About this trial
The goal of this observational study is to learn about the genetic factors influencing bruxism, a condition characterized by teeth grinding, in a group of participants. The main questions it aims to answer are:
* Is there a significant association between the rs6313 polymorphism of the HTR2A gene and bruxism? * Is there a significant association between the rs6280 polymorphism of the DRD3 gene and bruxism?
Participants will:
Provide DNA samples for genotyping of the DRD3 (rs6280) and HTR2A (rs6313) polymorphisms.
Provide RNA samples to assess changes in the expression of HTR2A and DRD3. Researchers will compare the genetic data and RNA expression levels between individuals with bruxism and those without (controls) to see if there are significant genetic differences and expression changes associated with bruxism.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
be above 18 years of age and have a confirmed diagnosis of bruxism
Disqualifiers
Systemic diseases,
orofacial dysfunction,
acute symptoms such as neurodegenerative diseases (specifically Parkinsons disease),
Taking medication such as anxiolytics
Trial population
A total of 170 participants will be included in this study.
Trial design
Case-control
Cross-sectional
Treatments tested in this trial
Genetic polymorphism
GeneticThe biological significance of HTR2A and DRD3 in bruxism remains unclear as molecular analyses, including genetic association studies, have not explored the mRNA expression of genes implicated in bruxism. This study aims to evaluate the influence of genetic polymorphisms affecting DRD3 (rs6280) and HTR2A (rs6313) on bruxism to identify potentially associated genotypes. Additionally, it aims to investigate the expression of HTR2A and DRD3 to elucidate their biological significance in bruxism.
Treatment groups
Trial outcomes
Primary outcomes
PCR-RFLP Analysis
Locations
Sponsors and contacts
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This trial is not recruiting at the moment. You can still explore other options: