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EVALUATION of GINGIVAL CREVICULAR FLUID and SERUM ASPROSIN LEVELS in OBESE and NORMAL-WEIGHT INDIVIDUALS with PERIODONTITIS

Evaluation of Serum and Gingival Crevicular Fluid Asprosin Levels in Obese and Normal-Weight Patients with Periodontitis

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06879951
Enrollment
60
Registered
2025-03-17
Start date
2023-08-08
Completion date
2024-08-10
Last updated
2025-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity, Periodontitis

Keywords

Periodontitis, Obesity, Asprosin, Chronic Inflammatory Diseases

Brief summary

Obesity and periodontitis are chronic inflammatory diseases that share common pathological mechanisms. Asprosin, a novel adipokine discovered in 2016, has not been extensively studied in relation to periodontal tissues. In our study, we investigate the levels of asprosin in both serum and gingival crevicular fluid of patients with obesity and those of normal weight who have periodontitis. Additionally, our research aims to clarify the pathophysiological mechanisms linking periodontitis and obesity by examining local and systemic levels of TNF-α, IL-6, and asprosin, alongside clinical periodontal parameters.

Interventions

Participants are not assigned an intervention as part of the study.

Sponsors

Gazi University Scientific Research Unit
CollaboratorUNKNOWN
Gazi University
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

1. Willingness to participate in the study. 2. Weight classification: * Obese individuals: Body mass index (BMI) of 30 kg/m² or higher. * Normal-weight individuals: BMI between 18.5 and 24.9 kg/m². 3. Periodontal health status: * Bleeding on probing: less than 10%. * Periodontal pocket depth: less than 3 mm. * No sites showing attachment loss or alveolar bone loss on radiographs. 4. For individuals with periodontitis: * At least two non-adjacent teeth must show signs of interdental attachment loss. * Periodontal pocket depth greater than 3 mm.

Exclusion criteria

1. Individuals who have received periodontal therapy, any oral decontamination treatment, or antibiotics or steroids in the six months prior to the start of the study. 2. Individuals who are pregnant or breastfeeding. 3. Individuals diagnosed with rheumatoid arthritis or lupus erythematosus. 4. Individuals with a medical history of radiation or cancer therapy. 5. Patients with diabetes, defined by: * Hemoglobin A1c (HbA1c) level greater than 6.5%. * Fasting blood glucose (FBG) greater than 126 mg/dL. * An abnormal oral glucose tolerance test (OGTT). 6. Smokers.

Design outcomes

Primary

MeasureTime frameDescription
Biyomarker levels08.10.2023-08.10.2024All groups' GCF and serum levels of asprosin, TNF-α, and IL-6 levels

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 8, 2026