Taurine in Periodontitis and Aging

October 9, 2024 updated by: Hadi Sayedyousef, Istanbul Medipol University Hospital

The Role of Taurine in Periodontitis and Aging: a Preliminary Study

Aging leads to a decline in physiological functions and increases the risk of chronic diseases. Periodontitis is a chronic inflammatory disease that causes progressive destruction of the tissues supporting the teeth. Taurine, an amino acid with anti-inflammatory and antioxidant effects, might impact both periodontitis and aging. This study investigated taurine, SIRT1, and TNF-α levels in saliva and blood of 66 healthy people in different age groups, with or without periodontal disease. The findings showed that young people with healthy periodontal status had higher levels of taurine and SIRT1 compared to others. TNF-α, a marker of inflammation, was linked to the severity of periodontitis and may help identifying it in younger individuals. Overall, higher TNF-α levels are associated with periodontal inflammation, while taurine levels decrease with age-related inflammation.

Study Overview

Status

Completed

Study Type

Interventional

Enrollment (Actual)

66

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Unkapani
      • Istanbul, Unkapani, Turkey
        • Istanbul Medipol University

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Exclusion Criteria:

  • ages 18-25 or 45-64
  • use of antibiotics, anti-inflammatory drugs, immunosuppressants, beta-blockers, calcium channel blockers, or anticoagulants within the last 6 months
  • presence of diabetes, rheumatoid arthritis, or other systemic conditions such as cardiovascular, renal, hepatic, and neurodegenerative disorders
  • pregnancy or lactation
  • alcoholism
  • smoking
  • nonsurgical periodontal treatment in the past 6 months or surgical treatment in the past 12 months
  • having less than 20 natural teeth, excluding third molars
  • use of orthodontic appliances

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Diagnostic
  • Allocation: Non-Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Young (25-44 years) with a healthy periodontium
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
  • Salivary Flow Rate
  • TNF-α Levels
  • SIRT1 Levels
  • Taurine Levels
Experimental: young (25-44 years) with Periodontitis
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
  • Salivary Flow Rate
  • TNF-α Levels
  • SIRT1 Levels
  • Taurine Levels
Experimental: Old (≥65 years) with a healthy periodontium
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
  • Salivary Flow Rate
  • TNF-α Levels
  • SIRT1 Levels
  • Taurine Levels
Experimental: Old (≥65 years) with Periodontitis
Saliva, serum and periodontal indexes were obtained from patients
Other Names:
  • Salivary Flow Rate
  • TNF-α Levels
  • SIRT1 Levels
  • Taurine Levels

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Taurine
Time Frame: 12 Weeks
Taurine levels in saliva and serum were measured
12 Weeks
SIRT1
Time Frame: 12 Weeks
SIRT1 levels in saliva and serum were measured
12 Weeks
TNF-α
Time Frame: 12 Weeks
TNF-α levels in saliva and serum were measured
12 Weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 21, 2023

Primary Completion (Actual)

May 1, 2024

Study Completion (Actual)

June 1, 2024

Study Registration Dates

First Submitted

October 4, 2024

First Submitted That Met QC Criteria

October 9, 2024

First Posted (Actual)

October 10, 2024

Study Record Updates

Last Update Posted (Actual)

October 10, 2024

Last Update Submitted That Met QC Criteria

October 9, 2024

Last Verified

October 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Due to patients data privacy

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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