Associations Between Temporomandibular Disorders and Brain Imaging-Derived Phenotypes
1Key Laboratory of Shaanxi Province for Craniofacial Precision Medicine Research, Testing Center of Stomatology, Xi'an Jiaotong University College of Stomatology, Xi'an, Shaanxi, China.
International Dental Journal
|February 16, 2024
Summary
This study used Mendelian randomization to find bidirectional causal links between temporomandibular disorders (TMD) and brain imaging phenotypes. Genetic evidence supports TMD influencing brain structure and vice versa.
Area of Science:
- Neuroscience
- Genetics
- Medical Science
Background:
- Temporomandibular disorders (TMD) are prevalent conditions impacting quality of life, with unclear underlying mechanisms.
- Observational studies suggest brain abnormalities in TMD patients, but lack causal inference.
- Magnetic resonance imaging (MRI) studies have indicated potential links between TMD and brain structure.
Purpose of the Study:
- To investigate the causal relationships between temporomandibular disorders (TMD) and brain imaging-derived phenotypes (IDPs).
- To employ Mendelian randomization (MR) to establish genetic evidence for bidirectional associations between TMD and brain changes.
- To explore potential neurobiological mechanisms contributing to TMD development.
Main Methods:
- Utilized genome-wide association study (GWAS) summary statistics for TMD and brain IDPs.
- Performed bidirectional 2-sample Mendelian randomization (MR) analyses using selected instrumental variables.
- Employed inverse-variance weighted analysis as the primary method and applied false discovery rate (FDR) correction for P-values.
Main Results:
- Identified eleven brain imaging-derived phenotypes (IDPs) with significant causal associations with TMD (P-FDR < .05).
- Forward MR revealed causal effects of left caudal middle frontal gyrus thickness and right superior frontal gyrus volume on TMD.
- Reverse MR indicated TMD causally affects 9 IDPs, including left medial orbitofrontal cortex thickness and left magnocellular nucleus volume.
Conclusions:
- This study provides robust genetic evidence for bidirectional causal associations between TMD and brain IDPs.
- Findings illuminate potential neurobiological pathways involved in TMD.
- The research contributes to understanding the complex relationship between TMD and brain structure.


