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Updated: Jan 29, 2026

Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Causal association between multiple sclerosis and trigeminal neuralgia: A Mendelian randomization study with
Esam Halboub1, Aisha A Al-Jamaei2,3, Abdulwahab Al-Amir1
1Department of Maxillofacial Surgery and Diagnostic Sciences, College of Dentistry, Jazan University, Jazan, Saudi Arabia.
Multiple sclerosis (MS) causally increases the risk of trigeminal neuralgia (TN). This genetic study found an 11% increased risk, confirming MS as a significant factor in TN development.
Area of Science:
- Neuroscience
- Genetics
- Epidemiology
Background:
- Multiple sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
- Trigeminal neuralgia (TN) is a neuropathic pain disorder characterized by severe facial pain.
- The etiological relationship between MS and TN requires further elucidation.
Purpose of the Study:
- To investigate the potential causal relationship between multiple sclerosis and trigeminal neuralgia.
- To leverage Mendelian randomization to assess genetic predisposition to MS as a risk factor for TN.
Main Methods:
- A two-sample Mendelian randomization (MR) meta-analysis was performed using genetic summary data.
- Eight MS genome-wide association studies (GWAS) served as exposures, and one TN GWAS as the outcome.
- Ten MR methods, including inverse-variance weighted (IVW) and MR-Egger regression, were utilized.
Main Results:
- Seven of eight MS exposure datasets demonstrated a positive causal association with TN.
- The meta-analysis indicated that MS significantly increases TN risk by 11% (IVW: 95% CI = 1.05-1.16; P < 0.001).
- Sensitivity analyses confirmed the robustness of findings, showing no significant pleiotropy or heterogeneity.
Conclusions:
- Genetic predisposition to multiple sclerosis is a causal factor for developing trigeminal neuralgia.
- These findings highlight a significant etiological link between MS and TN.
- Further research into biological pathways and diverse population validation is warranted.
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