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Dietary Inflammatory Index and Periodontal Status in Obese Patients

The Relationship Between Dietary Inflammatory Index and Periodontal Status in Obese Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07287553
Enrollment
200
Registered
2025-12-17
Start date
2025-11-22
Completion date
2026-06-03
Last updated
2026-06-05

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

Conditions

Obesity

Keywords

obesity, periodontal status, dietary inflammatory index

Brief summary

In this study aimed to investigate the effect of nutrition on periodontal status in individuals diagnosed with obesity and without any other systemic disease, and to investigate the relationship between DII and periodontal disease risk. A total of 200 participants will be included in the study. Participants' overall daily Dietary Inflammatory Index (DII) scores will be calculated. The obtained scores will be divided into four groups, from low to high: Q1 (n=50), Q2 (n=50), Q3 (n=50), and Q4 (n=50). According to the DII, groups Q1 and Q2, which include lower scores, represent individuals on an anti-inflammatory diet, while groups Q3 and Q4, which include higher scores, represent individuals on a pro-inflammatory diet. Interleukin (IL)-1β, IL-10, total oxidant status (TOS), and total antioxidant status (TAS) were collected from gingival crevicular fluid (GCF) and serum samples. The levels of biomarkers such as malondialdehyde (MDA), glutathione (GSH), leptin, adiponectin, tumor necrosis factor (TNF)-α and C-reactive protein (CRP) from serum samples alone will be analyzed by ELISA method at the Recep Tayyip Erdoğan University Medical Biochemistry Laboratory.

Interventions

OTHERPeriodontal indices will be obtained

Periodontal indices will be obtained from all participants

OTHERserum and crevicular fluid samples will be collected

Serum and gingival crevicular fluid samples will be collected from all participants.

Sponsors

Recep Tayyip Erdogan University Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years

Inclusion criteria

* Being diagnosed with obesity, * Not having any systemic conditions other than obesity (systemic diseases that may affect periodontal health, such as cardiovascular disease, chronic kidney disease, Type 1 diabetes, Type 2 diabetes, and hypertension (\>130/85 mmHg)), * Being between the ages of 18 and 65, * Not smoking or consuming alcohol, * Not having used anti-inflammatory medications in the last 3 months, or antibiotics or systemic corticosteroids in the last 6 months, * Not being pregnant or lactating, * Not having received periodontal treatment in the last 6 months, * Not having received nutritional advice in the last 3 months, * Obesity diagnosis: BMI \> 30 kg/m2 or waist circumference: \> 100 cm for men and \> 90 cm for women.

Exclusion criteria

* Non-obese * Having any systemic disease other than obesity (such as cardiovascular disease, chronic kidney disease, Type 1 diabetes, Type 2 diabetes, and hypertension (\>130/85 mmHg) that may affect periodontal health) * Being over 65 years old and under 18 years old * Smoking and alcohol use * Having used anti-inflammatory drugs in the last 3 months, antibiotics, or systemic corticosteroids in the last 6 months * Being pregnant or lactating * Having received periodontal treatment in the last 6 months * Having received nutritional advice in the last 3 months

Design outcomes

Primary

MeasureTime frameDescription
Periodontal pocket depthbaselineThe distance between the pocket base and the gingival margin will be measured. It will be measured from the six surfaces of each tooth and the average will be taken higher scores indicate worse outcome.
Clinical attachment lossbaselineIt will be calculated by measuring the distance between the cementoenemal border and the pocket base. It will be measured from the six surfaces of each tooth and the average will be taken higher scores indicate worse outcome.

Secondary

MeasureTime frameDescription
interleukin (IL)-1β levelbaselineIL-1β levels will be measured with biochemical kits.
interleukin (IL)-10 levelbaselineIL-10 levels will be measured with biochemical kits.
total oxidant status (TOS) levelbaselineTOS levels will be measured with biochemical kits.
total antioxidant status (TAS) levelbaselineTAS levels will be measured with biochemical kits.
serum leptin levelbaselineLeptin levels in serum will be measured with biochemical kits.
serum tumor necrosis factor (TNF)-α levelbaselineTNF-α levels in serum will be measured with biochemical kits.
serum adiponectin levelbaselineAdiponectin levels in serum will be measured with biochemical kits.
serum C-reactive protein (CRP) levelbaselineCRP levels in serum will be measured with biochemical kits.
serum malondialdehyde (MDA) levelbaselineMDA levels in serum will be measured with biochemical kits.
serum glutathione (GSH) levelbaselineGSH levels in serum will be measured with biochemical kits.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 6, 2026