- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06603207
Study of the Causal Link Between Rheumatoid Arthritis and Periodontitis Using Mendelian Randomization (RAPD-MR)
September 18, 2024 updated by: Zhibin Xu
Causal Association Between Rheumatoid Arthritis and Periodontitis: A Mendelian Randomization Study
This study aims to investigate the causal relationship between rheumatoid arthritis and periodontitis using Mendelian randomization.
Data will be sourced from genome-wide association studies (GWAS) to explore genetic associations and assess potential risk factors in an East Asian population.
Study Overview
Status
Not yet recruiting
Conditions
Detailed Description
The purpose of this study is to explore the causal association between rheumatoid arthritis (RA) and periodontitis using Mendelian randomization (MR).
RA and periodontitis share similar inflammatory pathways and immune responses, but their causal relationship remains unclear.
This study will utilize genome-wide association studies (GWAS) data from an East Asian population to identify single nucleotide polymorphisms (SNPs) associated with RA and assess their potential impact on the risk of developing periodontitis.
Statistical methods such as inverse-variance weighting, MR-Egger regression, and weighted median analysis will be employed to analyze the data.
The findings may provide insights into the shared genetic basis and causal relationships between these two conditions, offering potential targets for preventive strategies.
Study Type
Observational
Enrollment (Estimated)
220000
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
This study utilizes genetic data from an East Asian population, sourced from publicly available genome-wide association studies (GWAS) focused on rheumatoid arthritis and periodontitis.
Description
Inclusion Criteria:
- Participants included in the genome-wide association study (GWAS) database.
- Subjects with available genotypic data relevant to rheumatoid arthritis and periodontitis.
Exclusion Criteria:
- Individuals without complete genotypic data or those with missing critical phenotypic information.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Causal Association Between Rheumatoid Arthritis and Periodontitis
Time Frame: Data collected from 2023 to 2024.
|
This study uses Mendelian randomization to evaluate the causal relationship between rheumatoid arthritis (RA) and periodontitis in the East Asian population.
The analysis utilizes genome-wide association study (GWAS) data, employing inverse variance weighting (IVW), weighted median, and MR-Egger regression methods to assess the genetic relationship and the risk contribution of RA to the development of periodontitis.
|
Data collected from 2023 to 2024.
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Analysis of Genetic Pleiotropy and Confounders
Time Frame: 2023 to 2024
|
Evaluation of the presence of genetic pleiotropy and its potential effect on the association between rheumatoid arthritis and periodontitis.
|
2023 to 2024
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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 (Estimated)
October 1, 2024
Primary Completion (Estimated)
November 1, 2024
Study Completion (Estimated)
December 1, 2024
Study Registration Dates
First Submitted
September 17, 2024
First Submitted That Met QC Criteria
September 17, 2024
First Posted (Actual)
September 19, 2024
Study Record Updates
Last Update Posted (Actual)
September 20, 2024
Last Update Submitted That Met QC Criteria
September 18, 2024
Last Verified
September 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KY20240918-01
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
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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