels will be measured for biochemical verification of circadian rhythm status.

Gingivitis groups will receive standard periodontal treatment and be re-evaluated at 2 weeks post-treatment. A total of 116 participants (29 per group) are planned for enrollment.

Eligibility criteria

Qualifiers

Aged between 20 and 50 years

Systemically healthy

Diagnosed as periodontally healthy or with gingivitis based on clinical periodontal examination

Having at least 20 natural teeth in the oral cavity

Disqualifiers

Use of antioxidant or melatonin supplements

Presence of any systemic disease

Use of antibiotics, anti-inflammatory drugs, or immunosuppressants within the past 3 months

Having received periodontal treatment within the past 6 months

Trial design

Treatments tested in this trial

  • Standard Periodontal Treatment

Treatment groups

116 Participants
are divided into 4 treatment groups

Sponsors and collaborators

Inonu University

Lead sponsor

University of Minnesota

Collaborator

Harvard University

Collaborator

University of Turku

Collaborator